Lifestyle, genetic risk and incidence of cancer: a prospective cohort study of 13 cancer types

Author:

Byrne Stephanie123ORCID,Boyle Terry123,Ahmed Muktar1345,Lee Sang Hong123,Benyamin Beben123,Hyppönen Elina134ORCID

Affiliation:

1. Australian Centre for Precision Health, University of South Australia , Adelaide, SA, Australia

2. UniSA Allied Health & Human Performance, University of South Australia , Adelaide, SA, Australia

3. South Australian Health and Medical Research Institute , Adelaide, SA, Australia

4. UniSA Clinical and Health Sciences, University of South Australia , Adelaide, SA, Australia

5. Department of Epidemiology, Faculty of Public Health, Jimma University Institute of Health , Jimma, Ethiopia

Abstract

Abstract Background Genetic and lifestyle factors are associated with cancer risk. We investigated the benefits of adhering to lifestyle advice by the World Cancer Research Fund (WCRF) with the risk of 13 types of cancer and whether these associations differ according to genetic risk using data from the UK Biobank. Methods In 2006–2010, participants aged 37–73 years had their lifestyle assessed and were followed up for incident cancers until 2015–2019. Analyses were restricted to those of White European ancestry with no prior history of malignant cancer (n = 195 822). Polygenic risk scores (PRSs) were computed for 13 cancer types and these cancers combined (‘overall cancer’), and a lifestyle index was calculated from WCRF recommendations. Associations with cancer incidence were estimated using Cox regression, adjusting for relevant confounders. Additive and multiplicative interactions between lifestyle index and PRSs were assessed. Results There were 15 240 incident cancers during the 1 926 987 person-years of follow-up (median follow-up = 10.2 years). After adjusting for confounders, the lifestyle index was associated with a lower risk of overall cancer [hazard ratio per standard deviation increase (95% CI) = 0.89 (0.87, 0.90)] and of eight specific cancer types. There was no evidence of interactions on the multiplicative scale. There was evidence of additive interactions in risks for colorectal, breast, pancreatic, lung and bladder cancers, such that the recommended lifestyle was associated with greater change in absolute risk for persons at higher genetic risk (P < 0.0003 for all). Conclusions The recommended lifestyle has beneficial associations with most cancers. In terms of absolute risk, the protective association is greater for higher genetic risk groups for some cancers. These findings have important implications for persons most genetically predisposed to those cancers and for targeted strategies for cancer prevention.

Funder

Tour de Cure

Australian Government’s Medical Research Future Fund

Rapid Applied Research Translation

Health Translation SA

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Epidemiology

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