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      Increase in anticholinergic burden from 1990 to 2015: Age‐period‐cohort analysis in UK biobank

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          UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age

          Cathie Sudlow and colleagues describe the UK Biobank, a large population-based prospective study, established to allow investigation of the genetic and non-genetic determinants of the diseases of middle and old age.
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            glmmTMB Balances Speed and Flexibility Among Packages for Zero-inflated Generalized Linear Mixed Modeling

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              Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population

              Abstract The UK Biobank cohort is a population-based cohort of 500,000 participants recruited in the United Kingdom (UK) between 2006 and 2010. Approximately 9.2 million individuals aged 40–69 years who lived within 25 miles (40 km) of one of 22 assessment centers in England, Wales, and Scotland were invited to enter the cohort, and 5.5% participated in the baseline assessment. The representativeness of the UK Biobank cohort was investigated by comparing demographic characteristics between nonresponders and responders. Sociodemographic, physical, lifestyle, and health-related characteristics of the cohort were compared with nationally representative data sources. UK Biobank participants were more likely to be older, to be female, and to live in less socioeconomically deprived areas than nonparticipants. Compared with the general population, participants were less likely to be obese, to smoke, and to drink alcohol on a daily basis and had fewer self-reported health conditions. At age 70–74 years, rates of all-cause mortality and total cancer incidence were 46.2% and 11.8% lower, respectively, in men and 55.5% and 18.1% lower, respectively, in women than in the general population of the same age. UK Biobank is not representative of the sampling population; there is evidence of a “healthy volunteer” selection bias. Nonetheless, valid assessment of exposure-disease relationships may be widely generalizable and does not require participants to be representative of the population at large.
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                Author and article information

                Contributors
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                Journal
                British Journal of Clinical Pharmacology
                Brit J Clinical Pharma
                Wiley
                0306-5251
                1365-2125
                March 2022
                September 19 2021
                March 2022
                : 88
                : 3
                : 983-993
                Affiliations
                [1 ]Lothian Birth Cohorts Group, Department of Psychology University of Edinburgh Edinburgh UK
                [2 ]Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine University of Edinburgh Edinburgh UK
                [3 ]Alzheimer Scotland Dementia Research Centre University of Edinburgh Edinburgh UK
                [4 ]Edinburgh Dementia Prevention University of Edinburgh Edinburgh UK
                [5 ]Division of Psychiatry, Centre for Clinical Brain Science University of Edinburgh Edinburgh UK
                Article
                10.1111/bcp.15045
                34409635
                edec04ed-3964-4925-bdb9-55cfb9ce8218
                © 2022

                http://creativecommons.org/licenses/by/4.0/

                http://doi.wiley.com/10.1002/tdm_license_1.1

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