Genetic predictors of circulating 25-hydroxyvitamin D and risk of colorectal cancer

Linda T. Hiraki, Conghui Qu, Carolyn M. Hutter, John A. Baron, Sonja I. Berndt, Stéphane Bézieau, Hermann Brenner, Bette J. Caan, Graham Casey, Jenny Chang-Claude, Stephen J. Chanock, David V. Conti, David Duggan, Charles S. Fuchs, Steven Gallinger, Edward L. Giovannucci, Tabitha A. Harrison, Richard B. Hayes, Aditi Hazra, Brian HendersonMichael Hoffmeister, John L. Hopper, Thomas J. Hudson, Mark A. Jenkins, Sebastien Küry, Loic Le Marchand, Mathieu Lemire, Jing Ma, Jo Ann E. Manson, Hongmei Nan, Polly A. Newcomb, Kimmie Ng, John D. Potter, Robert E. Schoen, Fredrick R. Schumacher, Daniela Seminara, Martha L. Slattery, Jean Wactawski-Wende, Emily White, Kana Wu, Brent W. Zanke, Peter Kraft, Ulrike Peters, Andrew T. Chan

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Background: Experimental evidence has demonstrated an antineoplastic role for vitaminDin the colon, and higher circulating 25-hydroxyvitamin D [25(OH)D] levels are consistently associated with a lower risk of colorectal cancer. Genome-wide association studies have identified loci associated with levels of circulating 25(OH)D. The identified single-nucleotide polymorphisms (SNPs) from four gene regions collectively explain approximately 5% of the variance in circulating 25(OH)D. Methods:Weinvestigated whether five polymorphisms inGC, CYP2R1, CYP24A1, andDHCR7/NADSYN1, genes previously shown to be associated with circulating 25(OH)D levels, were associated with colorectal cancer risk in 10,061 cases and 12,768 controls drawn from 13 studies included in the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) and Colon Cancer Family Registry (CCFR). We conducted a meta-analysis of crude and multivariate- adjusted logistic regression models to calculate odds ratios and associated confidence intervals for SNPs individually, SNPs simultaneously, and for a vitamin D additive genetic risk score (GRS). Results:Wedid not observe a statistically significant association between the 25(OH)D-associated SNPs and colorectal cancer marginally, conditionally, or as a GRS, or for colon or rectal cancer separately. Conclusions: Our findings do not support an association between SNPs associated with circulating 25(OH)D and risk of colorectal cancer. Additional work is warranted to investigate the complex relationship between 25 (OH)D and colorectal cancer risk.

Original languageEnglish (US)
Pages (from-to)2037-2046
Number of pages10
JournalCancer Epidemiology Biomarkers and Prevention
Volume22
Issue number11
DOIs
StatePublished - Nov 2013
Externally publishedYes

ASJC Scopus subject areas

  • General Medicine

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