Reproducibility and associated regression dilution bias of accelerometer-derived physical activity and sleep in UK Biobank.
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BACKGROUND: Previous studies on the reproducibility of 7-day accelerometer measurements have been limited by small sample sizes and short follow-up periods. We aimed to assess the long-term reproducibility of accelerometer-derived physical activity and sleep, and to illustrate the impact of regression dilution bias on the association between daily step count and coronary heart disease (CHD) in UK Biobank. METHODS: We analysed data from 3138 UK Biobank participants in the main accelerometry sub-study with up to four repeat accelerometer measurements after 3-4 years. Nine physical activity and sleep phenotypes were extracted to capture different movement behaviours. Reproducibility was assessed by using intraclass correlation coefficients (ICCs). The impact on disease associations was illustrated by considering daily step count and incident CHD using Cox regression (87 038 participants; 3879 CHD events), before and after correction for regression dilution. RESULTS: Among the 3138 participants, 51% were women and the mean (SD) age was 63.1 (9.4) years. Reproducibility was good for overall activity, with an ICC (95% confidence interval) of 0.75 (0.74-0.76), and moderate for other phenotypes, with ICCs ranging from 0.58 (0.56-0.59) for sleep efficiency to 0.69 (0.68-0.70) for sedentary behaviour. In our example, the inverse association between daily step count and CHD showed a 20% lower risk of CHD per usual 4000 steps after correcting for regression dilution compared with 13% before correction. CONCLUSION: Accelerometer measurements are moderately reproducible and comparable to measures such as blood pressure. Correction for regression dilution bias is crucial to quantify associations of usual physical activity and sleep with disease risk.
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Acknowledgements: We thank Simon Sheard from the UK Biobank team for coordinating the repeat accelerometry sub-study, and Howard Callen and Janet Maccora for providing key information and guidance on its study design. This research was conducted by using the UK Biobank resource under application number 59070. We are grateful to all participants for generously contributing their data to advance research in population health. This work used data provided by patients and collected by the National Health Service (NHS) as part of their care and support. Computation was performed via the Oxford Biomedical Research Computing (BMRC) facility—a joint development between the Wellcome Centre for Human Genetics and the Big Data Institute supported by Health Data Research UK and the National Institute for Health and Care Research (NIHR) Oxford Biomedical Research Centre. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR, or the Department of Health.
Funder: UK Biobank
Funder: UK Medical Research Council (MRC)
Funder: University of Oxford from the UK MRC
Funder: Health Data Research (HDR) UK
Funder: HDR UK—an initiative funded by UK Research and Innovation (UKRI)
Funder: Department of Health and Social Care; doi: https://doi.org/10.13039/501100000276
Funder: Novo Nordisk and Swiss
Funder: MRC, Engineering and Physical Sciences Research Council (EPSRC)
Funder: Economic and Social Research Council; doi: https://doi.org/10.13039/501100000269
Funder: Department of Health and Social Care (England)
Funder: Chief Scientist Office of the Scottish Government Health and Social Care Directorates
Funder: Health and Social Care Research and Development Division (Welsh Government)
Funder: Public Health Agency (Northern Ireland); doi: https://doi.org/10.13039/501100001626
Funder: BHF, and Cancer Research UK
Funder: BHF, NIHR Oxford Biomedical Research Centre (BRC)
Funder: BHF Centre of Research Excellence, and the Nuffield Department of Population Health
Funder: Novo Nordisk, Swiss Re, Boehringer Ingelheim, National Institutes of Health’s Oxford Cambridge Scholars Program
Funder: Creative Commons Attribution (CC BY) licence to any Author Accepted Manuscript version arising
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1464-3685
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MRC (MC_UU_00006/4)

