41 results on '"Wark, P.A."'
Search Results
2. Animal and translational models of SARS-CoV-2 infection and COVID-19.
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McCaughan G.W., Rudloff I., Nold M.F., Hansbro N.G., Kim R.Y., Donovan C., Liu G., Faiz A., Short K.R., Lyons J.G., Tate M.D., Gorrell M.D., Cole A., Moreno C., Couteur D., Hesselson D., Triccas J., Neely G.G., Gamble J.R., Simpson S.J., Saunders B.M., Oliver B.G., Britton W.J., Wark P.A., Nold-Petry C.A., Hansbro P.M., Johansen M.D., Irving A., Montagutelli X., McCaughan G.W., Rudloff I., Nold M.F., Hansbro N.G., Kim R.Y., Donovan C., Liu G., Faiz A., Short K.R., Lyons J.G., Tate M.D., Gorrell M.D., Cole A., Moreno C., Couteur D., Hesselson D., Triccas J., Neely G.G., Gamble J.R., Simpson S.J., Saunders B.M., Oliver B.G., Britton W.J., Wark P.A., Nold-Petry C.A., Hansbro P.M., Johansen M.D., Irving A., and Montagutelli X.
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COVID-19 is causing a major once-in-a-century global pandemic. The scientific and clinical community is in a race to define and develop effective preventions and treatments. The major features of disease are described but clinical trials have been hampered by competing interests, small scale, lack of defined patient cohorts and defined readouts. What is needed now is head-to-head comparison of existing drugs, testing of safety including in the background of predisposing chronic diseases, and the development of new and targeted preventions and treatments. This is most efficiently achieved using representative animal models of primary infection including in the background of chronic disease with validation of findings in primary human cells and tissues. We explore and discuss the diverse animal, cell and tissue models that are being used and developed and collectively recapitulate many critical aspects of disease manifestation in humans to develop and test new preventions and treatments.Copyright © 2020, Society for Mucosal Immunology.
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- 2020
3. Cancer Epidemiology
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Wark, P.A., primary and Peto, J., additional
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- 2008
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4. Animal and translational models of SARS-CoV-2 infection and COVID-19
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Johansen, M.D., primary, Irving, A., additional, Montagutelli, X., additional, Tate, M.D., additional, Rudloff, I., additional, Nold, M.F., additional, Hansbro, N.G., additional, Kim, R.Y., additional, Donovan, C., additional, Liu, G., additional, Faiz, A., additional, Short, K.R., additional, Lyons, J.G., additional, McCaughan, G.W., additional, Gorrell, M.D., additional, Cole, A., additional, Moreno, C., additional, Couteur, D., additional, Hesselson, D., additional, Triccas, J., additional, Neely, G.G., additional, Gamble, J.R., additional, Simpson, S.J., additional, Saunders, B.M., additional, Oliver, B.G., additional, Britton, W.J., additional, Wark, P.A., additional, Nold-Petry, C.A., additional, and Hansbro, P.M., additional
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- 2020
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5. Changes in the Gut Microbiome in Chronic Obstructive Pulmonary Disease
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Rehman, S.F., primary, Bowerman, K.L., additional, Lachner, N., additional, Budden, K.F., additional, Kim, R., additional, Wood, D.L., additional, Gellatly, S.L., additional, Wark, P.A., additional, Hugenholtz, P., additional, and Hansbro, P.M., additional
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- 2020
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6. Protocol for a systematic review and qualitative synthesis of information quality frameworks in eHealth
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Fadahunsi, K.P., Akinlua, J.T., O'Connor, S., Wark, P.A., Gallagher, J., Carroll, C., Majeed, A., and O'Donoghue, J.
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education ,information quality ,Telemedicine ,quality in health care ,Patient safety ,systematic review ,Health information ,framework ,Information quality (IQ) ,digital heatlh ,Protocol ,Humans ,eHealth ,Public Health ,health informatics ,Delivery of Health Care ,Medical Informatics ,Qualitative Research ,Introduction Electronic health (eHealth) ,Systematic Reviews as Topic - Abstract
Introduction: Electronic health (eHealth) applications have become a very large repository of health information which informs critical decisions relating to the diagnosis, treatment and prognosis of patients. Poor information quality (IQ) within eHealth may compromise patient safety. Evaluation of IQ in eHealth is therefore necessary to promote patient safety. An IQ framework specifies what aspects of information to assess and how to conduct the assessment. This systematic review aims to identify dimensions within existing IQ frameworks in eHealth and develop a new IQ framework for assessment of eHealth. Method and Analysis: We will search EMBASE, Medline, PubMed, Cumulative Index to Nursing and Allied Health Literature (CINAHL), Maternity and Infant Care, PsycINFO, Global Health, Scopus, ProQuest Dissertations and Theses Global, Health Management Information Consortium and reference lists of relevant publications for articles published in English until November 2018. Studies will be selected by two independent reviewers based on pre-specified eligibility criteria. Two reviewers will independently extract data in each eligible study using a pre-piloted Microsoft Excel data extraction form. Thematic synthesis will be employed to define IQ dimensions and develop a new IQ framework for eHealth. Ethics and Dissemination: Ethical approval is not required for this systematic review as primary data will not be collected. The result of the review will be disseminated through publication in an academic journal and scientific conferences. Keywords: Quality in healthcare, health informatics, telemedicine, systematic review, information quality Review Registration: PROSPERO CRD42018097142
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- 2019
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7. Measuring Engagement in eHealth and mHealth Behavior Change Interventions: Viewpoint of Methodologies
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Short, C.E. (Camille E.), DeSmet, A. (Ann), Woods, C. (Catherine), Williams, S.L. (Susan L.), Maher, C. (Carol), Middelweerd, A. (Anouk), Müller, A.M. (Andre Matthias), Wark, P.A. (Petra A.), Vandelanotte, C., Poppe, L. (Louise), Hingle, M.D. (Melanie D.), Crutzen, R. (Rik), Short, C.E. (Camille E.), DeSmet, A. (Ann), Woods, C. (Catherine), Williams, S.L. (Susan L.), Maher, C. (Carol), Middelweerd, A. (Anouk), Müller, A.M. (Andre Matthias), Wark, P.A. (Petra A.), Vandelanotte, C., Poppe, L. (Louise), Hingle, M.D. (Melanie D.), and Crutzen, R. (Rik)
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Engagement in electronic health (eHealth) and mobile health (mHealth) behavior change interventions is thought to be important for intervention effectiveness, though what constitutes engagement and how it enhances efficacy has been somewhat unclear in the literature. Recently published detailed definitions and conceptual models of engagement have helped to build consensus around a definition of engagement and improve our understanding of how engagement may influence effectiveness. This work has helped to establish a clearer research agenda. However, to test the hypotheses generated by the conceptual modules, we need to know how to measure engagement in a valid and reliable way. The aim of this viewpoint is to provide an overview of engagement measurement options that can be employed in eHealth and mHealth behavior change intervention evaluations, discuss methodological considerations, and provide direction for future research. To identify measures, we used snowball sampling, starting from systematic reviews of engagement research as well as those utilized in studies known to the authors. A wide range of methods to measure engagement were identified, including qualitative measures, self-report questionnaires, ecological momentary assessments, system usage data, sensor data, social media data, and psychophysiological measures. Each measurement method is appraised and examples are provided to illustrate possible use in eHealth and mHealth behavior change research. Recommendations for future research are provided, based on the limitations of current methods and the heavy reliance on system usage data as the sole assessment of engagement. The validation and adoption of a wider range of engagement measurements and their thoughtful application to the study of engagement are encouraged.
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- 2018
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8. Persistent induction of goblet cell differentiation in the airways: Therapeutic approaches
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Reid, A.T., Veerati, P.C., Gosens, R., Bartlett, N.W., Wark, P.A., Grainge, C.L., Stick, S.M., Kicic, Anthony, Moheimani, F., Hansbro, P.M., Knight, D.A., Reid, A.T., Veerati, P.C., Gosens, R., Bartlett, N.W., Wark, P.A., Grainge, C.L., Stick, S.M., Kicic, Anthony, Moheimani, F., Hansbro, P.M., and Knight, D.A.
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© 2017 Dysregulated induction of goblet cell differentiation results in excessive production and retention of mucus and is a common feature of several chronic airways diseases. To date, therapeutic strategies to reduce mucus accumulation have focused primarily on altering the properties of the mucus itself, or have aimed to limit the production of mucus-stimulating cytokines. Here we review the current knowledge of key molecular pathways that are dysregulated during persistent goblet cell differentiation and highlights both pre-existing and novel therapeutic strategies to combat this pathology.
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- 2018
9. DIET@NET: Best Practice Guidelines for dietary assessment in health research
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Cade, J.E., Warthon-Medina, M., Albar, S., Alwan, N.A., Ness, A., Roe, M., Wark, P.A., Greathead, K., Burley, V.J., Finglas, P., Johnson, L., Page, P., Roberts, K., Steer, T., Hooson, J., Greenwood, D.C., Robinson, S., and Consortium, DIETNET
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Public health ,Biomedical Research ,Consensus ,Delphi Technique ,Dietary assessment methods ,Nutritional epidemiology ,lcsh:R ,lcsh:Medicine ,Guideline ,Guidelines ,Diet ,Nutrition Assessment ,Humans ,Nutrition - Abstract
Background Dietary assessment is complex, and strategies to select the most appropriate dietary assessment tool (DAT) in epidemiological research are needed. The DIETary Assessment Tool NETwork (DIET@NET) aimed to establish expert consensus on Best Practice Guidelines (BPGs) for dietary assessment using self-report. Methods The BPGs were developed using the Delphi technique. Two Delphi rounds were conducted. A total of 131 experts were invited, and of these 65 accepted, with 48 completing Delphi round I and 51 completing Delphi round II. In all, a total of 57 experts from North America, Europe, Asia and Australia commented on the 47 suggested guidelines. Results Forty-three guidelines were generated, grouped into the following four stages: Stage I. Define what is to be measured in terms of dietary intake (what? who? and when?); Stage II. Investigate different types of DATs; Stage III. Evaluate existing tools to select the most appropriate DAT by evaluating published validation studies; Stage IV. Think through the implementation of the chosen DAT and consider sources of potential biases. Conclusions The Delphi technique consolidated expert views on best practice in assessing dietary intake. The BPGs provide a valuable guide for health researchers to choose the most appropriate dietary assessment method for their studies. These guidelines will be accessible through the Nutritools website, www.nutritools.org. Electronic supplementary material The online version of this article (doi:10.1186/s12916-017-0962-x) contains supplementary material, which is available to authorized users.
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- 2017
10. Systematic review and website presentation of validated dietary assessment tools
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Warthon-Medina, M., primary, Hooson, J., additional, Hancock, N., additional, Gibson, L.E., additional, Bush, L.A., additional, Hutchinson, J., additional, Greenwood, D.C., additional, Robinson, S., additional, Burley, V.J., additional, Roe, M., additional, Steer, T., additional, Wark, P.A., additional, and Cade, J.E., additional
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- 2018
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11. Nutritools.org an innovative website including a Food Questionnaire Creator for dietary assessment in health research
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Warthon-Medina, M., primary, Hooson, J., additional, Hancock, N., additional, Hutchinson, J., additional, Vargas-Garcia, E., additional, Gibson, L.E., additional, Bush, L.A., additional, Greathead, K., additional, Knowles, B., additional, Margetts, B., additional, Robinson, S., additional, Ness, A., additional, Alwan, N.A., additional, Wark, P.A., additional, Roe, M., additional, Finglas, P., additional, Steer, T., additional, Page, P., additional, Key, T., additional, Johnson, L., additional, Roberts, K., additional, Amoutzopoulos, B., additional, Burley, V.J., additional, Greenwood, D.C., additional, and Cade, J.E., additional
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- 2018
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12. Sleep timing and vegetable intakes in UK adults: a cross-sectional study
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Noorwali, E.A., primary, Potter, G.D.M., additional, Ford, H.E., additional, Mulla, U.Z., additional, Murphy, D., additional, Wark, P.A., additional, Frost, G.S., additional, Hardie, L.J., additional, and Cade, J.E., additional
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- 2018
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13. Influenza epidemiology in patients admitted to sentinel Australian hospitals in 2015: the Influenza Complications Alert Network.
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Bowler S.D., Kelly P.M., Upham J., Lessing A., Kotsimbos T., Cheng A.C., Holmes M., Dwyer D.E., Irving L.B., Korman T.M., Senenayake S., Macartney K.K., Blyth C.C., Brown S., Waterer G., Hewer R., Friedman N.D., Wark P.A., Simpson G., Bowler S.D., Kelly P.M., Upham J., Lessing A., Kotsimbos T., Cheng A.C., Holmes M., Dwyer D.E., Irving L.B., Korman T.M., Senenayake S., Macartney K.K., Blyth C.C., Brown S., Waterer G., Hewer R., Friedman N.D., Wark P.A., and Simpson G.
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The Influenza Complications Alert Network (FluCAN) is a sentinel hospital-based surveillance program that operates at sites in all states and territories in Australia. This report summarises the epidemiology of hospitalisations with laboratory-confirmed influenza during the 2015 influenza season. In this observational study, cases were defined as patients admitted to one of the sentinel hospitals with an acute respiratory illness with influenza confirmed by nucleic acid detection. During the period 1 April to 30 October 2015 (the 2015 influenza season), 2,070 patients were admitted with confirmed influenza to one of 17 FluCAN sentinel hospitals. Of these, 46% were elderly (>= 65 years), 15% were children (< 16 years), 5% were Indigenous Australians, 2.1% were pregnant and 75% had chronic co-morbidities. A high proportion were due to influenza B (51%). There were a large number of hospital admissions detected with confirmed influenza in this national observational surveillance system in 2015 with case numbers similar to that reported in 2014. The national immunisation program is estimated to avert 46% of admissions from confirmed influenza across all at-risk groups, but more complete vaccination coverage in target groups could further reduce influenza admissions by as much as 14%.
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- 2017
14. Physical activity and risk of Amyotrophic Lateral Sclerosis in a prospective cohort study
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Gallo, V. Vanacore, N. Bueno-de-Mesquita, H.B. Vermeulen, R. Brayne, C. Pearce, N. Wark, P.A. Ward, H.A. Ferrari, P. Jenab, M. Andersen, P.M. Wennberg, P. Wareham, N. Katzke, V. Kaaks, R. Weiderpass, E. Peeters, P.H. Mattiello, A. Pala, V. Barricante, A. Chirlaque, M.-D. Travier, N. Travis, R.C. Sanchez, M.-J. Pessah-Rasmussen, H. Petersson, J. Tjønneland, A. Tumino, R. Quiros, J.R. Trichopoulou, A. Kyrozis, A. Oikonomidou, D. Masala, G. Sacerdote, C. Arriola, L. Boeing, H. Vigl, M. Claver-Chapelon, F. Middleton, L. Riboli, E. Vineis, P.
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Previous case–control studies have suggested a possible increased risk of Amyotrophic Lateral Sclerosis (ALS) with physical activity (PA), but this association has never been studied in prospective cohort studies. We therefore assessed the association between PA and risk of death from ALS in the European Prospective Investigation into Cancer and Nutrition. A total of 472,100 individuals were included in the analysis, yielding 219 ALS deaths. At recruitment, information on PA was collected thorough standardised questionnaires. Total PA was expressed by the Cambridge Physical Activity Index (CPAI) and analysed in relation to ALS mortality, using Cox hazard models. Interactions with age, sex, and anthropometric measures were assessed. Total PA was weakly inversely associated with ALS mortality with a borderline statistically significant trend across categories (p = 0.042), with those physically active being 33 % less likely to die from ALS compared to those inactive: HR = 0.67 (95 % CI 0.42–1.06). Anthropometric measures, sex, and age did not modify the association with CPAI. The present study shows a slightly decreased—not increased like in case–control studies—risk of dying from ALS in those with high levels of total PA at enrolment. This association does not appear confounded by age, gender, anthropometry, smoking, and education. Ours was the first prospective cohort study on ALS and physical activity. © 2016, The Author(s).
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- 2016
15. 238 Outcomes of a cohort of cystic fibrosis patients infected between 1985–1992 with an Australian epidemic strain of Burkholderia cenocepacia
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Wark, P.A., primary and Cookson, K., additional
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- 2017
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16. Diet, lifestyle and risk of K-ras mutation-positive and -negative colorectal adenomas
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Wark, P.A., Wark, P.A., van der Kuil, W., Ploemacher, J., van Muijen, G.N.P., Mulder, C.J., Weijenberg, M.P., Kok, F.J., Kampman, E., Wark, P.A., Wark, P.A., van der Kuil, W., Ploemacher, J., van Muijen, G.N.P., Mulder, C.J., Weijenberg, M.P., Kok, F.J., and Kampman, E.
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K-ras mutation-positive (K-ras+) and -negative (K-ras-) colorectal adenomas may differ clinically and pathologically. As environmental compounds may cause mutations in the growth-related K-ras oncogene or affect clonal selection depending on mutational status, we evaluated whether the aetiology of K-ras+ and K-ras- adenomas differs. K-ras mutations in codons 12 and 13 were assessed in colorectal adenoma tissue (K-ras+: n = 81, K-ras-: n = 453). Dietary and lifestyle data were collected through questionnaires that were also administered to 709 polyp-free controls. Multiple logistic regression analyses showed that intake of vitamin B2 and monounsaturated fat were differently associated with risk of K-ras+ and K-ras- adenomas; vitamin B2 was inversely associated with K-ras- (highest vs. lowest tertile: odds ratio (OR) = 0.70, 95% confidence interval (CI) = 0.50-0.97, p trend = 0.020), but not with K-ras+ adenomas, and a positive association with monounsaturated fat was confined to K-ras- adenomas (OR = 1.57, 95% CI = 1.06-2.34, p trend = 0.029). Besides, potential, not statistically significant, differences in risk arose because red meat was distinctly positively associated with K-ras+ adenomas (OR = 1.70, 95% CI = 0.94-3.09, p trend = 0.061); total dietary and polyunsaturated fat tended to be inversely associated with risk of K-ras+ but not of K-ras- adenomas; inverse associations with dairy products, calcium, protein and tea were confined to K-ras- adenomas, and smoking was more markedly positively associated with K-ras- adenomas. No differences in risk of K-ras+ and K-ras- adenomas could be detected for other factors. In conclusion, dietary and lifestyle factors may influence risk of K-ras+ and K-ras- adenomas differently. However, epidemiological literature on diet, lifestyle and colorectal K-ras mutations is inconsistent
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- 2006
17. Fruits, vegetables, and hMLH1 protein-deficient and -proficient colon cancer: The Netherlands cohort study
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Wark, P.A., Wark, P.A., Weijenberg, M.P., van 't Veer, P., van Wijhe, G., Luchtenborg, M., van Muijen, G.N.P., de Goeij, A.F., Goldbohm, R.A., van den Brandt, P.A., Wark, P.A., Wark, P.A., Weijenberg, M.P., van 't Veer, P., van Wijhe, G., Luchtenborg, M., van Muijen, G.N.P., de Goeij, A.F., Goldbohm, R.A., and van den Brandt, P.A.
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BACKGROUND: Clinical and pathologic differences exist between colon carcinomas deficient and proficient in the mismatch repair protein hMLH1. Animal and in vitro studies suggest that fruits, vegetables, folate, and antioxidants are associated with colonic expression of mismatch repair genes.METHODS: Associations between consumption of fruits and vegetables and hMLH1 protein-deficient and -proficient colon cancer were evaluated in the Netherlands Cohort Study on diet and cancer using a case-cohort approach. A self-administered food frequency questionnaire was completed, in 1986, by 120,852 individuals ages 55 to 69 years. Using immunohistochemistry, hMLH1 protein expression was assessed in colon cancer tissue obtained from 441 patients who were identified over 7.3 years of follow-up excluding the initial 2.3 years. Incidence rate ratios (RR) were estimated for hMLH1 protein-deficient and -proficient colon cancer.RESULTS: hMLH1 protein expression was absent in 54 tumors (12.2%) and present in 387 tumors. Fruit consumption was associated with hMLH1 protein-deficient colon cancer [highest versus lowest tertile, RR, 0.46; 95% confidence interval (95% CI), 0.23-0.90; P(trend) = 0.029] but not with hMLH1 protein-proficient tumors (highest versus lowest tertile, RR, 1.03; 95% CI, 0.78-1.35; P(trend) = 0.81). Total consumption of vegetables was not associated with either type of tumor (hMLH1 protein deficient: RR, 0.86; 95% CI, 0.45-1.65; P(trend) = 0.67; hMLH1 protein proficient: RR, 0.94; 95% CI, 0.72-1.23; P(trend) = 0.72). No associations were observed for folate, fiber, antioxidants, or subgroups of vegetables.CONCLUSION: These analyses indicate that an inverse association between consumption of fruits and colon cancer may be confined to the subgroup of tumors with a deficient mismatch repair system.
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- 2005
18. Plasma and dietary carotenoids and vitamins A, C and E and risk of colon and rectal cancer in the European Prospective Investigation into Cancer and Nutrition
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Leenders, M., Leufkens, A.M., Siersema, P.D., Duijnhoven, F.J.B. van, Vrieling, A., Hulshof, P.J., Gils, C.H. van, Overvad, K., Roswall, N., Kyro, C., Boutron-Ruault, M.C., Fagerhazzi, G., Cadeau, C., Kuhn, T., Johnson, T., Boeing, H., Aleksandrova, K., Trichopoulou, A., Klinaki, E., Androulidaki, A., Palli, D., Grioni, S., Sacerdote, C., Tumino, R., Panico, S., Bakker, M.F., Skeie, G., Weiderpass, E., Jakszyn, P., Barricarte, A., Huerta, J. Maria, Molina-Montes, E., Arguelles, M., Johansson, I., Ljuslinder, I., Key, T.J., Bradbury, K.E., Khaw, K.T., Wareham, N.J., Ferrari, P., Duarte-Salles, T., Jenab, M., Gunter, M.J., Vergnaud, A.C., Wark, P.A., Bueno-De-Mesquita, H.B., Leenders, M, Leufkens, Am, Siersema, Pd, van Duijnhoven, Fj, Vrieling, A, Hulshof, Pj, van Gils, Ch, Overvad, K, Roswall, N, Kyr?, C, Boutron Ruault, Mc, Fagerhazzi, G, Cadeau, C, K?hn, T, Johnson, T, Boeing, H, Aleksandrova, K, Trichopoulou, A, Klinaki, E, Androulidaki, A, Palli, D, Grioni, S, Sacerdote, C, Tumino, R, Panico, Salvatore, Bakker, Mf, Skeie, G, Weiderpass, E, Jakszyn, P, Barricarte, A, Mar?a Huerta, J, Molina Montes, E, Arg?elles, M, Johansson, I, Ljuslinder, I, Key, Tj, Bradbury, Ke, Khaw, Kt, Wareham, Nj, Ferrari, P, Duarte Salles, T, Jenab, M, Gunter, Mj, Vergnaud, Ac, Wark, Pa, Bueno de Mesquita, Hb, LS IRAS EEPI GRA (Gezh.risico-analyse), IRAS RATIA2, and Risk Assessment of Toxic and Immunomodulatory Agents
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Adult ,Male ,Ascorbic Acid ,Antioxidants ,Fruits and vegetables ,Body Mass Index ,Risk Factors ,Surveys and Questionnaires ,Odds Ratio ,Humans ,Vitamin E ,Vitamin A ,Aged ,Rectal Neoplasms ,Incidence ,Vitamins ,Middle Aged ,Colorectal cancer ,Carotenoids ,Diet ,Europe ,Oxidative Stress ,Urological cancers Radboud Institute for Health Sciences [Radboudumc 15] ,Case-Control Studies ,Colonic Neoplasms ,Multivariate Analysis ,Female - Abstract
Item does not contain fulltext Carotenoids and vitamins A, C and E are possibly associated with a reduced colorectal cancer (CRC) risk through antioxidative properties. The association of prediagnostic plasma concentrations and dietary consumption of carotenoids and vitamins A, C and E with the risk of colon and rectal cancer was examined in this case-control study, nested within the European Prospective Investigation into Cancer and Nutrition study. Plasma concentrations of carotenoids (alpha- and beta-carotene, canthaxanthin, beta-cryptoxanthin, lutein, lycopene, zeaxanthin) and vitamins A (retinol), C and E (alpha-, beta- and gamma- and delta-tocopherol) and dietary consumption of beta-carotene and vitamins A, C and E were determined in 898 colon cancer cases, 501 rectal cancer cases and 1,399 matched controls. Multivariable conditional logistic regression models were performed to estimate incidence rate ratios (IRR) and corresponding 95% confidence intervals (CIs). An association was observed between higher prediagnostic plasma retinol concentration and a lower risk of colon cancer (IRR for highest quartile = 0.63, 95% CI: 0.46, 0.87, p for trend = 0.01), most notably proximal colon cancer (IRR for highest quartile = 0.46, 95% CI: 0.27, 0.77, p for trend = 0.01). Additionally, inverse associations for dietary beta-carotene and dietary vitamins C and E with (distal) colon cancer were observed. Although other associations were suggested, there seems little evidence for a role of these selected compounds in preventing CRC through their antioxidative properties.
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- 2014
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19. A Systematic Review of Systematic Reviews of Validated Dietary Assessment Tools
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Hooson, J., primary, Hancock, N., additional, Greenwood, D.C., additional, Robinson, S., additional, Burley, V.J., additional, Roe, M., additional, Steer, T., additional, Wark, P.A., additional, and Cade, J.E., additional
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- 2016
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20. Influenza epidemiology, vaccine coverage and vaccine effectiveness in sentinel Australian hospitals in 2013: the Influenza Complications Alert Network.
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Cheng A.C., Holmes M., Irving L.B., Korman T.M., Hunter C., Hewagama S., Friedman N.D., Wark P.A., Simpson G., Upham J.W., Bowler S.D., Senenayake S.N., Kotsimbos T.C., Kelly P.M., Dwyer D.E., Brown S.G., Waterer G.W., Cheng A.C., Holmes M., Irving L.B., Korman T.M., Hunter C., Hewagama S., Friedman N.D., Wark P.A., Simpson G., Upham J.W., Bowler S.D., Senenayake S.N., Kotsimbos T.C., Kelly P.M., Dwyer D.E., Brown S.G., and Waterer G.W.
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The National Influenza Program aims to reduce serious morbidity and mortality from influenza by providing public funding for vaccination to at-risk groups. The Influenza Complications Alert Network (FluCAN) is a sentinel hospital-based surveillance program that operates at 14 sites in all states and territories in Australia. This report summarises the epidemiology of hospitalisations with confirmed influenza, estimates vaccine coverage and influenza vaccine protection against hospitalisation with influenza during the 2013 influenza season. In this observational study, cases were defined as patients admitted to one of the sentinel hospitals, with influenza confirmed by nucleic acid testing. Controls were patients who had acute respiratory illnesses who were test-negative for influenza. Vaccine effectiveness was estimated as 1 minus the odds ratio of vaccination in case patients compared with control patients, after adjusting for known confounders. During the period 5 April to 31 October 2012, 631 patients were admitted with confirmed influenza at the 14 FluCAN sentinel hospitals. Of these, 31% were more than 65 years of age, 9.5% were Indigenous Australians, 4.3% were pregnant and 77% had chronic co-morbidities. Influenza B was detected in 30% of patients. Vaccination coverage was estimated at 81% in patients more than 65 years of age but only 49% in patients aged less than 65 years with chronic comorbidities. Vaccination effectiveness against hospitalisation with influenza was estimated at 50% (95% confidence interval: 33%, 63%, P<0.001). We detected a significant number of hospital admissions with confirmed influenza in a national observational study. Vaccine coverage was incomplete in at-risk groups, particularly non-elderly patients with medical comorbidities. Our results suggest that the seasonal influenza vaccine was moderately protective against hospitalisation with influenza in the 2013 season.Copyright This work is copyright. You may download, display, print
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- 2015
21. The social network of cystic fibrosis centre care and shared Pseudomonas aeruginosa strain infection: A cross-sectional analysis.
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Armstrong D.S., Price D., Ramsay K., Reid D.W., Robinson P.J., Rose B.R., Ryan G., Serisier D.J., Sloots T.P., Smith D.J., Wainwright C.E., Wark P.A., Whitehead B.F., Wilson J.W., Kidd T.J., Magalhaes R.J.S., Paynter S., Bell S.C., Grimwood K., Bye P.T., Cooper P.J., Dakin C.J., Elkins M.R., Feather I.H., Greville H., Harbour C., Hu H., Jaffe A., Martin J.A., McKay K.O., Marks G.B., Morton J.M., Nissen M.D., Armstrong D.S., Price D., Ramsay K., Reid D.W., Robinson P.J., Rose B.R., Ryan G., Serisier D.J., Sloots T.P., Smith D.J., Wainwright C.E., Wark P.A., Whitehead B.F., Wilson J.W., Kidd T.J., Magalhaes R.J.S., Paynter S., Bell S.C., Grimwood K., Bye P.T., Cooper P.J., Dakin C.J., Elkins M.R., Feather I.H., Greville H., Harbour C., Hu H., Jaffe A., Martin J.A., McKay K.O., Marks G.B., Morton J.M., and Nissen M.D.
- Abstract
Background: Person-to-person transmission is a potential pathway of Pseudomonas aeruginosa acquisition in cystic fibrosis. Reports of cross-infection of shared cystic-fibrosis-specific P aeruginosa strains across large geographical distances are concerning. Therefore, we aimed to assess the extent to which patient movement between cystic fibrosis centres contributes to dissemination. Method(s): We did a cross-sectional study to assess movement of patients with cystic fibrosis who were infected with P aeruginosa between Sept 3, 2007, and June 16, 2010, at 18 Australian cystic fibrosis centres. We applied social network analysis to patient movement data from P aeruginosa-infected patients to assess the role of patient mobility in P aeruginosa genotype prevalence. We generated networks linking treatment centres based on the movement of patients attending adult and paediatric cystic fibrosis centres, and compared these with the movement of patients infected with all P aeruginosa strains, unique strains, and predominant Australian shared strains (AUST-01 and AUST-02). We summarised connectivity using degree centrality, in-degree centrality, out-degree centrality, and k-core estimates. Infection control and surveillance practices were also assessed by use of a questionnaire. Finding(s): 983 patients (mean age 25 years [SD 10]; 551 [56%] male) provided 2887 P aeruginosa isolates for ERIC-PCR genotyping, which yielded 531 distinct genotypes: 493 unique strains in 373 patients and 38 shared strains in 610 patients. AUST-01 infections were associated with higher in-degree centrality (p=0.004) and k-core (p=0.005) estimates and AUST-02 infections with higher degree centrality (p=0.002), out-degree centrality (p=0.002), and k-core (p=0.007) estimates for the previous health-care facilities; associations for the present cystic fibrosis centre were not significant. These findings were significant for adult patients (AUST-01 in-degree centrality p=0.004 and k-core p=0.005; AUST-02
- Published
- 2015
22. Pre-diagnostic concordance with the WCRF/AICR guidelines and survival in European colorectal cancer patients: a cohort study
- Author
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Romaguera, D., Ward, H., Wark, P.A., Vergnaud, A.C., Peeters, P.H.M., Gils, C.H. van, Ferrari, P., Fedirko, V., Jenab, M., Boutron-Ruault, M.C., Dossus, L., Dartois, L., Hansen, C.P., Dahm, C.C., Buckland, G., Sanchez, M.J., Dorronsoro, M., Navarro, C, Barricarte, A., Key, T.J., Trichopoulou, A., Tsironis, C., Lagiou, P., Masala, G., Pala, V., Tumino, R., Vineis, P., Panico, S., Bueno-de-Mesquita, H.B., Siersema, P.D., Ohlsson, B., Jirstrom, K., Wennberg, M., Nilsson, L.M., Weiderpass, E., Kuhn, T., Katzke, V., Khaw, K.T., Wareham, N.J., Tjonneland, A., Boeing, H., Quiros, J.R., Gunter, M.J., Riboli, E., Norat, T., Romaguera, D., Ward, H., Wark, P.A., Vergnaud, A.C., Peeters, P.H.M., Gils, C.H. van, Ferrari, P., Fedirko, V., Jenab, M., Boutron-Ruault, M.C., Dossus, L., Dartois, L., Hansen, C.P., Dahm, C.C., Buckland, G., Sanchez, M.J., Dorronsoro, M., Navarro, C, Barricarte, A., Key, T.J., Trichopoulou, A., Tsironis, C., Lagiou, P., Masala, G., Pala, V., Tumino, R., Vineis, P., Panico, S., Bueno-de-Mesquita, H.B., Siersema, P.D., Ohlsson, B., Jirstrom, K., Wennberg, M., Nilsson, L.M., Weiderpass, E., Kuhn, T., Katzke, V., Khaw, K.T., Wareham, N.J., Tjonneland, A., Boeing, H., Quiros, J.R., Gunter, M.J., Riboli, E., and Norat, T.
- Abstract
Contains fulltext : 152598.pdf (publisher's version ) (Open Access), BACKGROUND: Cancer survivors are advised to follow lifestyle recommendations on diet, physical activity, and body fatness proposed by the World Cancer Research Fund/American Institute of Cancer Research (WCRF/AICR) for cancer prevention. Previous studies have demonstrated that higher concordance with these recommendations measured using an index score (the WCRF/AICR score) was associated with lower cancer incidence and mortality. The aim of this study was to evaluate the association between pre-diagnostic concordance with WCRF/AICR recommendations and mortality in colorectal cancer (CRC) patients. METHODS: The association between the WCRF/AICR score (score range 0-6 in men and 0-7 in women; higher scores indicate greater concordance) assessed on average 6.4 years before diagnosis and CRC-specific (n = 872) and overall mortality (n = 1,113) was prospectively examined among 3,292 participants diagnosed with CRC in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort (mean follow-up time after diagnosis 4.2 years). Multivariable Cox proportional hazard models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for mortality. RESULTS: The HRs (95% CIs) for CRC-specific mortality among participants in the second (score range in men/women: 2.25-2.75/3.25-3.75), third (3-3.75/4-4.75), and fourth (4-6/5-7) categories of the score were 0.87 (0.72-1.06), 0.74 (0.61-0.90), and 0.70 (0.56-0.89), respectively (P for trend <0.0001), compared to participants with the lowest concordance with the recommendations (category 1 of the score: 0-2/0-3). Similar HRs for overall mortality were observed (P for trend 0.004). Meeting the recommendations on body fatness and plant food consumption were associated with improved survival among CRC cases in mutually adjusted models. CONCLUSIONS: Greater concordance with the WCRF/AICR recommendations on diet, physical activity, and body fatness prior to CRC diagnosis is associated with improved surv
- Published
- 2015
23. Prediagnostic body fat and risk of death from amyotrophic lateral sclerosis: The EPIC cohort
- Author
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Gallo, V. Wark, P.A. Jenab, M. Pearce, N. Brayne, C. Vermeulen, R. Andersen, P.M. Hallmans, G. Kyrozis, A. Vanacore, N. Vahdaninia, M. Grote, V. Kaaks, R. Mattiello, A. Bas Bueno-De-mesquita, H. Peeters, P.H. Travis, R.C. Petersson, J. Hansson, O. Arriola, L. Martin, J.-M.J. Tjønneland, A. Halkjær, J. Agnoli, C. Sacerdote, C. Bonet, C. Trichopoulou, A. Gavrila, D. Overvad, K. Weiderpass, E. Palli, D. Quirós, J.R. Tumino, R. Khaw, K.-T. Wareham, N. Barricante-Gurrea, A. Fedirko, V. Ferrari, P. Clavel-Chapelon, F. Ruault, M.-C.B. Boeing, H. Vigl, M. Middleton, L. Riboli, E. Vineis, P.
- Abstract
Objectives: The aim of this study was to investigate for the first time the association between body fat and risk of amyotrophic lateral sclerosis (ALS) with an appropriate prospective study design. Methods: The EPIC (European Prospective Investigation into Cancer and Nutrition) study included 518,108 individuals recruited from the general population across 10 Western European countries. At recruitment, information on lifestyle was collected and anthropometric characteristics were measured. Cox hazard models were fitted to investigate the associations between anthropometric measures and ALS mortality. Results: Two hundred twenty-two ALS deaths (79 men and 143 women) occurred during the followup period (mean follow-up 5 13 years). There was a statistically significant interaction between categories of body mass index and sex regarding ALS risk (p 5 0.009): in men, a significant linear decrease of risk per unit of body mass index was observed (hazard ratio 5 0.93, 95% confidence interval 0.86-0.99 per kg/m2); among women, the risk was more than 3-fold increased for underweight compared with normal-weight women. Among women, a significant risk reduction increasing the waist/hip ratio was also evident: women in the top quartile had less than half the risk of ALS compared with those in the bottom quartile (hazard ratio 5 0.48, 95% confidence interval 0.25-0.93) with a borderline significant p value for trend across quartiles (p 5 0.056). Conclusion: Increased prediagnostic body fat is associated with a decreased risk of ALS mortality. © 2013 American Academy of Neurology.
- Published
- 2013
24. Diet, lifestyle, heritable factors and colorectal carcinogenesis: associations with histopathological and molecular endpoints
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Wark, P.A., Wageningen University, Pieter van 't Veer, Frans Kok, and M.P. Weijenberg
- Subjects
Global Nutrition ,vegetables ,lifestyle ,Wereldvoeding ,Nutrition and Disease ,groenten ,histopathologie ,overerving ,dieet ,colorectal cancer ,fruit ,Voeding en Ziekte ,levensstijl ,histopathology ,inheritance ,colorectaal kanker ,diet ,carcinogenesis ,carcinogenese ,VLAG - Abstract
Background: Diet, lifestyle and heritable factors have been related to colorectal cancer risk; to date, their relevance to the overall scope of colorectal carcinogenesis, has not been clearly established.Aim and Methods: To evaluate whether distinguishing colorectal tissue by its histopathological and molecular characteristics sheds further light on the etiology of colorectal cancer. Five research questions addressed associations between diet, lifestyle and heritable factors, and specific tissue characteristics.Results: First, we observed that consumption of fruits, in particular citrus fruits, was associated with increased rectal glutathione S-transferase activity in a cross-sectional study of 94 Dutch individuals. Consumption of cruciferous vegetables was also associated with increased activity, but only among individuals who carried the GSTM1 genotype.Second, we observed that intake of vitamin B2 was inversely associated with adenomas with a K-ras mutation (n=81) but not with adenomas without a K-ras mutation (n=453) in a case-control study conducted in the Netherlands. A positive association with monounsaturated fat was confined to K-ras mutation-negative adenomas. We found indications for differential associations with some additional factors, but the epidemiological evidence on risk factors and K-ras mutations remains inconsistent.Third, in a cohort study of 26,769 American men, we observed that most risk factors were similarly associated with advanced (=1cm or with any villous characteristics or carcinoma in situ) and non-advanced colorectal adenomas after 17 years of follow-up. However, smoking had a stronger positive association with advanced adenomas than with non-advanced adenomas, and ahigh glycemic index was inversely associated with advanced but not with non-advanced adenomas.Fourth, associations with family history of colorectal cancer were stronger for men with multiple distal adenomas than for men with a single distal adenoma at first diagnosis, in the aforementioned cohort study among US men. Associations between family history, and advanced and non-advanced adenomas, were of similar strength, but a tendency towards a somewhat stronger association with non-advanced adenomas was found.Fifth, fruit consumption was inversely associated with hMLH1 protein-deficient colon cancer (n=54) but not with hMLH1 protein-proficient colon cancer (n=387) in a cohort study of 120,852 people who were followed-up over 7.3 years, while ignoring information from the initial 2.3 years of follow-up. Clear associations with consumption of vegetables, or nutrients related to fruits and vegetables, could not be detected.Conclusions: We showed that distinguishing colorectal tumors by their histopathological and molecular characteristics may indeed shed further light on the role of diet, lifestyle and heritable factors in colorectal carcinogenesis. Such an approach may alleviate some of the weaknesses of traditional epidemiology, but also adds another layer of complexity. It is a challenge for the future to develop a framework into which specific associations can be integrated, using risk markers signaling the molecular and biochemical pathways from normal to cancerous tissue.
- Published
- 2007
25. Mutations in APC, CTNNBI en K-ras genes and expression of hMLHI in sporadic colorectal carcinomas from the Netherlands Cohort Study
- Author
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Luchtenborg, M., Weijenberg, M.P., Wark, P.A., and Merdan Saritas, M.
- Subjects
polyposis-coli gene ,mismatch repair ,cell-lines ,Nutrition and Disease ,Voeding en Ziekte ,point mutations ,promoter hypermethylation ,somatic mutations ,microsatellite instability ,oncogene mutations ,tumor location ,adenomatous-polyposis ,VLAG - Abstract
Background - The early to intermediate stages of the majority of colorectal tumours are thought to be driven by aberrations in the Wnt (APC, CTNNB1) and Ras (K-ras) pathways. A smaller proportion of cancers shows mismatch repair deficiency. The aim of this study was to analyse the co-occurrence of these genetic alterations in relation to tumour and patient characteristics. Methods - In a group of 656 unselected sporadic colorectal cancer patients, aberrations in the APC, K-ras, CTNNB1 genes, and expression of hMLH1 were investigated. Additionally, tumours were divided in groups based on molecular features and compared with respect to patient's age at diagnosis, sex, family history of colorectal cancer, tumour sub-localisation, Dukes' stage and differentiation. Results - Mutations at the phosphorylation sites (codons 31, 33, 37, and 45) in the CTNNB1 gene were observed in tumours from only 5/464 patients. Tumours with truncating APC mutations and activating K-ras mutations in codons 12 and 13 occurred at similar frequencies (37% (245/656) and 36% (235/656), respectively). Seventeen percent of tumours harboured both an APC and a K-ras mutation (109/656). Nine percent of all tumours (58/656) lacked hMLH1 expression. Patients harbouring a tumour with absent hMLH1 expression were older, more often women, more often had proximal colon tumours that showed poorer differentiation when compared to patients harbouring tumours with an APC and/or K-ras mutation. Conclusion - CTNNB1 mutations seem to be of minor importance in sporadic colorectal cancer. The main differences in tumour and patient characteristics are found between groups of patients based on mismatch repair deficiency.
- Published
- 2005
26. Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres.
- Author
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Bye P.T., Martin A.J., McKay K.O., Morton J.M., Nissen M.D., Price D., Reid D.W., Ryan G., Serisier D.J., Sloots T.P., Smith D.J., Wark P.A., Whitehead B.F., Kidd T.J., Ramsay K.A., Hu H., Marks G.B., Wainwright C.E., Elkins M.R., Robinson P.J., Rose B.R., Wilson J.W., Grimwood K., Bell S.C., Armstrong D.S., Cooper P.J., Dakin C.J., Feather H Greville I.H., Harbour C., Jaffe A., Bye P.T., Martin A.J., McKay K.O., Morton J.M., Nissen M.D., Price D., Reid D.W., Ryan G., Serisier D.J., Sloots T.P., Smith D.J., Wark P.A., Whitehead B.F., Kidd T.J., Ramsay K.A., Hu H., Marks G.B., Wainwright C.E., Elkins M.R., Robinson P.J., Rose B.R., Wilson J.W., Grimwood K., Bell S.C., Armstrong D.S., Cooper P.J., Dakin C.J., Feather H Greville I.H., Harbour C., and Jaffe A.
- Abstract
Recent molecular-typing studies suggest cross-infection as one of the potential acquisition pathways for Pseudomonas aeruginosa in patients with cystic fibrosis (CF). In Australia, there is only limited evidence of unrelated patients sharing indistinguishable P. aeruginosa strains. We therefore examined the point-prevalence, distribution, diversity and clinical impact of P. aeruginosa strains in Australian CF patients nationally. 983 patients attending 18 Australian CF centres provided 2887 sputum P. aeruginosa isolates for genotyping by enterobacterial repetitive intergenic consensus-PCR assays with confirmation by multilocus sequence typing. Demographic and clinical details were recorded for each participant. Overall, 610 (62%) patients harboured at least one of 38 shared genotypes. Most shared strains were in small patient clusters from a limited number of centres. However, the two predominant genotypes, AUST-01 and AUST-02, were widely dispersed, being detected in 220 (22%) and 173 (18%) patients attending 17 and 16 centres, respectively. AUST-01 was associated with significantly greater treatment requirements than unique P. aeruginosa strains. Multiple clusters of shared P. aeruginosa strains are common in Australian CF centres. At least one of the predominant and widespread genotypes is associated with increased healthcare utilisation. Longitudinal studies are now needed to determine the infection control implications of these findings. Copyright ©ERS 2013.
- Published
- 2013
27. North-south gradients in plasma concentrations of B-vitamins and other components of one-carbon metabolism in Western Europe: results from the European Prospective Investigation into Cancer and Nutrition (EPIC) Study
- Author
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Eussen, S.J., Nilsen, R.M., Midttun, O., Hustad, S., N, I.J., Meyer, K., Fredriksen, A., Ulvik, A., Ueland, P.M., Brennan, P., Johansson, M., Bueno-de-Mesquita, B., Vineis, P., Chuang, S.C., Boutron-Ruault, M.C., Dossus, L., Perquier, F., Overvad, K., Teucher, B., Grote, V.A., Trichopoulou, A., Adarakis, G., Plada, M., Sieri, S., Tumino, R., Magistris, M.S. de, Ros, M.M., Peeters, P.H.M., Redondo, M.L., Zamora-Ros, R., Chirlaque, M.D., Ardanaz, E., Sonestedt, E., Ericson, U., Schneede, J., Guelpen, B. van, Wark, P.A., Gallo, V., Norat, T., Riboli, E., Vollset, S.E., Eussen, S.J., Nilsen, R.M., Midttun, O., Hustad, S., N, I.J., Meyer, K., Fredriksen, A., Ulvik, A., Ueland, P.M., Brennan, P., Johansson, M., Bueno-de-Mesquita, B., Vineis, P., Chuang, S.C., Boutron-Ruault, M.C., Dossus, L., Perquier, F., Overvad, K., Teucher, B., Grote, V.A., Trichopoulou, A., Adarakis, G., Plada, M., Sieri, S., Tumino, R., Magistris, M.S. de, Ros, M.M., Peeters, P.H.M., Redondo, M.L., Zamora-Ros, R., Chirlaque, M.D., Ardanaz, E., Sonestedt, E., Ericson, U., Schneede, J., Guelpen, B. van, Wark, P.A., Gallo, V., Norat, T., Riboli, E., and Vollset, S.E.
- Abstract
Item does not contain fulltext, Different lifestyle patterns across Europe may influence plasma concentrations of B-vitamins and one-carbon metabolites and their relation to chronic disease. Comparison of published data on one-carbon metabolites in Western European regions is difficult due to differences in sampling procedures and analytical methods between studies. The present study aimed, to compare plasma concentrations of one-carbon metabolites in Western European regions with one laboratory performing all biochemical analyses. We performed the present study in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort among 5446 presumptively healthy individuals. Quantile regression was used to compare sex-specific median concentrations between Northern (Denmark and Sweden), Central (France, Germany, The Netherlands and United Kingdom) and Southern (Greece, Spain and Italy) European regions. The lowest folate concentrations were observed in Northern Europe (men, 10.4 nmol/l; women, 10.7 nmol/l) and highest concentrations in Central Europe. Cobalamin concentrations were slightly higher in Northern Europe (men, 330 pmol/l; women, 352 pmol/l) compared with Central and Southern Europe, but did not show a clear north-south gradient. Vitamin B(2) concentrations were highest in Northern Europe (men, 22.2 nmol/l; women, 26.0 nmol/l) and decreased towards Southern Europe (P trend< 0.001). Vitamin B(6) concentrations were highest in Central Europe in men (77.3 nmol/l) and highest in the North among women (70.4 nmol/l), with decreasing concentrations towards Southern Europe in women (P trend< 0.001). In men, concentrations of serine, glycine and sarcosine increased from the north to south. In women, sarcosine increased from Northern to Southern Europe. These findings may provide relevant information for the study of regional differences of chronic disease incidence in association with lifestyle.
- Published
- 2013
28. Nort-South gradients in plasma concentrations of B-vitamins and other components of one-carbon metabolism in Western Europe: results from the European Prospective Investigation into Cancer and Nutrition (EPIC) Study
- Author
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Eussen, S.J.P.M., Nilsen, R.M., Midttun, O., Hustad, S., IJssenagger, N., Meyer, K., Fredriksen, A., Ulvik, A., Ueland, P.M., Brennan, P., Johansson, M., Bueno-de-Mesquita, B., Vineis, P., Chuang, S.C., Boutron-Ruault, M.C., Dossus, L., Perquier, F., Overvad, K., Teucher, B., Grote, V.A., Trichopoulou, A., Adarakis, G., Plada, M., Sieri, S., Tumino, R., Santucci de Magistris, M., Ros, M.M., Peeters, P.H.M., Redondo, M.L., Zamora-Ros, R., Chirlaque, M.D., Ardanaz, E., Sonestedt, E., Ericson, U., Schneede, J., Guelpen, B., Wark, P.A., Gallo, V., Norat, T., Riboli, E., Vollset, S.E., Eussen, S.J.P.M., Nilsen, R.M., Midttun, O., Hustad, S., IJssenagger, N., Meyer, K., Fredriksen, A., Ulvik, A., Ueland, P.M., Brennan, P., Johansson, M., Bueno-de-Mesquita, B., Vineis, P., Chuang, S.C., Boutron-Ruault, M.C., Dossus, L., Perquier, F., Overvad, K., Teucher, B., Grote, V.A., Trichopoulou, A., Adarakis, G., Plada, M., Sieri, S., Tumino, R., Santucci de Magistris, M., Ros, M.M., Peeters, P.H.M., Redondo, M.L., Zamora-Ros, R., Chirlaque, M.D., Ardanaz, E., Sonestedt, E., Ericson, U., Schneede, J., Guelpen, B., Wark, P.A., Gallo, V., Norat, T., Riboli, E., and Vollset, S.E.
- Abstract
Different lifestyle patterns across Europe may influence plasma concentrations of B-vitamins and one-carbon metabolites and their relation to chronic disease. Comparison of published data on one-carbon metabolites in Western European regions is difficult due to differences in sampling procedures and analytical methods between studies. The present study aimed, to compare plasma concentrations of one-carbon metabolites in Western European regions with one laboratory performing all biochemical analyses. We performed the present study in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort among 5446 presumptively healthy individuals. Quantile regression was used to compare sex-specific median concentrations between Northern (Denmark and Sweden), Central (France, Germany, The Netherlands and United Kingdom) and Southern (Greece, Spain and Italy) European regions. The lowest folate concentrations were observed in Northern Europe (men, 10·4 nmol/l; women, 10·7 nmol/l) and highest concentrations in Central Europe. Cobalamin concentrations were slightly higher in Northern Europe (men, 330 pmol/l; women, 352 pmol/l) compared with Central and Southern Europe, but did not show a clear north–south gradient. Vitamin B2 concentrations were highest in Northern Europe (men, 22·2 nmol/l; women, 26·0 nmol/l) and decreased towards Southern Europe (P trend <0·001). Vitamin B6 concentrations were highest in Central Europe in men (77·3 nmol/l) and highest in the North among women (70·4 nmol/l), with decreasing concentrations towards Southern Europe in women (P trend <0·001). In men, concentrations of serine, glycine and sarcosine increased from the north to south. In women, sarcosine increased from Northern to Southern Europe. These findings may provide relevant information for the study of regional differences of chronic disease incidence in association with lifestyle.
- Published
- 2013
29. Dietary factors, genetic susceptibility and somatic mutations in colorectal cancer : a prospective study
- Author
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Weijenberg, M.P., Brink, M., Luchtenborg, M., Wark, P.A., de Goeij, A.F.P.M., de Bruine, A.P., van 't Veer, P., Kampman, E., van Muijen, G.N.P., Goldbohm, R.A., van den Brandt, P.A., and TNO Voeding
- Subjects
Humane Voeding & Gezondheid ,Life Science ,Nutrition ,VLAG ,Human Nutrition & Health - Published
- 2002
30. Magnesium intake and colorectal tumor risk: a case-control study and meta-analysis.
- Author
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Wark, P.A., Lau, R., Norat, T., Kampman, E., Wark, P.A., Lau, R., Norat, T., and Kampman, E.
- Abstract
1 september 2012, Item does not contain fulltext, BACKGROUND: Dietary magnesium might be related to colorectal tumor risk through the pivotal roles of magnesium in cellular metabolism, insulin resistance, and systemic inflammation. OBJECTIVE: We evaluated the hypothesis of whether higher dietary magnesium intake is associated with reduced colorectal tumor risk. DESIGN: A case-control study on colorectal adenomas (768 cases; 709 polyp-free control subjects) and a meta-analysis of colorectal adenomas (3 case-control studies) and carcinomas (6 prospective cohort studies) were conducted. Dietary magnesium was estimated from food-frequency questionnaires in the case-control study and most studies in the meta-analyses. Data analysis comprised multiple logistic regression analysis (case-control study) and fixed- and random-effects meta-analyses. RESULTS: The case-control study showed a nonsignificant inverse association between dietary magnesium intake and risk of colorectal adenomas (OR for every 100-mg/d increase: 0.81; 95% CI: 0.62, 1.06). However, inverse associations were observed only in subjects with BMI (in kg/m(2)) >/=25, in subjects aged >/=55 y, and for advanced adenomas. Associations did not vary by the calcium-to-magnesium intake ratio. In the meta-analysis, every 100-mg/d increase in magnesium intake was associated with 13% lower risk of colorectal adenomas (OR: 0.87; 95% CI: 0.75, 1.00) and 12% lower risk of colorectal cancer (RR: 0.88; 95% CI: 0.81, 0.97). CONCLUSIONS: Our findings support the hypothesis that higher intakes of dietary magnesium are associated with lower risk of colorectal tumors. The consumption of magnesium-rich foods may be a new avenue to explore further in the search for cancer-prevention strategies.
- Published
- 2012
31. Effectiveness of H1N1/09 monovalent and trivalent influenza vaccines against hospitalization with laboratory-confirmed H1N1/09 influenza in Australia: A test-negative case control study.
- Author
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Kelly P.M., Paterson D.L., Wark P.A., Upham J.W., Korman T.M., Dwyer D.E., Waterer G.W., Cheng A.C., Kotsimbos T., Kelly H.A., Irving L.B., Bowler S.D., Brown S.G.A., Holmes M., Jenkins C.R., Thompson P., Simpson G., Wood-Baker R., Senanayake S.N., Brady S.J., Kelly P.M., Paterson D.L., Wark P.A., Upham J.W., Korman T.M., Dwyer D.E., Waterer G.W., Cheng A.C., Kotsimbos T., Kelly H.A., Irving L.B., Bowler S.D., Brown S.G.A., Holmes M., Jenkins C.R., Thompson P., Simpson G., Wood-Baker R., Senanayake S.N., and Brady S.J.
- Abstract
We aimed to estimate the effectiveness of H1N1/09 containing influenza vaccines against hospitalization from influenza in Australia. We performed a test-negative case control study in patients hospitalized in 15 sentinel Australian hospitals between March and November 2010, comparing influenza vaccination (H1N1/09 monovalent or 2010 seasonal trivalent) in hospitalized patients with PCR-confirmed influenza compared to PCR-negative controls. Between March and November 2010, 1169 hospitalized patients were tested for suspected influenza, of which influenza vaccine status was ascertained in 165/238 patients with H1N1/09 influenza, 40/64 with seasonal influenza and 558/867 test negative controls; 24% of H1N1/09 cases, 43% of seasonal influenza cases and 54% of controls were vaccinated. VE against hospitalisation with H1N1/09 influenza after adjusting for age, medical comorbidities and pregnancy status was estimated at 49% (95% CI: 13%, 70%). Influenza vaccination was associated with a reduction in hospitalisation caused by H1N1/09 influenza in the 2010 southern hemisphere winter season. © 2011 Elsevier Ltd.
- Published
- 2012
32. Dietary Fibre Intake and Risks of Cancers of the Colon and Rectum in the European Prospective Investigation into Cancer and Nutrition (EPIC)
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Murphy, N., Norat, T., Ferrari, P., Jenab, M., Bueno-de-Mesquita, B., Skeie, G., Dahm, C.C., Overvad, K., Olsen, A., Tjonneland, A., Clavel-Chapelon, F., Boutron-Ruault, M.C., Racine, A., Kaaks, R., Teucher, B., Boeing, H., Bergmann, M.M., Trichopoulou, A., Trichopoulos, D., Lagiou, P., Palli, D., Pala, V., Panico, S., Tumino, R., Vineis, P., Siersema, P., van Duijnhoven, F.J.B., Peeters, P.H.M., Hjartaker, A., Engeset, D., Gonzalez, C.A., Sanchez, M.J., Dorronsoro, M., Navarro, C., Ardanaz, E., Quiros, J.R., Sonestedt, E., Ericson, U., Nilsson, L., Palmqvist, R., Khaw, K.T., Wareham, N., Key, T.J., Crowe, F.L., Fedirko, V., Wark, P.A., Chuang, S.C., Riboli, E., Murphy, N., Norat, T., Ferrari, P., Jenab, M., Bueno-de-Mesquita, B., Skeie, G., Dahm, C.C., Overvad, K., Olsen, A., Tjonneland, A., Clavel-Chapelon, F., Boutron-Ruault, M.C., Racine, A., Kaaks, R., Teucher, B., Boeing, H., Bergmann, M.M., Trichopoulou, A., Trichopoulos, D., Lagiou, P., Palli, D., Pala, V., Panico, S., Tumino, R., Vineis, P., Siersema, P., van Duijnhoven, F.J.B., Peeters, P.H.M., Hjartaker, A., Engeset, D., Gonzalez, C.A., Sanchez, M.J., Dorronsoro, M., Navarro, C., Ardanaz, E., Quiros, J.R., Sonestedt, E., Ericson, U., Nilsson, L., Palmqvist, R., Khaw, K.T., Wareham, N., Key, T.J., Crowe, F.L., Fedirko, V., Wark, P.A., Chuang, S.C., and Riboli, E.
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Background: Earlier analyses within the EPIC study showed that dietary fibre intake was inversely associated with colorectal cancer risk, but results from some large cohort studies do not support this finding. We explored whether the association remained after longer follow-up with a near threefold increase in colorectal cancer cases, and if the association varied by gender and tumour location. Methodology/Principal Findings: After a mean follow-up of 11.0 years, 4,517 incident cases of colorectal cancer were documented. Total, cereal, fruit, and vegetable fibre intakes were estimated from dietary questionnaires at baseline. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated using Cox proportional hazards models stratified by age, sex, and centre, and adjusted for total energy intake, body mass index, physical activity, smoking, education, menopausal status, hormone replacement therapy, oral contraceptive use, and intakes of alcohol, folate, red and processed meats, and calcium. After multivariable adjustments, total dietary fibre was inversely associated with colorectal cancer (HR per 10 g/day increase in fibre 0.87, 95% CI: 0.79-0.96). Similar linear associations were observed for colon and rectal cancers. The association between total dietary fibre and risk of colorectal cancer risk did not differ by age, sex, or anthropometric, lifestyle, and dietary variables. Fibre from cereals and fibre from fruit and vegetables were similarly associated with colon cancer; but for rectal cancer, the inverse association was only evident for fibre from cereals. Conclusions/Significance: Our results strengthen the evidence for the role of high dietary fibre intake in colorectal cancer prevention.
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- 2012
33. Cigarette smoking and K-ras mutations in pancreas, lung and colorectal adenocarcinomas: etiopathogenic similarities, differences and paradoxes.
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Porta, M., Crous-Bou, M., Wark, P.A., Vineis, P., Real, F.X., Malats, N., Kampman, E., Porta, M., Crous-Bou, M., Wark, P.A., Vineis, P., Real, F.X., Malats, N., and Kampman, E.
- Abstract
Item does not contain fulltext, Surprisingly different frequencies and patterns of K-ras mutations are observed in human adenocarcinomas of the pancreas, colorectum and lung. Their respective relationships with smoking are apparently paradoxical. We evaluated all the available types of clinical and epidemiological studies on the relationship between tobacco smoking and the occurrence of K-ras mutations in human adenocarcinomas of the pancreas, colorectum and lung. We identified 8, 7 and 12 studies that analyzed the relationship between K-ras mutations and tobacco smoking in human neoplasms of the pancreas, colorectum and lung, respectively. A meta-analysis was undertaken for each site separately. In pancreatic adenocarcinomas lifetime history of tobacco consumption was not significantly associated with the frequency of K-ras mutations (OR=1.26; 95% CI=0.82-1.94). Similarly, no association was observed between smoking and K-ras mutations in colorectal adenocarcinomas (OR=0.94; CI=0.79-1.12), neither when colorectal adenomas and adenocarcinomas were jointly analyzed (OR=0.96; 95% CI=0.83-1.13). In lung adenocarcinoma, where only 15-25% of cases harbor a K-ras mutation, tumors from smokers were more likely to have K-ras mutations than tumors from non-smokers (OR=3.67; 95% CI=2.47-5.45). Furthermore, in lung adenocarcinomas K-ras mutations have a pattern different from that in pancreatic and colorectal adenocarcinomas. Results support the hypothesis that smoking influences the risk of pancreatic cancer - and possibly colorectal cancer - through events other than K-ras mutations. In adenocarcinoma of the lung, smoking may play a role in the occurrence of K-ras mutations. If the influence of tobacco products in the induction, acquisition and persistence of K-ras mutations had some tissue specificity, or was dependent on different factors in different organs, the corresponding mechanisms would deserve detailed research.
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- 2009
34. Diet, lifestyle, heritable factors and colorectal carcinogenesis: associations with histopathological and molecular endpoints
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van 't Veer, Pieter, Kok, Frans, Weijenberg, M.P., Wark, P.A., van 't Veer, Pieter, Kok, Frans, Weijenberg, M.P., and Wark, P.A.
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Background: Diet, lifestyle and heritable factors have been related to colorectal cancer risk; to date, their relevance to the overall scope of colorectal carcinogenesis, has not been clearly established.Aim and Methods: To evaluate whether distinguishing colorectal tissue by its histopathological and molecular characteristics sheds further light on the etiology of colorectal cancer. Five research questions addressed associations between diet, lifestyle and heritable factors, and specific tissue characteristics.Results: First, we observed that consumption of fruits, in particular citrus fruits, was associated with increased rectal glutathione S-transferase activity in a cross-sectional study of 94 Dutch individuals. Consumption of cruciferous vegetables was also associated with increased activity, but only among individuals who carried the GSTM1 genotype.Second, we observed that intake of vitamin B2 was inversely associated with adenomas with a K-ras mutation (n=81) but not with adenomas without a K-ras mutation (n=453) in a case-control study conducted in the Netherlands. A positive association with monounsaturated fat was confined to K-ras mutation-negative adenomas. We found indications for differential associations with some additional factors, but the epidemiological evidence on risk factors and K-ras mutations remains inconsistent.Third, in a cohort study of 26,769 American men, we observed that most risk factors were similarly associated with advanced (=1cm or with any villous characteristics or carcinoma in situ) and non-advanced colorectal adenomas after 17 years of follow-up. However, smoking had a stronger positive association with advanced adenomas than with non-advanced adenomas, and ahigh glycemic index was inversely associated with advanced but not with non-advanced adenomas.Fourth, associations with family history of colorectal cancer were stronger for men with multiple distal adenomas than for men with a single distal adenoma at first diagnosis, in
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- 2007
35. GSTP1 and GSTA1 polymorphisms interact with cruciferous vegetable intake in colorectal adenoma risk.
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Tijhuis, M.J., Wark, P.A., Aarts, J., Visker, M.H.P.W., Nagengast, F.M., Kok, F.J., Kampman, E., Tijhuis, M.J., Wark, P.A., Aarts, J., Visker, M.H.P.W., Nagengast, F.M., Kok, F.J., and Kampman, E.
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Item does not contain fulltext, The possible interplay between cruciferous vegetable consumption, functional genetic variations in glutathione S-transferases (GST) M1, T1, P1, and A1, and colorectal adenomas, was investigated in a Dutch case-control study. The GSTM1 and GSTT1 deletion polymorphisms, and the single nucleotide polymorphisms in GSTP1 (A313G) and in GSTA1 (C-69T) were assessed among 746 cases who developed colorectal adenomas and 698 endoscopy-based controls without any type of colorectal polyps. High and low cruciferous vegetable consumption was defined based on a median split in the control group. High consumption was slightly positively associated with colorectal adenomas [odds ratio (OR) 1.15; 95% confidence interval, 0.92-1.44]. For GSTP1, a positive association with higher cruciferous vegetable intake was only apparent in individuals with the low-activity GSTP1 genotype (GG genotype, OR 1.94; 95% confidence interval, 1.02-3.69). This interaction was more pronounced in men, with higher age and with higher meat intake. The GSTA1 polymorphism may have a modifying role as well: the OR for higher intake compared with lower intake was 1.57 (0.93-2.65) for individuals homozygous for the low expression variant (TT genotype). This seemed to be stronger with younger age and higher red meat intake. Cruciferous vegetable consumption and the combined GSTA1 and GSTP1 genotypes showed a statistically significant interaction (P = 0.034). The GSTM1 and GSTT1 genotypes did not seem to modify the association between cruciferous vegetable intake and colorectal adenomas. In conclusion, GSTP1 and GSTA1 genotypes might modulate the association between cruciferous vegetable intake and colorectal adenomas.
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- 2005
36. Mutations in APC, CTNNB1 and K-ras genes and expression of hMLH1 in sporadic colorectal carcinomas from the Netherlands Cohort Study
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Luchtenborg, M., Weijenberg, M.P., Wark, P.A., Saritas, A.M., Roemen, G.M., Muijen, G.N.P. van, Bruine, A.P. de, Brandt, P.A. van den, Goeij, A.F. de, Luchtenborg, M., Weijenberg, M.P., Wark, P.A., Saritas, A.M., Roemen, G.M., Muijen, G.N.P. van, Bruine, A.P. de, Brandt, P.A. van den, and Goeij, A.F. de
- Abstract
Contains fulltext : 48885.pdf ( ) (Open Access), BACKGROUND: The early to intermediate stages of the majority of colorectal tumours are thought to be driven by aberrations in the Wnt (APC, CTNNB1) and Ras (K-ras) pathways. A smaller proportion of cancers shows mismatch repair deficiency. The aim of this study was to analyse the co-occurrence of these genetic alterations in relation to tumour and patient characteristics. METHODS: In a group of 656 unselected sporadic colorectal cancer patients, aberrations in the APC, K-ras, CTNNB1 genes, and expression of hMLH1 were investigated. Additionally, tumours were divided in groups based on molecular features and compared with respect to patient's age at diagnosis, sex, family history of colorectal cancer, tumour sub-localisation, Dukes' stage and differentiation. RESULTS: Mutations at the phosphorylation sites (codons 31, 33, 37, and 45) in the CTNNB1 gene were observed in tumours from only 5/464 patients. Tumours with truncating APC mutations and activating K-ras mutations in codons 12 and 13 occurred at similar frequencies (37% (245/656) and 36% (235/656), respectively). Seventeen percent of tumours harboured both an APC and a K-ras mutation (109/656). Nine percent of all tumours (58/656) lacked hMLH1 expression. Patients harbouring a tumour with absent hMLH1 expression were older, more often women, more often had proximal colon tumours that showed poorer differentiation when compared to patients harbouring tumours with an APC and/or K-ras mutation. CONCLUSION: CTNNB1 mutations seem to be of minor importance in sporadic colorectal cancer. The main differences in tumour and patient characteristics are found between groups of patients based on mismatch repair deficiency.
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- 2005
37. Meat and Fish Consumption, APCGene Mutations and hMLH1 Expression in Colon and Rectal Cancer: a Prospective Cohort Study (The Netherlands)
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Luchtenborg, M., Luchtenborg, M., Weijenberg, M.P., de Goeij, A.F., Wark, P.A., Brink, M., Roemen, G.M.J.M., Lentjes, M.H.F.M., de Bruine, A.P., Goldbohm, R.A., van 't Veer, P., van den Brandt, P.A., Luchtenborg, M., Luchtenborg, M., Weijenberg, M.P., de Goeij, A.F., Wark, P.A., Brink, M., Roemen, G.M.J.M., Lentjes, M.H.F.M., de Bruine, A.P., Goldbohm, R.A., van 't Veer, P., and van den Brandt, P.A.
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Objective:The aim of this study was to investigate the associations between meat and fish consumption and APC mutation status and hMLH1 expression in colon and rectal cancer.Methods:The associations were investigated in the Netherlands Cohort Study, and included 434 colon and 154 rectal cancer patients on whom case-cohort analyses (subcohort n = 2948) were performed.Results:Total meat consumption was not associated with the endpoints studied. Meat product (i.e. processed meat) consumption showed a positive association with colon tumours harbouring a truncating APC mutation, whereas beef consumption was associated with an increased risk of colon tumours without a truncating APC mutation (incidence rate ratio (RR) highest versus lowest quartile of intake 1.61, 95% confidence interval (CI) 0.96-2.71, p-trend = 0.04 and 1.58, 95% CI 1.10-2.25, p-trend = 0.01, respectively). Consumption of other meat (horsemeat, lamb, mutton, frankfurters and deep-fried meat rolls) was associated with an increased risk of rectal cancer without a truncating APC mutation (RR intake versus no intake 1.79, 95% CI 1.10-2.90). No associations were observed for meat consumption and tumours lacking hMLH1 expression.Conclusions:Our data indicate that several types of meat may contribute differently to the aetiology of colon and rectal cancer, depending on APC mutation status but not hMLH1 expression of the tumour.
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- 2005
38. Habitual consumption of fruits and vegetables: associations with human rectal glutathione S-transferase.
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Wark, P.A., Grubben, M.J.A.L., Peters, W.H.M., Nagengast, F.M., Kampman, E., Kok, F.J., Veer, P. van 't, Wark, P.A., Grubben, M.J.A.L., Peters, W.H.M., Nagengast, F.M., Kampman, E., Kok, F.J., and Veer, P. van 't
- Abstract
Contains fulltext : 58333.pdf (publisher's version ) (Closed access), The glutathione (GSH)/glutathione S-transferase (GST) system is an important detoxification system in the gastrointestinal tract. A high activity of this system may benefit cancer prevention. The aim of the study was to assess whether habitual consumption of fruits and vegetables, especially citrus fruits and brassica and allium vegetables, is positively associated with parameters reflecting the activity of the GSH/GST enzyme system in human rectal mucosa. GST enzyme activity, GST isoenzyme levels of GST-alpha (A1-1, A1-2 and A2-2), -mu (M1-1) and -pi (P1-1), and GSH levels were measured in rectal biopsies from 94 subjects. Diet, lifestyle, GSTM1 and GSTT1 null polymorphisms were assessed. Mean GST enzyme activity was 237 nmol/min/mg protein (SD = 79). Consumption of citrus fruits was positively associated with GST enzyme activity [difference between high and low consumption: 28.9 (95% confidence interval (CI) = 9.3-48.6) nmol/min/mg protein], but was not associated with the other parameters. A positive association with brassica vegetables was found among carriers of the GSTM1-plus genotype [difference between high and low consumption: 22.6 (95% CI = 0.2-45.0) nmol/min/mg protein], but not among GSTM1-null individuals (-25.8 nmol/min/mg protein, 95% CI = -63.3-11.8). This is in line with a positive association between consumption of brassica vegetables and GSTM isoenzyme level [difference between high and low consumption: 67.5%, 95% CI = (6.8-162.7)]. Consumption of allium vegetables was not associated with GST enzyme activity, but negatively with GSTP1-1 levels [difference between high and low consumption: -23.3%, 95% CI = (-35.5; -8.6)]. Associations were similar among those with the GSTT1-plus and GSTT1-null genotype. In conclusion, variations in habitual consumption of fruits, particularly citrus fruits, and of vegetables, in particular brassica vegetables, among those with the GSTM1-plus genotype, may contribute to variations in human rectal GST enzyme activity
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- 2004
39. Development and usability of myfood24: an online 24-hour dietary assessment tool.
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Carter, M.C., Albar, S.A., Morris, M.A., Mulla, U.Z., Hancock, N., Evans, C.E.L., Alwan, N., Greenwood, D.C., Hardie, L.J., Frost, G.S., Wark, P.A., and Cade, J.E.
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CONFERENCES & conventions ,EXPERIMENTAL design ,RESEARCH methodology ,NUTRITIONAL assessment ,WORLD Wide Web - Published
- 2015
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40. Abdominal obesity, weight gain during adulthood and risk of liver and biliary tract cancer in a European cohort
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Schlesinger, S, Aleksandrova, K, Pischon, T, Fedirko, V, Jenab, M, Trepo, E, Boffetta, P, Dahm, CC, Overvad, K, Tjønneland, A, Halkjær, J, Fagherazzi, G, Boutron-Ruault, MC, Carbonnel, F, Kaaks, R, Lukanova, A, Boeing, H, Trichopoulou, A, Bamia, C, Lagiou, P, Palli, D, Grioni, S, Panico, S, Tumino, R, Vineis, P, Hb, BDM, Van Den Berg, S, Peeters, PHM, Braaten, T, Weiderpass, E, Quirós, JR, Travier, N, Sánchez, MJ, Navarro, C, Barricarte, A, Dorronsoro, M, Lindkvist, B, Regner, S, Werner, M, Sund, M, Khaw, KT, Wareham, N, Travis, RC, Norat, T, Wark, PA, Riboli, E, Nöthlings, U, Schlesinger, S, Aleksandrova, K, Pischon, T, Fedirko, V, Jenab, M, Trepo, E, Boffetta, P, Dahm, Cc, Overvad, K, Tj?nneland, A, Halkj?r, J, Fagherazzi, G, Boutron Ruault, Mc, Carbonnel, F, Kaaks, R, Lukanova, A, Boeing, H, Trichopoulou, A, Bamia, C, Lagiou, P, Palli, D, Grioni, S, Panico, Salvatore, Tumino, R, Vineis, P, Bueno de Mesquita, Hb, van den Berg, S, Peeters, Ph, Braaten, T, Weiderpass, E, Quir?s, Jr, Travier, N, S?nchez, Mj, Navarro, C, Barricarte, A, Dorronsoro, M, Lindkvist, B, Regner, S, Werner, M, Sund, M, Khaw, Kt, Wareham, N, Travis, Rc, Norat, T, Wark, Pa, Riboli, E, N?thlings, U., Schlesinger, S., Aleksandrova, K., Pischon, T., Fedirko, V., Jenab, M., Trepo, E., Boffetta, P., Dahm, C.C., Overvad, K., Tjønneland, A., Halkjær, J., Fagherazzi, G., Boutron-Ruault, M.-C., Carbonnel, F., Kaaks, R., Lukanova, A., Boeing, H., Trichopoulou, A., Bamia, C., Lagiou, P., Palli, D., Grioni, S., Panico, S., Tumino, R., Vineis, P., Hb, B.-D.-M., Van Den Berg, S., Peeters, P.H.M., Braaten, T., Weiderpass, E., Quirós, J.R., Travier, N., Sánchez, M.-J., Navarro, C., Barricarte, A., Dorronsoro, M., Lindkvist, B., Regner, S., Werner, M., Sund, M., Khaw, K.-T., Wareham, N., Travis, R.C., Norat, T., Wark, P.A., Riboli, E., Nöthlings, U., International Prevention Research Institute (IPRI), The Tisch Cancer Institute, and Icahn School of Medicine at Mount Sinai [New York] (MSSM)
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Male ,Cancer Research ,obesity ,Weight Gain ,Gastroenterology ,Body Mass Index ,Hepatocellular/*epidemiology/etiology Case-Control Studies Europe/epidemiology Female Hepatitis B/epidemiology Hepatitis C/epidemiology Humans Liver Neoplasms/*epidemiology/etiology Male Middle Aged Nutritional Status Obesity ,Biliary Tract Neoplasms/*epidemiology/etiology Body Composition Body Mass Index Body Weight Carcinoma ,hepatocellular carcinoma (HCC) ,0302 clinical medicine ,Waist–hip ratio ,intrahepatic (IBDC) ,Prospective Studies ,Prospective cohort study ,Abdominal/*epidemiology Proportional Hazards Models Prospective Studies Waist-Hip Ratio *Weight Gain ,Abdominal obesity ,extrahepatic bile duct system cancer ,2. Zero hunger ,Liver Neoplasms ,weight gain ,Middle Aged ,Hepatitis B ,Hepatitis C ,3. Good health ,European Prospective Investigation into Cancer and Nutrition ,Europe ,Biliary Tract Neoplasms ,Oncology ,030220 oncology & carcinogenesis ,Obesity, Abdominal ,Body Composition ,030211 gastroenterology & hepatology ,Female ,medicine.symptom ,medicine.medical_specialty ,Carcinoma, Hepatocellular ,adulthood ,liver and biliary tract cancer ,Nutritional Status ,abdominal obesity ,03 medical and health sciences ,Internal medicine ,medicine ,Humans ,Gallbladder cancer ,Proportional Hazards Models ,business.industry ,Waist-Hip Ratio ,Weight change ,Body Weight ,medicine.disease ,Endocrinology ,Relative risk ,Case-Control Studies ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,business ,Body mass index - Abstract
Schlesinger, Sabrina Aleksandrova, Krasimira Pischon, Tobias Fedirko, Veronika Jenab, Mazda Trepo, Elisabeth Boffetta, Paolo Dahm, Christina C Overvad, Kim Tjonneland, Anne Halkjaer, Jytte Fagherazzi, Guy Boutron-Ruault, Marie-Christine Carbonnel, Franck Kaaks, Rudolf Lukanova, Annekatrin Boeing, Heiner Trichopoulou, Antonia Bamia, Christina Lagiou, Pagona Palli, Domenico Grioni, Sara Panico, Salvatore Tumino, Rosario Vineis, Paolo Bueno-de-Mesquita, H B van den Berg, Saskia Peeters, Petra H M Braaten, Tonje Weiderpass, Elisabete Quiros, J Ramon Travier, Noemie Sanchez, Maria-Jose Navarro, Carmen Barricarte, Aurelio Dorronsoro, Miren Lindkvist, Bjorn Regner, Sara Werner, Marten Sund, Malin Khaw, Kay-Tee Wareham, Nicholas Travis, Ruth C Norat, Teresa Wark, Petra A Riboli, Elio Nothlings, Ute eng 11692/Cancer Research UK/United Kingdom G0401527/Medical Research Council/United Kingdom G1000143/Medical Research Council/United Kingdom MC_U106179471/Medical Research Council/United Kingdom British Heart Foundation/United Kingdom Cancer Research UK/United Kingdom Department of Health/United Kingdom Medical Research Council/United Kingdom Wellcome Trust/United Kingdom Research Support, Non-U.S. Gov't 2012/05/24 06:00 Int J Cancer. 2013 Feb 1;132(3):645-57. doi: 10.1002/ijc.27645. Epub 2012 Jun 13.; International audience; General obesity has been positively associated with risk of liver and probably with biliary tract cancer, but little is known about abdominal obesity or weight gain during adulthood. We used multivariable Cox proportional hazard models to investigate associations between weight, body mass index, waist and hip circumference, waist-to-hip and waist-to-height ratio (WHtR), weight change during adulthood and risk of hepatocellular carcinoma (HCC), intrahepatic (IBDC) and extrahepatic bile duct system cancer [EBDSC including gallbladder cancer (GBC)] among 359,525 men and women in the European Prospective Investigation into Cancer and Nutrition study. Hepatitis B and C virus status was measured in a nested case-control subset. During a mean follow-up of 8.6 years, 177 cases of HCC, 58 cases of IBDC and 210 cases of EBDSC, including 76 cases of GBC, occurred. All anthropometric measures were positively associated with risk of HCC and GBC. WHtR showed the strongest association with HCC [relative risk (RR) comparing extreme tertiles 3.51, 95% confidence interval (95% CI): 2.09-5.87; p(trend) < 0.0001] and with GBC (RR: 1.56, 95% CI: 1.12-2.16 for an increment of one unit in WHtR). Weight gain during adulthood was also positively associated with HCC when comparing extreme tertiles (RR: 2.48, 95% CI: 1.49-4.13
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- 2013
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41. Alcohol attributable burden of incidence of cancer in eight European countries based on results from prospective cohort study
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Antonio Agudo, Carla H. van Gils, Naomi E. Allen, Miren Dorronsoro, Tobias Pischon, Christina C. Dahm, Antonia Trichopoulou, Madlen Schütze, Sabine Rohrmann, Tara Kehoe, Nadia Slimani, Nicholas J. Wareham, Aurelio Barricarte, Paolo Boffetta, Kim Overvad, Rudolf Kaaks, Petra H.M. Peeters, María José Sánchez, Jürgen Rehm, Anja Olsen, Gerrit Gmel, Laudina Rodríguez, Manuela M. Bergmann, Françoise Clavel-Chapelon, Heiner Boeing, Franco Berrino, Petra A. Wark, Mazda Jenab, Elio Riboli, María Dolores Chirlaque, Vasiliki Benetou, Anne Tjønneland, Dora Romaguera, Kay-Tee Khaw, Rosario Tumino, Paolo Vineis, Marie-Christine Boutron-Ruault, Dimosthenis Zylis, Domenico Palli, Timothy J. Key, Schütze, M., Boeing, H., Pischon, T., Rehm, J., Kehoe, T., Gmel, G., Olsen, A., Tjønneland, A.M., Dahm, C.C., Overvad, K., Clavel-Chapelon, F., Boutron-Ruault, M.C., Trichopoulou, A., Benetou, V., Zylis, D., Kaaks, R., Rohrmann, S., Palli, D., Berrino, F., Tumino, R., Vineis, P., Rodríguez, L., Agudo, A., Sánchez, M.J., Dorronsoro, M., Chirlaque, M.D., Barricarte, A., Peeters, P.H., van Gils, C.H., Khaw, K.T., Wareham, N., Allen, N.E., Key, T.J., Boffetta, P., Slimani, N., Jenab, M., Romaguera, D., Wark, P.A., Riboli, E., Bergmann, M.M., [Schuetze,M, Boeing,H, Pischon,T, Bergmann,MM.] German Inst Human Nutr Potsdam Rehbrucke, Dept Epidemiol, Nuthetal, Germany. [Rehm,J, Kehoe,T, Gmel,G] CAMH, Toronto, ON, Canada. [Rehm, J] Tech Univ Dresden, Inst Clin Psychol & Psychotherapy, Dresden, Germany. [Olsen,A, Tjonneland,AM.] Danish Canc Soc, Inst Canc Epidemiol, Copenhagen, Denmark. [Dahm,CC] Aarhus Univ Hosp, Dept Clin Epidemiol, Aalborg, Denmark. [Overvad,K] Aarhus Univ, Sch Publ Hlth, Dept Epidemiol, Aarhus, Denmark. [Clavel-Chapelon,F, Boutron-Ruault,M-C] Inst Gustave Roussy, Ctr Res Epidemiol & Populat Hlth,Villejuif, France. [Clavel-Chapelon,F, Boutron-Ruault,MC] Paris S Univ, UMRS 1018, Villejuif, France. [Trichopoulou, A, Benetou,V, Zylis,D] Univ Athens, Sch Med, Dept Hyg Epidemiol & Med Stat, WHO Collaborating Ctr Food & Nutr Policies, Athens, Greece. [Kaaks,R, Rohrmann,S] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany. [Palli,D] Canc Res & Prevent Inst, Mol & Nutr Epidemiol Unit, Florence, Italy. [Berrino, Franco] Fdn IRCCS Ist Nazl Tumori, Dept Prevent & Predict Med, Epidemiol Unit, Milan, Italy. [Tumino,R] Civile MP Arezzo Hosp, Canc Registry, Ragusa, Italy. [Vineis, Paolo] Inst Sci Interchange Fdn, Turin, Italy. [Rodriguez,L] Hlth & Hlth Care Serv Council, Publ Hlth & Participat Directorate, Asturias, Spain. [Tumino,R] Civile MP Arezzo Hosp, Histopathol Unit, Ragusa, Italy. [Agudo,A] Catalan Inst Oncol IDIBELL, Canc Epidemiol Res Programme, Unit Nutr Environm & Canc, Barcelona, Spain. [Sanchez,MJ] Andalusian Sch Publ Hlth, Granada, Spain. [Sanchez,MJ, Dorronsoro,M, Chirlaque,MD, Barricarte,A] CIBERESP, San Sebastian, Spain. [Dorronsoro, Miren] Publ Hlth Dept Gipuzkoa, San Sebastian, Spain. [Chirlaque,MD] Murcia Reg Hlth Council, Dept Epidemiol, Murcia, Spain. [Peeters,PH., van Gils,CH.] Univ Med Ctr, Ctr Hlth Sci & Primary Care, Utrecht, Netherlands. [Khaw,K_T] Univ Cambridge, Dept Publ Hlth & Primary Care, Cambridge, England. [Wareham,N] MRC, Epidemiol Unit, Cambridge, England. [Allen,NE., Key,TJ.] Univ Oxford, Nuffield Dept Clin Med, Canc Epidemiol Unit, England. [Boffetta, P, Slimani,N, Jenab,M] Int Agcy Res Canc, Lyon, France. [Boffetta,P] Mt Sinai Sch Med, Tisch Canc Inst, New York, NY USA. [Vineis,P, Romaguera,D, Wark,PA., Riboli,E] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, Dept Epidemiol & Biostat, London, England., The work was performed (partly) within the coordinated action EPIC (SP23-CT-2005-006438), which has received research funding from the Community’s Sixth Framework Programme, as well as by the 'Europe Against Cancer' Programme of the European Commission (SANCO), Deutsche Krebshilfe, German Cancer Research Center, German Federal Ministry of Education and Research, Danish Cancer Society, Health Research Fund (FIS) of the Spanish Ministry of Health (grant No: Network RCESP C03/09), Spanish Regional Governments of Andalucia, Asturias, Basque Country, Murcia and Navarra, ISCIII, Red de Centros RETIC(RD06/0020) (grant No: C03/09), Cancer Research UK, Medical Research Council, UK, Stroke Association, UK, British Heart Foundation, Department of Health, UK, Food Standards Agency, UK, Wellcome Trust, UK, Italian Association for Research on Cancer (AIRC), Compagnia di San Paolo, Progetto Integrato Oncologia-PIO, Regione Toscana, Dutch Ministry of Public Health, Welfare and Sports, National Cancer Registry of the Netherlands, Greek Ministry of Health and Social Solidarity, and Hellenic Health Foundation and Stavros Niarchos Foundation
- Subjects
Male ,Alcohol drinking ,Alcohol use disorder ,burden ,0302 clinical medicine ,Breast cancer ,Cost of Illness ,Neoplasms ,Medicine ,Prospective Studies ,030212 general & internal medicine ,Prospective cohort study ,Health Education ,General Environmental Science ,Colon Cancer ,Incidence (epidemiology) ,Hazard ratio ,General Engineering ,General Medicine ,cohort ,Middle Aged ,Diseases::Neoplasms [Medical Subject Headings] ,Consumo de bebidas alcohólicas ,3. Good health ,European Prospective Investigation into Cancer and Nutrition ,Colon cancer ,Europe ,Oncology ,030220 oncology & carcinogenesis ,Female ,Incidencia ,Alcohol ,Cohort study ,Adult ,medicine.medical_specialty ,Alcohol Drinking ,Health Promotion ,03 medical and health sciences ,Health Care::Environment and Public Health::Public Health::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Cohort Studies [Medical Subject Headings] ,Breast Cancer ,Humans ,cancer ,Sex Distribution ,Aged ,Health Care::Health Care Facilities, Manpower, and Services::Health Services::Preventive Health Services::Health Education [Medical Subject Headings] ,business.industry ,Research ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques [Medical Subject Headings] ,prospective ,medicine.disease ,Surgery ,Epidemiologic Studies ,Cardiovascular and Metabolic Diseases ,Relative risk ,attributable ,Attributable risk ,Psychiatry and Psychology::Behavior and Behavior Mechanisms::Behavior::Drinking Behavior::Alcohol Drinking [Medical Subject Headings] ,incidence ,General Earth and Planetary Sciences ,Health Care::Environment and Public Health::Public Health::Epidemiologic Methods::Data Collection::Vital Statistics::Morbidity::Incidence [Medical Subject Headings] ,business ,Quantitative research ,Demography - Abstract
Objective To compute the burden of cancer attributable to current and former alcohol consumption in eight European countries based on direct relative risk estimates from a cohort study. Design Combination of prospective cohort study with representative population based data on alcohol exposure. Setting Eight countries (France, Italy, Spain, United Kingdom, the Netherlands, Greece, Germany, Denmark) participating in the European Prospective Investigation into Cancer and Nutrition (EPIC) study. Participants 109 118 men and 254 870 women, mainly aged 37-70. Main outcome measures Hazard rate ratios expressing the relative risk of cancer incidence for former and current alcohol consumption among EPIC participants. Hazard rate ratios combined with representative information on alcohol consumption to calculate alcohol attributable fractions of causally related cancers by country and sex. Partial alcohol attributable fractions for consumption higher than the recommended upper limit (two drinks a day for men with about 24 g alcohol, one for women with about 12 g alcohol) and the estimated total annual number of cases of alcohol attributable cancer. Results If we assume causality, among men and women, 10% (95% confidence interval 7 to 13%) and 3% (1 to 5%) of the incidence of total cancer was attributable to former and current alcohol consumption in the selected European countries. For selected cancers the figures were 44% (31 to 56%) and 25% (5 to 46%) for upper aerodigestive tract, 33% (11 to 54%) and 18% (−3 to 38%) for liver, 17% (10 to 25%) and 4% (−1 to 10%) for colorectal cancer for men and women, respectively, and 5.0% (2 to 8%) for female breast cancer. A substantial part of the alcohol attributable fraction in 2008 was associated with alcohol consumption higher than the recommended upper limit: 33 037 of 178 578 alcohol related cancer cases in men and 17 470 of 397 043 alcohol related cases in women. Conclusions In western Europe, an important proportion of cases of cancer can be attributable to alcohol consumption, especially consumption higher than the recommended upper limits. These data support current political efforts to reduce or to abstain from alcohol consumption to reduce the incidence of cancer.
- Published
- 2011
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