Modifiable pathways for colorectal cancer : a mendelian randomisation analysis

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Cornish , A J , Law , P J , Timofeeva , M , Palin , K , Farrington , S M , Palles , C , Jenkins , M A , Casey , G , Brenner , H , Chang-Claude , J , Hoffmeister , M , Kirac , I , Maughan , T , Brezina , S , Gsur , A , Cheadle , J P , Aaltonen , L A , Tomlinson , I , Dunlop , M G & Houlston , R S 2020 , ' Modifiable pathways for colorectal cancer : a mendelian randomisation analysis ' , The Lancet gastroenterology & hepatology , vol. 5 , no. 1 , pp. 55-62 . https://doi.org/10.1016/S2468-1253(19)30294-8

Title: Modifiable pathways for colorectal cancer : a mendelian randomisation analysis
Author: Cornish, Alex J.; Law, Philip J.; Timofeeva, Maria; Palin, Kimmo; Farrington, Susan M.; Palles, Claire; Jenkins, Mark A.; Casey, Graham; Brenner, Hermann; Chang-Claude, Jenny; Hoffmeister, Michael; Kirac, Iva; Maughan, Tim; Brezina, Stefanie; Gsur, Andrea; Cheadle, Jeremy P.; Aaltonen, Lauri A.; Tomlinson, Ian; Dunlop, Malcolm G.; Houlston, Richard S.
Contributor organization: Lauri Antti Aaltonen / Principal Investigator
Research Programs Unit
Medicum
Department of Medical and Clinical Genetics
University of Helsinki
Genome-Scale Biology (GSB) Research Program
HUS Helsinki and Uusimaa Hospital District
Date: 2020-01
Language: eng
Number of pages: 8
Belongs to series: The Lancet gastroenterology & hepatology
ISSN: 2468-1253
DOI: https://doi.org/10.1016/S2468-1253(19)30294-8
URI: http://hdl.handle.net/10138/309630
Abstract: Background Epidemiological studies have linked lifestyle, cardiometabolic, reproductive, developmental, and inflammatory factors to the risk of colorectal cancer. However, which specific factors affect risk and the strength of these effects are unknown. We aimed to examine the relationship between potentially modifiable risk factors and colorectal cancer. Methods We used a random-effects model to examine the relationship between 39 potentially modifiable risk factors and colorectal cancer in 26 397 patients with colorectal cancer and 41 481 controls (ie, people without colorectal cancer). These population data came from a genome-wide association study of people of European ancestry, which was amended to exclude UK BioBank data. In the model, we used genetic variants as instruments via two-sample mendelian randomisation to limit bias from confounding and reverse causation. We calculated odds ratios per genetically predicted SD unit increase in each putative risk factor (OR SD) for colorectal cancer risk. We did mendelian randomisation Egger regressions to identify evidence of potential violations of mendelian randomisation assumptions. A Bonferroni-corrected threshold of p=1.3 x 10(-3) was considered significant, and p values less than 0.05 were considered to be suggestive of an association. Findings No putative risk factors were significantly associated with colorectal cancer risk after correction for multiple testing. However, suggestive associations with increased risk were noted for genetically predicted body fat percentage (OR SD 1.14 [95% CI 1.03-1.25]; p=0.0086), body-mass index (1.09 [1.01-1.17]; p=0.023), waist circumference (1.13 [1.02-1.26]; p=0.018), basal metabolic rate (1.10 [1.03-1.18]; p=0.0079), and concentrations of LDL cholesterol (1.14 [1.04-1.25]; p=0.0056), total cholesterol (1.09 [1.01-1.18]; p=0.025), circulating serum iron (1.17 [1.00-1.36]; p=0.049), and serum vitamin B12 (1.21 [1.04-1.42]; p=0.016), although potential pleiotropy among genetic variants used as instruments for vitamin B12 constrains the finding. A suggestive association was also noted between adult height and increased risk of colorectal cancer (OR SD 1.04 [95% CI 1.00-1.08]; p=0.032). Low blood selenium concentration had a suggestive association with decreased risk of colorectal cancer (OR SD 0.85 [95% CI 0.75-0.96]; p=0.0078) based on a single variant, as did plasma concentrations of interleukin-6 receptor subunit a (also based on a single variant; 0.98 [0.96-1.00]; p=0.035). Risk of colorectal cancer was not associated with any sex hormone or reproductive factor, serum calcium, or circulating 25-hydroxyvitamin D concentrations. Interpretation This analysis identified several modifiable targets for primary prevention of colorectal cancer, including lifestyle, obesity, and cardiometabolic factors, that should inform public health policy. Copyright (C) 2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
Subject: INSTRUMENTS
ASSOCIATION
BIAS
3121 General medicine, internal medicine and other clinical medicine
3122 Cancers
Peer reviewed: Yes
Rights: cc_by
Usage restriction: openAccess
Self-archived version: publishedVersion


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