Folate intake, MTHFR polymorphisms, and the risk of colorectal cancer: A systematic review and meta-analysis

Deborah A. Kennedy, Seth J. Stern, Ilan Matok, Myla E. Moretti, Moumita Sarkar, Thomasin Adams-Webber, Gideon Koren*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

50 Scopus citations

Abstract

Background. The objective was to determine whether relationships exist between the methylene-tetrahydrofolate reductase (MTHFR) polymorphisms and risk of colorectal cancer (CRC) and examine whether the risk is modified by level of folate intake. Methods. MEDLINE, Embase, and SCOPUS were searched to May 2012 using the terms folic acid, folate, colorectal cancer, methylenetetrahydrofolate reductase, MTHFR. Observational studies were included which (1) assessed the risk of CRC for each polymorphism and/or (2) had defined levels of folate intake for each polymorphism and assessed the risk of CRC. Results. From 910 references, 67 studies met our criteria; hand searching yielded 10 studies. The summary risk estimate comparing the 677CT versus CC genotype was 1.02 (95 CI 0.951.10) and for 677TT versus CC was 0.88 (95 CI 0.800.96) both with heterogeneity. The summary risk estimates for A1298C polymorphisms suggested no reduced risk. The summary risk estimate for high versus low total folate for the 677CC genotype was 0.70 (95 CI 0.560.89) and the 677TT genotype 0.63 (95 CI 0.410.97). Conclusion. These results suggest that the 677TT genotype is associated with a reduced risk of developing CRC, under conditions of high total folate intake, and this associated risk remains reduced for both MTHFR 677 CC and TT genotypes.

Original languageAmerican English
Article number952508
JournalJournal of Cancer Epidemiology
DOIs
StatePublished - 2012
Externally publishedYes

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