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Observational and genetic associations between cardiorespiratory fitness and cancer: a UK Biobank and international consortia study.

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Peer-reviewed

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Abstract

BACKGROUND: The association of fitness with cancer risk is not clear. METHODS: We used Cox proportional hazards models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for risk of lung, colorectal, endometrial, breast, and prostate cancer in a subset of UK Biobank participants who completed a submaximal fitness test in 2009-12 (N = 72,572). We also investigated relationships using two-sample Mendelian randomisation (MR), odds ratios (ORs) were estimated using the inverse-variance weighted method. RESULTS: After a median of 11 years of follow-up, 4290 cancers of interest were diagnosed. A 3.5 ml O2⋅min-1⋅kg-1 total-body mass increase in fitness (equivalent to 1 metabolic equivalent of task (MET), approximately 0.5 standard deviation (SD)) was associated with lower risks of endometrial (HR = 0.81, 95% CI: 0.73-0.89), colorectal (0.94, 0.90-0.99), and breast cancer (0.96, 0.92-0.99). In MR analyses, a 0.5 SD increase in genetically predicted O2⋅min-1⋅kg-1 fat-free mass was associated with a lower risk of breast cancer (OR = 0.92, 95% CI: 0.86-0.98). After adjusting for adiposity, both the observational and genetic associations were attenuated. DISCUSSION: Higher fitness levels may reduce risks of endometrial, colorectal, and breast cancer, though relationships with adiposity are complex and may mediate these relationships. Increasing fitness, including via changes in body composition, may be an effective strategy for cancer prevention.

Description

Funder: Intramural Research Program of the National Institutes of Health

Journal Title

Br J Cancer

Conference Name

Journal ISSN

0007-0920
1532-1827

Volume Title

130

Publisher

Springer Nature

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
MRC (MC_UU_00006/4)
Cambridge University Hospitals NHS Foundation Trust (CUH) (146281)
MRC (MC_UU_00006/1)
MRC (MC_UU_00006/2)
National Institute for Health and Care Research (IS-BRC-1215-20014)
Medical Research Council (MR/N003284/1)
EW, SM, CM, PSM are supported by the Intramural Research Program of the National Institutes of Health (NIH). NW, TS, FRD, KW, TG and SB are supported by UK Medical Research Council [grant numbers MC_UU_00006/1, MC_UU_00006/2 and MC_UU_00006/4]. NW and SB are supported by the NIHR Biomedical Research Centre in Cambridge (IS-BRC-1215-20014). The NIHR Cambridge Biomedical Research Centre (BRC) is a partnership between Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge, funded by the National Institute for Health Research (NIHR). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care.