578 results on '"Sayer, Avan Aihie"'
Search Results
202. Nutrition and Muscle Strength, As the Key Component of Sarcopenia: An Overview of Current Evidence.
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Robinson, Sian, Granic, Antoneta, and Sayer, Avan Aihie
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Much has been achieved by recent research to increase understanding of the links between nutrition and muscle health. Focusing on muscle strength as the key component of sarcopenia, the aim of this overview was to evaluate its links to nutrition, both to variation in habitual diets in older populations, as well as considering supplementation effects in trials. A main message from the reviewed studies is that while many provide suggestive evidence of benefits of higher nutrient intakes and diets of higher quality, findings are inconsistent, and data on muscle strength are often lacking. To assess the potential of optimising diets as a strategy to promote and maintain muscle strength, gaps in current evidence need to be addressed. These include the need for (i) better understanding of individual differences in responsiveness to dietary change, and the need for targeted nutritional support; (ii) clearer distinction between protective and therapeutic actions of diet; and (iii) definition of the role of dietary patterns and their influence on muscle strength, to allow effects of changes in food consumption to be evaluated—particularly when combined with physical activity. Development of this evidence is needed to enable translation into appropriate dietary recommendations for older populations. [ABSTRACT FROM AUTHOR]
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- 2019
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203. Retinal vascular network architecture in lowbirthweight men
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Chapman, Neil, Mohamudally, Anthoulla, Cerutti, Alessia, Stanton, Alice, Sayer, Avan Aihie, Cooper, Cyrus, Barker, David, Rauf, Abdul, Evans, Jennifer, Wormald, Richard, Sever, Peter, Hughes, Alun, and Thom, Simon
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Low birth weight is associated with hypertension and increased cardiovascular mortality, but the mechanism of this association is not known. Hypertension is accompanied by abnormalities of the microvasculature including rarefaction.
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- 1997
204. The interrelationship between multiple long-term conditions (MLTC) and delirium: a scoping review.
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Richardson, Sarah Joanna, Cropp, Alexandria Danielle, Ellis, Samantha Wilhelmina, Gibbon, Jake, Sayer, Avan Aihie, and Witham, Miles David
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RISK assessment , *MEDICAL information storage & retrieval systems , *RESEARCH funding , *CINAHL database , *DESCRIPTIVE statistics , *CHRONIC diseases , *SYSTEMATIC reviews , *MEDLINE , *DELIRIUM , *LITERATURE reviews , *ONLINE information services , *COMORBIDITY , *PSYCHOLOGY information storage & retrieval systems , *DISEASE complications - Abstract
Introduction Delirium and multiple long-term conditions (MLTC) share numerous risk factors and have been shown individually to be associated with adverse outcomes following hospitalisation. However, the extent to which these common ageing syndromes have been studied together is unknown. This scoping review aims to summarise our knowledge to date on the interrelationship between MLTC and delirium. Methods Searches including terms for delirium and MLTC in adult human participants were performed in PubMed, EMBASE, Medline, Psycinfo and CINAHL. Descriptive analysis was used to summarise findings, structured according to Synthesis Without Meta-analysis reporting guidelines. Results After removing duplicates, 5256 abstracts were screened for eligibility, with 313 full-texts sought along with 17 additional full-texts from references in review articles. In total, 140 met inclusion criteria and were included in the final review. Much of the literature explored MLTC as a risk factor for delirium (n = 125). Fewer studies explored the impact of MLTC on delirium presentation (n = 5), duration (n = 3) or outcomes (n = 6) and no studies explored how MLTC impacts the treatment of delirium or whether having delirium increases risk of developing MLTC. The most frequently used measures of MLTC and delirium were the Charlson Comorbidity Index (n = 98/140) and Confusion Assessment Method (n = 81/140), respectively. Conclusion Existing literature largely evaluates MLTC as a risk factor for delirium. Major knowledge gaps identified include the impact of MLTC on delirium treatment and the effect of delirium on MLTC trajectories. Current research in this field is limited by significant heterogeneity in defining both MLTC and delirium. [ABSTRACT FROM AUTHOR]
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- 2024
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205. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
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Dastani, Zari, Hivert, Marie-France, Timpson, Nicholas, Perry, John RB, Yuan, Xin, Scott, Robert A, Henneman, Peter, Heid, Iris M, Kizer, Jorge R, Lyytikäinen, Leo-Pekka, Fuchsberger, Christian, Tanaka, Toshiko, Morris, Andrew P, Small, Kerrin, Isaacs, Aaron, Beekman, Marian, Coassin, Stefan, Lohman, Kurt, Qi, Lu, Kanoni, Stavroula, Pankow, James S, Uh, Hae-Won, Wu, Ying, Bidulescu, Aurelian, Rasmussen-Torvik, Laura J, Greenwood, Celia MT, Ladouceur, Martin, Grimsby, Jonna, Manning, Alisa K, Liu, Ching-Ti, Kooner, Jaspal, Mooser, Vincent E, Vollenweider, Peter, Kapur, Karen A, Chambers, John, Wareham, Nicholas J, Langenberg, Claudia, Frants, Rune, Willems-Vandijk, Ko, Oostra, Ben A, Willems, Sara M, Lamina, Claudia, Winkler, Thomas W, Psaty, Bruce M, Tracy, Russell P, Brody, Jennifer, Chen, Ida, Viikari, Jorma, Kähönen, Mika, Pramstaller, Peter P, Evans, David M, St Pourcain, Beate, Sattar, Naveed, Wood, Andrew R, Bandinelli, Stefania, Carlson, Olga D, Egan, Josephine M, Böhringer, Stefan, Van Heemst, Diana, Kedenko, Lyudmyla, Kristiansson, Kati, Nuotio, Marja-Liisa, Loo, Britt-Marie, Harris, Tamara, Garcia, Melissa, Kanaya, Alka, Haun, Margot, Klopp, Norman, Wichmann, H-Erich, Deloukas, Panos, Katsareli, Efi, Couper, David J, Duncan, Bruce B, Kloppenburg, Margreet, Adair, Linda S, Borja, Judith B, DIAGRAM+ Consortium, MAGIC Consortium, GLGC Investigators, MuTHER Consortium, Wilson, James G, Musani, Solomon, Guo, Xiuqing, Johnson, Toby, Semple, Robert, Teslovich, Tanya M, Allison, Matthew A, Redline, Susan, Buxbaum, Sarah G, Mohlke, Karen L, Meulenbelt, Ingrid, Ballantyne, Christie M, Dedoussis, George V, Hu, Frank B, Liu, Yongmei, Paulweber, Bernhard, Spector, Timothy D, Slagboom, P Eline, Ferrucci, Luigi, Jula, Antti, Perola, Markus, Raitakari, Olli, Florez, Jose C, Salomaa, Veikko, Eriksson, Johan G, Frayling, Timothy M, Hicks, Andrew A, Lehtimäki, Terho, Smith, George Davey, Siscovick, David S, Kronenberg, Florian, Van Duijn, Cornelia, Loos, Ruth JF, Waterworth, Dawn M, Meigs, James B, Dupuis, Josee, Richards, J Brent, Voight, Benjamin F, Scott, Laura J, Steinthorsdottir, Valgerdur, Dina, Christian, Welch, Ryan P, Zeggini, Eleftheria, Huth, Cornelia, Aulchenko, Yurii S, Thorleifsson, Gudmar, McCulloch, Laura J, Ferreira, Teresa, Grallert, Harald, Amin, Najaf, Wu, Guanming, Willer, Cristen J, Raychaudhuri, Soumya, McCarroll, Steve A, Hofmann, Oliver M, Segrè, Ayellet V, Van Hoek, Mandy, Navarro, Pau, Ardlie, Kristin, Balkau, Beverley, Benediktsson, Rafn, Bennett, Amanda J, Blagieva, Roza, Boerwinkle, Eric, Bonnycastle, Lori L, Boström, Kristina Bengtsson, Bravenboer, Bert, Bumpstead, Suzannah, Burtt, Noël P, Charpentier, Guillaume, Chines, Peter S, Cornelis, Marilyn, Crawford, Gabe, Doney, Alex SF, Elliott, Katherine S, Elliott, Amanda L, Erdos, Michael R, Fox, Caroline S, Franklin, Christopher S, Ganser, Martha, Gieger, Christian, Grarup, Niels, Green, Todd, Griffin, Simon, Groves, Christopher J, Guiducci, Candace, Hadjadj, Samy, Hassanali, Neelam, Herder, Christian, Isomaa, Bo, Jackson, Anne U, Johnson, Paul RV, Jørgensen, Torben, Kao, Wen HL, Kong, Augustine, Kraft, Peter, Kuusisto, Johanna, Lauritzen, Torsten, Li, Man, Lieverse, Aloysius, Lindgren, Cecilia M, Lyssenko, Valeriya, Marre, Michel, Meitinger, Thomas, Midthjell, Kristian, Morken, Mario A, Narisu, Narisu, Nilsson, Peter, Owen, Katharine R, Payne, Felicity, Petersen, Ann-Kristin, Platou, Carl, Proença, Christine, Prokopenko, Inga, Rathmann, Wolfgang, Rayner, N William, Robertson, Neil R, Rocheleau, Ghislain, Roden, Michael, Sampson, Michael J, Saxena, Richa, Shields, Beverley M, Shrader, Peter, Sigurdsson, Gunnar, Sparsø, Thomas, Strassburger, Klaus, Stringham, Heather M, Sun, Qi, Swift, Amy J, Thorand, Barbara, Tichet, Jean, Tuomi, Tiinamaija, Van Dam, Rob M, Van Haeften, Timon W, Van Herpt, Thijs, Van Vliet-Ostaptchouk, Jana V, Walters, G Bragi, Weedon, Michael N, Wijmenga, Cisca, Witteman, Jacqueline, Bergman, Richard N, Cauchi, Stephane, Collins, Francis S, Gloyn, Anna L, Gyllensten, Ulf, Hansen, Torben, Hide, Winston A, Hitman, Graham A, Hofman, Albert, Hunter, David J, Hveem, Kristian, Laakso, Markku, Morris, Andrew D, Palmer, Colin NA, Rudan, Igor, Sijbrands, Eric, Stein, Lincoln D, Tuomilehto, Jaakko, Uitterlinden, Andre, Walker, Mark, Watanabe, Richard M, Abecasis, Goncalo R, Boehm, Bernhard O, Campbell, Harry, Daly, Mark J, Hattersley, Andrew T, Pedersen, Oluf, Barroso, Inês, Groop, Leif, Sladek, Rob, Thorsteinsdottir, Unnur, Wilson, James F, Illig, Thomas, Froguel, Philippe, Van Duijn, Cornelia M, Stefansson, Kari, Altshuler, David, Boehnke, Michael, McCarthy, Mark I, Soranzo, Nicole, Wheeler, Eleanor, Glazer, Nicole L, Bouatia-Naji, Nabila, Mägi, Reedik, Randall, Joshua, Elliott, Paul, Rybin, Denis, Dehghan, Abbas, Hottenga, Jouke Jan, Song, Kijoung, Goel, Anuj, Lajunen, Taina, Doney, Alex, Cavalcanti-Proença, Christine, Kumari, Meena, Timpson, Nicholas J, Zabena, Carina, Ingelsson, Erik, An, Ping, O'Connell, Jeffrey, Luan, Jian'an, Elliott, Amanda, McCarroll, Steven A, Roccasecca, Rosa Maria, Pattou, François, Sethupathy, Praveen, Ariyurek, Yavuz, Barter, Philip, Beilby, John P, Ben-Shlomo, Yoav, Bergmann, Sven, Bochud, Murielle, Bonnefond, Amélie, Borch-Johnsen, Knut, Böttcher, Yvonne, Brunner, Eric, Bumpstead, Suzannah J, Chen, Yii-Der Ida, Chines, Peter, Clarke, Robert, Coin, Lachlan JM, Cooper, Matthew N, Crisponi, Laura, Day, Ian NM, De Geus, Eco JC, Delplanque, Jerome, Fedson, Annette C, Fischer-Rosinsky, Antje, Forouhi, Nita G, Franzosi, Maria Grazia, Galan, Pilar, Goodarzi, Mark O, Graessler, Jürgen, Grundy, Scott, Gwilliam, Rhian, Hallmans, Göran, Hammond, Naomi, Han, Xijing, Hartikainen, Anna-Liisa, Hayward, Caroline, Heath, Simon C, Hercberg, Serge, Hillman, David R, Hingorani, Aroon D, Hui, Jennie, Hung, Joe, Kaakinen, Marika, Kaprio, Jaakko, Kesaniemi, Y Antero, Kivimaki, Mika, Knight, Beatrice, Koskinen, Seppo, Kovacs, Peter, Kyvik, Kirsten Ohm, Lathrop, G Mark, Lawlor, Debbie A, Le Bacquer, Olivier, Lecoeur, Cécile, Li, Yun, Mahley, Robert, Mangino, Massimo, Martínez-Larrad, María Teresa, McAteer, Jarred B, McPherson, Ruth, Meisinger, Christa, Melzer, David, Meyre, David, Mitchell, Braxton D, Mukherjee, Sutapa, Naitza, Silvia, Neville, Matthew J, Orrù, Marco, Pakyz, Ruth, Paolisso, Giuseppe, Pattaro, Cristian, Pearson, Daniel, Peden, John F, Pedersen, Nancy L, Pfeiffer, Andreas FH, Pichler, Irene, Polasek, Ozren, Posthuma, Danielle, Potter, Simon C, Pouta, Anneli, Province, Michael A, Rayner, Nigel W, Rice, Kenneth, Ripatti, Samuli, Rivadeneira, Fernando, Rolandsson, Olov, Sandbaek, Annelli, Sandhu, Manjinder, Sanna, Serena, Sayer, Avan Aihie, Scheet, Paul, Seedorf, Udo, Sharp, Stephen J, Shields, Beverley, Sigurðsson, Gunnar, Sijbrands, Eric JG, Silveira, Angela, Simpson, Laila, Singleton, Andrew, Smith, Nicholas L, Sovio, Ulla, Swift, Amy, Syddall, Holly, Syvänen, Ann-Christine, Tönjes, Anke, Uitterlinden, André G, Van Dijk, Ko Willems, Varma, Dhiraj, Visvikis-Siest, Sophie, Vitart, Veronique, Vogelzangs, Nicole, Waeber, Gérard, Wagner, Peter J, Walley, Andrew, Ward, Kim L, Watkins, Hugh, Wild, Sarah H, Willemsen, Gonneke, Witteman, Jaqueline CM, Yarnell, John WG, Zelenika, Diana, Zethelius, Björn, Zhai, Guangju, Zhao, Jing Hua, Zillikens, M Carola, DIAGRAM Consortium, GIANT Consortium, Global B Pgen Consortium, Borecki, Ingrid B, Meneton, Pierre, Magnusson, Patrik KE, Nathan, David M, Williams, Gordon H, Silander, Kaisa, Bornstein, Stefan R, Schwarz, Peter, Spranger, Joachim, Karpe, Fredrik, Shuldiner, Alan R, Cooper, Cyrus, Serrano-Ríos, Manuel, Lind, Lars, Palmer, Lyle J, Franks, Paul W, Ebrahim, Shah, Marmot, Michael, Kao, WH Linda, Pramstaller, Peter Paul, Wright, Alan F, Stumvoll, Michael, Hamsten, Anders, Procardis Consortium, Buchanan, Thomas A, Valle, Timo T, Rotter, Jerome I, Penninx, Brenda WJH, Boomsma, Dorret I, Cao, Antonio, Scuteri, Angelo, Schlessinger, David, Uda, Manuela, Ruokonen, Aimo, Jarvelin, Marjo-Riitta, Peltonen, Leena, Mooser, Vincent, Sladek, Robert, MAGIC Investigators, GLGC Consortium, Musunuru, Kiran, Smith, Albert V, Edmondson, Andrew C, Stylianou, Ioannis M, Koseki, Masahiro, Pirruccello, James P, Chasman, Daniel I, Johansen, Christopher T, Fouchier, Sigrid W, Peloso, Gina M, Barbalic, Maja, Ricketts, Sally L, Bis, Joshua C, Feitosa, Mary F, Orho-Melander, Marju, Melander, Olle, Li, Xiaohui, Li, Mingyao, Cho, Yoon Shin, Go, Min Jin, Kim, Young Jin, Lee, Jong-Young, Park, Taesung, Kim, Kyunga, Sim, Xueling, Ong, Rick Twee-Hee, Croteau-Chonka, Damien C, Lange, Leslie A, Smith, Joshua D, Ziegler, Andreas, Zhang, Weihua, Zee, Robert YL, Whitfield, John B, Thompson, John R, Surakka, Ida, Spector, Tim D, Smit, Johannes H, Sinisalo, Juha, Scott, James, Saharinen, Juha, Sabatti, Chiara, Rose, Lynda M, Roberts, Robert, Rieder, Mark, Parker, Alex N, Pare, Guillaume, O'Donnell, Christopher J, Nieminen, Markku S, Nickerson, Deborah A, Montgomery, Grant W, McArdle, Wendy, Masson, David, Martin, Nicholas G, Marroni, Fabio, Lucas, Gavin, Luben, Robert, Lokki, Marja-Liisa, Lettre, Guillaume, Launer, Lenore J, Lakatta, Edward G, Laaksonen, Reijo, Kyvik, Kirsten O, König, Inke R, Khaw, Kay-Tee, Kaplan, Lee M, Johansson, Åsa, Janssens, A Cecile JW, Igl, Wilmar, Hovingh, G Kees, Hengstenberg, Christian, Havulinna, Aki S, Hastie, Nicholas D, Harris, Tamara B, Haritunians, Talin, Hall, Alistair S, Groop, Leif C, Gonzalez, Elena, Freimer, Nelson B, Erdmann, Jeanette, Ejebe, Kenechi G, Döring, Angela, Dominiczak, Anna F, Demissie, Serkalem, Deloukas, Panagiotis, De Faire, Ulf, Crawford, Gabriel, Chen, Yii-Der I, Caulfield, Mark J, Boekholdt, S Matthijs, Assimes, Themistocles L, Quertermous, Thomas, Seielstad, Mark, Wong, Tien Y, Tai, E-Shyong, Feranil, Alan B, Kuzawa, Christopher W, Taylor, Herman A, Gabriel, Stacey B, Holm, Hilma, Gudnason, Vilmundur, Krauss, Ronald M, Ordovas, Jose M, Munroe, Patricia B, Kooner, Jaspal S, Tall, Alan R, Hegele, Robert A, Kastelein, John JP, Schadt, Eric E, Strachan, David P, Reilly, Muredach P, Samani, Nilesh J, Schunkert, Heribert, Cupples, L Adrienne, Sandhu, Manjinder S, Ridker, Paul M, Rader, Daniel J, and Kathiresan, Sekar
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2. Zero hunger ,Male ,Waist-Hip Ratio ,Cholesterol, HDL ,Gene Expression ,Glucose Tolerance Test ,Polymorphism, Single Nucleotide ,White People ,3. Good health ,Black or African American ,Asian People ,Diabetes Mellitus, Type 2 ,Humans ,Female ,Genetic Predisposition to Disease ,Adiponectin ,Insulin Resistance ,Metabolic Networks and Pathways ,Genome-Wide Association Study - Abstract
Circulating levels of adiponectin, a hormone produced predominantly by adipocytes, are highly heritable and are inversely associated with type 2 diabetes mellitus (T2D) and other metabolic traits. We conducted a meta-analysis of genome-wide association studies in 39,883 individuals of European ancestry to identify genes associated with metabolic disease. We identified 8 novel loci associated with adiponectin levels and confirmed 2 previously reported loci (P = 4.5×10(-8)-1.2×10(-43)). Using a novel method to combine data across ethnicities (N = 4,232 African Americans, N = 1,776 Asians, and N = 29,347 Europeans), we identified two additional novel loci. Expression analyses of 436 human adipocyte samples revealed that mRNA levels of 18 genes at candidate regions were associated with adiponectin concentrations after accounting for multiple testing (p
206. Intrahepatic Lipid Content and Insulin Resistance Are More Strongly Associated with Impaired NEFA Suppression after Oral Glucose Loading Than with Fasting NEFA Levels in Healthy Older Individuals
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Finucane, Francis M, Sharp, Stephen J, Hatunic, Mensud, Sleigh, Alison, De Lucia Rolfe, Ema, Sayer, Avan Aihie, Cooper, Cyrus, Griffin, Simon J, Savage, David B, and Wareham, Nicholas J
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Prevention ,Diabetes ,1103 Clinical Sciences ,Metabolic and Endocrine ,3. Good health ,Clinical ,Clinical Medicine and Science ,Oral and Gastrointestinal ,Clinical Research ,5.1 Pharmaceuticals ,2.1 Biological and endogenous factors ,Obesity ,Digestive Diseases ,Nutrition - Abstract
Introduction. The mechanisms underlying the association between insulin resistance and intrahepatic lipid (IHL) accumulation are not completely understood. We sought to determine whether this association was explained by differences in fasting non-esterified fatty acid (NEFA) levels and/or NEFA suppression after oral glucose loading. Materials and Methods. We performed a cross-sectional analysis of 70 healthy participants in the Hertfordshire Physical Activity Trial (39 males, age 71.3 ± 2.4 years) who underwent oral glucose tolerance testing with glucose, insulin, and NEFA levels measured over two hours. IHL was quantified with magnetic resonance spectroscopy. Insulin sensitivity was measured with the oral glucose insulin sensitivity (OGIS) model, the leptin: adiponectin ratio (LAR), and the homeostasis model assessment (HOMA). Results. Measures of insulin sensitivity were not associated with fasting NEFA levels, but OGIS was strongly associated with NEFA suppression at 30 minutes and strongly inversely associated with IHL. Moreover, LAR was strongly inversely associated with NEFA suppression and strongly associated with IHL. This latter association (beta = 1.11 [1.01, 1.21], P = 0.026) was explained by reduced NEFA suppression (P = 0.24 after adjustment). Conclusions. Impaired postprandial NEFA suppression, but not fasting NEFA, contributes to the strong and well-established association between whole body insulin resistance and liver fat accumulation.
207. The dynamic relationship between cognitive function and walking speed: the English Longitudinal Study of Ageing
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Gale, Catharine R, Allerhand, Michael, Sayer, Avan Aihie, Cooper, Cyrus, and Deary, Ian J
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Aged, 80 and over ,Male ,Aging ,Walking ,Middle Aged ,Neuropsychological Tests ,Walking speed ,Article ,Executive Function ,Ageing ,Cognition ,Cross-Sectional Studies ,England ,Memory ,Cohort studies ,Humans ,Female ,Cognitive function ,Geriatrics and Gerontology ,human activities ,Aged ,Follow-Up Studies ,Retrospective Studies - Abstract
Cross-sectional studies show that older people with better cognition tend to walk faster. Whether this association reflects an influence of fluid cognition upon walking speed, vice versa, a bidirectional relationship or the effect of common causes is unclear. We used linear mixed effects models to examine the dynamic relationship between usual walking speed and fluid cognition, as measured by executive function, verbal memory and processing speed, in 2,654 men and women aged 60 to over 90 years from the English Longitudinal Study of Ageing. There was a bidirectional relationship between walking speed and fluid cognition. After adjusting for age and sex, better performance on executive function, memory and processing speed was associated with less yearly decline in walking speed over the 6-year follow-up period; faster walking speed was associated with less yearly decline in each cognitive domain; and less yearly decline in each cognitive domain was associated with less yearly decline in walking speed. Effect sizes were small. After further adjustment for other covariates, effect sizes were attenuated but most remained statistically significant. We found some evidence that walking speed and the fluid cognitive domains of executive function and processing speed may change in parallel with increasing age. Investigation of the association between walking speed and cognition earlier in life is needed to better understand the origins of this relation and inform the development and timing of interventions.
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208. Associations between APOE and low-density lipoprotein cholesterol genotypes and cognitive and physical capability: the HALCyon programme
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Alfred, Tamuno, Ben-Shlomo, Yoav, Cooper, Rachel, Hardy, Rebecca, Cooper, Cyrus, Deary, Ian J., Elliott, Jane, Gunnell, David, Harris, Sarah E., Kivimaki, Mika, Kumari, Meena, Martin, Richard M, Power, Chris, Sayer, Avan Aihie, Starr, John M., Kuh, Diana, and Day, Ian NM
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Adult ,Male ,Aging ,Polymorphism, Genetic ,Time Factors ,Apolipoprotein E4 ,Enzyme-Linked Immunosorbent Assay ,Cholesterol, LDL ,DNA ,Walking ,Middle Aged ,Article ,Single nucleotide polymorphism ,Ageing ,Cognition ,Phenotype ,Alzheimer Disease ,Humans ,Female ,lipids (amino acids, peptides, and proteins) ,Apolipoprotein E ,Prospective Studies ,Geriatrics and Gerontology ,Follow-Up Studies - Abstract
The APOE ε2/3/4 genotype has been associated with low-density lipoprotein cholesterol (LDL-C) and Alzheimer disease. However, evidence for associations with measures of cognitive performance in adults without dementia has been mixed, as it is for physical performance. Associations may also be evident in other genotypes implicated in LDL-C levels. As part of the Healthy Ageing across the Life Course (HALCyon) collaborative research programme, genotypic information was obtained for APOE ε2/3/4, rs515135 (APOB), rs2228671 (LDLR) and rs629301 (SORT1) from eight cohorts of adults aged between 44 and 90 + years. We investigated associations with four measures of cognitive (word recall, phonemic fluency, semantic fluency and search speed) and physical capability (grip strength, get up and go/walk speed, timed chair rises and ability to balance) using meta-analyses. Overall, little evidence for associations between any of the genotypes and measures of cognitive capability was observed (e.g. pooled beta for APOE ε4 effect on semantic fluency z score = −0.02; 95 % CI = −0.05 to 0.02; p value = 0.3; n = 18,796). However, there was borderline evidence within studies that negative effects of APOE ε4 on nonverbal ability measures become more apparent with age. Few genotypic associations were observed with physical capability measures. The findings from our large investigation of middle-aged to older adults in the general population suggest that effects of APOE on cognitive capability are at most modest and are domain- and age-specific, while APOE has little influence on physical capability. In addition, other LDL-C-related genotypes have little impact on these traits. Electronic supplementary material The online version of this article (doi:10.1007/s11357-014-9673-9) contains supplementary material, which is available to authorized users.
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209. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
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Global BPgen Consrotium, Sovio, Ulla, Shuldiner, Alan R., Dedoussis, George V., Bonnycastle, Lori L., Hercberg, Serge, Chen, Yii-Der Ida, Visvikis-Siest, Sophie, Kumari, Meena, Meneton, Pierre, Ariyurek, Yavuz, Egan, Josephine M., Ben-Shlomo, Yoav, Forouhi, Nita G., Graessler, Jurgen, Rudan, Igor, Pedersen, Nancy L., Lindgren, Cecilia M., Chines, Peter, Stringham, Heather M., Meisinger, Christa, Pattaro, Cristian, Vogelzangs, Nicole, DIAGRAM Consortium, Illig, Thomas, Langenberg, Claudia, Zethelius, Bjorn, Sayer, Avan Aihie, Laakso, Markku, Li, Man, Clarke, Robert, Isomaa, Bo, McAteer, Jarred B., Doney, Alex, Pedersen, Oluf, Jorgensen, Torben, Bottcher, Yvonne, Ebrahim, Shah, Schwarz, Peter, Lecoeur, Cecile, Psaty, Bruce M., Shrader, Peter, Knight, Beatrice, Beilby, John P., Gieger, Christian, Ripatti, Samuli, Zhao, Jing Hua, Herder, Christian, Morken, Mario A., Kesaniemi, Y. Antero, Orru, Marco, Mitchell, Braxton D., Thorand, Barbara, Lyssenko, Valeriya, Manning, Alisa K., Sethupathy, Praveen, Meyre, David, Hansen, Torben, Rayner, Nigel W., Hammond, Naomi, Timpson, Nicholas J., Sanna, Serena, Brunner, Eric, Zhai, Guangju, Witteman, Jacqueline C.M., Rybin, Denis, Cornelis, Marilyn, Zabena, Carina, Willemson, Gonneke, Kaakinen, Marika, Perry, John R.B., Zelenika, Diana, Walters, G. Bragi, Heath, Simon C., Oostra, Ben A., Salomaa, Veikko, Ward, Kim L., van Dijk, Ko Willems, Williams, Gordon H., Karpe, Fredrik, Wagner, Peter J., Magi, Reedik, Fischer-Rosinsky, Antje, Hallmans, Goran, Lajunen, Taina, Qi, Lu, Navarro, Paul, Grallert, Harald, Pramstaller, Peter Paul, Kaprio, Jaakko, Smith, Nicholas L., Hayward, Caroline, Sandbaek, Annelli, Sparso, Thomas, Dina, Christian, Paolisso, Giuseppe, Wright, Alan F., Mangino, Massimo, Henneman, Peter, Smith, George Davey, Boerwinkle, Eric, Prokopenko, Inga, Jackson, Anne U., Grarup, Niels, Walley, Andrew, Hofman, Albert, Hadjadj, Samy, Hu, Frank B., Hung, Joe, Li, Yun, Gwilliam, Rhian, Thorleifsson, Gudmar, Singleton, Andrew, Ardlie, Kristin, Kivimaki, Mika, Syvanen, Ann-Christine, Zillikens, M. Carola, Day, Ian N.M., Rice, Kenneth, Silander, Kaisa, Bergmann, Sven, Simpson, Laila, Scott, Laura J., Melzer, David, Neville, Matthew J., Watkins, Hugh, Ingelsson, Erik, Lathrop, G. Mark, Scheet, Paul, Hottenga, Jouke Jan, Song, Kijoung, Benediktsson, Rafn, de Geus, Eco J. C., Le Bacquer, Olivier, Hillman, David R., Koskinen, Seppo, Frants, Rune, Lind, Lars, Kanoni, Stavroula, Sandhu, Manjinder, Crawford, Gabe, Sigurdsson, Gunnar, Pfeiffer, Andreas F.H., Pattou, Francois, Pankow, James S., Wilson, James F., Bennett, Amanda J., Dupuis, Josee, Potter, Simon C., Elliott, Amanda, Province, Michael A., Perola, Markus, Serrano-Rios, Manuel, Kyvik, Kirsten Ohm, Yarnell, John W.G., Pakyz, Ruth, Johnson, Paul R.V., Borch-Johnsen, Knut, Saxena, Richa, Steinthorsdottir, Valgerdur, Tanaka, Toshiko, Campbell, Harry, Barter, Philip, Franzosi, Maria Grazia, GIANT Consortium, Han, Xijing, Cavalcanti-Proenca, Christine, Glazer, Nicole L., Kovacs, Peter, Stumvoll, Michael, Syddall, Holly, Hingorani, Aroon D., Morris, Andrew P., O'Connell, Jeffrey, Payne, Felicity, Galan, Pilar, Rivadeneira, Fernando, Wild, Sarah H., McPherson, Ruth, Sijbrands, Eric J.G., Hicks, Andrew A., Dehghan, Abbas, Elliott, Paul, Cooper, Matthew N., Sharp, Stephen J., Balkau, Beverley, Voight, Benjamin F., Roden, Michael, Tuomi, Tiinamaija, Franklin, Christopher S., Swift, Amy, Pichler, Irene, Narisu, Narisu, Goodarzi, Mark O., Franks, Paul W., An, Ping, Bumpstead, Suzannah J., Bochud, Murielle, Rathmann, Wolfgang, Randall, Joshua, Bouatia-Naji, Nabila, von Hoek, Mandy, Kuusisto, Johanna, Sampson, Michael J., Wichmann, H. Erich, Vitart, Veronique, Tichet, Jean, Spranger, Joachim, Fedson, Annette C., Waeber, Gerard, Wheeler, Eleanor, Polasek, Ozren, Coin, Lachlan J.M., Varma, Dhiraj, Pearson, Daniel, Hartikainen, Anna-Liisa, Loos, Ruth J.F., Grundy, Scott, Martinez-Larrad, Maria Teresa, Jula, Antti, Palmer, Colin N.A., Mukherjee, Sutapa, Bornstein, Stefan R., Gyllensten, Ulf, Roccasecca, Rosa Maria, Johnson, Toby, Crisponi, Laura, Weedon, Michael N., Hamsten, Anders, Bonnefond, Amelie, Nathan, David M., Silveira, Angela, Borecki, Ingrid B., Hassanali, Neelam, Pouta, Anneli, Fox, Caroline S., Cooper, Cyrus, McCulloch, Laura J., Hattersley, Andrew T., Seedorf, Udo, Zeggini, Eleftheria, Lawlor, Debbie A., Uitterlinden, Andre G., Rocheleau, Ghislain, Kao, W.H. Linda, Goel, Anuj, Palmer, Lyel J., Magnusson, Patrik K.E., Shields, Beverley, Tonjes, Anke, Soranzo, Nicole, Groves, Christopher J., Gloyn, Anna L., Charpentier, Guillaume, Erdos, Michael R., Posthuma, Danielle, Marmot, Michael, Morris, Andrew D., Luan, Jian'an, Delplanque, Jerome, Naitza, Silvia, Mahley, Robert, McCarroll, Steven A., Hui, Jennie, Rolandsson, Olov, and Peden, John F.
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3. Good health - Abstract
Levels of circulating glucose are tightly regulated. To identify new loci influencing glycemic traits, we performed meta-analyses of 21 genome-wide association studies informative for fasting glucose, fasting insulin and indices of beta-cell function (HOMA-B) and insulin resistance (HOMA-IR) in up to 46,186 nondiabetic participants. Follow-up of 25 loci in up to 76,558 additional subjects identified 16 loci associated with fasting glucose and HOMA-B and two loci associated with fasting insulin and HOMA-IR. These include nine loci newly associated with fasting glucose (in or near ADCY5, MADD, ADRA2A, CRY2, FADS1, GLIS3, SLC2A2, PROX1 and C2CD4B) and one influencing fasting insulin and HOMA-IR (near IGF1). We also demonstrated association of ADCY5, PROX1, GCK, GCKR and DGKB-TMEM195 with type 2 diabetes. Within these loci, likely biological candidate genes influence signal transduction, cell proliferation, development, glucose-sensing and circadian regulation. Our results demonstrate that genetic studies of glycemic traits can identify type 2 diabetes risk loci, as well as loci containing gene variants that are associated with a modest elevation in glucose levels but are not associated with overt diabetes.
210. Introduction to the Age and Ageing sarcopenia collection.
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WITHAM, MILES D. and SAYER, AVAN AIHIE
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ADVERSE health care events , *ACCIDENTAL falls , *SERIAL publications , *SARCOPENIA , *PATIENT-centered care - Abstract
The article discusses the contents of the papers about sarcopenia published in online "Age and Ageing" magazine. Topic covered include evolution of the definition of sarcopenia, evidence on the causes, prevalence and adverse effects of sarcopenia, evaluation of existing therapy for the disease and marginal decrease in muscle mass and reduction in grip strength of older people.
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- 2016
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211. Sarcopenia the new geriatric giant: time to translate research findings into clinical practice.
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Sayer, Avan Aihie
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MUSCULAR atrophy , *ELDER care , *DIET therapy , *EXERCISE therapy , *THERAPEUTICS - Abstract
The authors reflect on the immobility and instability as geriatric giants sarcopenia and the significance of changes in ageing skeletal muscle. The authors state the research and clinical practice on the loss of skeletal muscle mass and function with age. The author also emphasizes the standardised approach and methodology adopted in prevalence studies on the interventions for sarcopenia.
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- 2014
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212. OBITUARIES.
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Sayer, Avan Aihie, Stanbridge, Rex, Cowmeadow, Richard, Mounty, Jane, Edmondson, Pat, Crawford, Michael, and Mills, Penelope Riches
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PHYSICAL therapists , *PHYSICIANS - Abstract
Obituaries for several peoples are presented including British public health consultant Pamela Aihie, British consultant cardiothoracic surgeon Lance Lee Bromley and General practitioner Audrey Finnegan.
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- 2013
213. Sarcopenia: A research agenda has been set, but recognition in clinical practice is lagging behind.
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Sayer, Avan Aihie
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SARCOPENIA , *MUSCLE strength , *MUSCULOSKELETAL diseases in old age , *DISEASE diagnosis in older people , *ISOMETRIC exercise - Abstract
The author reflects on the recognition of sarcopenia or the loss of skeletal muscle mass and strength in relation to age in clinical practice. He cites the factors that should be looked for when diagnosing sarcopenia. He discusses the use of resistance exercise to improve muscle mass and strength in adults, along with the role of nutrition in sarcopenia prevention and treatment. The author also argues that sarcopenia needs to be recognized in clinical practice.
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- 2010
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214. Finding the right outcome measures for care home research.
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Roberts, Helen C., Sayer, Avan Aihie, Anderson, Frazer, and Bowman, Clive
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LETTERS to the editor , *HEALTH outcome assessment - Abstract
A letter to the editor is presented in response to the article regarding the appropriate outcome measures for care home populations, by Thomas J. Hoppitt, Cath Sackley and Chris Wright in the January 2010 issue.
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- 2010
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215. Insulin-like growth factor-I genotype and birthweight.
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Day, Ian NM, King, Tabitha HT, Chen, Xiao-he, Voropanov, Anca M, Ye, Shu, Syddall, Holly E, Sayer, Avan Aihie, Cooper, Cyrus, Barker, David J, and Phillips, David IW
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- 2002
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216. Pamela Aihie
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Sayer, Avan Aihie
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- 2013
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217. Sarcopenia
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Sayer, Avan Aihie
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- 2010
218. Dysregulation of the hypothalamic pituitary adrenal (HPA) axis and physical performance at older ages: An individual participant meta-analysis
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Gardner, Michael P., Lightman, Stafford, Sayer, Avan Aihie, Cooper, Cyrus, Cooper, Rachel, Deeg, Dorly, Ebrahim, Shah, Gallacher, John, Kivimaki, Mika, Kumari, Meena, Kuh, Diana, Martin, Richard M., Peeters, Geeske, and Ben-Shlomo, Yoav
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HYPOTHALAMIC-pituitary-adrenal axis , *OLD age , *META-analysis , *CIRCADIAN rhythms , *HYDROCORTISONE , *PHYSICAL fitness , *LOGISTIC regression analysis - Abstract
Summary: The association between functioning of the hypothalamic pituitary adrenal (HPA) axis and physical performance at older ages remains poorly understood. We carried out meta-analyses to test the hypothesis that dysregulation of the HPA axis, as indexed by patterns of diurnal cortisol release, is associated with worse physical performance. Data from six adult cohorts (ages 50–92 years) were included in a two stage meta-analysis of individual participant data. We analysed each study separately using linear and logistic regression models and then used meta-analytic methods to pool the results. Physical performance outcome measures were walking speed, balance time, chair rise time and grip strength. Exposure measures were morning (serum and salivary) and evening (salivary) cortisol. Total sample sizes in meta-analyses ranged from n =2146 for associations between morning Cortisol Awakening Response and balance to n =8448 for associations between morning cortisol and walking speed. A larger diurnal drop was associated with faster walking speed (standardised coefficient per SD increase 0.052, 95% confidence interval (CI) 0.029, 0.076, p <0.001; age and gender adjusted) and a quicker chair rise time (standardised coefficient per SD increase −0.075, 95% CI −0.116, −0.034, p <0.001; age and gender adjusted). There was little evidence of associations with balance or grip strength. Greater diurnal decline of the HPA axis is associated with better physical performance in later life. This may reflect a causal effect of the HPA axis on performance or that other ageing-related factors are associated with both reduced HPA reactivity and performance. [ABSTRACT FROM AUTHOR]
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- 2013
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219. Does Cognitive Impairment Affect Rehabilitation Outcome?
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Poynter, Lynn, Kwan, Joseph, Sayer, Avan Aihie, and Vassallo, Michael
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GERIATRIC assessment , *ANALYSIS of variance , *COGNITION disorders , *LENGTH of stay in hospitals , *LONGITUDINAL method , *SCIENTIFIC observation , *REHABILITATION , *STATISTICS , *DATA analysis , *ACTIVITIES of daily living , *MULTIPLE regression analysis - Abstract
Objectives To assess how cognitive impairment affects rehabilitation outcomes and to determine whether individual benefit regardless of cognition. Design Prospective open observational study. Setting Two rehabilitation wards admitting older adults after admissions with medical or surgical problems. Participants Two hundred forty-one individuals admitted to two rehabilitation wards, 144 female, mean age 84.4 ± 7.3 (range: 59-103). Measurements The Mini-Mental State Examination ( MMSE) was administered, and participants were categorized into four groups: cognitively intact ( MMSE score: 27-30), mildly impaired ( MMSE score: 21-26), moderately impaired ( MMSE score: 11-20), and severely impaired ( MMSE score: 0-10). Barthel activity of daily living score was calculated on admission, at 2 and 6 weeks (if appropriate), and at discharge to assess level of independence and improvement or deterioration in function. Information relating to mortality, discharge destination, and length of stay was also collected. Results After adjusting for comorbidities and age, all four groups showed improvement in Barthel score from admission to discharge. This improvement was highly significant ( P = .005) in participants with normal cognition and mild to moderate impairment. Severely impaired participants also made significant improvement ( P = .01). Length of stay was significantly longer for participants with lower cognitive scores. Discharge of 50% of participants occurred by 26, 28, 38, and 47 days for Groups 1 to 4, respectively ( P = .001). Higher rates of institutionalization and mortality ( P = .02) were associated with lower MMSE score. Conclusion All participants improved functionally regardless of cognition. Likelihood of institutionalization, mortality, length of stay, and adverse incidents was higher with lower MMSE scores. [ABSTRACT FROM AUTHOR]
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- 2011
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220. Growth in early life predicts bone strength in late adulthood: The Hertfordshire Cohort Study
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Oliver, Helen, Jameson, Karen A., Sayer, Avan Aihie, Cooper, Cyrus, and Dennison, Elaine M.
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GROWTH , *ADULTS , *COHORT analysis , *BONES - Abstract
Abstract: Infant growth is a determinant of adult bone mass, and poor childhood growth is a risk factor for adult hip fracture. Peripheral quantitative computed tomography (pQCT) allows non-invasive assessment of bone strength. We utilised this technology to examine relationships between growth in early life and bone strength. We studied 313 men and 318 women born in Hertfordshire between 1931 and 1939 who were still resident there in adult life, for whom detailed early life records were available. Lifestyle factors were evaluated by questionnaire, anthropometric measurements made, and peripheral QCT examination of the radius and tibia performed (Stratec 4500). Birthweight and conditional weight at 1 year were strongly related to radial and tibial length in both sexes (p <0.001) and to measures of bone strength [fracture load X, fracture load Y, polar strength strain index (SSI)] at both the radius and tibia. These relationships were robust to adjustment for age, body mass index (BMI), social class, cigarette and alcohol consumption, physical activity, dietary calcium intake, HRT use, and menopausal status in women. Among men, BMI was strongly positively associated with radial (r =0.46, p =0.001) and tibial (r =0.24, p =0.006) trabecular bone mineral density (BMD). Current smoking was associated with lower cortical (radius: p =0.0002; tibia: p =0.08) and trabecular BMD (radius: p =0.08; tibia: p =0.04) in males. Similar trends of BMD with these anthropometric and lifestyle variables were seen in women but they were non-significant. Current HRT use was associated with greater female cortical (radius: p =0.0002; tibia: p =0.001) and trabecular (radius: p =0.008; tibia: p =0.04) BMD. Current HRT use was also associated with greater radial strength (polar SSI: p =0.006; fracture load X: p =0.005; fracture load Y: p =0.02) in women. Women who had sustained any fracture since the age of 45 years had lower radial total (p =0.0001), cortical (p <0.005) and trabecular (p =0.0002) BMD, poorer forearm bone strength [polar SSI (p =0.006), fracture load X and Y (p =0.02)], and lower tibial total (p <0.001), cortical (p =0.008), and trabecular (p =0.0001) BMD. We have shown that growth in early life is associated with bone size and strength in a UK population aged 65–73 years. Lifestyle factors were associated with volumetric bone density in this population. [Copyright &y& Elsevier]
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- 2007
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221. Long-term conditions, multimorbidity, lifestyle factors and change in grip strength over 9 years of follow-up: Findings from 44,315 UK biobank participants.
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Hurst, Christopher, Murray, James C, Granic, Antoneta, Hillman, Susan J, Cooper, Rachel, Sayer, Avan Aihie, Robinson, Sian M, and Dodds, Richard M
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LIFESTYLES , *GRIP strength , *PATIENT aftercare , *CONFIDENCE intervals , *SARCOPENIA , *RISK assessment , *PHYSICAL activity , *DESCRIPTIVE statistics , *MUSCLE strength , *LOGISTIC regression analysis , *ODDS ratio , *BODY mass index , *COMORBIDITY - Abstract
Background Weak grip strength is associated with a range of adverse health outcomes and an accelerated decline in grip strength confers an even greater risk. The factors associated with change in grip strength in mid-life remain to be fully determined. Methods We used data from 44,315 UK Biobank participants who had grip strength measured at baseline (2006-10) and a subsequent visit approximately nine years later. At baseline, participants' long-term conditions (LTCs) were categorised against a hierarchy, with multimorbidity characterised by the number of LTC categories. Lifestyle factors were assessed. Change in grip strength was grouped into four patterns: decline, stable low, stable high or reference (no change or increase) and used as the outcome in multinomial logistic regression. Results Most LTC categories were associated with adverse patterns of change in grip strength (stable low and/or decline): for example, musculoskeletal/trauma conditions were associated with an increased risk of the stable low pattern (Relative Risk Ratio [RRR] = 1.63; 95% confidence interval [CI]: 1.49-1.79). Multimorbidity and lifestyle factors had independent associations with grip strength change. Those with 3+ categories of LTCs were more likely to experience decline in grip strength (RRR = 1.18; 95% CI: 1.08-1.28) compared to those with none. Low physical activity was associated with adverse patterns of grip strength, while raised body mass index (BMI) had divergent associations. Conclusions Individuals living with multimorbidity and those with lifestyle risk factors such as low physical activity are at increased risk of low muscle strength and the loss of strength over time. [ABSTRACT FROM AUTHOR]
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- 2021
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222. Associations Between Objectively Measured Physical Activity, Body Composition and Sarcopenia: Findings from the Hertfordshire Sarcopenia Study (HSS).
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Westbury, Leo D., Dodds, Richard M., Syddall, Holly E., Baczynska, Alicja M., Shaw, Sarah C., Dennison, Elaine M., Roberts, Helen C., Sayer, Avan Aihie, Cooper, Cyrus, and Patel, Harnish P.
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SARCOPENIA , *PHYSICAL activity , *HUMAN body composition , *ACCELEROMETERS , *DUAL-energy X-ray absorptiometry - Abstract
Regular physical activity (PA) is associated with reduced risk of the development and progression of musculoskeletal, metabolic and vascular disease. However, PA declines with age and this can contribute to multiple adverse outcomes. The aims of this study were to describe the relationship between accelerometer-determined PA, body composition and sarcopenia (the loss of muscle mass and function with age). Seven-day PA was measured using the GENEactiv accelerometer among 32 men and 99 women aged 74-84 years who participated in the Hertfordshire Sarcopenia Study. We measured mean daily acceleration and minutes/day spent in non-sedentary and moderate-to-vigorous physical activity (MVPA) levels. Body composition was measured by dual-energy X-ray absorptiometry, muscle strength by grip dynamometry and function by gait speed. Sarcopenia was defined according to the EWGSOP diagnostic algorithm. Men and women spent a median (inter-quartile range) of 138.8 (82, 217) and 186 (122, 240) minutes/day engaging in non-sedentary activity but only 14.3 (1.8, 30.2) and 9.5 (2.1, 18.6) min in MVPA, respectively. Higher levels of PA were associated with reduced adiposity, faster walking speed and decreased risk of sarcopenia. For example, a standard deviation (SD) increase in mean daily acceleration was associated with an increase in walking speed of 0.25 (95% CI 0.05, 0.45) SDs and a reduction in the risk of sarcopenia of 35% (95% CI 1, 57%) in fully adjusted analyses. PA was not associated with hand grip strength. Community-dwelling older adults in this study were largely sedentary but there was evidence that higher levels of activity were associated with reduced adiposity and improved function. PA at all intensity levels in later life may help maintain physical function and protect against sarcopenia. [ABSTRACT FROM AUTHOR]
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- 2018
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223. Personality and Risk of Frailty: the English Longitudinal Study of Ageing.
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Gale, Catharine, Mõttus, René, Deary, Ian, Cooper, Cyrus, Sayer, Avan, Gale, Catharine R, Mõttus, René, Deary, Ian J, and Sayer, Avan Aihie
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FRAGILITY (Psychology) , *PERSONALITY , *AGE factors in disease , *NEUROTICISM , *EXTRAVERSION - Abstract
Background: There is evidence that the personality traits conscientiousness, extraversion and neuroticism are associated with health behaviours and with risk of various health outcomes. We hypothesised that people who are lower in conscientiousness or extraversion or higher in neuroticism may be at greater risk of frailty in later life.Methods: We used general linear models to examine the prospective relation between personality, assessed using the Midlife Development Inventory, and change in frailty, modelled by a frailty index, in 5314 men and women aged 60 to over 90 years from the English Longitudinal Study of Ageing.Results: Men and women with higher levels of neuroticism or lower levels of extraversion or conscientiousness had an increased frailty index score at follow-up. After adjustment for potential confounding or mediating variables, including frailty index score at baseline, the frailty index score at follow-up-which potentially ranges from 0 to 1-was higher by 0.035 (95 % confidence interval 0.018, 0.052) for a standard deviation increase in neuroticism and lower by 0.061 (0.031, 0.091) or 0.045 (0.020, 0.071) for a standard deviation increase in extraversion or conscientiousness, respectively. There was some evidence that the association between extraversion and frailty may be due to reverse causation whereby poorer health affected responses to items in the personality inventory.Conclusions: Higher levels of neuroticism or lower levels of conscientiousness or extraversion may be risk factors for the onset or progression of frailty. Future studies need to replicate these observations in other populations and explore the mechanisms underlying these associations. [ABSTRACT FROM AUTHOR]- Published
- 2017
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224. Global variation in grip strength: a systematic review and meta-analysis of normative data.
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DODDS, RICHARD M., SYDDALL, HOLLY E., COOPER, RACHEL, KUH, DIANA, COOPER, CYRUS, and SAYER, AVAN AIHIE
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CONFIDENCE intervals , *FRAIL elderly , *GRIP strength , *MEDICAL information storage & retrieval systems , *MEDLINE , *META-analysis , *REFERENCE values , *RESEARCH funding , *WORLD health , *SYSTEMATIC reviews , *SARCOPENIA , *DATA analysis software , *DESCRIPTIVE statistics , *OLD age - Abstract
Background: weak grip strength is a key component of sarcopenia and is associated with subsequent disability and mortality. We have recently established life course normative data for grip strength in Great Britain, but it is unclear whether the cut points we derived for weak grip strength are suitable for use in other settings. Our objective was to investigate differences in grip strength by world region using our data as a reference standard. Methods: we searched MEDLINE and EMBASE for reporting age- and gender-stratified normative data for grip strength. We extracted each item of normative data and converted it on to a Z-score scale relative to our British centiles. We performed meta-regression to pool the Z-scores and compare them by world region. Findings: our search returned 806 abstracts. Sixty papers met inclusion criteria and reported on 63 different samples. Seven UN regions were represented, although most samples (n = 44) were based in developed regions. We extracted 726 normative data items relating to 96,537 grip strength observations. Normative data from developed regions were broadly similar to our British centiles, with a pooled Z-score 0.12 SDs (95% CI: 0.07, 0.17) above the corresponding British centiles. By comparison, normative data from developing regions were clearly lower, with a pooled Z-score of -0.85 SDs (95% CI: -0.94, -0.76). Interpretation: our findings support the use of our British grip strength centiles and their associated cut points in consensus definitions for sarcopenia and frailty across developed regions, but highlight the need for different cut points in developing regions. [ABSTRACT FROM AUTHOR]
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- 2016
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225. Understanding poor health behaviours as predictors of different types of hospital admission in older people: findings from the Hertfordshire Cohort Study.
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Syddall, Holly E., Westbury, Leo D., Simmonds, Shirley J., Robinson, Sian, Cooper, Cyrus, and Sayer, Avan Aihie
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AGE distribution , *CONFIDENCE intervals , *DIET , *EMERGENCY medical services , *HEALTH behavior , *HOSPITAL care , *LENGTH of stay in hospitals , *POISSON distribution , *PROBABILITY theory , *RESEARCH funding , *SMOKING , *SURVIVAL analysis (Biometry) , *INDEPENDENT living , *PHYSICAL activity , *DATA analysis software , *DESCRIPTIVE statistics - Abstract
Background Rates of hospital admission are increasing, particularly among older people. Poor health behaviours cluster but their combined impact on risk of hospital admission among older people in the UK is unknown. Methods 2997 community-dwelling men and women (aged 59-73) participated in the Hertfordshire Cohort Study (HCS). We scored (from 0 to 4) number of poor health behaviours engaged in at baseline (1998-2004) out of: current smoking, high weekly alcohol, low customary physical activity and poor diet. We linked HCS with Hospital Episode Statistics and mortality data to 31/ 03/2010 and analysed associations between the score and risk of different types of hospital admission: any; elective; emergency; long stay (>7 days); 30-day readmission (any, or emergency). Results 32%, 40%, 20% and 7% of men engaged in 0, 1, 2 and 3/4 poor health behaviours; corresponding percentages for women 51%, 38%, 9%, 2%. 75% of men (69% women) experienced at least one hospital admission. Among men and women, increased number of poor health behaviours was strongly associated (p<0.01) with greater risk of long stay and emergency admissions, and 30-day emergency readmissions. Hazard ratios (HRs) for emergency admission for 3/4 poor health behaviours in comparison with none were: men, 1.37 (95% CI 1.11 to 1.69); women, 1.84 (95% CI 1.22 to 2.77). Associations were unaltered by adjustment for age, body mass index and comorbidity. Conclusions Clustered poor health behaviours are associated with increased risk of hospital admission among older people in the UK. Lifecourse interventions to reduce number of poor health behaviours could have substantial beneficial impact on health and use of healthcare in later life. [ABSTRACT FROM AUTHOR]
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- 2016
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226. Self-Reported Walking Speed: A Useful Marker of Physical Performance Among Community-Dwelling Older People?
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Syddall, Holly E., Westbury, Leo D., Cooper, Cyrus, and Sayer, Avan Aihie
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SARCOPENIA , *GERIATRIC assessment , *CONFIDENCE intervals , *DIAGNOSIS , *FRAIL elderly , *GAIT in humans , *LIFE skills , *LONGITUDINAL method , *RESEARCH methodology , *MORTALITY , *PROBABILITY theory , *RESEARCH funding , *SELF-evaluation , *SOCIOECONOMIC factors , *LIFESTYLES , *DESCRIPTIVE statistics - Abstract
Background Walking speed is central to emerging consensus definitions of sarcopenia and frailty as well as being a major predictor of future health outcomes in its own right. However, measurement is not always feasible in clinical settings. We hypothesized that self-reported walking speed might be a good marker of objectively measured walking speed for use in this context. Methods We investigated the relationship between self-reported and measured walking speed and their associations with clinical characteristics and mortality using data from 730 men and 999 women, aged 61 to 73 years, who participated in the Hertfordshire Cohort Study. Walking speed was measured over 3 meters. Participants rated their walking speed as “unable to walk,” “very slow,” “stroll at an easy pace,” “normal speed,” “fairly brisk,” or “fast.” Results Self-reported walking speed was strongly associated with measured walking speed among men and women ( P < .001). Average walking speeds ranged from 0.78 m/s (95% CI 0.73–0.83) among men with “very slow” self-reported walking speed to 0.98 m/s (95% CI 0.93–1.03) among “fast” walkers (corresponding figures for women were 0.72 m/s [95% CI 0.68–0.75] and 1.01 m/s [95% CI 0.98–1.05]). Self-reported and measured walking speeds were similarly associated with clinical characteristics and mortality; among men and women, slower self-reported and measured walking speeds were associated ( P < .05) with increased likelihood of poor physical function, having more systems medicated and with increased mortality risk, with and without adjustment for sociodemographic and lifestyle factors (hazard ratios for mortality per slower band of self-reported walking speed, adjusted for sociodemographic and lifestyle characteristics: men 1.44 [95% CI 1.11–1.87]; women 1.35 [95% CI 1.02–1.81]). Conclusion and Implications Self-reported walking speed is a good marker of measured walking speed and could serve as a useful marker of physical performance in consensus definitions of sarcopenia and frailty when direct measurement of walking speed is not feasible. [ABSTRACT FROM AUTHOR]
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- 2015
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227. ACE inhibitors, statins and thiazides: no association with change in grip strength among community dwelling older men and women from the Hertfordshire Cohort Study.
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Witham, Miles D., Syddall, Holly E., Dennison, Elaine, Cooper, Cyrus, McMurdo, Marion E. T., and Sayer, Avan Aihie
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Background: vascular disease has been postulated to contribute to muscle dysfunction in old age. Previous studies examining the effects of cardiovascular drugs on muscle function have shown conflicting results. We therefore examined the association of angiotensin converting enzyme (ACE) inhibitor, thiazide and statin use with decline in grip strength in a well-characterised cohort.Methods: we analysed prospectively collected data from the Hertfordshire Cohort Study (HCS). For each medication, participants were divided into no baseline use/no use at follow-up, baseline use/no use at follow-up, no baseline use but use at follow-up and use at baseline and follow-up. For each group, annualised decline in grip strength (kg per year) was calculated, then adjusted for baseline age, height, weight, baseline grip strength, indices of ischaemic heart disease and hypertension. Analyses were conducted separately for males and females.Results: 639 participants were included in the analysis, mean age 65 years. 321 (50%) were male; mean follow-up time was 4.4 years. There were no differences in baseline grip between baseline users and non-users of any drug class. Adjusted grip strength change per year was similar for each group of ACE inhibitor use (P > 0.05). Similar analyses revealed no significant between-group differences for statin or thiazide use. Analysis of dropout rates by medication use revealed no evidence of selection bias.Conclusion: use of ACE inhibitors, statins or thiazides was not associated with differences in grip strength decline in healthy older people in the HCS. [ABSTRACT FROM AUTHOR]
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- 2014
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228. Gender and telomere length: Systematic review and meta-analysis.
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Gardner, Michael, Bann, David, Wiley, Laura, Cooper, Rachel, Hardy, Rebecca, Nitsch, Dorothea, Martin-Ruiz, Carmen, Shiels, Paul, Sayer, Avan Aihie, Barbieri, Michelangela, Bekaert, Sofie, Bischoff, Claus, Brooks-Wilson, Angela, Chen, Wei, Cooper, Cyrus, Christensen, Kaare, De Meyer, Tim, Deary, Ian, Der, Geoff, and Roux, Ana Diez
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TELOMERES , *SYSTEMATIC reviews , *META-analysis , *MEASUREMENT errors , *SCIENTIFIC observation ,SEX differences (Biology) - Abstract
Abstract: Background: It is widely believed that females have longer telomeres than males, although results from studies have been contradictory. Methods: We carried out a systematic review and meta-analyses to test the hypothesis that in humans, females have longer telomeres than males and that this association becomes stronger with increasing age. Searches were conducted in EMBASE and MEDLINE (by November 2009) and additional datasets were obtained from study investigators. Eligible observational studies measured telomeres for both females and males of any age, had a minimum sample size of 100 and included participants not part of a diseased group. We calculated summary estimates using random-effects meta-analyses. Heterogeneity between studies was investigated using sub-group analysis and meta-regression. Results: Meta-analyses from 36 cohorts (36,230 participants) showed that on average females had longer telomeres than males (standardised difference in telomere length between females and males 0.090, 95% CI 0.015, 0.166; age-adjusted). There was little evidence that these associations varied by age group (p=1.00) or cell type (p=0.29). However, the size of this difference did vary by measurement methods, with only Southern blot but neither real-time PCR nor Flow-FISH showing a significant difference. This difference was not associated with random measurement error. Conclusions: Telomere length is longer in females than males, although this difference was not universally found in studies that did not use Southern blot methods. Further research on explanations for the methodological differences is required. [Copyright &y& Elsevier]
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- 2014
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229. Grip strength and its determinants among older people in different healthcare settings.
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Roberts, Helen C., Syddall, Holly Emma, Sparkes, Jonathan, Ritchie, Jan, Butchart, Joe, Kerr, Alastair, Cooper, Cyrus, and Sayer, Avan Aihie
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Background: low muscle strength is central to geriatric syndromes including sarcopenia and frailty. It is well described in community-dwelling older people, but the epidemiology of grip strength of older people in rehabilitation or long-term care has been little explored.Objective: to describe grip strength of older people in rehabilitation and nursing home settings.Design: cross-sectional epidemiological study.Setting: three healthcare settings in one town.Subjects: hundred and one inpatients on a rehabilitation ward, 47 community rehabilitation referrals and 100 nursing home residents.Methods: grip strength, age, height, weight, body mass index, number of co-morbidities and medications, Barthel score, Mini-Mental State Examination (MMSE), nutritional status and number of falls in the last year were recorded.Results: grip strength differed substantially between healthcare settings for both men and women (P < 0.0001). Nursing home residents had the lowest age-adjusted mean grip strength and community rehabilitation referrals the highest. Broadly higher grip strength was associated in univariate analyses with younger age, greater height and weight, fewer comorbidities, higher Barthel score, higher MMSE score, better nutritional status and fewer falls. However, after mutual adjustment for these factors, the difference in grip strength between settings remained significant. The Barthel score was the characteristic most strongly associated with grip strength.Conclusions: older people in rehabilitation and care home settings had lower grip strength than reported for those living at home. Furthermore grip strength varied widely between healthcare settings independent of known major influences. Further research is required to ascertain whether grip strength may help identify people at risk of adverse health outcomes within these settings. [ABSTRACT FROM AUTHOR]
- Published
- 2014
230. Lower Maternal Body Condition During Pregnancy Affects Skeletal Muscle Structure and Glut-4 Protein Levels But Not Glucose Tolerance in Mature Adult Sheep.
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Costello, Paula M., Hollis, Lisa J., Cripps, Roselle L., Bearpark, Natasha, Patel, Harnish P., Sayer, Avan Aihie, Cooper, Cyrus, Hanson, Mark A., Ozanne, Susan E., and Green, Lucy R.
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METABOLIC disorders , *HOMEOSTASIS , *MATERNAL nutrition , *GLUCOSE , *SKELETAL muscle - Abstract
Suboptimal maternal nutrition and body composition are implicated in metabolic disease risk in adult offspring. We hypothesized that modest disruption of glucose homeostasis previously observed in young adult sheep offspring from ewes of a lower body condition score (BCS) would deteriorate with age, due to changes in skeletal muscle structure and insulin signaling mechanisms. Ewes were fed to achieve a lower (LBCS, n = 10) or higher (HBCS, n = 14) BCS before and during pregnancy. Baseline plasma glucose, glucose tolerance and basal glucose uptake into isolated muscle strips were similar in male offspring at 210 ± 4 weeks. Vastus total myofiber density (HBCS, 343 ± 15; LBCS, 294 ± 14 fibers/mm2, P < .05) and fast myofiber density (HBCS, 226 ± 10; LBCS 194 ± 10 fibers/mm2, P < .05), capillary to myofiber ratio (HBCS, 1.5 ± 0.1; LBCS 1.2 ± 0.1 capillary:myofiber, P < .05) were lower in LBCS offspring. Vastus protein levels of Akt1 were lower (83% ± 7% of HBCS, P < .05), and total glucose transporter 4 was increased (157% ± 6% of HBCS, P < .001) in LBCS offspring, Despite the reduction in total myofiber density in LBCS offspring, glucose tolerance was normal in mature adult life. However, such adaptations may lead to complications in metabolic control in an overabundant postnatal nutrient environment. [ABSTRACT FROM AUTHOR]
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- 2013
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231. Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programme
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Alfred, Tamuno, Ben-Shlomo, Yoav, Cooper, Rachel, Hardy, Rebecca, Cooper, Cyrus, Deary, Ian J., Gunnell, David, Harris, Sarah E., Kumari, Meena, Martin, Richard M., Sayer, Avan Aihie, Starr, John M., Kuh, Diana, and Day, Ian N.M.
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GENETIC markers , *OLDER people physiology , *PHYSICAL fitness , *BONE density , *MORTALITY , *OSTEOARTHRITIS - Abstract
Abstract: Background: Good bone and joint health is essential for the physical tasks of daily living and poorer indicators of physical capability in older adults have been associated with increased mortality rates. Genetic variants of indicators of bone and joint health may be associated with measures of physical capability. Methods: As part of the Healthy Ageing across the Life Course (HALCyon) programme, men and women aged between 52 and 90+ years from six UK cohorts were genotyped for a polymorphism associated with serum calcium (rs1801725, CASR), two polymorphisms associated with bone mineral density (BMD) (rs2941740, ESR1 and rs9594759, RANKL) and one associated with osteoarthritis risk rs3815148 (COG5). Meta-analysis was used to pool within-study effects of the associations between each of the polymorphisms and measures of physical capability: grip strength, timed walk or get up and go, chair rises and standing balance. Results: Few important associations were observed among the several tests. We found that carriers of the serum calcium-raising allele had poorer grip strength compared with non-carriers (pooled p =0.05, n =11,239) after adjusting for age and sex. Inconsistent results were observed for the two variants associated with BMD and we found no evidence for an association between rs3815148 (COG5) and any of the physical capability measures. Conclusion: Our findings suggest elevated serum calcium levels may lead to lower grip strength, though this requires further replication. Our results do not provide evidence for a substantial influence of these variants in ESR1, RANKL and COG5 on physical capability in older adults. [Copyright &y& Elsevier]
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- 2013
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232. Muscle Strength in Older Community-Dwelling Men Is Related to Type of Milk Feeding in Infancy.
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Robinson, Siân M., Simmonds, Shirley J., Jameson, Karen A., Syddall, Holly E., Dennison, Elaine M., Cooper, Cyrus, and Sayer, Avan Aihie
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BREASTFEEDING , *INFANT nutrition , *MUSCLE growth , *MUSCLE strength , *ADULTS - Abstract
Background. There is a growing literature that links greater duration and exclusivity of breastfeeding to beneficial effects on adult health outcomes. Muscle growth in the neonatal period may be very sensitive to variations in early nutrition, but little is known about long-term effects of infant feeding on muscle strength. Methods. In 2,983 community-dwelling older men and women born 1931–1939, we examined the relationship between their type of milk feeding in infancy and their muscle strength in adult life. Information about milk feeding for each participant was abstracted from their infant record; grip strength was measured using a Jamar dynamometer. Results. Sixty percent (1,783) of the participants were breastfed only, 31% (926) were breast- and bottle-fed, and 9% (274) were bottle-fed only. There were no differences in type of milk feeding between men and women or according to social class at birth. Among the men studied, grip strength was related to the type of milk feeding, such that greater exposure to breast milk in infancy was associated with greater grip strength in adult life (p = .023). This association remained after adjustment for the effects of a range of confounding influences (birthweight, infant growth, height, age at measurement, adult diet, and level of physical activity). In contrast, the type of milk feeding in infancy was not related to grip strength among the women studied (p = .807). Conclusions. These data suggest that in men, differences in nutritional exposure in the early postnatal period may have lifelong implications for muscle strength. [ABSTRACT FROM PUBLISHER]
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- 2012
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233. A review of the measurement of grip strength in clinical and epidemiological studies: towards a standardised approach.
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Roberts, Helen C., Denison, Hayley J., Martin, Helen J., Patel, Harnish P., Syddall, Holly, Cooper, Cyrus, and Sayer, Avan Aihie
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- 2011
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234. Neighbourhood environment and positive mental health in older people: The Hertfordshire Cohort Study
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Gale, Catharine R., Dennison, Elaine M., Cooper, Cyrus, and Sayer, Avan Aihie
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ENVIRONMENTAL psychology , *MENTAL health , *COHORT analysis , *PSYCHOLOGICAL well-being , *CROSS-sectional method , *SOCIAL classes , *NEIGHBORHOODS , *DEPRIVATION (Psychology) - Abstract
Abstract: Little is known about the potential effects of neighbourhood environment on positive mental health in older people. We examined cross-sectional associations between the index of multiple deprivation score of the census area of residence, perceptions of neighbourhood cohesion and neighbourhood problems and mental wellbeing, as measured by the Warwick–Edinburgh Mental Wellbeing Scale, in 1157 men and women aged 69–78 years from Hertfordshire, UK. We found no association between area-level deprivation and mental wellbeing. People who felt a stronger sense of cohesion within their neighbourhood and reported fewer neighbourhood problems had higher levels of mental wellbeing, independently of social class, income, presence of limiting illness or disability, mobility problems, and perceived social support. Adjustment for emotional stability attenuated the associations between mental wellbeing and both of these measures of perceived neighbourhood environment, particularly in the case of neighbourhood problems. How older people feel about their neighbourhood may be important for positive mental health in later life. [Copyright &y& Elsevier]
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- 2011
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235. A systematic review of the use of volunteers to improve mealtime care of adult patients or residents in institutional settings.
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Green, Sue M., Martin, Helen J., Roberts, Helen C., and Sayer, Avan Aihie
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PREVENTION of malnutrition , *CINAHL database , *NUTRITION for people with disabilities , *INFORMATION storage & retrieval systems , *MEDICAL information storage & retrieval systems , *NURSING databases , *MEDLINE , *VOLUNTEERS , *SYSTEMATIC reviews ,MALNUTRITION risk factors - Abstract
The objective of this review was to locate and assess the evidence obtained from articles reporting empirical research that volunteers improve mealtime care of adults in institutional settings. Malnutrition in adult patients or residents in institutional care settings is common. Poor standards of mealtime care have been suggested to contribute to the development of malnutrition. A systematic review of the literature was undertaken. Key words were identified and used separately and in combination to search the electronic databases MEDLINE, CINHAL, BNI and EMBASE and the internet for relevant articles. Searches were undertaken in August 2008, April 2009 and July 1010. Ten studies fulfilled the criteria for inclusion. The methodologies of five of the 10 studies were unclear due to the brevity of the reports. The validity of the design of the other five studies varied. Generally the results suggested the use of volunteers in mealtime care increased satisfaction of patients, relatives, volunteers and staff concerning meal-time assistance (assessed using methods such as questionnaires and focus groups) and three studies found increased nutritional intake in groups assisted by volunteers. However, few well designed and reported studies were identified. There is some evidence that volunteers can improve mealtime care of adult patients or residents in institutional settings, however few well designed studies are reported. This review demonstrates that there is limited evidence that the use of volunteers improves mealtime care of adult patients or relatives in institutional settings. [ABSTRACT FROM AUTHOR]
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- 2011
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236. Prevalence of and risk factors for falls in older people in an urban community in South Africa
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Kalula, Sebastiana Zimba, Swingler, George H, and Sayer, Avan Aihie
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InformationSystems_INFORMATIONSTORAGEANDRETRIEVAL ,ComputingMethodologies_DOCUMENTANDTEXTPROCESSING ,Medicine ,GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries) - Abstract
Includes abstract. Includes bibliographical references.
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- 2012
237. Scientific Business Abstracts.
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Cooles F, Vidal-Pedrola G, Naamane N, Pratt A, Barron-Millar B, Anderson A, Hilkens C, Casement J, Bondet V, Duffy D, Zhang F, Shukla R, Isaacs J, Little M, Payne M, Coupe N, Fairfax B, Taylor CA, Mackay S, Milotay G, Bos S, Hunter B, Mcdonald D, Merces G, Sheldon G, Pradère P, Majo J, Pulle J, Vanstapel A, Vanaudenaerde BM, Vos R, Filby AJ, Fisher AJ, Collier J, Lambton J, Suomi F, Prigent M, Guissart C, Erskine D, Rozanska A, Mccorvie T, Trimouille A, Imam A, Hobson E, Mccullagh H, Frengen E, Misceo D, Bjerre A, Smeland M, Klingenberg C, Alkuraya F, Mcfarland R, Alston C, Yue W, Legouis R, Koenig M, Lako M, Mcwilliams T, Oláhová M, Taylor R, Newman W, Harkness R, McDermott J, Metcalfe K, Khan N, Macken W, Pitceathly R, Record C, Maroofian R, Sabir A, Santra S, Urquhart J, Demain L, Byers H, Beaman G, Yue W, Taylor R, Durmusalioglu E, Atik T, Isik E, Cogulu O, Reunert J, Marquardt T, Ryba L, Buchert-Lo R, Haack T, Lassuthova P, Polavarapu K, Lochmuller H, Horvath R, Jamieson P, Reilly M, O'Keefe R, Boggan R, Ng YS, Franklin I, Alston C, Blakely E, Büchner B, Bugiardini E, Colclough K, Feeney C, Hanna M, Hattersley A, Klopstock T, Kornblum C, Mancuso M, Patel K, Pitceathly R, Pizzamiglio C, Prokisch H, Schäfer J, Schaefer A, Shepherd M, Thaele A, Thomas R, Turnbull D, Gorman G, Woodward C, McFarland R, Taylor R, Cordell H, Pickett S, Tsilifis C, Pearce M, Gennery A, Daly A, Darlay R, Zatorska M, Worthington S, Anstee Q, Cordell H, Reeves H, Nizami S, Mauricio-Muir J, McCain M, Singh R, Wordsworth J, Kadharusman M, Watson R, Masson S, McPherson S, Burt A, Tiniakos D, Littler P, Nsengimana J, Zhang S, Mann D, Jamieson D, Leslie J, Shukla R, Wilson C, Betts J, Croall I, Hoggard N, Bennett J, Naamane N, Hollingsworth KG, Pratt AG, Egail M, Feeney C, Di Leo V, Taylor RW, Dodds R, Anderson AE, Sayer AA, Isaacs JD, McCracken C, Condurache DG, Szabo L, Elghazaly H, Walter F, Meade A, Chakraverty R, Harvey N, Manisty C, Petersen S, Neubauer S, Raisi-Estabragh Z, Allen L, Taylor P, Carlsson A, Hagopian W, Hedlund E, Hill A, Jones A, Ludvigsson J, Onengut-Gumuscu S, Redondo M, Rich S, Gillespie K, Dayan C, Oram R, Resteu A, Wonders K, Schattenberg J, Straub B, Ekstedt M, Berzigotti A, Geier A, Francque S, Driessen A, Boursier J, Yki-Jarvinen H, Arola J, Aithal G, Holleboom A, Verheij J, Yunis C, Trylesinski A, Papatheodoridis G, Petta S, Romero-Gomez M, Bugianesi E, Paradis V, Ratziu V, Tiniakos D, Anstee Q, Burton J, Ciminata G, Geue C, Quinn T, Glover E, Morais M, Reynolds G, Denby L, Ali S, Lennon R, Sheerin N, Yang F, Zounemat-Kermani N, Dixey P, Adcock IM, Bloom CI, Chung KF, Govaere O, Hasoon M, Alexander L, Cockell S, Tiniakos D, Ekstedt M, Schattenberg JM, Boursier J, Bugianesi E, Ratziu V, Daly AK, and Anstee QM
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- 2024
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238. Recovery from Resistance Exercise in Older Adults: A Systematic Scoping Review.
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Hayes EJ, Stevenson E, Sayer AA, Granic A, and Hurst C
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Background: Resistance exercise is recommended for maintaining muscle mass and strength in older adults. However, little is known about exercise-induced muscle damage and recovery from resistance exercise in older adults. This may have implications for exercise prescription. This scoping review aimed to identify and provide a broad overview of the available literature, examine how this research has been conducted, and identify current knowledge gaps relating to exercise-induced muscle damage and recovery from resistance exercise in older adults., Methods: Studies were included if they included older adults aged 65 years and over, and reported any markers of exercise-induced muscle damage after performing a bout of resistance exercise. The following electronic databases were searched using a combination of MeSH terms and free text: MEDLINE, Scopus, Embase, SPORTDiscus and Web of Science. Additionally, reference lists of identified articles were screened for eligible studies. Data were extracted from eligible studies using a standardised form. Studies were collated and are reported by emergent theme or outcomes., Results: A total of 10,976 possible articles were identified and 27 original research articles were included. Findings are reported by theme; sex differences in recovery from resistance exercise, symptoms of exercise-induced muscle damage, and biological markers of muscle damage., Conclusions: Despite the volume of available data, there is considerable variability in study protocols and inconsistency in findings reported. Across all measures of exercise-induced muscle damage, data in women are lacking when compared to males, and rectifying this discrepancy should be a focus of future studies. Current available data make it challenging to provide clear recommendations to those prescribing resistance exercise for older people., (© 2023. The Author(s).)
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- 2023
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239. Sarcopenia definition, diagnosis and treatment: consensus is growing.
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Sayer AA and Cruz-Jentoft A
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- Humans, Aged, Muscle Strength physiology, Consensus, Geriatric Assessment, Muscle, Skeletal, Hand Strength, Sarcopenia diagnosis, Sarcopenia epidemiology, Sarcopenia therapy
- Abstract
Sarcopenia is a skeletal muscle disorder that commonly occurs with advancing age as well as with a number of long-term conditions. Recognition in clinical practice is relatively recent but important because of the association between sarcopenia and a range of adverse effects on health including impaired mobility, increased morbidity and mortality. Originally characterised as loss of muscle mass, the definition has evolved to focus on loss of skeletal muscle function, particularly strength, through a number of international definitions such as that of the European Working Group on Sarcopenia in Older People most recently revised in 2019. Progress in the decades ahead is likely to be seen with regard to use of routine health data, prescription of resistance exercise, translation of biology and epidemiology into first in man studies for new treatments, and focus on sarcopenia in low and middle-income countries. Immediate next steps include the newly formed Global Leadership Initiative on Sarcopenia to develop international consensus on definition and diagnosis., (© The Author(s) 2022. Published by Oxford University Press on behalf of the British Geriatrics Society.)
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- 2022
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240. Recovery from resistance exercise in older adults: a protocol for a scoping review.
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Hayes EJ, Stevenson E, Sayer AA, Granic A, and Hurst C
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Introduction: Resistance exercise has been shown to improve muscle health in older adults and is recommended as a front-line treatment for many health conditions, including sarcopenia and frailty. However, despite considerable research detailing the potential benefits of resistance exercise programmes, little is known about how older adults recover from individual exercise sessions. This scoping review will examine the current evidence surrounding the acute post-exercise effects of resistance exercise and the exercise recovery process in older adults to inform future research and exercise prescription guidelines for older adults., Methods and Analysis: The methodological framework of Arksey and O'Malley (2005) will be applied for this scoping review. A systematic search of five online databases and the hand-searching of reference lists of identified articles will be used to identify relevant papers. Studies that aim to measure exercise-induced muscle damage or exercise recovery following a resistance exercise session in participants aged 65 years and over will be included. Qualitative and quantitative data from relevant studies will be presented in a tabular format. Results will be summarised in narrative format. Key findings will be discussed concerning resistance exercise prescription in older adults., Dissemination: This review will be used to direct further research surrounding the exercise recovery process from resistance exercise in older adults and will also aid in designing specific exercise prescription guidelines for an older population. Findings will be relevant to researchers, clinicians, health workers and policy-makers and disseminated through publications and presentations., Competing Interests: Competing interests: None declared., (© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.)
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- 2022
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241. Micronutrients and sarcopenia: current perspectives.
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Robinson S, Granic A, and Sayer AA
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- Aged, Cross-Sectional Studies, Humans, Micronutrients, Muscle Strength, Muscle, Skeletal, Prospective Studies, Sarcopenia prevention & control, Vitamin B Complex
- Abstract
Sarcopenia, a skeletal muscle disorder that is characterised by loss of muscle strength and mass, is common in older populations and associated with poorer health outcomes. Although the individual and economic costs of sarcopenia are widely recognised, current understanding of its pathophysiology is incomplete, limiting efforts to translate research evidence into effective preventive and treatment strategies. While nutrition is a key field of sarcopenia research, the role of differences in habitual diets, and the effectiveness of dietary change as a prevention or treatment strategy, is uncertain. There is a growing evidence base that links low micronutrient intakes to sarcopenia risk and/or its components (low muscle strength and mass, impaired physical performance), although there remain many gaps in understanding. There is some consistency in findings across studies highlighting potential roles for antioxidant nutrients, B vitamins and magnesium; however, the evidence is largely observational and from cross-sectional studies, often describing associations with different muscle outcomes. As low intakes of some micronutrients are common in older populations, there is a need for new research, particularly from well-characterised prospective cohorts, to improve the understanding of their role and importance in the aetiology of sarcopenia and to generate the evidence needed to inform dietary guidelines to promote muscle health.
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- 2021
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242. How clinical practitioners assess frailty in their daily practice: an international survey.
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Bruyère O, Buckinx F, Beaudart C, Reginster JY, Bauer J, Cederholm T, Cherubini A, Cooper C, Cruz-Jentoft AJ, Landi F, Maggi S, Rizzoli R, Sayer AA, Sieber C, Vellas B, and Cesari M
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- Adult, Aged, European Union, Female, Gait, Geriatrics, Humans, Male, Middle Aged, Surveys and Questionnaires, Frail Elderly, Frailty diagnosis, Geriatric Assessment methods
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Introduction: Various operational definitions have been proposed to assess the frailty condition among older individuals. Our objective was to assess how practitioners measure the geriatric syndrome of frailty in their daily routine., Methods: An online survey was sent to national geriatric societies affiliated to the European Union Geriatric Medicine Society (EUGMS) and to members of the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO)., Results: A total of 388 clinicians from 44 countries answered to the survey. Most of them were medical doctors (93%), and their primary field of practice was geriatrics (83%). Two hundred and five clinicians (52.8%) always assessed frailty in their daily practice, 38.1% reported to "sometimes" measure it, and 9.1% never assess it. A substantial proportion of clinicians (64.9%) diagnose frailty using more than one instrument. The most widely used tool was the gait speed test, adopted by 43.8% of the clinicians, followed by clinical frailty scale (34.3%), the SPPB test (30.2%), the frailty phenotype (26.8%) and the frailty index (16.8%)., Conclusion: A variety of tools is used to assess frailty of older patients in clinical practice highlighting the need for standardisation and guidelines.
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- 2017
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243. Sleep disturbance and the older worker: findings from the Health and Employment after Fifty study.
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Palmer KT, D'Angelo S, Harris EC, Linaker C, Sayer AA, Gale CR, Evandrou M, van Staa T, Cooper C, and Coggon D
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- Achievement, Age Factors, England epidemiology, Female, Humans, Job Satisfaction, Male, Middle Aged, Prevalence, Risk Factors, Sex Factors, Surveys and Questionnaires, Workplace, Employment psychology, Occupational Exposure adverse effects, Sleep Initiation and Maintenance Disorders epidemiology
- Abstract
Objectives The aim of this study was to characterize the descriptive epidemiology of insomnia in midlife and explore the relative importance of different occupational risk factors for insomnia among older workers. Methods A questionnaire was mailed to all adults aged 50-64 years registered with 24 English general practices. Insomnia was defined as having at least one of four problems with sleep severely in the past three months. Subjects were also asked about employment conditions, feelings concerning work, and their health. Associations were assessed by logistic regression and population attributable fractions (PAF) calculated. Results Analysis was based on 8067 respondents (5470 in paid work), 18.8% of whom reported insomnia. It was more common among women, smokers, obese individuals, those living alone, and those in financial hardship, and less prevalent among the educated, those in South-East England, and those with friendships and leisure-time pursuits. Occupational risk factors included unemployment, shift working, lack of control and support at work, job insecurity, job dissatisfaction and several of its determinants (lacking a sense of achievement, feeling unappreciated, having difficult work colleagues, feeling unfairly criticized). Population burden of insomnia was associated more strongly with difficulties in coping with work demands, job insecurity, difficult colleagues, and lack of friendships at work [population attributable fraction (PAF) 15-33%] than shift work and lack of autonomy or support (PAF 5-7%). It was strongly associated with seven measures of poorer self-assessed health. Conclusions Employment policies aimed at tackling insomnia among older workers may benefit from focusing particularly on job-person fit, job security and relationships in the workplace.
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- 2017
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244. Job dissatisfaction and the older worker: baseline findings from the Health and Employment After Fifty study.
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D'Angelo S, Coggon D, Harris EC, Linaker C, Sayer AA, Gale CR, Evandrou M, van Staa T, Cooper C, Walker-Bone K, and Palmer KT
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- Achievement, Age Factors, Cross-Sectional Studies, England, Female, Health, Humans, Logistic Models, London, Male, Middle Aged, Odds Ratio, Risk Factors, Sex Factors, Stress, Psychological, Employment psychology, Job Satisfaction, Occupational Exposure, Work, Workplace
- Abstract
Objectives: Demographic changes are requiring people to work longer. Labour force participation might be promoted by tackling sources of job dissatisfaction. We aimed to describe the epidemiology of job dissatisfaction in older British workers, to explore which perceptions of work contribute most importantly, and to assess possible impacts on health., Methods: Participants aged 50-64 years were recruited from 24 English general practices. At baseline, those currently in work (N=5437) reported on their demographic and employment circumstances, overall job satisfaction, perceptions of their work that might contribute to dissatisfaction, and their general health, mood and well-being. Associations of job dissatisfaction with risk factors and potential health outcomes were assessed cross-sectionally by logistic regression, and the potential contributions of different negative perceptions to overall dissatisfaction were summarised by population attributable fractions (PAFs)., Results: Job dissatisfaction was more common among men, below age 60 years, those living in London and the South East, in the more educated and in those working for larger employers. The main contributors to job dissatisfaction among employees were feeling unappreciated and/or lacking a sense of achievement (PAF 55-56%), while in the self-employed, job insecurity was the leading contributor (PAF 79%). Job dissatisfaction was associated with all of the adverse health outcomes examined (ORs of 3-5), as were most of the negative perceptions of work that contributed to overall dissatisfaction., Conclusions: Employment policies aimed at improving job satisfaction in older workers may benefit from focussing particularly on relationships in the workplace, fairness, job security and instilling a sense of achievement., (Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/)
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- 2016
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245. A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and height.
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North TL, Ben-Shlomo Y, Cooper C, Deary IJ, Gallacher J, Kivimaki M, Kumari M, Martin RM, Pattie A, Sayer AA, Starr JM, Wong A, Kuh D, Rodriguez S, and Day IN
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- Alleles, Cystic Fibrosis epidemiology, Cystic Fibrosis pathology, Europe, Female, Forced Expiratory Volume genetics, Genotype, HMGA2 Protein genetics, Heterozygote, Humans, Male, Phenotype, Phenylketonurias epidemiology, Phenylketonurias genetics, Phenylketonurias pathology, Polymorphism, Genetic, Pulmonary Disease, Chronic Obstructive epidemiology, Pulmonary Disease, Chronic Obstructive pathology, alpha 1-Antitrypsin Deficiency epidemiology, alpha 1-Antitrypsin Deficiency pathology, Cystic Fibrosis genetics, Pulmonary Disease, Chronic Obstructive genetics, alpha 1-Antitrypsin genetics, alpha 1-Antitrypsin Deficiency genetics
- Abstract
Background: Several recessive Mendelian disorders are common in Europeans, including cystic fibrosis (CFTR), medium-chain-acyl-Co-A-dehydrogenase deficiency (ACADM), phenylketonuria (PAH) and alpha 1-antitrypsin deficiency (SERPINA1)., Methods: In a multicohort study of >19,000 older individuals, we investigated the relevant phenotypes in heterozygotes for these genes: lung function (forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC)) for CFTR and SERPINA1; cognitive measures for ACADM and PAH; and physical capability for ACADM, PAH and SERPINA1., Results: Findings were mostly negative but lung function in SERPINA1 (protease inhibitor (PI) Z allele, rs28929474) showed enhanced FEV1 and FVC (0.13 z-score increase in FEV1 (p=1.7 × 10(-5)) and 0.16 z-score increase in FVC (p=5.2 × 10(-8))) in PI-MZ individuals. Height adjustment (a known, strong correlate of FEV1 and FVC) revealed strong positive height associations of the Z allele (1.50 cm increase in height (p=3.6 × 10(-10)))., Conclusions: The PI-MZ rare (2%) SNP effect is nearly four times greater than the 'top' common height SNP in HMGA2. However, height only partially attenuates the SERPINA1-FEV1 or FVC association (around 50%) and vice versa. Height SNP variants have recently been shown to be positively selected collectively in North versus South Europeans, while the Z allele high frequency is localised to North Europe. Although PI-ZZ is clinically disadvantageous to lung function, PI-MZ increases both height and respiratory function; potentially a balanced polymorphism. Partial blockade of PI could conceivably form part of a future poly-therapeutic approach in very short children. The notion that elastase inhibition should benefit patients with chronic obstructive pulmonary disease may also merit re-evaluation. PI is already a therapeutic target: our findings invite a reconsideration of the optimum level in respiratory care and novel pathway potential for development of agents for the management of growth disorders., (Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/)
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- 2016
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246. Accumulation of risk factors associated with poor bone health in older adults.
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Zhang J, Jameson K, Sayer AA, Robinson S, Cooper C, and Dennison E
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- Aged, Alcohol Drinking adverse effects, Alcohol Drinking epidemiology, Bone Density physiology, Bone Diseases epidemiology, Bone Diseases physiopathology, Cohort Studies, Cross-Sectional Studies, Diet, Exercise physiology, Female, Femur physiology, Fractures, Bone epidemiology, Fractures, Bone physiopathology, Hand Strength physiology, Humans, Lumbar Vertebrae physiology, Male, Middle Aged, Risk Factors, Smoking adverse effects, Smoking epidemiology, Bone Diseases etiology, Fractures, Bone etiology
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Unlabelled: Clustering of factors linked with poor bone health is common in older adults and is associated with lower bone density and increased fracture risk in women., Purpose: Many factors are associated with bone mineral density, which in turn is strongly linked with risk of fragility fracture. We assessed how commonly clustering of risk factors occurs and related such clustering to bone mineral density in a population of older community-dwelling men and women., Method: This is a cross-sectional study with 498 men and 498 women aged 59 to 72 years, who were participants in the Hertfordshire Cohort Study, in whom incident fracture was recorded. Physical activity, diet quality, history of prior fracture, family history of fracture, cigarette and alcohol consumption and comorbidities were obtained through baseline questionnaire. Measurements of grip strength and bone mineral density of the lumbar spine and total femur were also taken., Results: Clustering of risk factors was common, with over 30% having two or more. In women, a graded association between the number of risk factors and low bone density was seen, and strong relationships were also seen between the number of risk factors and incident fracture; women with three or more risk factors had an adjusted hazard ratio (HR) of incident fracture of 5.98 (1.67, 21.43; p = 0.006) compared to women with no risk factors; women with two risk factors had an adjusted HR of 2.97 (1.14, 7.74; p = 0.03) and those with one, 2.28 (0.90, 5.75; p = 0.08)., Conclusion: Clustering of risk factors for poor bone health is common in community-dwelling older adults and is associated with increased risk of fracture and adverse bone health in women., Competing Interests: Compliance with ethical standards The East and North Hertfordshire Ethical Committees granted ethical approval for the study, and all participants gave written informed consent. Conflicts of interest Elaine Dennison has received speaker fees from Lilly; Cyrus Cooper has received consultancy fees/honoraria from Servier, Eli Lilly, Merck, Amgen, Novartis and Medtronic. Jean Zhang, Karen Jameson, Avan Aihie Sayer and Sian Robinson declare that they have no conflict of interest. Funding The Hertfordshire Cohort Study is funded by grants from the Medical Research Council and Arthritis Research UK.
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- 2016
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247. The Epidemiology of Sarcopenia.
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Dodds RM, Roberts HC, Cooper C, and Sayer AA
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- Humans, Prevalence, Sarcopenia physiopathology, Sarcopenia epidemiology
- Abstract
The aim of this review is to describe the epidemiology of sarcopenia, specifically prevalence, health outcomes, and factors across the life course that have been linked to its development. Sarcopenia definitions involve a range of measures (muscle mass, strength, and physical performance), which tend to decline with age, and hence sarcopenia becomes increasingly prevalent with age. Less is known about prevalence in older people in hospital and care homes, although it is likely to be higher than in community settings. The range of measures used, and the cutpoints suggested for each, presents a challenge for comparing prevalence estimates between studies. The importance of sarcopenia is highlighted by the range of adverse health outcomes that strength and physical performance (and to a lesser extent, muscle mass) have been linked to. This is shown most strikingly by the finding of increased all-cause mortality rates among those with weaker grip strength and slower gait speed. A life course approach broadens the window for our understanding of the etiology of sarcopenia and hence the potential intervention. An example is physical activity, with increased levels across midadulthood appearing to increase muscle mass and strength in early old age. Epidemiologic studies will continue to make an important contribution to our understanding of sarcopenia and possible avenues for intervention and prevention., (Copyright © 2015 The International Society for Clinical Densitometry. Published by Elsevier Inc. All rights reserved.)
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- 2015
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248. Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals.
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Nead KT, Li A, Wehner MR, Neupane B, Gustafsson S, Butterworth A, Engert JC, Davis AD, Hegele RA, Miller R, den Hoed M, Khaw KT, Kilpeläinen TO, Wareham N, Edwards TL, Hallmans G, Varga TV, Kardia SL, Smith JA, Zhao W, Faul JD, Weir D, Mi J, Xi B, Quinteros SC, Cooper C, Sayer AA, Jameson K, Grøntved A, Fornage M, Sidney S, Hanis CL, Highland HM, Häring HU, Heni M, Lasky-Su J, Weiss ST, Gerhard GS, Still C, Melka MM, Pausova Z, Paus T, Grant SF, Hakonarson H, Price RA, Wang K, Scherag A, Hebebrand J, Hinney A, Franks PW, Frayling TM, McCarthy MI, Hirschhorn JN, Loos RJ, Ingelsson E, Gerstein HC, Yusuf S, Beyene J, Anand SS, and Meyre D
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- Alleles, Humans, Obesity diagnosis, Odds Ratio, Polymorphism, Single Nucleotide, Body Mass Index, Genetic Predisposition to Disease, Genetic Variation, Obesity epidemiology, Obesity genetics, Proprotein Convertase 1 genetics
- Abstract
Polymorphisms rs6232 and rs6234/rs6235 in PCSK1 have been associated with extreme obesity [e.g. body mass index (BMI) ≥ 40 kg/m(2)], but their contribution to common obesity (BMI ≥ 30 kg/m(2)) and BMI variation in a multi-ethnic context is unclear. To fill this gap, we collected phenotypic and genetic data in up to 331 175 individuals from diverse ethnic groups. This process involved a systematic review of the literature in PubMed, Web of Science, Embase and the NIH GWAS catalog complemented by data extraction from pre-existing GWAS or custom-arrays in consortia and single studies. We employed recently developed global meta-analytic random-effects methods to calculate summary odds ratios (OR) and 95% confidence intervals (CIs) or beta estimates and standard errors (SE) for the obesity status and BMI analyses, respectively. Significant associations were found with binary obesity status for rs6232 (OR = 1.15, 95% CI 1.06-1.24, P = 6.08 × 10(-6)) and rs6234/rs6235 (OR = 1.07, 95% CI 1.04-1.10, P = 3.00 × 10(-7)). Similarly, significant associations were found with continuous BMI for rs6232 (β = 0.03, 95% CI 0.00-0.07; P = 0.047) and rs6234/rs6235 (β = 0.02, 95% CI 0.00-0.03; P = 5.57 × 10(-4)). Ethnicity, age and study ascertainment significantly modulated the association of PCSK1 polymorphisms with obesity. In summary, we demonstrate evidence that common gene variation in PCSK1 contributes to BMI variation and susceptibility to common obesity in the largest known meta-analysis published to date in genetic epidemiology., (© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
- Published
- 2015
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249. Prevalence of frailty and disability: findings from the English Longitudinal Study of Ageing.
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Gale CR, Cooper C, and Sayer AA
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- Activities of Daily Living, Age Factors, Aged, Aged, 80 and over, Dependent Ambulation, England epidemiology, Female, Health Surveys, Humans, Longitudinal Studies, Male, Middle Aged, Mobility Limitation, Physical Examination, Predictive Value of Tests, Prevalence, Risk Assessment, Risk Factors, Sex Factors, Surveys and Questionnaires, Time Factors, Aging, Disability Evaluation, Frail Elderly, Geriatric Assessment methods
- Abstract
Objective: to examine the prevalence of frailty and disability in people aged 60 and over and the proportion of those with disabilities who receive help or use assistive devices., Methods: participants were 5,450 people aged 60 and over from the English Longitudinal Study of Ageing. Frailty was defined according to the Fried criteria. Participants were asked about difficulties with mobility or other everyday activities. Those with difficulties were asked whether they received help or used assistive devices., Results: the overall weighted prevalence of frailty was 14%. Prevalence rose with increasing age, from 6.5% in those aged 60-69 years to 65% in those aged 90 or over. Frailty occurred more frequently in women than in men (16 versus 12%). Mobility difficulties were very common: 93% of frail individuals had such difficulties versus 58% of the non-frail individuals. Among frail individuals, difficulties in performing activities or instrumental activities of daily living were reported by 57 or 64%, respectively, versus 13 or 15%, respectively, among the non-frail individuals. Among those with difficulties with mobility or other daily activities, 71% of frail individuals and 31% of non-frail individuals said that they received help. Of those with difficulties, 63% of frail individuals and 20% of non-frail individuals used a walking stick, but the use of other assistive devices was uncommon., Conclusions: frailty becomes increasingly common in older age groups and is associated with a sizeable burden as regards difficulties with mobility and other everyday activities., (© The Author 2014. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
- Published
- 2015
- Full Text
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250. [Role of primary care professionals in the management of sarcopenia].
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Monteserín R, Roberts HC, and Sayer AA
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- Humans, Health Personnel, Primary Health Care, Professional Role, Sarcopenia therapy
- Published
- 2014
- Full Text
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