Associations of “Weekend Warrior” Physical Activity With Incident Disease and Cardiometabolic Health
Abstract
BACKGROUND:
Achievement of guideline-recommended levels of physical activity (≥150 minutes of moderate-to-vigorous physical activity per week) is associated with lower risk of adverse cardiovascular events and represents an important public health priority. Although physical activity commonly follows a “weekend warrior” pattern, in which most moderate-to-vigorous physical activity is concentrated in 1 or 2 days rather than spread more evenly across the week (regular), the effects of physical activity pattern across a range of incident diseases, including cardiometabolic conditions, are unknown.
METHODS:
We tested associations between physical activity pattern and incidence of 678 conditions in 89 573 participants (62±8 years of age; 56% women) of the UK Biobank prospective cohort study who wore an accelerometer for 1 week between June 2013 and December 2015. Models were adjusted for multiple baseline clinical factors, and P value thresholds were corrected for multiplicity.
RESULTS:
When compared to inactive (<150 minutes moderate-to-vigorous physical activity/week), both weekend warrior (267 total associations; 264 [99%] with lower disease risk; hazard ratio [HR] range, 0.35–0.89) and regular activity (209 associations; 205 [98%] with lower disease risk; HR range, 0.41–0.88) were broadly associated with lower risk of incident disease. The strongest associations were observed for cardiometabolic conditions such as incident hypertension (weekend warrior: HR, 0.77 [95% CI, 0.73–0.80]; P=1.2×10-27; regular: HR, 0.72 [95% CI, 0.68–0.77]; P=4.5×10-28), diabetes (weekend warrior: HR, 0.57 [95% CI, 0.51–0.62]; P=3.9×10-32; regular: HR, 0.54 [95% CI, 0.48–0.60]; P=8.7×10-26), obesity (weekend warrior: HR, 0.55 [95% CI, 0.50–0.60]; P=2.4×10-43, regular: HR, 0.44 [95% CI, 0.40–0.50]; P=9.6×10-47), and sleep apnea (weekend warrior: HR, 0.57 [95% CI, 0.48–0.69]; P=1.6×10-9; regular: HR, 0.49 [95% CI, 0.39–0.62]; P=7.4×10-10). When weekend warrior and regular activity were compared directly, there were no conditions for which effects differed significantly. Observations were similar when activity was thresholded at the sample median (≥230.4 minutes of moderate-to-vigorous physical activity/week).
CONCLUSIONS:
Achievement of measured physical activity volumes consistent with guideline recommendations is associated with lower risk for >200 diseases, with prominent effects on cardiometabolic conditions. Associations appear similar whether physical activity follows a weekend warrior pattern or is spread more evenly throughout the week.
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© 2024 American Heart Association, Inc.
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History
Received: 5 January 2024
Accepted: 17 July 2024
Published online: 26 September 2024
Published in print: 15 October 2024
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Disclosures
P.T.E. receives sponsored research support from Bayer AG, Bristol Myers Squibb, Pfizer, and Novo Nordisk; he has also served on advisory boards or consulted for Bayer AG. S.A.L. is an employee of Novartis as of July 2022. S.A.L. received sponsored research support from Bristol Myers Squibb, Pfizer, Boehringer Ingelheim, Fitbit, Medtronic, Premier, and IBM, and has consulted for Bristol Myers Squibb, Pfizer, Blackstone Life Sciences, and Invitae. The other authors report no conflicts.
Sources of Funding
S. Kany is supported by the Walter Benjamin Fellowship from the Deutsche Forschungsgemeinschaft (521832260). J.T.R. is supported by a research fellowship from the Sigrid Jusélius Foundation. J.P.P. is supported by the National Institutes of Health (NIH; K08HL159346). T.W.C. is supported by NIH (K23HL159262-01A1). J.S.G. is supported by the American Heart Association (AHA; 19AMFDP34990046) and the president and fellows of Harvard College (5KL2TR002542-04). P.T.E. is supported by grants from NIH (1RO1HL092577 and 1R01HL157635), from AHA (18SFRN34230127 and 961045), and from the European Union (MAESTRIA 965286). S.A.L. previously received support from NIH grants R01HL139731 and R01HL157635 and AHA grant 18SFRN34250007. M.A.A.-A. is supported by NIH (T32HL007208). S. Khurshid is supported by NIH (K23HL169839-01) and AHA (2023CDA1050571).
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