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Identification of potential mediators of the relationship between body mass index and colorectal cancer: a Mendelian randomization analysis.

Authors :
Bouras, Emmanouil
Gill, Dipender
Zuber, Verena
Murphy, Neil
Dimou, Niki
Aleksandrova, Krasimira
Lewis, Sarah J
Martin, Richard M
Yarmolinsky, James
Albanes, Demetrius
Brenner, Hermann
Castellví-Bel, Sergi
Chan, Andrew T
Cheng, Iona
Gruber, Stephen
Guelpen, Bethany Van
Li, Christopher I
Marchand, Loic Le
Newcomb, Polly A
Ogino, Shuji
Source :
International Journal of Epidemiology; Jun2024, Vol. 53 Issue 3, p1-8, 8p
Publication Year :
2024

Abstract

Background Colorectal cancer (CRC) is the third-most-common cancer worldwide and its rates are increasing. Elevated body mass index (BMI) is an established risk factor for CRC, although the molecular mechanisms behind this association remain unclear. Using the Mendelian randomization (MR) framework, we aimed to investigate the mediating effects of putative biomarkers and other CRC risk factors in the association between BMI and CRC. Methods We selected as mediators biomarkers of established cancer-related mechanisms and other CRC risk factors for which a plausible association with obesity exists, such as inflammatory biomarkers, glucose homeostasis traits, lipids, adipokines, insulin-like growth factor 1 (IGF1), sex hormones, 25-hydroxy-vitamin D, smoking, physical activity (PA) and alcohol consumption. We used inverse-variance weighted MR in the main univariable analyses and performed sensitivity analyses (weighted-median, MR–Egger, Contamination Mixture). We used multivariable MR for the mediation analyses. Results Genetically predicted BMI was positively associated with CRC risk [odds ratio per SD (5 kg/m<superscript>2</superscript>) = 1.17, 95% CI: 1.08–1.24, P -value = 1.4 × 10<superscript>−5</superscript>] and robustly associated with nearly all potential mediators. Genetically predicted IGF1, fasting insulin, low-density lipoprotein cholesterol, smoking, PA and alcohol were associated with CRC risk. Evidence for attenuation was found for IGF1 [explained 7% (95% CI: 2–13%) of the association], smoking (31%, 4–57%) and PA (7%, 2–11%). There was little evidence for pleiotropy, although smoking was bidirectionally associated with BMI and instruments were weak for PA. Conclusions The effect of BMI on CRC risk is possibly partly mediated through plasma IGF1, whereas the attenuation of the BMI–CRC association by smoking and PA may reflect confounding and shared underlying mechanisms rather than mediation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03005771
Volume :
53
Issue :
3
Database :
Complementary Index
Journal :
International Journal of Epidemiology
Publication Type :
Academic Journal
Accession number :
177774123
Full Text :
https://doi.org/10.1093/ije/dyae067