250 results on '"Cougnard-Grégoire, A."'
Search Results
52. Predicting Progression to Advanced Age-Related Macular Degeneration from Clinical, Genetic, and Lifestyle Factors Using Machine Learning
- Author
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Soufiane Ajana, Audrey Cougnard-Grégoire, Johanna M. Colijn, Bénédicte M.J. Merle, Timo Verzijden, Paulus T.V.M. de Jong, Albert Hofman, Johannes R. Vingerling, Boris P. Hejblum, Jean-François Korobelnik, Magda A. Meester-Smoor, Marius Ueffing, Hélène Jacqmin-Gadda, Caroline C.W. Klaver, Cécile Delcourt, Erkin I. Acar, Blanca Arango-Gonzalez, Angela Armento, Franz Badura, Vaibhav Bhatia, Shomi S. Bhattacharya, Marc Biarnés, Anna Borrell, Sofia M. Calado, Sascha Dammeier, Anita de Breuk, Berta De la Cerda, Anneke I. den Hollander, Francisco J. Diaz-Corrales, Sigrid Diether, Eszter Emri, Tanja Endermann, Lucia L. Ferraro, Míriam Garcia, Thomas J. Heesterbeek, Sabina Honisch, Carel B. Hoyng, Ellen Kilger, Elod Kortvely, Claire Lastrucci, Hanno Langen, Imre Lengyel, Phil Luthert, Jordi Monés, Everson Nogoceke, Tunde Peto, Frances M. Pool, Eduardo Rodriguez-Bocanegra, Luis Serrano, Jose Sousa, Eric Thee, Karl U. Ulrich Bartz-Schmidt, Markus Zumbansen, Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Erasmus University Medical Center [Rotterdam] (Erasmus MC), University of Amsterdam [Amsterdam] (UvA), Statistics In System biology and Translational Medicine (SISTM), Inria Bordeaux - Sud-Ouest, Institut National de Recherche en Informatique et en Automatique (Inria)-Institut National de Recherche en Informatique et en Automatique (Inria)- Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Vaccine Research Institute (VRI), Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Institut de Santé Publique, d'Epidémiologie et de Développement (ISPED), Université Bordeaux Segalen - Bordeaux 2, The EYE-RISK project was supported by the European Union’s Horizon 2020 Research and Innovation Programme (grant n°: 634479). The Rotterdam Study is funded by Erasmus Medical Center and Erasmus University, Rotterdam, The Netherlands, the Organization for the Health Research and Development (ZonMw), the Research Institute for Diseases in the Elderly (RIDE), the Ministry of Education, Culture and Science, the Ministry for Health, Welfare and Sports, the European Commission (DG XII), and the Municipality of Rotterdam, Rotterdam, The Netherlands. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Additionally, the ophthalmic research within the Rotterdam Study was supported by the following foundations: Oogfonds, Bartiméus Sonneheerdt Vereniging, LandelijkeStichting voor Blinden en Slechtzienden, Algemene Nederlandse Vereniging Ter Voorkoming Van Blindheid, Novartis Foundation, and MaculaFonds, which contributed through UitZicht (grant nos.: 2015-36 and 2016-19). The Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires (ALIENOR) Study was funded by Laboratoires Théa, Fondation Voir et Entendre, Retina France, Agence Nationale de la Recherche (ANR-2010-PRSP-011 VISA), Programme Hospitalier de Recherche Clinique (PHRC) (ECLAIR project-2012), CFSR Recherche, the French Speaking Retina Specialists’ Club and Caisse Nationale pour la Solidarité et l’Autonomie. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Laboratoires Théa participated in the design of the Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires (ALIENOR) Study, but none of the sponsors of this study participated in the collection, management, statistical analysis, or interpretation of the data, or in the preparation, review, or approval of the present manuscript., European Project: 634479,H2020,H2020-PHC-2014-two-stage,EYE-RISK(2015), Hejblum, Boris, Exploring the combined role of genetic and non-genetic factors for developing Age-Related Macular Degeneration: A systems level analysis of disease subgroups, risk factors, and pathways - EYE-RISK - - H20202015-05-01 - 2019-04-30 - 634479 - VALID, Ophthalmology, Epidemiology, Netherlands Institute for Neuroscience (NIN), and Vaccine Research Institute [Créteil, France] (VRI)
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Male ,computer.software_genre ,Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12] ,Machine Learning ,Rotterdam Study ,Macular Degeneration ,0302 clinical medicine ,[STAT.AP] Statistics [stat]/Applications [stat.AP] ,Risk Factors ,Cumulative incidence ,ComputingMilieux_MISCELLANEOUS ,0303 health sciences ,education.field_of_study ,[STAT.AP]Statistics [stat]/Applications [stat.AP] ,Smoking ,Middle Aged ,3. Good health ,Phenotype ,Area Under Curve ,Disease Progression ,Female ,Cohort study ,Genotype ,Population ,Clinical Decision-Making ,Retinal Drusen ,Machine learning ,03 medical and health sciences ,medicine ,Genetics ,Humans ,education ,Life Style ,Survival analysis ,030304 developmental biology ,Aged ,Nutrition ,Receiver operating characteristic ,business.industry ,Age-related macular degeneration ,Macular degeneration ,Models, Theoretical ,medicine.disease ,Lifestyle ,Personalized medicine ,Confidence interval ,eye diseases ,Ophthalmology ,[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie ,030221 ophthalmology & optometry ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,Artificial intelligence ,business ,Prediction ,computer - Abstract
Contains fulltext : 245098.pdf (Publisher’s version ) (Closed access) PURPOSE: Current prediction models for advanced age-related macular degeneration (AMD) are based on a restrictive set of risk factors. The objective of this study was to develop a comprehensive prediction model applying a machine learning algorithm allowing selection of the most predictive risk factors automatically. DESIGN: Two population-based cohort studies. PARTICIPANTS: The Rotterdam Study I (RS-I; training set) included 3838 participants 55 years of age or older, with a median follow-up period of 10.8 years, and 108 incident cases of advanced AMD. The Antioxydants, Lipids Essentiels, Nutrition et Maladies Oculaires (ALIENOR) study (test set) included 362 participants 73 years of age or older, with a median follow-up period of 6.5 years, and 33 incident cases of advanced AMD. METHODS: The prediction model used the bootstrap least absolute shrinkage and selection operator (LASSO) method for survival analysis to select the best predictors of incident advanced AMD in the training set. Predictive performance of the model was assessed using the area under the receiver operating characteristic curve (AUC). MAIN OUTCOME MEASURES: Incident advanced AMD (atrophic, neovascular, or both), based on standardized interpretation of retinal photographs. RESULTS: The prediction model retained (1) age, (2) a combination of phenotypic predictors (based on the presence of intermediate drusen, hyperpigmentation in one or both eyes, and Age-Related Eye Disease Study simplified score), (3) a summary genetic risk score based on 49 single nucleotide polymorphisms, (4) smoking, (5) diet quality, (6) education, and (7) pulse pressure. The cross-validated AUC estimation in RS-I was 0.92 (95% confidence interval [CI], 0.88-0.97) at 5 years, 0.92 (95% CI, 0.90-0.95) at 10 years, and 0.91 (95% CI, 0.88-0.94) at 15 years. In ALIENOR, the AUC reached 0.92 at 5 years (95% CI, 0.87-0.98). In terms of calibration, the model tended to underestimate the cumulative incidence of advanced AMD for the high-risk groups, especially in ALIENOR. CONCLUSIONS: This prediction model reached high discrimination abilities, paving the way toward making precision medicine for AMD patients a reality in the near future.
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- 2020
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- View/download PDF
53. Genetic Risk, Lifestyle, and Age-Related Macular Degeneration in Europe: The EYE-RISK Consortium
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Johanna M, Colijn, Magda, Meester-Smoor, Timo, Verzijden, Anita, de Breuk, Rufino, Silva, Benedicte M J, Merle, Audrey, Cougnard-Grégoire, Carel B, Hoyng, Sascha, Fauser, Anthonius, Coolen, Catherine, Creuzot-Garcher, Hans-Werner, Hense, Marius, Ueffing, Cecile, Delcourt, Anneke I, den Hollander, and Caroline C W, Klaver
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Male ,Incidence ,Middle Aged ,Polymorphism, Single Nucleotide ,Risk Assessment ,Europe ,Macular Degeneration ,Cross-Sectional Studies ,Gene Frequency ,Risk Factors ,Case-Control Studies ,Population Surveillance ,Humans ,Female ,Genetic Predisposition to Disease ,Life Style ,Aged - Abstract
Age-related macular degeneration (AMD) is a common multifactorial disease in the elderly with a prominent genetic basis. Many risk variants have been identified, but the interpretation remains challenging. We investigated the genetic distribution of AMD-associated risk variants in a large European consortium, calculated attributable and pathway-specific genetic risks, and assessed the influence of lifestyle on genetic outcomes.Pooled analysis of cross-sectional data from the European Eye Epidemiology Consortium.Seventeen thousand one hundred seventy-four individuals 45 years of age or older participating in 6 population-based cohort studies, 2 clinic-based studies, and 1 case-control study.Age-related macular degeneration was diagnosed and graded based on fundus photographs. Data on genetics, lifestyle, and diet were harmonized. Minor allele frequencies and population-attributable fraction (PAF) were calculated. A total genetic risk score (GRS) and pathway-specific risk scores (complement, lipid, extra-cellular matrix, other) were constructed based on the dosage of SNPs and conditional β values; a lifestyle score was constructed based on smoking and diet.Intermediate and late AMD.The risk variants with the largest difference between late AMD patients and control participants and the highest PAFs were located in ARMS2 (rs3750846) and CHF (rs570618 and rs10922109). Combining all genetic variants, the total genetic risk score ranged from -3.50 to 4.63 and increased with AMD severity. Of the late AMD patients, 1581 of 1777 (89%) showed a positive total GRS. The complement pathway and ARMS2 were by far the most prominent genetic pathways contributing to late AMD (positive GRS, 90% of patients with late disease), but risk in 3 pathways was most frequent (35% of patients with late disease). Lifestyle was a strong determinant of the outcome in each genetic risk category; unfavorable lifestyle increased the risk of late AMD at least 2-fold.Genetic risk variants contribute to late AMD in most patients. However, lifestyle factors have a strong influence on the outcome of genetic risk and should be a strong focus in patient management. Genetic risks in ARMS2 and the complement pathway are present in most late AMD patients but are mostly combined with risks in other pathways.
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- 2020
54. Predicting Progression to Advanced Age-Related Macular Degeneration from Clinical, Genetic, and Lifestyle Factors Using Machine Learning
- Author
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Ajana, Soufiane, Cougnard-Grégoire, Audrey, Colijn, Johanna M, Merle, Bénédicte M J, Verzijden, Timo, de Jong, Paulus T V M, Hofman, Albert, Vingerling, Johannes R, Hejblum, Boris P, Korobelnik, Jean-François, Meester-Smoor, Magda A, Ueffing, Marius, Jacqmin-Gadda, Hélène, Klaver, Caroline C W, Delcourt, Cécile, EYE-RISK consortium, Ajana, Soufiane, Cougnard-Grégoire, Audrey, Colijn, Johanna M, Merle, Bénédicte M J, Verzijden, Timo, de Jong, Paulus T V M, Hofman, Albert, Vingerling, Johannes R, Hejblum, Boris P, Korobelnik, Jean-François, Meester-Smoor, Magda A, Ueffing, Marius, Jacqmin-Gadda, Hélène, Klaver, Caroline C W, Delcourt, Cécile, and EYE-RISK consortium
- Abstract
PURPOSE: Current prediction models for advanced age-related macular degeneration (AMD) are based on a restrictive set of risk factors. The objective of this study was to develop a comprehensive prediction model applying a machine learning algorithm allowing selection of the most predictive risk factors automatically.DESIGN: Two population-based cohort studies.PARTICIPANTS: The Rotterdam Study I (RS-I; training set) included 3838 participants 55 years of age or older, with a median follow-up period of 10.8 years, and 108 incident cases of advanced AMD. The Antioxydants, Lipids Essentiels, Nutrition et Maladies Oculaires (ALIENOR) study (test set) included 362 participants 73 years of age or older, with a median follow-up period of 6.5 years, and 33 incident cases of advanced AMD.METHODS: The prediction model used the bootstrap least absolute shrinkage and selection operator (LASSO) method for survival analysis to select the best predictors of incident advanced AMD in the training set. Predictive performance of the model was assessed using the area under the receiver operating characteristic curve (AUC).MAIN OUTCOME MEASURES: Incident advanced AMD (atrophic, neovascular, or both), based on standardized interpretation of retinal photographs.RESULTS: The prediction model retained (1) age, (2) a combination of phenotypic predictors (based on the presence of intermediate drusen, hyperpigmentation in one or both eyes, and Age-Related Eye Disease Study simplified score), (3) a summary genetic risk score based on 49 single nucleotide polymorphisms, (4) smoking, (5) diet quality, (6) education, and (7) pulse pressure. The cross-validated AUC estimation in RS-I was 0.92 (95% confidence interval [CI], 0.88-0.97) at 5 years, 0.92 (95% CI, 0.90-0.95) at 10 years, and 0.91 (95% CI, 0.88-0.94) at 15 years. In ALIENOR, the AUC reached 0.92 at 5 years (95% CI, 0.87-0.98). In terms of calibration, the model tended to underestimate the cumulative i
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- 2021
55. Genetic Risk, Lifestyle, and Age-Related Macular Degeneration in Europe: The EYE-RISK Consortium
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Colijn, J.M., Meester-Smoor, M., Verzijden, T., Breuk, A. de, Silva, R. de, Merle, B.M.J., Cougnard-Grégoire, A., Hoyng, C.B., Fauser, S., Coolen, A., Creuzot-Garcher, C., Hense, H.W., Ueffing, M., Delcourt, C, Hollander, A.I. den, Klaver, C.C.W., Colijn, J.M., Meester-Smoor, M., Verzijden, T., Breuk, A. de, Silva, R. de, Merle, B.M.J., Cougnard-Grégoire, A., Hoyng, C.B., Fauser, S., Coolen, A., Creuzot-Garcher, C., Hense, H.W., Ueffing, M., Delcourt, C, Hollander, A.I. den, and Klaver, C.C.W.
- Abstract
Item does not contain fulltext, PURPOSE: Age-related macular degeneration (AMD) is a common multifactorial disease in the elderly with a prominent genetic basis. Many risk variants have been identified, but the interpretation remains challenging. We investigated the genetic distribution of AMD-associated risk variants in a large European consortium, calculated attributable and pathway-specific genetic risks, and assessed the influence of lifestyle on genetic outcomes. DESIGN: Pooled analysis of cross-sectional data from the European Eye Epidemiology Consortium. PARTICIPANTS: Seventeen thousand one hundred seventy-four individuals 45 years of age or older participating in 6 population-based cohort studies, 2 clinic-based studies, and 1 case-control study. METHODS: Age-related macular degeneration was diagnosed and graded based on fundus photographs. Data on genetics, lifestyle, and diet were harmonized. Minor allele frequencies and population-attributable fraction (PAF) were calculated. A total genetic risk score (GRS) and pathway-specific risk scores (complement, lipid, extra-cellular matrix, other) were constructed based on the dosage of SNPs and conditional β values; a lifestyle score was constructed based on smoking and diet. MAIN OUTCOME MEASURES: Intermediate and late AMD. RESULTS: The risk variants with the largest difference between late AMD patients and control participants and the highest PAFs were located in ARMS2 (rs3750846) and CHF (rs570618 and rs10922109). Combining all genetic variants, the total genetic risk score ranged from -3.50 to 4.63 and increased with AMD severity. Of the late AMD patients, 1581 of 1777 (89%) showed a positive total GRS. The complement pathway and ARMS2 were by far the most prominent genetic pathways contributing to late AMD (positive GRS, 90% of patients with late disease), but risk in 3 pathways was most frequent (35% of patients with late disease). Lifestyle was a strong determinant of the outcome in each genetic risk category; unfavorable lifestyle incre
- Published
- 2021
56. Predicting Progression to Advanced Age-Related Macular Degeneration from Clinical, Genetic, and Lifestyle Factors Using Machine Learning
- Author
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Ajana, S., Cougnard-Grégoire, A., Colijn, J.M., Merle, B.M.J., Verzijden, T., Jong, p de, Hofman, A., Vingerling, J.R., Hejblum, B.P., Korobelnik, J.F., Meester-Smoor, M.A., Ueffing, M., Jacqmin-Gadda, H., Hollander, A.I. den, Klaver, C.C.W., Delcourt, C, Ajana, S., Cougnard-Grégoire, A., Colijn, J.M., Merle, B.M.J., Verzijden, T., Jong, p de, Hofman, A., Vingerling, J.R., Hejblum, B.P., Korobelnik, J.F., Meester-Smoor, M.A., Ueffing, M., Jacqmin-Gadda, H., Hollander, A.I. den, Klaver, C.C.W., and Delcourt, C
- Abstract
Item does not contain fulltext, PURPOSE: Current prediction models for advanced age-related macular degeneration (AMD) are based on a restrictive set of risk factors. The objective of this study was to develop a comprehensive prediction model applying a machine learning algorithm allowing selection of the most predictive risk factors automatically. DESIGN: Two population-based cohort studies. PARTICIPANTS: The Rotterdam Study I (RS-I; training set) included 3838 participants 55 years of age or older, with a median follow-up period of 10.8 years, and 108 incident cases of advanced AMD. The Antioxydants, Lipids Essentiels, Nutrition et Maladies Oculaires (ALIENOR) study (test set) included 362 participants 73 years of age or older, with a median follow-up period of 6.5 years, and 33 incident cases of advanced AMD. METHODS: The prediction model used the bootstrap least absolute shrinkage and selection operator (LASSO) method for survival analysis to select the best predictors of incident advanced AMD in the training set. Predictive performance of the model was assessed using the area under the receiver operating characteristic curve (AUC). MAIN OUTCOME MEASURES: Incident advanced AMD (atrophic, neovascular, or both), based on standardized interpretation of retinal photographs. RESULTS: The prediction model retained (1) age, (2) a combination of phenotypic predictors (based on the presence of intermediate drusen, hyperpigmentation in one or both eyes, and Age-Related Eye Disease Study simplified score), (3) a summary genetic risk score based on 49 single nucleotide polymorphisms, (4) smoking, (5) diet quality, (6) education, and (7) pulse pressure. The cross-validated AUC estimation in RS-I was 0.92 (95% confidence interval [CI], 0.88-0.97) at 5 years, 0.92 (95% CI, 0.90-0.95) at 10 years, and 0.91 (95% CI, 0.88-0.94) at 15 years. In ALIENOR, the AUC reached 0.92 at 5 years (95% CI, 0.87-0.98). In terms of calibration, the model tended to underestimate the cumulative incidence of advanced AMD for the
- Published
- 2021
57. Predicting Progression to Advanced Age-Related Macular Degeneration from Clinical, Genetic, and Lifestyle Factors Using Machine Learning
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Ajana, Soufiane, primary, Cougnard-Grégoire, Audrey, additional, Colijn, Johanna M., additional, Merle, Bénédicte M.J., additional, Verzijden, Timo, additional, de Jong, Paulus T.V.M., additional, Hofman, Albert, additional, Vingerling, Johannes R., additional, Hejblum, Boris P., additional, Korobelnik, Jean-François, additional, Meester-Smoor, Magda A., additional, Ueffing, Marius, additional, Jacqmin-Gadda, Hélène, additional, Klaver, Caroline C.W., additional, Delcourt, Cécile, additional, Acar, Erkin I., additional, Arango-Gonzalez, Blanca, additional, Armento, Angela, additional, Badura, Franz, additional, Bhatia, Vaibhav, additional, Bhattacharya, Shomi S., additional, Biarnés, Marc, additional, Borrell, Anna, additional, Calado, Sofia M., additional, Dammeier, Sascha, additional, de Breuk, Anita, additional, De la Cerda, Berta, additional, den Hollander, Anneke I., additional, Diaz-Corrales, Francisco J., additional, Diether, Sigrid, additional, Emri, Eszter, additional, Endermann, Tanja, additional, Ferraro, Lucia L., additional, Garcia, Míriam, additional, Heesterbeek, Thomas J., additional, Honisch, Sabina, additional, Hoyng, Carel B., additional, Kilger, Ellen, additional, Kortvely, Elod, additional, Lastrucci, Claire, additional, Langen, Hanno, additional, Lengyel, Imre, additional, Luthert, Phil, additional, Monés, Jordi, additional, Nogoceke, Everson, additional, Peto, Tunde, additional, Pool, Frances M., additional, Rodriguez-Bocanegra, Eduardo, additional, Serrano, Luis, additional, Sousa, Jose, additional, Thee, Eric, additional, Ulrich Bartz-Schmidt, Karl U., additional, and Zumbansen, Markus, additional
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- 2021
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58. Incidence and Risk Factors of Reticular Pseudodrusen Using Multimodal Imaging
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Dutheil, Cyril, primary, Le Goff, Mélanie, additional, Cougnard-Grégoire, Audrey, additional, Gattoussi, Sarra, additional, Korobelnik, Jean-François, additional, Rougier, Marie-Bénédicte, additional, Schweitzer, Cédric, additional, Delcourt, Cécile, additional, and Delyfer, Marie-Noëlle, additional
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- 2020
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59. Trajectories of recall memory as predictive of hearing impairment: A longitudinal cohort study
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Maharani, Asri, Dawes, Piers, Nazroo, James, Tampubolon, Gindo, Pendleton, Neil, Bertelsen, Geir, Cosh, Suzanne, Cougnard-Grégoire, Audrey, Delcourt, Cécile, Constantinidou, Fofi, Goedegebure, Andre, Helmer, Catherine, Arfan Ikram, M., Klaver, Caroline C.W., Meester-Smoor, Magda, Nael, Virginie, Oosterloo, Neelke, Schirmer, Henrik, Tiemeier, Henning, Otorhinolaryngology and Head and Neck Surgery, Ophthalmology, Epidemiology, and Child and Adolescent Psychiatry / Psychology
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Male ,ResearchInstitutes_Networks_Beacons/global_development_institute ,Longitudinal study ,Aging ,Physiology ,Social Sciences ,Otology ,Audiology ,Deafness ,Cohort Studies ,0302 clinical medicine ,Cognition ,Learning and Memory ,Hearing ,Medicine and Health Sciences ,Psychology ,Public and Occupational Health ,Longitudinal Studies ,030223 otorhinolaryngology ,Hearing Disorders ,Aged, 80 and over ,Cognitive Impairment ,Multidisciplinary ,VDP::Medisinske Fag: 700::Helsefag: 800::Samfunnsmedisin, sosialmedisin: 801 ,medicine.diagnostic_test ,Cognitive Neurology ,Hearing Tests ,Middle Aged ,England ,Neurology ,Memory Recall ,Medicine ,Female ,Sensory Perception ,Anatomy ,Cohort study ,Research Article ,medicine.medical_specialty ,Science ,Cognitive Neuroscience ,03 medical and health sciences ,Memory ,medicine ,otorhinolaryngologic diseases ,Humans ,Cognitive Dysfunction ,Association (psychology) ,Hearing Loss ,Aged ,Memory Disorders ,Recall ,Biology and Life Sciences ,Physical Activity ,Global Development Institute ,Otorhinolaryngology ,Ageing ,Ears ,Mental Recall ,Hearing test ,Cognitive Science ,VDP::Medical disciplines: 700::Health sciences: 800::Community medicine, Social medicine: 801 ,Physiological Processes ,Organism Development ,Head ,030217 neurology & neurosurgery ,Neuroscience ,Developmental Biology - Abstract
Objectives - Accumulating evidence points to a relationship between hearing function and cognitive ability in later life. However, the exact mechanisms of this relationship are still unclear. This study aimed to characterise latent cognitive trajectories in recall memory and identify their association with subsequent risk of hearing impairment. Methods - We analysed data from the English Longitudinal Study of Ageing Wave 1 (2002/03) until Wave 7 (2014/15). The study population consisted of 3,615 adults aged 50+ who participated in the first wave of the English Longitudinal Study of Ageing, who had no self-reported hearing impairment in Wave 1, and who underwent a hearing test in Wave 7. Respondents were classified as having hearing impairment if they failed to hear tones quieter than 35 dB HL in the better ear. Results - The trajectories of recall memory scores were grouped using latent class growth mixture modelling and were related to the presence of hearing impairment in Wave 7. Models estimating 1-class through 5-class recall memory trajectories were compared and the best-fitting models were 4-class trajectories. The different recall memory trajectories represent different starting points and mean of the memory scores. Compared to respondents with the highest recall memory trajectory, other trajectories were increasingly likely to develop later hearing impairment. Conclusions - Long-term changes in cognitive ability predict hearing impairment. Further research is required to identify the mechanisms explaining the association between cognitive trajectories and hearing impairment, as well as to determine whether intervention for maintenance of cognitive function also give benefit on hearing function among older adults.
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- 2019
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60. Trends in eye care use in adults treated for diabetes between 2008 and 2017 in France: a nationwide study
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Audrey Cougnard-Grégoire, Korobelnik, Jean-Francois, Delyfer, Marie-Noelle, Rigalleau, Vincent, Daien, Vincent, Creuzot-Garcher, Catherine, Delcourt, Cecile, Université de Bordeaux (UB), CHU de Bordeaux Pellegrin [Bordeaux], CHU Bordeaux [Bordeaux], Centre Hospitalier Universitaire de Montpellier (CHU Montpellier ), Centre des Sciences du Goût et de l'Alimentation [Dijon] (CSGA), Institut National de la Recherche Agronomique (INRA)-Université de Bourgogne (UB)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Centre National de la Recherche Scientifique (CNRS), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Université Bourgogne Franche-Comté [COMUE] (UBFC), and ProdInra, Migration
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[SDV.MHEP.EM] Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism ,[SDV.MHEP.OS] Life Sciences [q-bio]/Human health and pathology/Sensory Organs ,[SDV.MHEP.EM]Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism ,[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs - Published
- 2019
61. Increased High-Density Lipoprotein Levels Associated with Age-Related Macular Degeneration: Evidence from the EYE-RISK and European Eye Epidemiology Consortia
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Colijn, Johanna M, den Hollander, Anneke I, Demirkan, Ayse, Cougnard-Grégoire, Audrey, Verzijden, Timo, Kersten, Eveline, Meester-Smoor, Magda A, Merle, Benedicte M J, Papageorgiou, Grigorios, Ahmad, Shahzad, Mulder, Monique T, Costa, Miguel Angelo, Benlian, Pascale, Bertelsen, Geir, Bron, Alain M, Claes, Birte, Creuzot-Garcher, Catherine, Erke, Maja Gran, Fauser, Sascha, Foster, Paul J, Hammond, Christopher J, Hense, Hans-Werner, Hoyng, Carel B, Khawaja, Anthony P, Korobelnik, Jean-Francois, Piermarocchi, Stefano, Segato, Tatiana, Silva, Rufino, Souied, Eric H, Williams, Katie M, van Duijn, Cornelia M, Bergen, Arthur, ANS - Complex Trait Genetics, ARD - Amsterdam Reproduction and Development, ANS - Amsterdam Neuroscience, and Human Genetics
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Aged, 80 and over ,Male ,Cholesterol, HDL/blood ,Magnetic Resonance Spectroscopy ,genetic structures ,Middle Aged ,Lipid Metabolism ,Polymorphism, Single Nucleotide ,eye diseases ,Triglycerides/blood ,Cross-Sectional Studies ,Cholesterol, LDL/blood ,European Continental Ancestry Group/statistics & numerical data ,Risk Factors ,Cholesterol Ester Transfer Proteins/blood ,Odds Ratio ,Humans ,Metabolomics ,lipids (amino acids, peptides, and proteins) ,Female ,sense organs ,European Union ,Macular Degeneration/blood ,Aged - Abstract
PURPOSE: Genetic and epidemiologic studies have shown that lipid genes and high-density lipoproteins (HDLs) are implicated in age-related macular degeneration (AMD). We studied circulating lipid levels in relationship to AMD in a large European dataset. DESIGN: Pooled analysis of cross-sectional data. PARTICIPANTS: Individuals (N = 30 953) aged 50 years or older participating in the European Eye Epidemiology (E3) consortium and 1530 individuals from the Rotterdam Study with lipid subfraction data. METHODS: AMD features were graded on fundus photographs using the Rotterdam classification. Routine blood lipid measurements, genetics, medication, and potential confounders were extracted from the E3 database. In a subgroup of the Rotterdam Study, lipid subfractions were identified by the Nightingale biomarker platform. Random-intercepts mixed-effects models incorporating confounders and study site as a random effect were used to estimate associations. MAIN OUTCOME MEASURES: AMD features and stage; lipid measurements. RESULTS: HDL was associated with an increased risk of AMD (odds ratio [OR], 1.21 per 1-mmol/l increase; 95% confidence interval [CI], 1.14-1.29), whereas triglycerides were associated with a decreased risk (OR, 0.94 per 1-mmol/l increase; 95% CI, 0.91-0.97). Both were associated with drusen size. Higher HDL raised the odds of larger drusen, whereas higher triglycerides decreases the odds. LDL cholesterol reached statistical significance only in the association with early AMD (P = 0.045). Regarding lipid subfractions, the concentration of extra-large HDL particles showed the most prominent association with AMD (OR, 1.24; 95% CI, 1.10-1.40). The cholesteryl ester transfer protein risk variant (rs17231506) for AMD was in line with increased HDL levels (P = 7.7 × 10-7), but lipase C risk variants (rs2043085, rs2070895) were associated in an opposite way (P = 1.0 × 10-6 and P = 1.6 × 10-4). CONCLUSIONS: Our study suggested that HDL cholesterol is associated with increased risk of AMD and that triglycerides are negatively associated. Both show the strongest association with early AMD and drusen. Extra-large HDL subfractions seem to be drivers in the relationship with AMD, and variants in lipid genes play a more ambiguous role in this association. Whether systemic lipids directly influence AMD or represent lipid metabolism in the retina remains to be answered.
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- 2019
62. Mediterranean Diet and Incidence of Advanced Age-Related Macular Degeneration: The EYE-RISK Consortium
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Merle, B. nédicte M. J., Colijn, Johanna M., Cougnard-Grégoire, Audrey, de Koning-Backus, Alexandra P. M., Delyfer, Marie-Noëlle, Kiefte-de Jong, Jessica C., Meester-Smoor, Magda, Féart, Catherine, Verzijden, Timo, Samieri, C. cilia, Franco, Oscar H., Korobelnik, Jean-François, Klaver, Caroline C. W., Delcourt, C. cile, Ajana, Soufiane, Arango-Gonzalez, Blanca, Armento, Angela, Arndt, Verena, Bhatia, Vaibhav, Bhattacharya, Shomi S., Biarnés, Marc, Borrell, Anna, Bühren, Sebastian, Calado, Sofia M., Dammeier, Sascha, de Jong, Eiko K., de la Cerda, Berta, den Hollander, Anneke I., Diaz-Corrales, Francisco J., Diether, Sigrid, Emri, Eszter, Endermann, Tanja, Ferraro, Lucia L., Garcia, M. riam, Heesterbeek, Thomas J., Honisch, Sabina, Hoyng, Carel B., Kersten, Eveline, Kilger, Ellen, Langen, Hanno, Lengyel, Imre, Luthert, Phil, Maugeais, Cyrille, van Leeuwen, Elisabeth M., Zumbansen, Markus, Vasiliev, Vassil, Experimental Immunology, and AII - Inflammatory diseases
- Abstract
Purpose: To investigate associations of adherence to the Mediterranean diet (MeDi) with incidence of advanced age-related macular degeneration (AMD; the symptomatic form of AMD) in 2 European population-based prospective cohorts. Design: Prospective cohort study of the Rotterdam Study I (RS-I) and the Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires (Alienor) Study populations. Participants: Four thousand four hundred forty-six participants 55 years of age or older from the RS-I (The Netherlands) and 550 French adults 73 years of age or older from the Alienor Study with complete ophthalmologic and dietary data were included in the present study. Methods: Examinations were performed approximately every 5 years over a 21-year period (1990–2011) in RS-I and every 2 years over a 4-year period (2006–2012) in the Alienor Study. Adherence to the MeDi was evaluated using a 9-component score based on intake of vegetables, fruits, legumes, cereals, fish, meat, dairy products, alcohol, and the monounsaturated-to-saturated fatty acids ratio. Associations of incidence of AMD with MeDi were estimated using multivariate Cox proportional hazard models. Main Outcomes Measures: Incidence of advanced AMD based on retinal fundus photographs. Results: Among the 4996 included participants, 155 demonstrated advanced incident AMD (117 from the RS-I and 38 from the Alienor Study). The mean follow-up time was 9.9 years (range, 0.6–21.7 years) in the RS-I and 4.1 years (range, 2.5–5.0 years) in the Alienor Study. Pooling data for both the RS-I and Alienor Study, participants with a high (range, 6–9) MeDi score showed a significantly reduced risk for incident advanced AMD compared with participants with a low (range, 0–3) MeDi score in the fully adjusted Cox model (hazard ratio, 0.59; 95% confidence interval, 0.37–0.95; P = 0.04 for trend). Conclusions: Pooling data from the RS-I and Alienor Study, higher adherence to the MeDi was associated with a 41% reduced risk of incident advanced AMD. These findings support the role of a diet rich in healthful nutrient-rich foods such as fruits, vegetables, legumes, and fish in the prevention of AMD.
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- 2019
63. Associations between self-reported sensory impairment and risk of cognitive decline and impairment in the health and retirement study cohort
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Maharani, Asri, Dawes, Piers, Nazroo, James, Tampubolon, Gindo, Pendleton, Neil, Bertelsen, Geir, Cosh, Suzanne, Cougnard-Grégoire, Audrey, Delcourt, Cécile, Constantinidou, Fofi, Goedegebure, Andre, Helmer, Catherine, Arfan Ikram, M., Klaver, Caroline C.W., Meester-Smor, Magda, Nael, Virginie, Oosterloo, Neelke, Schirmer, Henrik, Tiemeier, Henning, Maharani, Asri, Dawes, Piers, Nazroo, James, Tampubolon, Gindo, Pendleton, Neil, Bertelsen, Geir, Cosh, Suzanne, Cougnard-Grégoire, Audrey, Delcourt, Cécile, Constantinidou, Fofi, Goedegebure, Andre, Helmer, Catherine, Arfan Ikram, M., Klaver, Caroline C.W., Meester-Smor, Magda, Nael, Virginie, Oosterloo, Neelke, Schirmer, Henrik, and Tiemeier, Henning
- Abstract
Objectives: We aimed to determine whether self-assessed single (hearing or visual) and dual sensory (hearing and visual) impairments are associated with cognitive decline and incident possible cognitive impairment, no dementia (CIND) and probable dementia. Method: Data were drawn from the 1996-2014 surveys of the Health and Retirement Study (HRS), involving 19,618 respondents who had no probable dementia and who were aged 50 years or older at the baseline. We used linear mixed models to test the association between self-assessed sensory impairment and cognitive decline followed by a Cox proportional hazard model to estimate the relative risk of incident possible CIND and probable dementia associated with the presence of sensory impairment. Results: Respondents with self-assessed single and dual sensory impairment performed worse in cognitive tests than those without sensory impairment. The fully adjusted incidence of developing possible CIND was 17% higher for respondents with hearing impairment than those without hearing impairment. Respondents with visual impairment had 35% and 25% higher risk for developing possible CIND and probable dementia, respectively, than those without visual impairment. Respondents with dual sensory impairment at baseline were 38% and 26% more likely to develop possible CIND and probable dementia, respectively, than those with no sensory impairment. Discussion: Self-assessed sensory impairment is independently associated with cognitive decline and incident possible CIND and probable dementia. Further studies are needed to identify the mechanism underlying this association and to determine whether treatment of sensory impairment could ameliorate cognitive decline and delay the onset of dementia among older adults.
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- 2020
64. Trajectories of recall memory as predictive of hearing impairment:A longitudinal cohort study
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Maharani, Asri, Dawes, Piers, Nazroo, James, Tampubolon, Gindo, Pendleton, Neil, Bertelsen, Geir, Cosh, Suzanne, Cougnard-Grégoire, Audrey, Delcourt, Cécile, Constantinidou, Fofi, Goedegebure, Andre, Helmer, Catherine, Arfan Ikram, M., Klaver, Caroline C.W., Meester-Smoor, Magda, Nael, Virginie, Oosterloo, Neelke, Schirmer, Henrik, Tiemeier, Henning, Maharani, Asri, Dawes, Piers, Nazroo, James, Tampubolon, Gindo, Pendleton, Neil, Bertelsen, Geir, Cosh, Suzanne, Cougnard-Grégoire, Audrey, Delcourt, Cécile, Constantinidou, Fofi, Goedegebure, Andre, Helmer, Catherine, Arfan Ikram, M., Klaver, Caroline C.W., Meester-Smoor, Magda, Nael, Virginie, Oosterloo, Neelke, Schirmer, Henrik, and Tiemeier, Henning
- Abstract
Objectives Accumulating evidence points to a relationship between hearing function and cognitive ability in later life. However, the exact mechanisms of this relationship are still unclear. This study aimed to characterise latent cognitive trajectories in recall memory and identify their association with subsequent risk of hearing impairment. Methods We analysed data from the English Longitudinal Study of Ageing Wave 1 (2002/03) until Wave 7 (2014/15). The study population consisted of 3,615 adults aged 50+ who participated in the first wave of the English Longitudinal Study of Ageing, who had no self-reported hearing impairment in Wave 1, and who underwent a hearing test in Wave 7. Respondents were classified as having hearing impairment if they failed to hear tones quieter than 35 dB HL in the better ear. Results The trajectories of recall memory scores were grouped using latent class growth mixture modelling and were related to the presence of hearing impairment in Wave 7. Models estimating 1-class through 5-class recall memory trajectories were compared and the best-fitting models were 4-class trajectories. The different recall memory trajectories represent different starting points and mean of the memory scores. Compared to respondents with the highest recall memory trajectory, other trajectories were increasingly likely to develop later hearing impairment. Conclusions Long-term changes in cognitive ability predict hearing impairment. Further research is required to identify the mechanisms explaining the association between cognitive trajectories and hearing impairment, as well as to determine whether intervention for maintenance of cognitive function also give benefit on hearing function among older adults.
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- 2020
65. Metabolomics in serum of patients with non-advanced age-related macular degeneration reveals aberrations in the glutamine pathway
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Kersten, Eveline, Dammeier, Sascha, Ajana, Soufiane, Groenewoud, Joannes M.M., Codrea, Marius, Klose, Franziska, Lechanteur, Yara T., Fauser, Sascha, Ueffing, Marius, Delcourt, Cécile, Hoyng, Carel B., de Jong, Eiko, Den Hollander, Anneke I., Arango-Gonzalez, Blanca, Arndt, Verena, Bhatia, Vaibhav, Bhatta-Charya, Shomi S., Biarnés, Marc, Borrell, Anna, Bühren, Sebastian, Calado, Sofia M., Colijn, Johanna M., Cougnard-Grégoire, Audrey, De la Cerda, Berta, Del-Court, Cécile, Diaz-Corrales, F. J., Diether, Sigrid, Emri, Eszter, Ender-Mann, Tanja, Ferraro, Lucia, Garcia, Míriam, Heesterbeek, Thomas J., Honisch, Sabina, Iacone, Roberto, Kilger, Ellen, Klaver, Caroline C.W., Langen, Hanno, Lengyel, Imre, Luthert, Phil, Maugeais, Cyrille, Meester-Smoor, Magda, Merle, Benedicte, Monés, Jordi, Nogoceke, Everson, Peto, Tunde, Pool, Fran, Rodríguez, Eduardo, Bartz-Schmidt, Karl Ulrich, Verzijden, Timo, Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Ophthalmology, and Epidemiology
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0301 basic medicine ,genetic structures ,Metabolite ,Glutamine ,Stress-related disorders Donders Center for Medical Neuroscience [Radboudumc 13] ,Disease ,Bioinformatics ,Biochemistry ,Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12] ,chemistry.chemical_compound ,Macular Degeneration ,0302 clinical medicine ,Medicine and Health Sciences ,Metabolites ,Geriatric Ophthalmology ,Amino Acids ,Multidisciplinary ,Agricultural and Biological Sciences(all) ,Organic Compounds ,Retinal Degeneration ,Acidic Amino Acids ,Discriminant Analysis ,Neurochemistry ,Neurotransmitters ,Middle Aged ,3. Good health ,Chemistry ,Physical Sciences ,Biomarker (medicine) ,Medicine ,Retinal Disorders ,Female ,Metabolic Pathways ,Glutamate ,Metabolic Networks and Pathways ,Research Article ,Science ,03 medical and health sciences ,Metabolomics ,Age related ,medicine ,Humans ,Least-Squares Analysis ,General ,Nutrition ,Aged ,Glutaminolysis ,business.industry ,Biochemistry, Genetics and Molecular Biology(all) ,Organic Chemistry ,Chemical Compounds ,Biology and Life Sciences ,Proteins ,Macular degeneration ,medicine.disease ,eye diseases ,Diet ,Ophthalmology ,030104 developmental biology ,Metabolism ,chemistry ,Geriatrics ,Macular Disorders ,030221 ophthalmology & optometry ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,sense organs ,business ,Biomarkers ,Neuroscience - Abstract
Contains fulltext : 205500.pdf (Publisher’s version ) (Open Access) Age-related macular degeneration (AMD) is a common, progressive multifactorial vision-threatening disease and many genetic and environmental risk factors have been identified. The risk of AMD is influenced by lifestyle and diet, which may be reflected by an altered metabolic profile. Therefore, measurements of metabolites could identify biomarkers for AMD, and could aid in identifying high-risk individuals. Hypothesis-free technologies such as metabolomics have a great potential to uncover biomarkers or pathways that contribute to disease pathophysiology. To date, only a limited number of metabolomic studies have been performed in AMD. Here, we aim to contribute to the discovery of novel biomarkers and metabolic pathways for AMD using a targeted metabolomics approach of 188 metabolites. This study focuses on non-advanced AMD, since there is a need for biomarkers for the early stages of disease before severe visual loss has occurred. Targeted metabolomics was performed in 72 patients with early or intermediate AMD and 72 control individuals, and metabolites predictive for AMD were identified by a sparse partial least squares discriminant analysis. In our cohort, we identified four metabolite variables that were most predictive for early and intermediate stages of AMD. Increased glutamine and phosphatidylcholine diacyl C28:1 levels were detected in non-advanced AMD cases compared to controls, while the rate of glutaminolysis and the glutamine to glutamate ratio were reduced in non-advanced AMD. The association of glutamine with non-advanced AMD corroborates a recent report demonstrating an elevated glutamine level in early AMD using a different metabolomics technique. In conclusion, this study indicates that metabolomics is a suitable method for the discovery of biomarker candidates for AMD. In the future, larger metabolomics studies could add to the discovery of novel biomarkers in yet unknown AMD pathways and expand our insights in AMD pathophysiology.
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- 2019
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66. Response to Comment on Foussard et al. Skin Autofluorescence of Pregnant Women With Diabetes Predicts the Macrosomia of Their Children. Diabetes 2019;68:1663–1669
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Foussard, Ninon, primary, Cougnard-Grégoire, Audrey, additional, Rajaobelina, Kalina, additional, Delcourt, Cécile, additional, Helmer, Catherine, additional, Lamireau, Thierry, additional, Gonzalez, Concepcion, additional, Grouthier, Virginie, additional, Haissaguerre, Magalie, additional, Blanco, Laurence, additional, Alexandre, Laure, additional, Mohammedi, Kamel, additional, and Rigalleau, Vincent, additional
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- 2020
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67. Trends in the Use of Eye Care Services in Adults Treated for Diabetes between 2008 and 2017 in France: A Nationwide Study
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Cougnard-Grégoire, Audrey, primary, Korobelnik, Jean-François, additional, Delyfer, Marie-Noëlle, additional, Rigalleau, Vincent, additional, Daien, Vincent, additional, Creuzot-Garcher, Catherine, additional, and Delcourt, Cécile, additional
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- 2020
- Full Text
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68. Mediterranean Diet and Incidence of Advanced Age-Related Macular Degeneration: The EYE-RISK Consortium
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Merle, Bénédicte M. J., Colijn, Johanna M., Cougnard-Grégoire, Audrey, Koning-Backus, Alexandra de, Delyfer, Marie Nöelle, Kiefte-de Jong, Jessica, Meester-Smoor, Magda, Féart, Catherine, Verzijden, Timo, Samieri, Cécilia, Franco, Oscar H., Korobelnik, Jean-François, Klaver, Caroline C. W., Delcourt, Cécilia, EYE-RISK Consortium, Laboratoires Théa, Nestlé, Essilor, Bayer, Alcon, IVERIC bio, Notal Vision, Novartis, Roche, Optos, European Commission, Erasmus University Rotterdam, Netherlands Organisation for Health Research and Development, Ministry of Education, Culture and Science (The Netherlands), Ministry of Health, Welfare and Sport (The Netherlands), Fondation Voir et Entendre, Retina France, and Agence Nationale de la Recherche (France)
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Aged, 80 and over ,Male ,Incidence ,Middle Aged ,Diet, Mediterranean ,Diet Records ,White People ,Macular Degeneration ,Risk Factors ,Humans ,Female ,France ,Prospective Studies ,Aged ,Netherlands ,Proportional Hazards Models - Abstract
Purpose: To investigate associations of adherence to the Mediterranean diet (MeDi) with incidence of advanced age-related macular degeneration (AMD; the symptomatic form of AMD) in 2 European population-based prospective cohorts. Design: Prospective cohort study of the Rotterdam Study I (RS-I) and the Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires (Alienor) Study populations. Participants: Four thousand four hundred forty-six participants 55 years of age or older from the RS-I (The Netherlands) and 550 French adults 73 years of age or older from the Alienor Study with complete ophthalmologic and dietary data were included in the present study. Methods: Examinations were performed approximately every 5 years over a 21-year period (1990–2011) in RS-I and every 2 years over a 4-year period (2006–2012) in the Alienor Study. Adherence to the MeDi was evaluated using a 9-component score based on intake of vegetables, fruits, legumes, cereals, fish, meat, dairy products, alcohol, and the monounsaturated-to-saturated fatty acids ratio. Associations of incidence of AMD with MeDi were estimated using multivariate Cox proportional hazard models. Main Outcomes Measures: Incidence of advanced AMD based on retinal fundus photographs. Results: Among the 4996 included participants, 155 demonstrated advanced incident AMD (117 from the RS-I and 38 from the Alienor Study). The mean follow-up time was 9.9 years (range, 0.6–21.7 years) in the RS-I and 4.1 years (range, 2.5–5.0 years) in the Alienor Study. Pooling data for both the RS-I and Alienor Study, participants with a high (range, 6–9) MeDi score showed a significantly reduced risk for incident advanced AMD compared with participants with a low (range, 0–3) MeDi score in the fully adjusted Cox model (hazard ratio, 0.59; 95% confidence interval, 0.37–0.95; P = 0.04 for trend). Conclusions: Pooling data from the RS-I and Alienor Study, higher adherence to the MeDi was associated with a 41% reduced risk of incident advanced AMD. These findings support the role of a diet rich in healthful nutrient-rich foods such as fruits, vegetables, legumes, and fish in the prevention of AMD., The author(s) have made the following disclosure(s): B.M.J.M.: Consultant e Bausch & Lomb (Rochester, New York); Financial support e Laboratoires Théa (Clermont-Ferrand, France). A.C.-G.: Financial support e Laboratoires Théa (Clermont-Ferrand, France). M.-N.D.: Consultant e Bayer (Leverkusen, Germany), Allergan (Irvine, California), Novartis (Basel, Switzerland); Board membership e Bayer (Leverkusen, Germany), Allergan (Irvine, California), Novartis (Basel, Switzerland). O.H.F.: Financial support e Nestle (Vevey, Switzerland). J.-F.K.: Consultant e Alcon (Hünenberg, Switzerland), Alimera (Alpharetta, Georgia), Novartis (Basel, Switzerland), Roche (Basel, Switzerland), Thea (Clermont-Ferrand, France), Zeiss (Oberkochen, Germany), Bayer (Leverkusen, Germany). C.C.W.K.: Consultant e Bayer (Leverkusen, Germany); Lecturer e Novartis (Basel, Switzerland), Thea Pharma (Clermont-Ferrand, France). C.D.: Consultant e Allergan (Irvine, California), Bausch & Lomb (Rochester, New York), Laboratoires Théa (Clermont-Ferrand, France), Novartis (Basel, Switzerland), Roche (Basel, Switzerland); Financial support e Laboratoires Théa (Clermont-Ferrand, France), Essilor (Charenton le Pont, France). M.B.: Travel fees e Bayer (Leverkusen, Germany); Consultant e Roche (Basel, Switzerland). R.I., H.L., C.M., and E.N.: Employees e F. Hoffmann-La Roche Ltd (Basel, Switzerland). J.M.: Financial support e Bayer (Leverkusen, Germany), Alcon (Hünenberg, Switzerland), Ophthotech (New-York, NY), Notal Vision (Manassas, VA), Novartis (Basel, Switzerland), Roche (Basel, Switzerland). I.L.: Unrestricted research support e OPTOS Plc (Dunfermline, UK). Competing financial interest of members of the EYE-RISK consortium not otherwise disclosed: Verena Arndt, Sebastian Bühren, Tanja Endermann, and Markus Zumbansen are employees of AYOXXA. The EYE-RISK project is supported by the European Union’s Horizon 2020 Research and Innovation Programme (grant no.: 634479). The Rotterdam Study is funded by Erasmus Medical Center and Erasmus University, Rotterdam, The Netherlands; the Organization for the Health Research and Development (ZonMw); the Research Institute for Diseases in the Elderly (RIDE); the Ministry of Education, Culture and Science; the Ministry for Health, Welfare and Sports; the European Commission (DG XII), and the Municipality of Rotterdam, Rotterdam, The Netherlands. Additionally, the ophthalmic research within the Rotterdam Study was supported by the following foundations: Oogfonds; Bartiméus Sonneheerdt Vereniging; Landelijke Stichting voor Blinden en Slechtzienden; Algemene Nederlandse Vereniging Ter Voorkoming Van Blindheid; Novartis Foundation; and MaculaFonds, which contributed through UitZicht (grant nos.: 2015-36 and 2016-19). The funding organizations had no role in the design or conduct of this research and provided unrestricted grants. The Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires Study is funded by Laboratoires Théa; Fondation Voir et Entendre; Retina France; Agence Nationale de la Recherche (ANR 2010-PRSP-011 VISA); and Caisse Nationale pour la Solidarité et l’Autonomie.
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- 2018
69. Mediterranean diet and incidence of advanced AMD: The EYE-RISK CONSORTIUM
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Merle, B.M.J., Colijn, J.M., Cougnard-Grégoire, A., Koning-Backus, A.P.M. de, Delyfer, M.N., Kiefte-de Jong, J.C., Meester-Smoor, M., Féart, C., Verzijden, T., Samieri, C., Franco, O.H., Korobelnik, J.F., Klaver, C.C.W., Delcourt, C., and EYE-RISK consortium.
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- 2018
70. Associations Between Self-Reported Sensory Impairment and Risk of Cognitive Decline and Impairment in the Health and Retirement Study Cohort
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Maharani, Asri, Dawes, Piers, Nazroo, James, Tampubolon, Gindo, Pendleton, Neil, Bertelsen, Geir, Cosh, Suzanne, Cougnard-Grégoire, Audrey, Delcourt, Cécile, Constantinidou, Fofi, Goedegebure, Andre, Helmer, Catherine, Ikram, M Arfan, Klaver, Caroline C W, Leroi, Iracema, Meester-Smor, Magda, Nael, Virginie, Oosterloo, Neelke, Schirmer, Henrik, Tiemeier, Henning, von Hanno, Therese, Constantinidou, Fofi [0000-0002-7928-8363], Dawes, Piers [0000-0003-3180-9884], Maharani, Asri [0000-0002-5931-8692], Tampubolon, Gindo [0000-0002-9081-2349], Otorhinolaryngology and Head and Neck Surgery, Ophthalmology, Epidemiology, and Child and Adolescent Psychiatry / Psychology
- Subjects
Male ,ResearchInstitutes_Networks_Beacons/global_development_institute ,medicine.medical_specialty ,Social Psychology ,Hearing loss ,Visual impairment ,Vision Disorders ,Audiology ,Cohort Studies ,03 medical and health sciences ,Diagnostic Self Evaluation ,0302 clinical medicine ,Risk Factors ,mental disorders ,Medicine ,Dementia ,Humans ,Cognitive Dysfunction ,030212 general & internal medicine ,Longitudinal Studies ,Cognitive decline ,Correlation of Data ,Hearing Loss ,Aged ,Retirement ,business.industry ,Proportional hazards model ,Incidence ,Middle Aged ,medicine.disease ,Mental Status and Dementia Tests ,Cognitive test ,Clinical Psychology ,Global Development Institute ,Relative risk ,Cohort ,Female ,Geriatrics and Gerontology ,medicine.symptom ,business ,Gerontology ,030217 neurology & neurosurgery - Abstract
Objectives We aimed to determine whether self-assessed single (hearing or visual) and dual sensory (hearing and visual) impairments are associated with cognitive decline and incident possible cognitive impairment, no dementia (CIND) and probable dementia. Method Data were drawn from the 1996–2014 surveys of the Health and Retirement Study (HRS), involving 19,618 respondents who had no probable dementia and who were aged 50 years or older at the baseline. We used linear mixed models to test the association between self-assessed sensory impairment and cognitive decline followed by a Cox proportional hazard model to estimate the relative risk of incident possible CIND and probable dementia associated with the presence of sensory impairment. Results Respondents with self-assessed single and dual sensory impairment performed worse in cognitive tests than those without sensory impairment. The fully adjusted incidence of developing possible CIND was 17% higher for respondents with hearing impairment than those without hearing impairment. Respondents with visual impairment had 35% and 25% higher risk for developing possible CIND and probable dementia, respectively, than those without visual impairment. Respondents with dual sensory impairment at baseline were 38% and 26% more likely to develop possible CIND and probable dementia, respectively, than those with no sensory impairment. Discussion Self-assessed sensory impairment is independently associated with cognitive decline and incident possible CIND and probable dementia. Further studies are needed to identify the mechanism underlying this association and to determine whether treatment of sensory impairment could ameliorate cognitive decline and delay the onset of dementia among older adults.
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- 2018
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71. Mediterranean Diet and Incidence of Advanced Age-Related Macular Degeneration: The EYE-RISK Consortium
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Bénédicte M J, Merle, Johanna M, Colijn, Audrey, Cougnard-Grégoire, Alexandra P M, de Koning-Backus, Marie-Noëlle, Delyfer, Jessica C, Kiefte-de Jong, Magda, Meester-Smoor, Catherine, Féart, Timo, Verzijden, Cécilia, Samieri, Oscar H, Franco, Jean-François, Korobelnik, Caroline C W, Klaver, Cécile, Delcourt, and Vassil, Vasiliev
- Subjects
Aged, 80 and over ,Male ,Incidence ,Middle Aged ,Diet, Mediterranean ,Diet Records ,White People ,Macular Degeneration ,Risk Factors ,Humans ,Female ,France ,Prospective Studies ,Aged ,Netherlands ,Proportional Hazards Models - Abstract
To investigate associations of adherence to the Mediterranean diet (MeDi) with incidence of advanced age-related macular degeneration (AMD; the symptomatic form of AMD) in 2 European population-based prospective cohorts.Prospective cohort study of the Rotterdam Study I (RS-I) and the Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires (Alienor) Study populations.Four thousand four hundred forty-six participants 55 years of age or older from the RS-I (The Netherlands) and 550 French adults 73 years of age or older from the Alienor Study with complete ophthalmologic and dietary data were included in the present study.Examinations were performed approximately every 5 years over a 21-year period (1990-2011) in RS-I and every 2 years over a 4-year period (2006-2012) in the Alienor Study. Adherence to the MeDi was evaluated using a 9-component score based on intake of vegetables, fruits, legumes, cereals, fish, meat, dairy products, alcohol, and the monounsaturated-to-saturated fatty acids ratio. Associations of incidence of AMD with MeDi were estimated using multivariate Cox proportional hazard models.Incidence of advanced AMD based on retinal fundus photographs.Among the 4996 included participants, 155 demonstrated advanced incident AMD (117 from the RS-I and 38 from the Alienor Study). The mean follow-up time was 9.9 years (range, 0.6-21.7 years) in the RS-I and 4.1 years (range, 2.5-5.0 years) in the Alienor Study. Pooling data for both the RS-I and Alienor Study, participants with a high (range, 6-9) MeDi score showed a significantly reduced risk for incident advanced AMD compared with participants with a low (range, 0-3) MeDi score in the fully adjusted Cox model (hazard ratio, 0.59; 95% confidence interval, 0.37-0.95; P = 0.04 for trend).Pooling data from the RS-I and Alienor Study, higher adherence to the MeDi was associated with a 41% reduced risk of incident advanced AMD. These findings support the role of a diet rich in healthful nutrient-rich foods such as fruits, vegetables, legumes, and fish in the prevention of AMD.
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- 2018
72. Markers of glycation and neonatal hypoglycaemia in gestational diabetes mellitus
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Foussard, N., primary, Baillet‐Blanco, L., additional, Poupon, P., additional, Monlun, M., additional, Mohammedi, K., additional, Cougnard‐Grégoire, A., additional, Delcourt, C., additional, Helmer, C., additional, and Rigalleau, V., additional
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- 2019
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73. Skin Autofluorescence of Pregnant Women With Diabetes Predicts the Macrosomia of Their Children
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Foussard, Ninon, primary, Cougnard-Grégoire, Audrey, additional, Rajaobelina, Kalina, additional, Delcourt, Cécile, additional, Helmer, Catherine, additional, Lamireau, Thierry, additional, Gonzalez, Concepcion, additional, Grouthier, Virginie, additional, Haissaguerre, Magalie, additional, Blanco, Laurence, additional, Alexandre, Laure, additional, Mohammedi, Kamel, additional, and Rigalleau, Vincent, additional
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- 2019
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74. A parental history of diabetes is associated with a high risk of retinopathy in patients with type 2 diabetes
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Lapeyre, G., Cougnard-Grégoire, A., Delyfer, M.-N., Delcourt, C., Hadjadj, S., Blanco, L., Pupier, E., Rougier, M.-B., Rajaobelina, K., Mohammedi, K., Hugo, M., Korobelnik, J.F., and Rigalleau, V.
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- 2017
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75. Predicting the retinal content in omega‐3 fatty acids for age‐related macular‐degeneration.
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Acar, Niyazi, Merle, Bénédicte M. J., Ajana, Soufiane, He, Zhiguo, Grégoire, Stéphane, Hejblum, Boris P., Martine, Lucy, Buaud, Benjamin, Bron, Alain M., Creuzot‐Garcher, Catherine P., Korobelnik, Jean‐François, Berdeaux, Olivier, Jacqmin‐Gadda, Hélène, Bretillon, Lionel, Delcourt, Cécile, Bron, Alain, Cabaret, Stéphanie, Gain, Philippe, Cougnard‐Grégoire, Audrey, and Creuzot‐Garcher, Catherine
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OMEGA-3 fatty acids ,MONOUNSATURATED fatty acids ,BLOOD lipids ,HDL cholesterol ,LDL cholesterol ,FISH oils ,ZEAXANTHIN ,LIPID metabolism - Abstract
Adjusted differences black squares and 95% confidence intervals (CIs) (horizontal lines) of observed and predicted retinal -3 PUFAs contents for age-related macular degeneration in donor eyes and humans patients. Interestingly, cholesteryl esters species with -3 PUFAs contributed positively to the estimation of retinal -3 PUFAs content whereas those with -6 PUFAs lowered the prediction index, which is consistent with the well-established competitive metabolism of -3 and -6 PUFAs. Current treatments for age-related macular degeneration (AMD)-the leading cause of blindness in industrialized countries-are restricted to a single form of the disease and cannot always avoid severe visual loss.1 Among emerging preventive strategies, -3 polyunsaturated fatty acids (PUFAs) are enjoying interest as they promote normal retinal structure and function, reduce incidence, and slow progression of AMD, consistently with their abundance in retinal neurons. [Extracted from the article]
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- 2021
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76. Mediterranean Diet and Incidence of Advanced Age-Related Macular Degeneration: The EYE-RISK Consortium
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Laboratoires Théa, Nestlé, Essilor, Bayer, Alcon, IVERIC bio, Notal Vision, Novartis, Roche, Optos, European Commission, Erasmus University Rotterdam, Netherlands Organisation for Health Research and Development, Ministry of Education, Culture and Science (The Netherlands), Ministry of Health, Welfare and Sport (The Netherlands), Fondation Voir et Entendre, Retina France, Agence Nationale de la Recherche (France), Merle, Bénédicte M. J., Colijn, Johanna M., Cougnard-Grégoire, Audrey, Koning-Backus, Alexandra de, Delyfer, Marie Nöelle, Kiefte-de Jong, Jessica, Meester-Smoor, Magda, Féart, Catherine, Verzijden, Timo, Samieri, Cécilia, Franco, Oscar H., Korobelnik, Jean-François, Klaver, Caroline C. W., Delcourt, Cécilia, EYE-RISK Consortium, Laboratoires Théa, Nestlé, Essilor, Bayer, Alcon, IVERIC bio, Notal Vision, Novartis, Roche, Optos, European Commission, Erasmus University Rotterdam, Netherlands Organisation for Health Research and Development, Ministry of Education, Culture and Science (The Netherlands), Ministry of Health, Welfare and Sport (The Netherlands), Fondation Voir et Entendre, Retina France, Agence Nationale de la Recherche (France), Merle, Bénédicte M. J., Colijn, Johanna M., Cougnard-Grégoire, Audrey, Koning-Backus, Alexandra de, Delyfer, Marie Nöelle, Kiefte-de Jong, Jessica, Meester-Smoor, Magda, Féart, Catherine, Verzijden, Timo, Samieri, Cécilia, Franco, Oscar H., Korobelnik, Jean-François, Klaver, Caroline C. W., Delcourt, Cécilia, and EYE-RISK Consortium
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Purpose: To investigate associations of adherence to the Mediterranean diet (MeDi) with incidence of advanced age-related macular degeneration (AMD; the symptomatic form of AMD) in 2 European population-based prospective cohorts. Design: Prospective cohort study of the Rotterdam Study I (RS-I) and the Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires (Alienor) Study populations. Participants: Four thousand four hundred forty-six participants 55 years of age or older from the RS-I (The Netherlands) and 550 French adults 73 years of age or older from the Alienor Study with complete ophthalmologic and dietary data were included in the present study. Methods: Examinations were performed approximately every 5 years over a 21-year period (1990–2011) in RS-I and every 2 years over a 4-year period (2006–2012) in the Alienor Study. Adherence to the MeDi was evaluated using a 9-component score based on intake of vegetables, fruits, legumes, cereals, fish, meat, dairy products, alcohol, and the monounsaturated-to-saturated fatty acids ratio. Associations of incidence of AMD with MeDi were estimated using multivariate Cox proportional hazard models. Main Outcomes Measures: Incidence of advanced AMD based on retinal fundus photographs. Results: Among the 4996 included participants, 155 demonstrated advanced incident AMD (117 from the RS-I and 38 from the Alienor Study). The mean follow-up time was 9.9 years (range, 0.6–21.7 years) in the RS-I and 4.1 years (range, 2.5–5.0 years) in the Alienor Study. Pooling data for both the RS-I and Alienor Study, participants with a high (range, 6–9) MeDi score showed a significantly reduced risk for incident advanced AMD compared with participants with a low (range, 0–3) MeDi score in the fully adjusted Cox model (hazard ratio, 0.59; 95% confidence interval, 0.37–0.95; P = 0.04 for trend). Conclusions: Pooling data from the RS-I and Alienor Study, higher adherence to the MeDi was associated with a 41% reduced risk of incident
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- 2019
77. Systemic and Ocular Determinants of Peripapillary Retinal Nerve Fiber Layer Thickness Measurements in the European Eye Epidemiology (E3) Population
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Matthias M. Mauschitz, Pieter W.M. Bonnemaijer, Kersten Diers, Franziska G. Rauscher, Tobias Elze, Christoph Engel, Markus Loeffler, Johanna Maria Colijn, M. Arfan Ikram, Johannes R. Vingerling, Katie M. Williams, Christopher J. Hammond, Catherine Creuzot-Garcher, Alain M. Bron, Rufino Silva, Sandrina Nunes, Cécile Delcourt, Audrey Cougnard-Grégoire, Frank G. Holz, Caroline C.W. Klaver, Monique M.B. Breteler, Robert P. Finger, Niyazi Acar, Eleftherios Anastosopoulos, Augusto Azuara-Blanco, Tos Berendschot, Arthur Bergen, Geir Bertelsen, Christine Binquet, Alan Bird, Martin Bobak, Morten Bøgelund Larsen, Camiel Boon, Rupert Bourne, Lionel Brétillon, Rebecca Broe, Alain Bron, Gabrielle Buitendijk, Maria Luz Cachulo, Vittorio Capuano, Isabelle Carrière, Usha Chakravarthy, Michelle Chan, Petrus Chang, Johanna Colijn, Angela Cree, Phillippa Cumberland, José Cunha-Vaz, Vincent Daien, Eiko De Jong, Gabor Deak, Marie-Noëlle Delyfer, Anneke den Hollander, Martha Dietzel, Maja Gran Erke, Pedro Faria, Claudia Farinha, Sascha Fauser, Robert Finger, Astrid Fletcher, Paul Foster, Panayiota Founti, Theo Gorgels, Jakob Grauslund, Franz Grus, Christopher Hammond, Hans-Werner Hense, Manuel Hermann, René Hoehn, Ruth Hogg, Frank Holz, Carel Hoyng, Nomdo Jansonius, Sarah Janssen, Eveline Kersten, Anthony Khawaja, Caroline Klaver, Jean-François Korobelnik, Julia Lamparter, Mélanie Le Goff, Yara Lechanteur, Terho Lehtimäki, Irene Leung, Andrew Lotery, Matthias Mauschitz, Magda Meester, Bénédicte Merle, Verena Meyer zu Westrup, Edoardo Midena, Stefania Miotto, Alireza Mirshahi, Sadek Mohan-Saïd, Michael Mueller, Alyson Muldrew, Joaquim Murta, Stefan Nickels, Christopher Owen, Tunde Peto, Norbert Pfeiffer, Stefano Piermarocchi, Elena Prokofyeva, Jugnoo Rahi, Olli Raitakari, Franziska Rauscher, Luisa Ribeiro, Marie-Bénédicte Rougier, Alicja Rudnicka, José Sahel, Aggeliki Salonikiou, Clarisa Sanchez, Steffen Schmitz-Valckenberg, Alexander Schuster, Cédric Schweitzer, Tatiana Segato, Jasmin Shehata, Giuliana Silvestri, Christian Simader, Eric Souied, Martynas Speckauskas, Henriet Springelkamp, Robyn Tapp, Fotis Topouzis, Elisa van Leeuwen, Virginie Verhoeven, Timo Verzijden, Therese Von Hanno, Peter Wiedemann, Katie Williams, Christian Wolfram, Jennifer Yip, Jennyfer Zerbib, OEil, nutrition et signalisation cellulaire [CSGA], Centre des Sciences du Goût et de l'Alimentation [Dijon] (CSGA), Institut National de la Recherche Agronomique (INRA)-Université de Bourgogne (UB)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Recherche Agronomique (INRA)-Université de Bourgogne (UB)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Centre National de la Recherche Scientifique (CNRS), Service d'Ophtalmologie (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Neuropsychiatrie : recherche épidémiologique et clinique, Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Neuropsychiatrie : recherche épidémiologique et clinique (PSNREC), Université Montpellier 1 (UM1)-Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM), Montrachet Study: Funding was provided by an Inter-regional grant (PHRC) and the Regional Council of Burgundy. Funded by INRA, CNRS, Université de Bourgogne, Regional Council of Burgundy France (PARI Agrale 1), FEDER (European Funding for Regional Economic Development), and French Government grant managed by the French National Research Agency (ANR) as part of the 'Investissements d’Avenir' program (reference ANR-11-LABX-0021-01-LipSTIC Labex)., Human Genetics, ANS - Cellular & Molecular Mechanisms, RS: NUTRIM - R1 - Obesity, diabetes and cardiovascular health, RS: MHeNs - R3 - Neuroscience, Oogheelkunde, MUMC+: MA UECM Oogartsen MUMC (9), Perceptual and Cognitive Neuroscience (PCN), Epidemiology, and Ophthalmology
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Retinal Ganglion Cells ,Cross-Sectional Studies ,Disease Progression ,Europe ,Glaucoma ,Humans ,Intraocular Pressure ,Nerve Fibers ,Optic Disk ,Population Surveillance ,Tomography, Optical Coherence ,methods [Tomography, Optical Coherence] ,Intraocular pressure ,OPTICAL COHERENCE TOMOGRAPHY ,Cross-sectional study ,Nerve Fibers/pathology ,ANYANG CHILDHOOD EYE ,AXIAL LENGTH ,Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12] ,INTRAOCULAR-PRESSURE ,Tomography, Optical Coherence/methods ,Rotterdam Study ,0302 clinical medicine ,physiopathology [Glaucoma] ,GLAUCOMA ,epidemiology [Glaucoma] ,Tomography ,education.field_of_study ,GANGLION-CELL LAYER ,epidemiology [Europe] ,pathology [Nerve Fibers] ,ASSOCIATION ,3. Good health ,ALZHEIMERS-DISEASE ,Population Surveillance/methods ,pathology [Optic Disk] ,methods [Population Surveillance] ,Optic Disk/pathology ,Cohort study ,Glaucoma/diagnosis ,medicine.medical_specialty ,Population ,physiology [Intraocular Pressure] ,Retinal Ganglion Cells/pathology ,pathology [Retinal Ganglion Cells] ,Europe/epidemiology ,03 medical and health sciences ,Ophthalmology ,medicine ,ddc:610 ,Intraocular Pressure/physiology ,education ,business.industry ,diagnosis [Glaucoma] ,CONSORTIUM ,medicine.disease ,Confidence interval ,ta3125 ,Optical Coherence ,030221 ophthalmology & optometry ,DISC SIZE ,business ,Body mass index ,030217 neurology & neurosurgery ,[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology - Abstract
Purpose: To investigate systemic and ocular determinants of peripapillary retinal nerve fiber layer thickness (pRNFLT) in the European population.Design: Cross-sectional meta-analysis.Participants: A total of 16 084 European adults from 8 cohort studies (mean age range, 56.9 +/- 12.3-82.1 +/- 4.2 years) of the European Eye Epidemiology (E3) consortium.Methods: We examined associations with pRNFLT measured by spectral-domain OCT in each study using multivariable linear regression and pooled results using random effects meta-analysis.Main Outcome Measures: Determinants of pRNFLT.Results: Mean pRNFLT ranged from 86.8 +/- 21.4 mu m in the Rotterdam Study I to 104.7 +/- 12.5 mu m in the Rotterdam Study III. We found the following factors to be associated with reduced pRNFLT: Older age (beta = -0.38 mu m/year; 95% confidence interval [CI], -0.57 to -0.18), higher intraocular pressure (10P) (beta = -0.36 mu m/mmHg; 95% CI, -0.56 to -0.15), visual impairment (beta = -5.50 mu m; 95% CI, -9.37 to -1.64), and history of systemic hypertension (beta = -0.54 mu m; 95% CI, -1.01 to -0.07) and stroke (beta = -1.94 mu m; 95% CI, -3.17 to -0.72). A suggestive, albeit nonsignificant, association was observed for dementia (beta = -3.11 mu m; 95% CI, -6.22 to 0.01). Higher pRNFLT was associated with more hyperopic spherical equivalent (beta = 1.39 mu m/diopter; 95% CI, 1.19-1.59) and smoking (beta = 1.53 mu m; 95% CI, 1.00-2.06 for current smokers compared with never-smokers).Conclusions: In addition to previously described determinants such as age and refraction, we found that systemic vascular and neurovascular diseases were associated with reduced pRNFLT. These may be of clinical relevance, especially in glaucoma monitoring of patients with newly occurring vascular comorbidities. (C) 2018 by the American Academy of Ophthalmology
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- 2018
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78. Prevalence of Age-Related Macular Degeneration in Europe
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Johanna M. Colijn, Gabriëlle H.S. Buitendijk, Elena Prokofyeva, Dalila Alves, Maria L. Cachulo, Anthony P. Khawaja, Audrey Cougnard-Gregoire, Bénédicte M.J. Merle, Christina Korb, Maja G. Erke, Alain Bron, Eleftherios Anastasopoulos, Magda A. Meester-Smoor, Tatiana Segato, Stefano Piermarocchi, Paulus T.V.M. de Jong, Johannes R. Vingerling, Fotis Topouzis, Catherine Creuzot-Garcher, Geir Bertelsen, Norbert Pfeiffer, Astrid E. Fletcher, Paul J. Foster, Rufino Silva, Jean-François Korobelnik, Cécile Delcourt, Caroline C.W. Klaver, Soufiane Ajana, Blanca Arango-Gonzalez, Verena Arndt, Vaibhav Bhatia, Shomi S. Bhattacharya, Marc Biarnés, Anna Borrell, Sebastian Bühren, Sofia M. Calado, Audrey Cougnard-Grégoire, Sascha Dammeier, Eiko K. de Jong, Berta De la Cerda, Anneke I. den Hollander, Francisco J. Diaz-Corrales, Sigrid Diether, Eszter Emri, Tanja Endermann, Lucia L. Ferraro, Míriam Garcia, Thomas J. Heesterbeek, Sabina Honisch, Carel B. Hoyng, Eveline Kersten, Ellen Kilger, Hanno Langen, Imre Lengyel, Phil Luthert, Cyrille Maugeais, Magda Meester-Smoor, Jordi Monés, Everson Nogoceke, Tunde Peto, Frances M. Pool, Eduardo Rodríguez, Marius Ueffing, Karl U. Ulrich Bartz-Schmidt, Elisabeth M. van Leeuwen, Timo Verzijden, Markus Zumbansen, Niyazi Acar, Eleftherios Anastosopoulos, Augusto Azuara-Blanco, Arthur Bergen, Christine Binquet, Alan Bird, Lionel Brétillon, Gabrielle Buitendijk, Maria Luz Cachulo, Usha Chakravarthy, Michelle Chan, Petrus Chang, Johanna Colijn, Philippa Cumberland, José Cunha-Vaz, Vincent Daien, Gabor Deak, Marie-Noëlle Delyfer, Anneke den Hollander, Martha Dietzel, Maja Gran Erke, Sascha Fauser, Robert Finger, Astrid Fletcher, Paul Foster, Panayiota Founti, Arno Göbel, Theo Gorgels, Jakob Grauslund, Franz Grus, Christopher Hammond, Catherine Helmer, Hans-Werner Hense, Manuel Hermann, René Hoehn, Ruth Hogg, Frank Holz, Carel Hoyng, Nomdo Jansonius, Sarah Janssen, Anthony Khawaja, Caroline Klaver, Julia Lamparter, Mélanie Le Goff, Sergio Leal, Yara Lechanteur, Terho Lehtimäki, Andrew Lotery, Irene Leung, Matthias Mauschitz, Bénédicte Merle, Verena Meyer zu Westrup, Edoardo Midena, Stefania Miotto, Alireza Mirshahi, Sadek Mohan-Saïd, Michael Mueller, Alyson Muldrew, Sandrina Nunes, Konrad Oexle, Jugnoo Rahi, Olli Raitakari, Luisa Ribeiro, Marie-Bénédicte Rougier, José Sahel, Aggeliki Salonikiou, Clarisa Sanchez, Steffen Schmitz-Valckenberg, Cédric Schweitzer, Jasmin Shehata, Giuliana Silvestri, Christian Simader, Eric Souied, Henriet Springelkamp, Robyn Tapp, Virginie Verhoeven, Therese Von Hanno, Stela Vujosevic, Katie Williams, Christian Wolfram, Jennifer Yip, Jennyfer Zerbib, Isabella Zwiener, Erasmus University Rotterdam, Scientific Institute for Public Health, Federal Agency for Medicines and Health Products, Partenaires INRAE, Association for Innovation and Biomedical Research on Light and Image (AIBILI), Universidade de Coimbra, Coimbra University Hospital (CHUC), University of Cambridge [UK] (CAM), Moorfields Eye Hospital NHS Foundation Trust, Institut National de la Santé et de la Recherche Médicale (INSERM), Université de Bordeaux (UB), Mainz University Medical Center, Oslo University Hospital [Oslo], Centre des Sciences du Goût et de l'Alimentation [Dijon] (CSGA), Institut National de la Recherche Agronomique (INRA)-Université de Bourgogne (UB)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Centre National de la Recherche Scientifique (CNRS), Department of Ophthalmology, Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Aristotle University of Thessaloniki, Universitad de Padua, Univ Padua, Dept Ophthalmol, Padua, Italy, Royal Netherlands Academy of Arts and Sciences (KNAW), University Hospital of North Norway [Tromsø] (UNN), London School of Hygiene and Tropical Medicine (LSHTM), Institute of Ophthalmology, University of Messina, CHU Bordeaux [Bordeaux], Radboud University Medical Center [Nijmegen], The European Eye Epidemiology (E3) Consortium, Epidemiology, Ophthalmology, Erasmus MC other, Other departments, ANS - Complex Trait Genetics, Human Genetics, and Genome Analysis
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0301 basic medicine ,medicine.medical_specialty ,Visual acuity ,OPTICAL COHERENCE TOMOGRAPHY ,MACULOPATHY ,genetic structures ,Population ,Prevalence ,HEART-DISEASE ,choroidal neovascularization ,Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12] ,03 medical and health sciences ,Rotterdam Study ,0302 clinical medicine ,All institutes and research themes of the Radboud University Medical Center ,BEAVER DAM EYE ,Epidemiology ,geographic atrophy ,medicine ,VISUAL IMPAIRMENT ,[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs ,education ,POPULATION ,education.field_of_study ,BIRTH COHORT ,business.industry ,Macular degeneration ,medicine.disease ,TRENDS ,Confidence interval ,eye diseases ,3. Good health ,European Prospective Investigation into Cancer and Nutrition ,Ophthalmology ,030104 developmental biology ,Age-related Macular Degeneration ,ENDOTHELIAL GROWTH-FACTOR ,BLINDNESS ,030221 ophthalmology & optometry ,Optometry ,Age-related Macular Degeneration, choroidal neovascularization, geographic atrophy ,sense organs ,medicine.symptom ,business ,[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology ,Demography - Abstract
Manuscript no. 2016-1147 Supplemental material is available at www.aaojournal.org/; International audience; [u]Purpose:[/u] Age-related macular degeneration (AMD) is a frequent, complex disorder in elderly of European ancestry. Risk profiles and treatment options have changed considerably over the years, which may have affected disease prevalence and outcome. We determined the prevalence of early and late AMD in Europe from 1990 to 2013 using the European Eye Epidemiology (E3) consortium, and made projections for the future. [u]Design:[/u] Meta-analysis of prevalence data. [u]Participants:[/u] A total of 42 080 individuals 40 years of age and older participating in 14 population-based cohorts from 10 countries in Europe. [u]Methods:[/u] AMD was diagnosed based on fundus photographs using the Rotterdam Classification. Prevalence of early and late AMD was calculated using random-effects meta-analysis stratified for age, birth cohort, gender, geographic region, and time period of the study. Best-corrected visual acuity (BCVA) was compared between late AMD subtypes; geographic atrophy (GA) and choroidal neovascularization (CNV). [u]Main Outcome Measures:[/u] Prevalence of early and late AMD, BCVA, and number of AMD cases. [u]Results:[/u] Prevalence of early AMD increased from 3.5% (95% confidence interval [CI] 2.1% -5.0%) in those aged 55-59 years to 17.6% (95% CI 13.6%-21.5%) in those aged >= 85 years; for late AMD these figures were 0.1% (95% CI 0.04%-0.3%) and 9.8% (95% CI 6.3%-13.3%), respectively. We observed a decreasing prevalence of late AMD after 2006, which became most prominent after age 70. Prevalences were similar for gender across all age groups except for late AMD in the oldest age category, and a trend was found showing a higher prevalence of CNV in Northern Europe. After 2006, fewer eyes and fewer >= 80-year-old subjects with CNV were visually impaired (P = 0.016). Projections of AMD showed an almost doubling of affected persons despite a decreasing prevalence. By 2040, the number of individuals in Europe with early AMD will range between 14.9 and 21.5 million, and for late AMD between 3.9 and 4.8 million. [u]Conclusion:[/u] We observed a decreasing prevalence of AMD and an improvement in visual acuity in CNV occuring over the past 2 decades in Europe. Healthier lifestyles and implementation of anti-vascular endothelial growth factor treatment are the most likely explanations. Nevertheless, the numbers of affected subjects will increase considerably in the next 2 decades. AMD continues to remain a significant public health problem among Europeans.
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- 2017
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79. Vitreomacular Adhesion and Its Association With Age-Related Macular Degeneration in a Population-Based Setting: The Alienor Study
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Sarra, Gattoussi, Audrey, Cougnard-Grégoire, Marie-Noëlle, Delyfer, Marie-Bénédicte, Rougier, Cédric, Schweitzer, Cécile, Delcourt, and Jean-François, Korobelnik
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Aged, 80 and over ,Male ,Incidence ,Vitreous Detachment ,Risk Assessment ,Macular Degeneration ,Risk Factors ,Population Surveillance ,Prevalence ,Humans ,Female ,France ,Prospective Studies ,Tomography, Optical Coherence ,Aged ,Follow-Up Studies - Abstract
The purpose of this study was to describe vitreomacular adhesion (VMA), diagnosed with spectral-domain optical coherence tomography (SD-OCT), its risk factors, and its association with AMD in a population-based study of French elderly subjects.Six hundred twenty-two of 624 (99.7%) participants of the Alienor study (Bordeaux, France), ≥75 years of age, had gradable SD-OCT scans of the macula in at least one eye. VMA was defined as visible perifoveal vitreous separation with remaining vitreomacular attachment and unperturbed foveal morphologic features. Late AMD was classified from retinal color photographs, SD-OCT, and ophthalmologic history. Early AMD was classified from retinal photographs and defined by the presence of large drusen and/or reticular drusen and/or pigmentary abnormalities.The prevalence of VMA was 15.8%, decreased with age (18.1% in subjects 75 to 84 years of age versus 8.9% after 85 years of age), and was higher in men than women (20.6% vs. 12.8%). VMA also tended to be less frequent in eyes with a history of cataract surgery (odds ratio [OR] = 0.66, P = 0.05), after adjustment for age and sex. No associations of VMA with other risk factors (cardiovascular risk factors, dietary intake of omega-3 fatty acids, lifetime ultraviolet radiation exposure, major AMD genetic polymorphisms) were found. After multivariate adjustment, VMA was not significantly associated with early or late AMD (OR = 1.14, P = 0.70 and OR = 0.78, P = 0.51 for early and late AMD, respectively).VMA was visible on SD-OCT in 16% in this sample of elderly French subjects but was not associated with AMD. Prospective studies of the associations of VMA with AMD are needed.
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- 2017
80. CHOROIDAL THICKNESS, VASCULAR FACTORS, AND AGE-RELATED MACULAR DEGENERATION
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Gattoussi, Sarra, primary, Cougnard-Grégoire, Audrey, additional, Korobelnik, Jean-François, additional, Rougier, Marie-Bénédicte, additional, Delyfer, Marie-Noëlle, additional, Schweitzer, Cédric, additional, Le Goff, Mélanie, additional, Merle, Bénédicte M.J., additional, Dartigues, Jean-François, additional, and Delcourt, Cécile, additional
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- 2019
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81. Prevalence and Associated Factors of Uncorrected Refractive Error in Older Adults in a Population-Based Study in France
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Naël, Virginie, primary, Moreau, Gwendoline, additional, Monfermé, Solène, additional, Cougnard-Grégoire, Audrey, additional, Scherlen, Anne-Catherine, additional, Arleo, Angelo, additional, Korobelnik, Jean-François, additional, Delcourt, Cécile, additional, and Helmer, Catherine, additional
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- 2019
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82. Systemic and Ocular Determinants of Peripapillary Retinal Nerve Fiber Layer Thickness Measurements in the European Eye Epidemiology (E3) Population
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Mauschitz, Matthias M., primary, Bonnemaijer, Pieter W.M., additional, Diers, Kersten, additional, Rauscher, Franziska G., additional, Elze, Tobias, additional, Engel, Christoph, additional, Loeffler, Markus, additional, Colijn, Johanna Maria, additional, Ikram, M. Arfan, additional, Vingerling, Johannes R., additional, Williams, Katie M., additional, Hammond, Christopher J., additional, Creuzot-Garcher, Catherine, additional, Bron, Alain M., additional, Silva, Rufino, additional, Nunes, Sandrina, additional, Delcourt, Cécile, additional, Cougnard-Grégoire, Audrey, additional, Holz, Frank G., additional, Klaver, Caroline C.W., additional, Breteler, Monique M.B., additional, Finger, Robert P., additional, Acar, Niyazi, additional, Anastosopoulos, Eleftherios, additional, Azuara-Blanco, Augusto, additional, Berendschot, Tos, additional, Bergen, Arthur, additional, Bertelsen, Geir, additional, Binquet, Christine, additional, Bird, Alan, additional, Bobak, Martin, additional, Larsen, Morten Bøgelund, additional, Boon, Camiel, additional, Bourne, Rupert, additional, Brétillon, Lionel, additional, Broe, Rebecca, additional, Bron, Alain, additional, Buitendijk, Gabrielle, additional, Cachulo, Maria Luz, additional, Capuano, Vittorio, additional, Carrière, Isabelle, additional, Chakravarthy, Usha, additional, Chan, Michelle, additional, Chang, Petrus, additional, Colijn, Johanna, additional, Cree, Angela, additional, Cumberland, Phillippa, additional, Cunha-Vaz, José, additional, Daien, Vincent, additional, De Jong, Eiko, additional, Deak, Gabor, additional, Delyfer, Marie-Noëlle, additional, Hollander, Anneke den, additional, Dietzel, Martha, additional, Erke, Maja Gran, additional, Faria, Pedro, additional, Farinha, Claudia, additional, Fauser, Sascha, additional, Finger, Robert, additional, Fletcher, Astrid, additional, Foster, Paul, additional, Founti, Panayiota, additional, Gorgels, Theo, additional, Grauslund, Jakob, additional, Grus, Franz, additional, Hammond, Christopher, additional, Hense, Hans-Werner, additional, Hermann, Manuel, additional, Hoehn, René, additional, Hogg, Ruth, additional, Holz, Frank, additional, Hoyng, Carel, additional, Jansonius, Nomdo, additional, Janssen, Sarah, additional, Kersten, Eveline, additional, Khawaja, Anthony, additional, Klaver, Caroline, additional, Korobelnik, Jean-François, additional, Lamparter, Julia, additional, Le Goff, Mélanie, additional, Lechanteur, Yara, additional, Lehtimäki, Terho, additional, Leung, Irene, additional, Lotery, Andrew, additional, Mauschitz, Matthias, additional, Meester, Magda, additional, Merle, Bénédicte, additional, Meyer zu Westrup, Verena, additional, Midena, Edoardo, additional, Miotto, Stefania, additional, Mirshahi, Alireza, additional, Mohan-Saïd, Sadek, additional, Mueller, Michael, additional, Muldrew, Alyson, additional, Murta, Joaquim, additional, Nickels, Stefan, additional, Owen, Christopher, additional, Peto, Tunde, additional, Pfeiffer, Norbert, additional, Piermarocchi, Stefano, additional, Prokofyeva, Elena, additional, Rahi, Jugnoo, additional, Raitakari, Olli, additional, Rauscher, Franziska, additional, Ribeiro, Luisa, additional, Rougier, Marie-Bénédicte, additional, Rudnicka, Alicja, additional, Sahel, José, additional, Salonikiou, Aggeliki, additional, Sanchez, Clarisa, additional, Schmitz-Valckenberg, Steffen, additional, Schuster, Alexander, additional, Schweitzer, Cédric, additional, Segato, Tatiana, additional, Shehata, Jasmin, additional, Silvestri, Giuliana, additional, Simader, Christian, additional, Souied, Eric, additional, Speckauskas, Martynas, additional, Springelkamp, Henriet, additional, Tapp, Robyn, additional, Topouzis, Fotis, additional, van Leeuwen, Elisa, additional, Verhoeven, Virginie, additional, Verzijden, Timo, additional, Von Hanno, Therese, additional, Wiedemann, Peter, additional, Williams, Katie, additional, Wolfram, Christian, additional, Yip, Jennifer, additional, and Zerbib, Jennyfer, additional
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- 2018
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83. The Decreasing Prevalence of Nonrefractive Visual Impairment in Older Europeans
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Delcourt, Cécile, primary, Le Goff, Mélanie, additional, von Hanno, Therese, additional, Mirshahi, Alireza, additional, Khawaja, Anthony P., additional, Verhoeven, Virginie J.M., additional, Hogg, Ruth E., additional, Anastosopoulos, Eleftherios, additional, Cachulo, Maria Luz, additional, Höhn, René, additional, Wolfram, Christian, additional, Bron, Alain, additional, Miotto, Stefania, additional, Carrière, Isabelle, additional, Colijn, Johanna M., additional, Buitendijk, Gabriëlle H.S., additional, Evans, Jennifer, additional, Nitsch, Dorothea, additional, Founti, Panayiota, additional, Yip, Jennifer L.Y., additional, Pfeiffer, Norbert, additional, Creuzot-Garcher, Catherine, additional, Silva, Rufino, additional, Piermarocchi, Stefano, additional, Topouzis, Fotis, additional, Bertelsen, Geir, additional, Foster, Paul J., additional, Fletcher, Astrid, additional, Klaver, Caroline C.W., additional, Korobelnik, Jean-François, additional, Acar, Niyazi, additional, Azuara-Blanco, Augusto, additional, Berendschot, Tos, additional, Bergen, Arthur, additional, Binquet, Christine, additional, Bird, Alan, additional, Bobak, Martin, additional, Boon, Camiel, additional, Brétillon, Lionel, additional, Broe, Rebecca, additional, Buitendijk, Gabrielle, additional, Capuano, Vittorio, additional, Chakravarthy, Usha, additional, Chan, Michelle, additional, Chang, Petrus, additional, Colijn, Johanna, additional, Cougnard-Grégoire, Audrey, additional, Cree, Angela, additional, Cumberland, Phillippa, additional, Cunha-Vaz, José, additional, Daien, Vincent, additional, De Jong, Eiko, additional, Deak, Gabor, additional, Delcourt, Cécile, additional, Delyfer, Marie-Noëlle, additional, den Hollander, Anneke, additional, Dietzel, Martha, additional, Erke, Maja Gran, additional, Faria, Pedro, additional, Farinha, Claudia, additional, Fauser, Sascha, additional, Finger, Robert, additional, Foster, Paul, additional, Gorgels, Theo, additional, Grauslund, Jakob, additional, Grus, Franz, additional, Hammond, Christopher, additional, Hansen, Morten, additional, Helmer, Catherine, additional, Hense, Hans-Werner, additional, Hermann, Manuel, additional, Hoehn, René, additional, Hogg, Ruth, additional, Holz, Frank, additional, Hoyng, Carel, additional, Jansonius, Nomdo, additional, Janssen, Sarah, additional, Kersten, Eveline, additional, Khawaja, Anthony, additional, Klaver, Caroline, additional, Lamparter, Julia, additional, Lechanteur, Yara, additional, Lehtimäki, Terho, additional, Leung, Irene, additional, Lotery, Andrew, additional, Mauschitz, Matthias, additional, Meester, Magda, additional, Merle, Bénédicte, additional, Meyer zu Westrup, Verena, additional, Midena, Edoardo, additional, Mohan-Saïd, Sadek, additional, Mueller, Michael, additional, Muldrew, Alyson, additional, Murta, Joaquim, additional, Nickels, Stefan, additional, Nunes, Sandrina, additional, Owen, Christopher, additional, Peto, Tunde, additional, Prokofyeva, Elena, additional, Rahi, Jugnoo, additional, Raitakari, Olli, additional, Rauscher, Franziska, additional, Ribeiro, Luisa, additional, Rougier, Marie-Bénédicte, additional, Rudnicka, Alicja, additional, Sahel, José, additional, Salonikiou, Aggeliki, additional, Sanchez, Clarisa, additional, Schmitz-Valckenberg, Steffen, additional, Schouten, Johannes, additional, Schuster, Alexander, additional, Schweitzer, Cédric, additional, Segato, Tatiana, additional, Shehata, Jasmin, additional, Silvestri, Giuliana, additional, Simader, Christian, additional, Souied, Eric, additional, Speckauskas, Martynas, additional, Springelkamp, Henriet, additional, Tapp, Robyn, additional, van Leeuwen, Elisa, additional, Verhoeven, Virginie, additional, Verzijden, Timo, additional, Von Hanno, Therese, additional, Vujosevic, Stela, additional, Wiedemann, Peter, additional, Williams, Katie, additional, Yip, Jennifer, additional, and Zerbib, Jennyfer, additional
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- 2018
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84. Incidence of and Risk Factors Associated With Age-Related Macular Degeneration
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Saunier, Valentine, primary, Merle, Bénédicte M. J., additional, Delyfer, Marie-Noëlle, additional, Cougnard-Grégoire, Audrey, additional, Rougier, Marie-Bénédicte, additional, Amouyel, Philippe, additional, Lambert, Jean-Charles, additional, Dartigues, Jean-François, additional, Korobelnik, Jean-François, additional, and Delcourt, Cécile, additional
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- 2018
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85. Unhealthy behaviours and risk of visual impairment: The CONSTANCES population-based cohort
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Merle, Bénédicte M. J., primary, Moreau, Gwendoline, additional, Ozguler, Anna, additional, Srour, Bernard, additional, Cougnard-Grégoire, Audrey, additional, Goldberg, Marcel, additional, Zins, Marie, additional, and Delcourt, Cécile, additional
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- 2018
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86. Associations with intraocular pressure across Europe: The European Eye Epidemiology (E3) Consortium
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Khawaja, Anthony P, Springelkamp, Henriët, Creuzot-Garcher, Catherine, Delcourt, Cécile, Hofman, Albert, Höhn, René, Iglesias, Adriana I, Wolfs, Roger CW, Korobelnik, Jean-François, Silva, Rufino, Topouzis, Fotis, Williams, Katie M, Bron, Alain M, Buitendijk, Gabriëlle HS, Cachulo, Maria Da Luz, Cougnard-Grégoire, Audrey, Dartigues, Jean-François, Hammond, Christopher J, Pfeiffer, Norbert, Salonikiou, Angeliki, Van Duijn, Cornelia M, Vingerling, Johannes R, Luben, Robert N, Mirshahi, Alireza, Lamparter, Julia, Klaver, Caroline CW, Jansonius, Nomdo M, Foster, Paul J, European Eye Epidemiology (E³) Consortium, Khawaja, Anthony P [0000-0001-6802-8585], and Apollo - University of Cambridge Repository
- Subjects
Aged, 80 and over ,Male ,genetic structures ,Epidemiology ,Intraocular pressure ,Age Factors ,Glaucoma ,Middle Aged ,eye diseases ,Cohort Studies ,Europe ,Refractive errors ,Cross-Sectional Studies ,Blood pressure ,Humans ,Female ,Ocular Hypertension ,sense organs ,Body mass index ,Aged - Abstract
Raised intraocular pressure (IOP) is the most important risk factor for developing glaucoma, the second commonest cause of blindness globally. Understanding associations with IOP and variations in IOP between countries may teach us about mechanisms underlying glaucoma. We examined cross-sectional associations with IOP in 43,500 European adults from 12 cohort studies belonging to the European Eye Epidemiology (E3) consortium. Each study conducted multivariable linear regression with IOP as the outcome variable and results were pooled using random effects meta-analysis. The association of standardized study IOP with latitude was tested using meta-regression. Higher IOP was observed in men (0.18 mmHg; 95 % CI 0.06, 0.31; P = 0.004) and with higher body mass index (0.21 mmHg per 5 kg/m2; 95 % CI 0.14, 0.28; P < 0.001), shorter height (-0.17 mmHg per 10 cm; 95 % CI -0.25, -0.08; P < 0.001), higher systolic blood pressure (0.17 mmHg per 10 mmHg; 95 % CI 0.12, 0.22; P < 0.001) and more myopic refraction (0.06 mmHg per Dioptre; 95 % CI 0.03, 0.09; P < 0.001). An inverted U-shaped trend was observed between age and IOP, with IOP increasing up to the age of 60 and decreasing in participants older than 70 years. We found no significant association between standardized IOP and study location latitude (P = 0.76). Novel findings of our study include the association of lower IOP in taller people and an inverted-U shaped association of IOP with age. We found no evidence of significant variation in IOP across Europe. Despite the limited range of latitude amongst included studies, this finding is in favour of collaborative pooling of data from studies examining environmental and genetic determinants of IOP in Europeans.
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- 2016
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87. Prevalence of Age-Related Macular Degeneration in Europe
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Colijn, Johanna M., primary, Buitendijk, Gabriëlle H.S., additional, Prokofyeva, Elena, additional, Alves, Dalila, additional, Cachulo, Maria L., additional, Khawaja, Anthony P., additional, Cougnard-Gregoire, Audrey, additional, Merle, Bénédicte M.J., additional, Korb, Christina, additional, Erke, Maja G., additional, Bron, Alain, additional, Anastasopoulos, Eleftherios, additional, Meester-Smoor, Magda A., additional, Segato, Tatiana, additional, Piermarocchi, Stefano, additional, de Jong, Paulus T.V.M., additional, Vingerling, Johannes R., additional, Topouzis, Fotis, additional, Creuzot-Garcher, Catherine, additional, Bertelsen, Geir, additional, Pfeiffer, Norbert, additional, Fletcher, Astrid E., additional, Foster, Paul J., additional, Silva, Rufino, additional, Korobelnik, Jean-François, additional, Delcourt, Cécile, additional, Klaver, Caroline C.W., additional, Ajana, Soufiane, additional, Arango-Gonzalez, Blanca, additional, Arndt, Verena, additional, Bhatia, Vaibhav, additional, Bhattacharya, Shomi S., additional, Biarnés, Marc, additional, Borrell, Anna, additional, Bühren, Sebastian, additional, Calado, Sofia M., additional, Colijn, Johanna M., additional, Cougnard-Grégoire, Audrey, additional, Dammeier, Sascha, additional, de Jong, Eiko K., additional, De la Cerda, Berta, additional, den Hollander, Anneke I., additional, Diaz-Corrales, Francisco J., additional, Diether, Sigrid, additional, Emri, Eszter, additional, Endermann, Tanja, additional, Ferraro, Lucia L., additional, Garcia, Míriam, additional, Heesterbeek, Thomas J., additional, Honisch, Sabina, additional, Hoyng, Carel B., additional, Kersten, Eveline, additional, Kilger, Ellen, additional, Langen, Hanno, additional, Lengyel, Imre, additional, Luthert, Phil, additional, Maugeais, Cyrille, additional, Meester-Smoor, Magda, additional, Monés, Jordi, additional, Nogoceke, Everson, additional, Peto, Tunde, additional, Pool, Frances M., additional, Rodríguez, Eduardo, additional, Ueffing, Marius, additional, Ulrich Bartz-Schmidt, Karl U., additional, van Leeuwen, Elisabeth M., additional, Verzijden, Timo, additional, Zumbansen, Markus, additional, Acar, Niyazi, additional, Anastosopoulos, Eleftherios, additional, Azuara-Blanco, Augusto, additional, Bergen, Arthur, additional, Binquet, Christine, additional, Bird, Alan, additional, Brétillon, Lionel, additional, Buitendijk, Gabrielle, additional, Cachulo, Maria Luz, additional, Chakravarthy, Usha, additional, Chan, Michelle, additional, Chang, Petrus, additional, Colijn, Johanna, additional, Cumberland, Philippa, additional, Cunha-Vaz, José, additional, Daien, Vincent, additional, Deak, Gabor, additional, Delyfer, Marie-Noëlle, additional, den Hollander, Anneke, additional, Dietzel, Martha, additional, Erke, Maja Gran, additional, Fauser, Sascha, additional, Finger, Robert, additional, Fletcher, Astrid, additional, Foster, Paul, additional, Founti, Panayiota, additional, Göbel, Arno, additional, Gorgels, Theo, additional, Grauslund, Jakob, additional, Grus, Franz, additional, Hammond, Christopher, additional, Helmer, Catherine, additional, Hense, Hans-Werner, additional, Hermann, Manuel, additional, Hoehn, René, additional, Hogg, Ruth, additional, Holz, Frank, additional, Hoyng, Carel, additional, Jansonius, Nomdo, additional, Janssen, Sarah, additional, Khawaja, Anthony, additional, Klaver, Caroline, additional, Lamparter, Julia, additional, Le Goff, Mélanie, additional, Leal, Sergio, additional, Lechanteur, Yara, additional, Lehtimäki, Terho, additional, Lotery, Andrew, additional, Leung, Irene, additional, Mauschitz, Matthias, additional, Merle, Bénédicte, additional, Meyer zu Westrup, Verena, additional, Midena, Edoardo, additional, Miotto, Stefania, additional, Mirshahi, Alireza, additional, Mohan-Saïd, Sadek, additional, Mueller, Michael, additional, Muldrew, Alyson, additional, Nunes, Sandrina, additional, Oexle, Konrad, additional, Rahi, Jugnoo, additional, Raitakari, Olli, additional, Ribeiro, Luisa, additional, Rougier, Marie-Bénédicte, additional, Sahel, José, additional, Salonikiou, Aggeliki, additional, Sanchez, Clarisa, additional, Schmitz-Valckenberg, Steffen, additional, Schweitzer, Cédric, additional, Shehata, Jasmin, additional, Silvestri, Giuliana, additional, Simader, Christian, additional, Souied, Eric, additional, Springelkamp, Henriet, additional, Tapp, Robyn, additional, Verhoeven, Virginie, additional, Von Hanno, Therese, additional, Vujosevic, Stela, additional, Williams, Katie, additional, Wolfram, Christian, additional, Yip, Jennifer, additional, Zerbib, Jennyfer, additional, and Zwiener, Isabella, additional
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- 2017
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88. Vitreomacular Adhesion and Its Association With Age-Related Macular Degeneration in a Population-Based Setting: The Alienor Study
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Gattoussi, Sarra, primary, Cougnard-Grégoire, Audrey, additional, Delyfer, Marie-Noëlle, additional, Rougier, Marie-Bénédicte, additional, Schweitzer, Cédric, additional, Delcourt, Cécile, additional, and Korobelnik, Jean-François, additional
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- 2017
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89. Prevalence of Age-Related Macular Degeneration in Europe: The Past and the Future
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Colijn, J.M. (Johanna), Buitendijk, G.H.S. (Gabrielle), Prokofyeva, E. (Elena), Alves, D. (Dalila), Cachulo, M.L. (Maria L.), Khawaja, A.P. (Anthony), Cougnard-Grégoire, A. (Audrey), Merle, B.M.J. (Bénédicte M.J.), Korb, C. (Christina), Erke, M.G. (Maja Gran), Bron, A. (Alain), Anastasopoulos, E. (Eleftherios), Meester-Smoor, M.A. (Magda), Segato, T. (Tatiana), Piermarocchi, S. (Stefano), Jong, P.T.V.M. (Paulus) de, Vingerling, J.R. (Hans), Topouzis, F. (Fotis), Creuzot-Garcher, C. (Catherine), Bertelsen, G. (Geir), Pfeiffer, A.F.H. (Andreas), Fletcher, A.E. (Astrid E.), Foster, P.J. (Paul), Silva, R. (Rufino), Korobelnik, J.-F. (Jean-François), Delcourt, C. (Cécile), Klaver, C.C.W. (Caroline), Ajana, S. (Soufiane), Arango-Gonzalez, B. (Blanca), Arndt, V. (Verena), Bhatia, V. (Vaibhav), Bhattacharya, S.S. (Shomi S.), Biarnés, M. (Marc), Borrell, A. (Anna), Bühren, S. (Sebastian), Calado, S.M. (Sofia M.), Colijn, J.M. (Johanna M.), Dammeier, S. (Sascha), Jong, E.K. (Eiko) de, De la Cerda, B. (Berta), den Hollander, A.I. (Anneke I.), Diaz-Corrales, F.J. (Francisco J.), Diether, S. (Sigrid), Emri, E. (Eszter), Endermann, T. (Tanja), Ferraro, L.L. (Lucia L.), Garcia, M. (Míriam), Heesterbeek, T.J. (Thomas J.), Honisch, S. (Sabina), Hoyng, C.B. (Carel B.), Kersten, E. (Eveline), Kilger, E. (Ellen), Klaver, C.C.W. (Caroline C.W.), Langen, H. (Hanno), Lengyel, I. (Imre), Luthert, P. (Phil), Maugeais, C. (Cyrille), Meester-Smoor, M. (Magda), Monés, J. (Jordi), Nogoceke, E. (Everson), Peto, T. (Tunde), Pool, F.M. (Frances M.), Rodríguez, E. (Eduardo), Ueffing, M. (Marius), Ulrich Bartz-Schmidt, K.U. (Karl U.), van Leeuwen, E.M. (Elisabeth M.), Verzijden, T. (Timo), Zumbansen, M. (Markus), Acar, N. (Niyazi), Anastosopoulos, E. (Eleftherios), Azuara-Blanco, A. (Augusto), Bergen, A.A.B. (Arthur), Binquet, C. (Christine), Bird, A.C. (Alan), Bretillon, L. (Lionel), Buitendijk, G. (Gabrielle), Cachulo, M.L. (Maria Luz), Chakravarthy, U. (Usha), Chan, M. (Michelle), Chang, P. (Petrus), Colijn, J. (Johanna), Cumberland, P. (Phillippa), Cunha-Vaz, J. (José), Daien, V. (Vincent), Deak, G. (Gabor), Delyfer, M.-N. (Marie-Noëlle), Hollander, A.I. (Anneke), Dietzel, M. (Martha), Fauser, S. (Sascha), Finger, R. (Robert), Fletcher, A. (Astrid), Foster, P.J. (Paul J.), Founti, P. (Panayiota), Göbel, A. (Arno), Gorgels, T.G.M.F. (Theo), Grauslund, J. (Jakob), Grus, F. (Franz), Hammond, C.J. (Christopher), Helmer, C. (Catherine), Hense, H.-W. (Hans-Werner), Hermann, M. (Manuel), Hoehn, R. (René), Hogg, R. (Ruth), Holz, F.G. (Frank), Hoyng, C.B. (Carel), Jansonius, N.M. (Nomdo), Janssen, S.F. (Sarah), Khawaja, A. (Anthony), Lamparter, J. (Julia), Le Goff, M. (Mélanie), Leal, S. (Sergio), Lechanteur, Y.T.E. (Yara T. E.), Lehtimäki, T. (Terho), Lotery, A.J. (Andrew), Leung, I. (Irene), Mauschitz, M. (Matthias), Merle, B. (Bénédicte), Meyer zu Westrup, V. (Verena), Midena, E. (Edoardo), Miotto, S. (Stefania), Mirshahi, A. (Alireza), Mohan-Saïd, S. (Sadek), Mueller, M. (Michael), Muldrew, A. (Alyson), Nunes, S. (Sandrina), Oexle, K. (Konrad), Peto, T. (Tünde), Rahi, J. (Jugnoo), Raitakari, O. (Olli), Ribeiro, L. (Luisa), Rougier, M.-B. (Marie-Bénédicte), Sahel, J.-A. (José-Alain), Salonikiou, A. (Aggeliki), Sanchez, C. (Clarisa), Schmitz-Valckenberg, S. (Steffen), Schweitzer, C.M.C. (C. M C), Shehata, J. (Jasmin), Silvestri, G. (Giuliana), Simader, C. (Christian), Souied, E.H. (Eric), Springelkamp, H. (Henriët), Tapp, R. (Robyn), Verhoeven, V. (Virginie), Von Hanno, T. (Therese), Vujosevic, S. (Stela), Williams, K. (Katie), Wolfram, C. (Christian), Yip, J. (Jennifer), Zerbib, J. (Jennyfer), Zwiener, I. (Isabella), Colijn, J.M. (Johanna), Buitendijk, G.H.S. (Gabrielle), Prokofyeva, E. (Elena), Alves, D. (Dalila), Cachulo, M.L. (Maria L.), Khawaja, A.P. (Anthony), Cougnard-Grégoire, A. (Audrey), Merle, B.M.J. (Bénédicte M.J.), Korb, C. (Christina), Erke, M.G. (Maja Gran), Bron, A. (Alain), Anastasopoulos, E. (Eleftherios), Meester-Smoor, M.A. (Magda), Segato, T. (Tatiana), Piermarocchi, S. (Stefano), Jong, P.T.V.M. (Paulus) de, Vingerling, J.R. (Hans), Topouzis, F. (Fotis), Creuzot-Garcher, C. (Catherine), Bertelsen, G. (Geir), Pfeiffer, A.F.H. (Andreas), Fletcher, A.E. (Astrid E.), Foster, P.J. (Paul), Silva, R. (Rufino), Korobelnik, J.-F. (Jean-François), Delcourt, C. (Cécile), Klaver, C.C.W. (Caroline), Ajana, S. (Soufiane), Arango-Gonzalez, B. (Blanca), Arndt, V. (Verena), Bhatia, V. (Vaibhav), Bhattacharya, S.S. (Shomi S.), Biarnés, M. (Marc), Borrell, A. (Anna), Bühren, S. (Sebastian), Calado, S.M. (Sofia M.), Colijn, J.M. (Johanna M.), Dammeier, S. (Sascha), Jong, E.K. (Eiko) de, De la Cerda, B. (Berta), den Hollander, A.I. (Anneke I.), Diaz-Corrales, F.J. (Francisco J.), Diether, S. (Sigrid), Emri, E. (Eszter), Endermann, T. (Tanja), Ferraro, L.L. (Lucia L.), Garcia, M. (Míriam), Heesterbeek, T.J. (Thomas J.), Honisch, S. (Sabina), Hoyng, C.B. (Carel B.), Kersten, E. (Eveline), Kilger, E. (Ellen), Klaver, C.C.W. (Caroline C.W.), Langen, H. (Hanno), Lengyel, I. (Imre), Luthert, P. (Phil), Maugeais, C. (Cyrille), Meester-Smoor, M. (Magda), Monés, J. (Jordi), Nogoceke, E. (Everson), Peto, T. (Tunde), Pool, F.M. (Frances M.), Rodríguez, E. (Eduardo), Ueffing, M. (Marius), Ulrich Bartz-Schmidt, K.U. (Karl U.), van Leeuwen, E.M. (Elisabeth M.), Verzijden, T. (Timo), Zumbansen, M. (Markus), Acar, N. (Niyazi), Anastosopoulos, E. (Eleftherios), Azuara-Blanco, A. (Augusto), Bergen, A.A.B. (Arthur), Binquet, C. (Christine), Bird, A.C. (Alan), Bretillon, L. (Lionel), Buitendijk, G. (Gabrielle), Cachulo, M.L. (Maria Luz), Chakravarthy, U. (Usha), Chan, M. (Michelle), Chang, P. (Petrus), Colijn, J. (Johanna), Cumberland, P. (Phillippa), Cunha-Vaz, J. (José), Daien, V. (Vincent), Deak, G. (Gabor), Delyfer, M.-N. (Marie-Noëlle), Hollander, A.I. (Anneke), Dietzel, M. (Martha), Fauser, S. (Sascha), Finger, R. (Robert), Fletcher, A. (Astrid), Foster, P.J. (Paul J.), Founti, P. (Panayiota), Göbel, A. (Arno), Gorgels, T.G.M.F. (Theo), Grauslund, J. (Jakob), Grus, F. (Franz), Hammond, C.J. (Christopher), Helmer, C. (Catherine), Hense, H.-W. (Hans-Werner), Hermann, M. (Manuel), Hoehn, R. (René), Hogg, R. (Ruth), Holz, F.G. (Frank), Hoyng, C.B. (Carel), Jansonius, N.M. (Nomdo), Janssen, S.F. (Sarah), Khawaja, A. (Anthony), Lamparter, J. (Julia), Le Goff, M. (Mélanie), Leal, S. (Sergio), Lechanteur, Y.T.E. (Yara T. E.), Lehtimäki, T. (Terho), Lotery, A.J. (Andrew), Leung, I. (Irene), Mauschitz, M. (Matthias), Merle, B. (Bénédicte), Meyer zu Westrup, V. (Verena), Midena, E. (Edoardo), Miotto, S. (Stefania), Mirshahi, A. (Alireza), Mohan-Saïd, S. (Sadek), Mueller, M. (Michael), Muldrew, A. (Alyson), Nunes, S. (Sandrina), Oexle, K. (Konrad), Peto, T. (Tünde), Rahi, J. (Jugnoo), Raitakari, O. (Olli), Ribeiro, L. (Luisa), Rougier, M.-B. (Marie-Bénédicte), Sahel, J.-A. (José-Alain), Salonikiou, A. (Aggeliki), Sanchez, C. (Clarisa), Schmitz-Valckenberg, S. (Steffen), Schweitzer, C.M.C. (C. M C), Shehata, J. (Jasmin), Silvestri, G. (Giuliana), Simader, C. (Christian), Souied, E.H. (Eric), Springelkamp, H. (Henriët), Tapp, R. (Robyn), Verhoeven, V. (Virginie), Von Hanno, T. (Therese), Vujosevic, S. (Stela), Williams, K. (Katie), Wolfram, C. (Christian), Yip, J. (Jennifer), Zerbib, J. (Jennyfer), and Zwiener, I. (Isabella)
- Abstract
Purpose Age-related macular degeneration (AMD) is a frequent, complex disorder in elderly of European ancestry. Risk profiles and treatment options have changed considerably over the years, which may have affected disease prevalence and outcome. We determined the prevalence of early and late AMD in Europe from 1990 to 2013 using the European Eye Epidemiology (E3) consortium, and made projections for the future. Design Meta-analysis of prevalence data. Participants A total of 42 080 individuals 40 years of age and older participating in 14 population-based cohorts from 10 countries in Europe. Methods AMD was diagnosed based on fundus photographs using the Rotterdam Classification. Prevalence of early and late AMD was calculated using random-effects meta-analysis stratified for age, birth cohort, gender, geographic region, and time period of the study. Best-corrected visual acuity (BCVA) was compared between late AMD subtypes; geographic atrophy (GA) and choroidal neovascularization (CNV). Main Outcome Measures Prevalence of early and late AMD, BCVA, and number of AMD cases. Results Prevalence of early AMD increased from 3.5% (95% confidence interval [CI] 2.1%–5.0%) in those aged 55–59 years to 17.6% (95% C
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- 2017
- Full Text
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90. Associations with intraocular pressure across Europe: The European Eye Epidemiology (E3) Consortium
- Author
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Khawaja, A.P. (Anthony), Springelkamp, H. (Henriët), Creuzot-Garcher, C. (Catherine), Delcourt, C. (Cécile), Hofman, A. (Albert), Höhn, R. (René), Iglesias González, A.I. (Adriana), Wolfs, R.C.W. (Roger), Korobelnik, J.-F. (Jean-François), Silva, R. (Rufino), Topouzis, F. (Fotis), Williams, K.M. (Katie M.), Bron, A. (Alain), Buitendijk, G.H.S. (Gabrielle), Cachulo, M.L. (Maria da Luz), Cougnard-Grégoire, A. (Audrey), Dartigues, J.-F., Hammond, C.J. (Christopher J.), Pfeiffer, A.F.H. (Andreas), Salonikiou, A. (Angeliki), van Duijn, C.M. (Cornelia M.), Vingerling, J.R. (Hans), Luben, R.N. (Robert), Mirshahi, A. (Alireza), Lamparter, J. (Julia), Klaver, C.C.W. (Caroline), Jansonius, N.M. (Nomdo M.), Foster, P.J. (Paul), Khawaja, A.P. (Anthony), Springelkamp, H. (Henriët), Creuzot-Garcher, C. (Catherine), Delcourt, C. (Cécile), Hofman, A. (Albert), Höhn, R. (René), Iglesias González, A.I. (Adriana), Wolfs, R.C.W. (Roger), Korobelnik, J.-F. (Jean-François), Silva, R. (Rufino), Topouzis, F. (Fotis), Williams, K.M. (Katie M.), Bron, A. (Alain), Buitendijk, G.H.S. (Gabrielle), Cachulo, M.L. (Maria da Luz), Cougnard-Grégoire, A. (Audrey), Dartigues, J.-F., Hammond, C.J. (Christopher J.), Pfeiffer, A.F.H. (Andreas), Salonikiou, A. (Angeliki), van Duijn, C.M. (Cornelia M.), Vingerling, J.R. (Hans), Luben, R.N. (Robert), Mirshahi, A. (Alireza), Lamparter, J. (Julia), Klaver, C.C.W. (Caroline), Jansonius, N.M. (Nomdo M.), and Foster, P.J. (Paul)
- Abstract
Raised intraocular pressure (IOP) is the most important risk factor for developing glaucoma, the second commonest cause of blindness globally. Understanding associations with IOP and variations in IOP between countries may teach us about mechanisms underlying glaucoma. We examined cross-sectional associations with IOP in 43,500 European adults from 12 cohort studies belonging to the European Eye Epidemiology (E3) consortium. Each study conducted multivariable linear regression with IOP as the outcome variable and results were pooled using random effects meta-analysis. The association of standardized study IOP with latitude was tested using meta-regression. Higher IOP was observed in men (0.18 mmHg; 95 % CI 0.06, 0.31; P = 0.004) and with higher body mass index (0.21 mmHg per 5 kg/m2; 95 % CI 0.14, 0.28; P < 0.001), shorter height (−0.17 mmHg per 10 cm; 95 % CI –0.25, −0.08; P < 0.001), higher systolic blood pressure (0.17 mmHg per 10 mmHg; 95 % CI 0.12, 0.22; P < 0.001) and more myopic refraction (0.06 mmHg per Dioptre; 95 % CI 0.03, 0.09; P < 0.001). An inverted U-shaped trend was observed between age and IOP, with IOP increasing up to the age of 60 and decreasing in participants older than 70 years. We found no significant association between standardized IOP and study location latitude (P = 0.76). Novel findings of our study include the association of lower IOP in taller people and an inverted-U shaped association of IOP with age. We found no evidence of significant variation in IOP across Europe. Despite the limited range of latitude amongst included studies, this finding is in favour of collaborative pooling of data from studies examining environmental and genetic determinants of IOP in Europeans.
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- 2016
- Full Text
- View/download PDF
91. Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
- Author
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Fan, Q. (Qiao), Verhoeven, V.J.M. (Virginie), Wojciechowski, R. (Robert), Barathi, V.A. (Veluchamy), Hysi, P.G. (Pirro), Guggenheim, J. (Jean), Höhn, R. (René), Vitart, V. (Veronique), Khawaja, A.P. (Anthony P.), Yamashiro, K. (Kenji), Hosseini, S.M. (S Mohsen), Lehtimäki, T. (Terho), Lu, Y. (Yi), Haller, T. (Toomas), Xie, J. (Jing), Delcourt, C. (Cécile), Pirastu, M. (Mario), Wedenoja, J. (Juho), Gharahkhani, P. (Puya), Venturini, C. (Cristina), Miyake, M. (Masahiro), Hewit, A.W. (Alex), Guo, X. (Xiaobo), Mazur, J. (Johanna), Huffman, J.E. (Jenifer E.), Williams, K.M. (Katie M.), Polasek, O. (Ozren), Campbell, H. (Harry), Rudan, I. (Igor), Vatavuk, Z. (Zoran), Wilson, J.F. (James F), Joshi, P.K. (Peter), Mcmahon, G. (George), St Pourcain, B. (Beate), Evans, D.M. (David), Simpson, C.L. (Claire), Schwantes-An, T.-H. (Tae-Hwi), Igo Jr., R.P. (Robert), Mirshahi, A. (Alireza), Cougnard-Grégoire, A. (Audrey), Bellenguez, C. (Céline), Blettner, M. (Maria), Raitakari, O. (Olli), Kähönen, M. (Mika), Seppälä, I. (Ilkka), Zeller, T. (Tanja), Meitinger, T. (Thomas), Ried, J.S. (Janina), Gieger, C. (Christian), Portas, L. (Laura), Leeuwen, E.M. (Elisa) van, Amin, N. (Najaf), Uitterlinden, A.G. (André), Rivadeneira Ramirez, F. (Fernando), Hofman, A. (Albert), Vingerling, J.R. (Hans), Wang, Y. (Ying), Wang, X. (Xu), Tai-Hui Boh, E. (Eileen), Ikram, M.K. (Kamran), Sabanayagam, C. (Charumathi), Gupta, P. (Preeti), Tan, V. (Vincent), Zhou, L. (Lei), Ho, C.E.H. (Candice E. H.), Lim, W. (Wan'E), Beuerman, R.W. (Roger W.), Siantar, R. (Rosalynn), Tai, E.-S. (E-Shyong), Vithana, E.N. (Eranga), Mihailov, E. (Evelin), Khor, C.C., Hayward, C. (Caroline), Luben, R.N. (Robert), Foster, P.J. (Paul), Klein, B.E.K. (Barbara), Klein, R. (Ronald), Wong, H.-S. (Hoi-Suen), Mitchell, P. (Paul), Metspalu, A. (Andres), Aung, T. (Tin), Young, T.L. (Terri L.), He, M. (Mingguang), Pärssinen, O. (Olavi), Duijn, C.M. (Cornelia) van, Jin Wang, J. (Jie), Williams, C. (Cathy), Jonas, J.B. (Jost B.), Teo, Y.Y. (Yik Ying), Mackey, D.A. (David), Oexle, K. (Konrad), Yoshimura, N., Paterson, A.D. (Andrew D.), Pfeiffer, N. (Norbert), Wong, T.Y. (Tien Yin), Baird, P.N. (Paul), Stambolian, D. (Dwight), Wilson, J.E.B. (Joan E. Bailey), Cheng, C-Y. (Ching-Yu), Hammond, C.J. (Christopher J.), Klaver, C.C.W. (Caroline), Saw, S-M. (Seang-Mei), Rahi, J.S. (Jugnoo), Korobelnik, J.-F. (Jean-François), Kemp, J.P. (John), Timpson, N.J. (Nicholas), Smith, A.V. (Davey), Craig, J.E. (Jamie E.), Burdon, K.P. (Kathryn P.), Fogarty, R. (Rhys), Iyengar, S.K. (Sudha), Chew, E.Y. (Emily), Janmahasatian, S. (Sarayut), Martin, N.G. (Nicholas), MacGregor, S. (Stuart), Xu, L. (Liang), Schache, M. (Maria), Nangia, M. (Monika), Panda-Jonas, S. (Songhomitra), Wright, A.F. (Alan), Fondran, J.R. (Jeremy R.), Lass, J.H. (Jonathan H.), Feng, S. (Sheng), Zhao, J.H. (Jing Hua), Khaw, K.T., Wareham, N.J. (Nick), Rantanen, T. (Taina), Kaprio, J. (Jaakko), Pang, C.P. (Chi Pui), Chen, L.J. (Li Jia), Tam, P.O. (Pancy O.), Jhanji, V. (Vishal), Young, A.L. (Alvin L.), Döring, A. (Angela), Raffel, L.J. (Leslie), Cotch, M.-F. (Mary-Frances), Li, X. (Xiaohui), Yip, S.P. (Shea Ping), Yap, M.K.H. (Maurice K.H.), Biino, G. (Ginevra), Vaccargiu, S. (Simona), Fossarello, M. (Maurizio), Fleck, B. (Brian), Yazar, S. (Seyhan), Tideman, J.W.L. (Willem), Tedja, M. (Milly), Léveillard, T. (Thierry), Morrison, M.A. (Margaux A.), Farrer, L.A. (Lindsay), Zhou, X. (Xiangtian), Chen, W. (Wei), Mizuki, N. (Nobuhisa), Meguro, A. (Akira), Makela, K.M. (Kari Matti), Fan, Q. (Qiao), Verhoeven, V.J.M. (Virginie), Wojciechowski, R. (Robert), Barathi, V.A. (Veluchamy), Hysi, P.G. (Pirro), Guggenheim, J. (Jean), Höhn, R. (René), Vitart, V. (Veronique), Khawaja, A.P. (Anthony P.), Yamashiro, K. (Kenji), Hosseini, S.M. (S Mohsen), Lehtimäki, T. (Terho), Lu, Y. (Yi), Haller, T. (Toomas), Xie, J. (Jing), Delcourt, C. (Cécile), Pirastu, M. (Mario), Wedenoja, J. (Juho), Gharahkhani, P. (Puya), Venturini, C. (Cristina), Miyake, M. (Masahiro), Hewit, A.W. (Alex), Guo, X. (Xiaobo), Mazur, J. (Johanna), Huffman, J.E. (Jenifer E.), Williams, K.M. (Katie M.), Polasek, O. (Ozren), Campbell, H. (Harry), Rudan, I. (Igor), Vatavuk, Z. (Zoran), Wilson, J.F. (James F), Joshi, P.K. (Peter), Mcmahon, G. (George), St Pourcain, B. (Beate), Evans, D.M. (David), Simpson, C.L. (Claire), Schwantes-An, T.-H. (Tae-Hwi), Igo Jr., R.P. (Robert), Mirshahi, A. (Alireza), Cougnard-Grégoire, A. (Audrey), Bellenguez, C. (Céline), Blettner, M. (Maria), Raitakari, O. (Olli), Kähönen, M. (Mika), Seppälä, I. (Ilkka), Zeller, T. (Tanja), Meitinger, T. (Thomas), Ried, J.S. (Janina), Gieger, C. (Christian), Portas, L. (Laura), Leeuwen, E.M. (Elisa) van, Amin, N. (Najaf), Uitterlinden, A.G. (André), Rivadeneira Ramirez, F. (Fernando), Hofman, A. (Albert), Vingerling, J.R. (Hans), Wang, Y. (Ying), Wang, X. (Xu), Tai-Hui Boh, E. (Eileen), Ikram, M.K. (Kamran), Sabanayagam, C. (Charumathi), Gupta, P. (Preeti), Tan, V. (Vincent), Zhou, L. (Lei), Ho, C.E.H. (Candice E. H.), Lim, W. (Wan'E), Beuerman, R.W. (Roger W.), Siantar, R. (Rosalynn), Tai, E.-S. (E-Shyong), Vithana, E.N. (Eranga), Mihailov, E. (Evelin), Khor, C.C., Hayward, C. (Caroline), Luben, R.N. (Robert), Foster, P.J. (Paul), Klein, B.E.K. (Barbara), Klein, R. (Ronald), Wong, H.-S. (Hoi-Suen), Mitchell, P. (Paul), Metspalu, A. (Andres), Aung, T. (Tin), Young, T.L. (Terri L.), He, M. (Mingguang), Pärssinen, O. (Olavi), Duijn, C.M. (Cornelia) van, Jin Wang, J. (Jie), Williams, C. (Cathy), Jonas, J.B. (Jost B.), Teo, Y.Y. (Yik Ying), Mackey, D.A. (David), Oexle, K. (Konrad), Yoshimura, N., Paterson, A.D. (Andrew D.), Pfeiffer, N. (Norbert), Wong, T.Y. (Tien Yin), Baird, P.N. (Paul), Stambolian, D. (Dwight), Wilson, J.E.B. (Joan E. Bailey), Cheng, C-Y. (Ching-Yu), Hammond, C.J. (Christopher J.), Klaver, C.C.W. (Caroline), Saw, S-M. (Seang-Mei), Rahi, J.S. (Jugnoo), Korobelnik, J.-F. (Jean-François), Kemp, J.P. (John), Timpson, N.J. (Nicholas), Smith, A.V. (Davey), Craig, J.E. (Jamie E.), Burdon, K.P. (Kathryn P.), Fogarty, R. (Rhys), Iyengar, S.K. (Sudha), Chew, E.Y. (Emily), Janmahasatian, S. (Sarayut), Martin, N.G. (Nicholas), MacGregor, S. (Stuart), Xu, L. (Liang), Schache, M. (Maria), Nangia, M. (Monika), Panda-Jonas, S. (Songhomitra), Wright, A.F. (Alan), Fondran, J.R. (Jeremy R.), Lass, J.H. (Jonathan H.), Feng, S. (Sheng), Zhao, J.H. (Jing Hua), Khaw, K.T., Wareham, N.J. (Nick), Rantanen, T. (Taina), Kaprio, J. (Jaakko), Pang, C.P. (Chi Pui), Chen, L.J. (Li Jia), Tam, P.O. (Pancy O.), Jhanji, V. (Vishal), Young, A.L. (Alvin L.), Döring, A. (Angela), Raffel, L.J. (Leslie), Cotch, M.-F. (Mary-Frances), Li, X. (Xiaohui), Yip, S.P. (Shea Ping), Yap, M.K.H. (Maurice K.H.), Biino, G. (Ginevra), Vaccargiu, S. (Simona), Fossarello, M. (Maurizio), Fleck, B. (Brian), Yazar, S. (Seyhan), Tideman, J.W.L. (Willem), Tedja, M. (Milly), Léveillard, T. (Thierry), Morrison, M.A. (Margaux A.), Farrer, L.A. (Lindsay), Zhou, X. (Xiangtian), Chen, W. (Wei), Mizuki, N. (Nobuhisa), Meguro, A. (Akira), and Makela, K.M. (Kari Matti)
- Abstract
Myopia is the most common human eye disorder and it results from complex genetic and environmental causes. The rapidly increasing prevalence of myopia poses a major public health challenge. Here, the CREAM consortium performs a joint meta-analysis to test single-nucleotide polymorphism (SNP) main effects and SNP × education interaction effects on refractive error in 40,036 adults from 25 studies of European ancestry and 10,315 adults from 9 studies of Asian ancestry. In European ancestry individuals, we identify six novel loci (FAM150B-ACP1, LINC00340, FBN1, DIS3L-MAP2K1, ARID2-SNAT1 and SLC14A2) associated with refractive error. In Asian populations, three genome-wide significant loci AREG, GABRR1 and PDE10A also exhibit strong interactions with education (P<8.5 × 10-5), whereas the interactions are less evident in Europeans. The discovery of these loci represents an important advance in understanding how gene and environment interactions contribute to the heterogeneity of myopia.
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- 2016
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92. Associations with intraocular pressure across Europe: The European Eye Epidemiology (E3) Consortium.
- Author
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Khawaja, AP, Springelkamp, H, Creuzot-Garcher, C, Delcourt, C, Hofman, A, Höhn, R, Iglesias, AI, Wolfs, RCW, Korobelnik, J-F, Silva, R, Topouzis, F, Williams, KM, Bron, AM, Buitendijk, GHS, Cachulo, MDL, Cougnard-Grégoire, A, Dartigues, J-F, Hammond, CJ, Pfeiffer, N, Salonikiou, A, van Duijn, CM, Vingerling, JR, Luben, RN, Mirshahi, A, Lamparter, J, Klaver, CCW, Jansonius, NM, Foster, PJ, European Eye Epidemiology (E³) Consortium, Khawaja, AP, Springelkamp, H, Creuzot-Garcher, C, Delcourt, C, Hofman, A, Höhn, R, Iglesias, AI, Wolfs, RCW, Korobelnik, J-F, Silva, R, Topouzis, F, Williams, KM, Bron, AM, Buitendijk, GHS, Cachulo, MDL, Cougnard-Grégoire, A, Dartigues, J-F, Hammond, CJ, Pfeiffer, N, Salonikiou, A, van Duijn, CM, Vingerling, JR, Luben, RN, Mirshahi, A, Lamparter, J, Klaver, CCW, Jansonius, NM, Foster, PJ, and European Eye Epidemiology (E³) Consortium
- Abstract
Raised intraocular pressure (IOP) is the most important risk factor for developing glaucoma, the second commonest cause of blindness globally. Understanding associations with IOP and variations in IOP between countries may teach us about mechanisms underlying glaucoma. We examined cross-sectional associations with IOP in 43,500 European adults from 12 cohort studies belonging to the European Eye Epidemiology (E3) consortium. Each study conducted multivariable linear regression with IOP as the outcome variable and results were pooled using random effects meta-analysis. The association of standardized study IOP with latitude was tested using meta-regression. Higher IOP was observed in men (0.18 mmHg; 95 % CI 0.06, 0.31; P = 0.004) and with higher body mass index (0.21 mmHg per 5 kg/m2; 95 % CI 0.14, 0.28; P < 0.001), shorter height (-0.17 mmHg per 10 cm; 95 % CI -0.25, -0.08; P < 0.001), higher systolic blood pressure (0.17 mmHg per 10 mmHg; 95 % CI 0.12, 0.22; P < 0.001) and more myopic refraction (0.06 mmHg per Dioptre; 95 % CI 0.03, 0.09; P < 0.001). An inverted U-shaped trend was observed between age and IOP, with IOP increasing up to the age of 60 and decreasing in participants older than 70 years. We found no significant association between standardized IOP and study location latitude (P = 0.76). Novel findings of our study include the association of lower IOP in taller people and an inverted-U shaped association of IOP with age. We found no evidence of significant variation in IOP across Europe. Despite the limited range of latitude amongst included studies, this finding is in favour of collaborative pooling of data from studies examining environmental and genetic determinants of IOP in Europeans.
- Published
- 2016
93. Optic Radiations Microstructural Changes in Glaucoma and Association With Severity: A Study Using 3Tesla-Magnetic Resonance Diffusion Tensor Imaging
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Tellouck, Laury, primary, Durieux, Muriel, additional, Coupé, Pierrick, additional, Cougnard-Grégoire, Audrey, additional, Tellouck, Joy, additional, Tourdias, Thomas, additional, Munsch, Fanny, additional, Garrigues, Arnaud, additional, Helmer, Catherine, additional, Malet, Florence, additional, Dartigues, Jean-François, additional, Dousset, Vincent, additional, Delcourt, Cécile, additional, and Schweitzer, Cédric, additional
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- 2016
- Full Text
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94. Olive Oil Consumption and Age-Related Macular Degeneration: The Alienor Study
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Cougnard-Grégoire, Audrey, primary, Merle, Bénédicte M. J., additional, Korobelnik, Jean-François, additional, Rougier, Marie-Bénédicte, additional, Delyfer, Marie-Noëlle, additional, Le Goff, Mélanie, additional, Samieri, Cécilia, additional, Dartigues, Jean-François, additional, and Delcourt, Cécile, additional
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- 2016
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95. Multimodal Imaging of Reticular Pseudodrusen in a Population-Based Setting: The Alienor Study
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Chan, Hélène, primary, Cougnard-Grégoire, Audrey, additional, Delyfer, Marie-Noëlle, additional, Combillet, France, additional, Rougier, Marie-Bénédicte, additional, Schweitzer, Cédric, additional, Dartigues, Jean-François, additional, Korobelnik, Jean-François, additional, and Delcourt, Cécile, additional
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- 2016
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96. P240 Accumulation de produits de glycation avancée et maladie rénale chronique chez les patients diabétiques de type 2
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C. Gonzalez, S. Nov, E. Maury, A. Cougnard-Grégoire, S. Lorrain, H. Gin, and P. Barberger-Gateau
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Endocrinology ,Endocrinology, Diabetes and Metabolism ,Internal Medicine ,General Medicine - Abstract
Introduction Avec l’âge, les produits de glycation avancee (AGE) s’accumulent, en cas de diabete par production acceleree, ou d’insuffisance renale par l’elimination reduite de leurs precurseurs. Notre objectif etait d’analyser si l’autofluorescence cutanee (AF), marqueur du depot tissulaire des AGE, etait elevee chez les patients diabetiques de type 2 (DT2) porteurs de maladie renale chronique (MRC). Patients et methodes Nous avons mesure l’AF (AGE-Reader, Diagnoptics) chez 472 patients hospitalises pour DT2. Nous avons recueilli leur excretion urinaire d’albumine (EUA), debit de filtration glomerulaire (DFG, EPI-CKD), la presence d’un traitement bloqueur du SRA ainsi que d’une macroangiopathie (infarctus, AVC, gangrene ou revascularisation). L’association entre l’atteinte renale et l’AF a ete etudiee par regression lineaire ajustee sur l’âge. Les resultats sont exprimes en moyenne (ET). Resultats Les 472 patients (hommes 58 %), âges de 62 (10) ans, avaient un diabete depuis 13 (9) ans, un BMI de 32,5 (5,9) kg/m 2 , une HbA1C a 8,9 (1,8) %. Les 191 patients porteurs d’une MRC avaient une AF elevee : 2,67 (0,66) A.U. vs 2,37 (0,50) (p 130 mL/min/1,73 m 2 , AF = 1,43 (0,46), p Conclusion L’autofluorescence cutanee est associee a l’atteinte renale des patients DT2. L’accumulation des AGE favorise les lesions renales et l’albuminurie, puis s’aggrave avec l’insuffisance renale, contribuant a la macroangiopathie.
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- 2014
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97. Prevalence of refractive error in Europe: the European Eye Epidemiology (E3) Consortium
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Williams, K.M. (Katie M.), Verhoeven, V.J.M. (Virginie), Cumberland, P. (Phillippa), Bertelsen, G. (Geir), Wolfram, C. (Christian), Buitendijk, G.H.S. (Gabrielle), Hofman, A. (Albert), Duijn, C.M. (Cornelia) van, Vingerling, J.R. (Hans), Kuijpers, R.W.A.M. (Robert), Höhn, R. (René), Mirshahi, A. (Alireza), Khawaja, A.P. (Anthony P.), Luben, R.N. (Robert N.), Erke, M.G. (Maja Gran), Von Hanno, T. (Therese), Mahroo, O. (Omar), Hogg, R. (Ruth), Gieger, C. (Christian), Cougnard-Grégoire, A. (Audrey), Anastasopoulos, E. (Eleftherios), Bron, A. (Alain), Dartigues, J.-F., Korobelnik, J.-F. (Jean-François), Creuzot-Garcher, C. (Catherine), Topouzis, F. (Fotis), Delcourt, C. (Cécile), Rahi, J.S. (Jugnoo), Meitinger, T. (Thomas), Fletcher, A. (Astrid), Foster, P.J. (Paul J.), Pfeiffer, N. (Norbert), Klaver, C.C.W. (Caroline), Hammond, C.J. (Christopher), Williams, K.M. (Katie M.), Verhoeven, V.J.M. (Virginie), Cumberland, P. (Phillippa), Bertelsen, G. (Geir), Wolfram, C. (Christian), Buitendijk, G.H.S. (Gabrielle), Hofman, A. (Albert), Duijn, C.M. (Cornelia) van, Vingerling, J.R. (Hans), Kuijpers, R.W.A.M. (Robert), Höhn, R. (René), Mirshahi, A. (Alireza), Khawaja, A.P. (Anthony P.), Luben, R.N. (Robert N.), Erke, M.G. (Maja Gran), Von Hanno, T. (Therese), Mahroo, O. (Omar), Hogg, R. (Ruth), Gieger, C. (Christian), Cougnard-Grégoire, A. (Audrey), Anastasopoulos, E. (Eleftherios), Bron, A. (Alain), Dartigues, J.-F., Korobelnik, J.-F. (Jean-François), Creuzot-Garcher, C. (Catherine), Topouzis, F. (Fotis), Delcourt, C. (Cécile), Rahi, J.S. (Jugnoo), Meitinger, T. (Thomas), Fletcher, A. (Astrid), Foster, P.J. (Paul J.), Pfeiffer, N. (Norbert), Klaver, C.C.W. (Caroline), and Hammond, C.J. (Christopher)
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To estimate the prevalence of refractive error in adults across Europe. Refractive data (mean spherical equivalent) collected between 1990 and 2013 from fifteen population-based cohort and cross-sectional studies of the European Eye Epidemiology (E3) Consortium were combined in a random effects meta-analysis stratified by 5-year age intervals and gender. Participants were excluded if they were identified as having had cataract surgery, retinal detachment, refractive surgery or other factors that might influence refraction. Estimates of refractive error prevalence were obtained including the following classifications: myopia ≤−0.75 diopters (D), high myopia ≤−6D, hyperopia ≥1D and astigmatism ≥1D. Meta-analysis of refractive error was performed for 61,946 individuals from fifteen studies with median age ranging from 44 to 81 and minimal ethnic variation (98 % European ancestry). The age-standardised prevalences (using the 2010 European Standard Population, limited to those ≥25 and <90 years old) were: myopia 30.6 % [95 % confidence interval (CI) 30.4–30.9], high myopia 2.7 % (95 % CI 2.69–2.73), hyperopia 25.2 % (95 % CI 25.0–25.4) and astigmatism 23.9 % (95 % CI 23.7–24.1). Age-specific estimates revealed a high prevalence of myopia in younger participants [47.2 % (CI 41.8–52.5) in 25–29 years-olds]. Refractive error affects just over a half of European adults. The greatest burden of refractive error is due to myopia, with high prevalence rates in young adults. Using the 2010 European population estimates, we estimate there are 227.2 million people with myopia across Europe.
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- 2015
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98. Increasing Prevalence of Myopia in Europe and the Impact of Education
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Williams, K.M. (Katie M.), Bertelsen, G. (Geir), Cumberland, P. (Phillippa), Wolfram, C. (Christian), Verhoeven, V.J.M. (Virginie), Anastasopoulos, E. (Eleftherios), Buitendijk, G.H.S. (Gabrielle), Cougnard-Grégoire, A. (Audrey), Creuzot-Garcher, C. (Catherine), Erke, M.G. (Maja Gran), Hogg, R. (Ruth), Höhn, R. (René), Hysi, P.G. (Pirro), Khawaja, A.P. (Anthony P.), Korobelnik, J.-F. (Jean-François), Ried, J.S. (Janina), Vingerling, J.R. (Hans), Bron, A. (Alain), Dartigues, J.-F. (Jean-François), Fletcher, A. (Astrid), Hofman, A. (Albert), Kuijpers, R.W.A.M. (Robert), Luben, R.N. (Robert N.), Oxele, K. (Konrad), Topouzis, F. (Fotis), Von Hanno, T. (Therese), Mirshahi, A. (Alireza), Foster, P.J. (Paul J.), Duijn, C.M. (Cornelia) van, Pfeiffer, A.F.H. (Andreas), Delcourt, C. (Cécile), Klaver, C.C.W. (Caroline), Rahi, J.S. (Jugnoo), Hammond, C.J. (Christopher), Williams, K.M. (Katie M.), Bertelsen, G. (Geir), Cumberland, P. (Phillippa), Wolfram, C. (Christian), Verhoeven, V.J.M. (Virginie), Anastasopoulos, E. (Eleftherios), Buitendijk, G.H.S. (Gabrielle), Cougnard-Grégoire, A. (Audrey), Creuzot-Garcher, C. (Catherine), Erke, M.G. (Maja Gran), Hogg, R. (Ruth), Höhn, R. (René), Hysi, P.G. (Pirro), Khawaja, A.P. (Anthony P.), Korobelnik, J.-F. (Jean-François), Ried, J.S. (Janina), Vingerling, J.R. (Hans), Bron, A. (Alain), Dartigues, J.-F. (Jean-François), Fletcher, A. (Astrid), Hofman, A. (Albert), Kuijpers, R.W.A.M. (Robert), Luben, R.N. (Robert N.), Oxele, K. (Konrad), Topouzis, F. (Fotis), Von Hanno, T. (Therese), Mirshahi, A. (Alireza), Foster, P.J. (Paul J.), Duijn, C.M. (Cornelia) van, Pfeiffer, A.F.H. (Andreas), Delcourt, C. (Cécile), Klaver, C.C.W. (Caroline), Rahi, J.S. (Jugnoo), and Hammond, C.J. (Christopher)
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Purpose To investigate whether myopia is becoming more common across Europe and explore whether increasing education levels, an important environmental risk factor for myopia, might explain any temporal trend. Design Meta-analysis of population-based, cross-sectional studies from the European Eye Epidemiology (E3) Consortium. Participants The E3 Consortium is a collaborative network of epidemiological studies of common eye diseases in adults across Europe. Refractive data were available for 61 946 participants from 15 population-based studies performed between 1990 and 2013; participants had a range of median ages from 44 to 78 years. Methods Noncycloplegic refraction, year of birth, and highest educational level achieved were obtained for all participants. Myopia was defined as a mean spherical equivalent ≤-0.75 diopters. A random-effects meta-analysis of age-specific myopia prevalence was performed, with sequential analyses stratified by year of birth and highest level of educational attainment. Main Outcome Measures Variation in age-specific myopia prevalence for differing years of birth and educational level. Results There was a significant cohort effect for increasing myopia prevalence across more recent birth decades; age-standardized myopia prevalence increased from 17.8% (95% confidence interval [CI], 17.6-18.1) to 23.5% (95% CI, 23.2-23.7) in those born between 1910 and 1939 compared with 1940 and 1979 (P = 0.03). Education was significantly associated with myopia; for those completing primary, secondary, and higher education, the age-standardized prevalences were 25.4% (CI, 25.0-25.8), 29.1% (CI, 28.8-29.5), and 36.6% (CI, 36.1-37.2), respectively. Although more recent birth cohorts were more educated, this did not fully explain the cohort effect. Compared with the reference risk of participants born in the 1920s with only primary education, higher education or being born in the 1960s doubled the myopia prevalence ratio-2.43 (CI, 1.26
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- 2015
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99. Markers of glycation and neonatal hypoglycaemia in gestational diabetes mellitus.
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Foussard, N., Baillet‐Blanco, L., Poupon, P., Monlun, M., Mohammedi, K., Cougnard‐Grégoire, A., Delcourt, C., Helmer, C., and Rigalleau, V.
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BIOMARKERS ,BLOOD sugar monitoring ,GESTATIONAL diabetes ,FASTING ,GESTATIONAL age ,GLUCOSE tolerance tests ,GLYCOSYLATED hemoglobin ,HYPOGLYCEMIA ,NEONATAL diseases ,NEONATAL jaundice ,PREGNANCY complications ,RISK assessment ,ADVANCED glycation end-products ,GLYCEMIC control ,DISEASE complications ,DISEASE risk factors - Abstract
The authors discuss a report about the risk factors for neonatal hypoglycaemia in 767 women with gestational diabetes mellitus (GDM). Topics mentioned include intrauterine epigenetic modifications driven by early hyperglycaemia, an increase in advanced glycation end-products from no diabetes to early and regular GDM, and attributes of mothers with gestational diabetes according to the presence of neonatal hypoglycaemia in their newborn.
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- 2020
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100. Lifetime Exposure to Ambient Ultraviolet Radiation and the Risk for Cataract Extraction and Age-Related Macular Degeneration: The Alienor Study
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Delcourt, Cécile, primary, Cougnard-Grégoire, Audrey, additional, Boniol, Mathieu, additional, Carrière, Isabelle, additional, Doré, Jean-François, additional, Delyfer, Marie-Noëlle, additional, Rougier, Marie-Bénédicte, additional, Le Goff, Mélanie, additional, Dartigues, Jean-François, additional, Barberger-Gateau, Pascale, additional, and Korobelnik, Jean-François, additional
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- 2014
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