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Joint associations of device-measured step count and sleep duration with incident major adverse cardiovascular events: prospective analysis of the UK Biobank

Abstract:
BackgroundThe interaction between physical activity and sleep with cardiovascular disease remains poorly understood, despite both being key risk factors. This study investigated the independent and joint associations of device-measured step count and sleep duration with incident major adverse cardiovascular events (MACE).MethodsProspective analysis of UK Biobank participants who wore a wrist-based accelerometer for seven days between 2013 and 2015. Open-source machine learning algorithms derived daily step count and overnight sleep duration. The outcome was incident MACE (cardiovascular death, non-fatal myocardial infarction or stroke, or revascularisation procedure), identified through electronic health record linkage. Cox proportional hazards models were used to examine independent and joint associations of median daily step count (low [11,000]) and median overnight sleep duration (short [7.5 h]) with incident MACE.FindingsAmong 88,012 participants (mean age 62.2 years [standard deviation, SD 7.8]), 3817 were diagnosed with MACE during follow-up (median 7.9 years [interquartile range, IQR 7.3-8.4]). Low step count and short sleep duration were independently associated with a higher risk of MACE, but there was no evidence of an interaction between step count and sleep duration (P for interaction = 0.42). Compared with the reference group-participants with high step count and intermediate sleep duration-the highest risk of MACE was observed in participants with both low step count and short sleep duration (hazard ratio, HR: 1.84, 95% CI: 1.62-2.10, p < 0.0001).InterpretationThe results of this study show that higher daily step count does not fully attenuate the higher risk of cardiovascular disease associated with short sleep duration, reinforcing the importance of sufficient levels of both daily step count and sleep for the prevention of cardiovascular disease.FundingWellcome Trust (223100/Z/21/Z).
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.eclinm.2026.103769

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Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Big Data Institute
Role:
Author
ORCID:
0000-0001-5941-9795
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Big Data Institute
Role:
Author
ORCID:
0009-0004-4493-0426
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Big Data Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Big Data Institute
Role:
Author


More from this funder
Funder identifier:
10.13039/100010269
Grant:
223100/Z/21/Z
More from this funder
Funder identifier:
10.13039/501100000274
Grant:
RE/18/3/34214
More from this funder
Funder identifier:
10.13039/501100004191
More from this funder
Funder identifier:
10.13039/100008349
More from this funder
Funder identifier:
10.13039/100000002


Publisher:
Elsevier
Journal:
EClinicalMedicine More from this journal
Volume:
92
Pages:
103769
Article number:
103769
Publication date:
2026-01-29
Acceptance date:
2026-01-08
DOI:
EISSN:
2589-5370
ISSN:
2589-5370
Pmid:
41660364


Language:
English
Keywords:
Pubs id:
2374390
Local pid:
pubs:2374390
Source identifiers:
3769154
Deposit date:
2026-02-18
ARK identifier:
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