Evaluating the effect of metabolic traits on oral and oropharyngeal cancer risk using Mendelian randomization

Author:

Gormley Mark12ORCID,Dudding Tom2,Thomas Steven J2,Tyrrell Jessica3,Ness Andrew R4,Pring Miranda2,Legge Danny5ORCID,Davey Smith George1ORCID,Richmond Rebecca C1,Vincent Emma E15ORCID,Bull Caroline15ORCID

Affiliation:

1. MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol

2. Bristol Dental Hospital and School, University of Bristol

3. University of Exeter Medical School, RILD Building, RD&E Hospital

4. University Hospitals Bristol and Weston NHS Foundation Trust National Institute for Health Research Bristol Biomedical Research Centre, University of Bristol

5. Translational Health Sciences, Bristol Medical School, University of Bristol

Abstract

A recent World Health Organization report states that at least 40% of all cancer cases may be preventable, with smoking, alcohol consumption, and obesity identified as three of the most important modifiable lifestyle factors. Given the significant decline in smoking rates, particularly within developed countries, other potentially modifiable risk factors for head and neck cancer warrant investigation. Obesity and related metabolic disorders such as type 2 diabetes (T2D) and hypertension have been associated with head and neck cancer risk in multiple observational studies. However, adiposity has also been correlated with smoking, with bias, confounding or reverse causality possibly explaining these findings. To overcome the challenges of observational studies, we conducted two-sample Mendelian randomization (inverse variance weighted [IVW] method) using genetic variants which were robustly associated with adiposity, glycaemic and blood pressure traits in genome-wide association studies (GWAS). Outcome data were taken from the largest available GWAS of 6034 oral and oropharyngeal cases, with 6585 controls. We found limited evidence of a causal effect of genetically proxied body mass index (BMI; OR IVW = 0.89, 95% CI 0.72–1.09, p = 0.26 per 1 standard deviation in BMI [4.81kg/m2]) on oral and oropharyngeal cancer risk. Similarly, there was limited evidence for related traits including T2D and hypertension. Small effects cannot be excluded given the lack of power to detect them in currently available GWAS.

Funder

Wellcome Trust

Diabetes UK

National Institute for Health and Care Research

Cancer Research UK

National Institute of Dental and Craniofacial Research

World Cancer Research Fund

Medical Research Council

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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