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While dietary fat has been established as a risk factor for colorectal cancer (CRC), associations between fatty acids (FAs) and CRC have been inconsistent. Using Mendelian randomisation (MR), we sought to evaluate associations between polyunsaturated (PUFA), monounsaturated (MUFA) and saturated FAs (SFAs) and CRC risk.We analysed genotype data on 9254 CRC cases and 18,386 controls of European ancestry. Externally weighted polygenic risk scores were generated and used to evaluate associations with CRC per one standard deviation increase in genetically defined plasma FA levels.Risk reduction was observed for oleic and palmitoleic MUFAs (OROA = 0.77, 95% CI: 0.65-0.92, P = 3.9 × 10-3; ORPOA = 0.36, 95% CI: 0.15-0.84, P = 0.018). PUFAs linoleic and arachidonic acid had negative and positive associations with CRC respectively (ORLA = 0.95, 95% CI: 0.93-0.98, P = 3.7 × 10-4; ORAA = 1.05, 95% CI: 1.02-1.07, P = 1.7 × 10-4). The SFA stearic acid was associated with increased CRC risk (ORSA = 1.17, 95% CI: 1.01-1.35, P = 0.041).Results from our analysis are broadly consistent with a pro-inflammatory FA profile having a detrimental effect in terms of CRC risk.

Original publication

DOI

10.1016/j.ejca.2017.07.034

Type

Journal article

Journal

European journal of cancer (Oxford, England : 1990)

Publication Date

10/2017

Volume

84

Pages

228 - 238

Addresses

Division of Genetics and Epidemiology, The Institute of Cancer Research, London, SW7 3RP, UK.

Keywords

Humans, Colorectal Neoplasms, Genetic Predisposition to Disease, Fatty Acids, Inflammation Mediators, Diet, Odds Ratio, Risk Assessment, Risk Factors, Case-Control Studies, Risk Reduction Behavior, Diet, Mediterranean, Phenotype, Polymorphism, Single Nucleotide, European Continental Ancestry Group, Genome-Wide Association Study, Mendelian Randomization Analysis, Gene-Environment Interaction, Protective Factors, Biomarkers, Tumor, Healthy Diet