Vigorous physical activity, incident heart disease, and cancer: how little is enough?

Author:

Ahmadi Matthew N1ORCID,Clare Philip J123,Katzmarzyk Peter T4,del Pozo Cruz Borja5ORCID,Lee I Min67,Stamatakis Emmanuel1ORCID

Affiliation:

1. Charles Perkins Centre, School of Health Sciences, Faculty of Medicine and Health, The University of Sydney , NSW , Australia

2. Prevention Research Collaboration, School of Public Health, Faculty of Medicine and Health, The University of Sydney , NSW , Australia

3. National Drug and Alcohol Research Centre, UNSW Sydney , NSW , Australia

4. Population and Public Health Sciences, Pennington Biomedical Research Center , Baton Rouge, LA , USA

5. Department of Sports Science and Clinical Biomechanics, University of Southern Denmark , Odense , Denmark

6. Division of Preventive Medicine, Brigham & Women’s Hospital, Harvard Medical School , Boston , USA

7. Department of Epidemiology, Harvard T.H. Chan School of Public Health , Boston, MA , USA

Abstract

Abstract Aims Vigorous physical activity (VPA) is a time-efficient way to achieve recommended physical activity levels. There is a very limited understanding of the minimal and optimal amounts of vigorous physical activity in relation to mortality and disease incidence. Methods and results A prospective study in 71 893 adults [median age (IQR): 62.5 years (55.3, 67.7); 55.9% female] from the UK Biobank cohort with wrist-worn accelerometry. VPA volume (min/week) and frequency of short VPA bouts (≤2 min) were measured. The dose–response associations of VPA volume and frequency with mortality [all-cause, cardiovascular disease (CVD) and cancer], and CVD and cancer incidence were examined after excluding events occurring in the first year. During a mean post-landmark point follow-up of 5.9 years (SD ± 0.8), the adjusted 5-year absolute mortality risk was 4.17% (95% confidence interval: 3.19%, 5.13%) for no VPA, 2.12% (1.81%, 2.44%) for >0 to <10 min, 1.78% (1.53%, 2.03%) for 10 to <30 min, 1.47% (1.21%, 1.73%) for 30 to <60 min, and 1.10% (0.84%, 1.36%) for ≥60 min. The ‘optimal dose’ (nadir of the curve) was 53.6 (50.5, 56.7) min/week [hazard ratio (HR): 0.64 (0.54, 0.77)] relative to the 5th percentile reference (2.2 min/week). There was an inverse linear dose-response association of VPA with CVD mortality. The ‘minimal’ volume dose (50% of the optimal dose) was ∼15 (14.3, 16.3) min/week for all-cause [HR: 0.82 (0.75, 0.89)] and cancer [HR: 0.84 (0.74, 0.95)] mortality, and 19.2 (16.5, 21.9) min/week [HR: 0.60 (0.50, 0.72)] for CVD mortality. These associations were consistent for CVD and cancer incidence. There was an inverse linear association between VPA frequency and CVD mortality. 27 (24, 30) bouts/week was associated with the lowest all-cause mortality [HR: 0.73 (0.62, 0.87)]. Conclusion VPA of 15–20 min/week were associated with a 16–40% lower mortality HR, with further decreases up to 50–57 min/week. These findings suggest reduced health risks may be attainable through relatively modest amounts of VPA accrued in short bouts across the week.

Funder

Australian National Health and Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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