Volume 129, Issue 1 pp. 192-203
Epidemiology

Folic acid and prevention of colorectal adenomas: A combined analysis of randomized clinical trials

Jane C. Figueiredo

Jane C. Figueiredo

Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA

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Leila A. Mott

Leila A. Mott

Department of Community and Family Medicine, Dartmouth Medical School, Hanover, NH

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Edward Giovannucci

Edward Giovannucci

Department of Epidemiology, Harvard School of Public Health, Boston, MA

Department of Nutrition, Harvard School of Public Health, Boston, MA

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Kana Wu

Kana Wu

Department of Nutrition, Harvard School of Public Health, Boston, MA

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Bernard Cole

Bernard Cole

Department of Mathematics and Statistics, University of Vermont, Burlington, VT

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Matthew J. Grainge

Matthew J. Grainge

Division of Epidemiology and Public Health, University of Nottingham, University Hospital, Nottingham, United Kingdom

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Richard F. Logan

Richard F. Logan

Division of Epidemiology and Public Health, University of Nottingham, University Hospital, Nottingham, United Kingdom

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John A. Baron

Corresponding Author

John A. Baron

Department of Medicine, Dartmouth Medical School, Hanover, NH

Department of Community and Family Medicine, Dartmouth Medical School, Hanover, NH

Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CASearch for more papers by this author
First published: 17 December 2010
Citations: 64

Disclosure: Wyeth (now Pfizer) provided folic acid and placebo tablets for the Aspirin/Folate Polyp Prevention Study, one of the trials included in this combined analysis.

Abstract

Observational data suggest that lower folate status is associated with an increased risk of colorectal neoplasia, implying that folate may be useful as a chemopreventive agent. We conducted a combined analysis of three large randomized trials of folic acid supplementation for the prevention of metachronous adenomas in patients with an adenoma history. Participants included 2,632 men and women who had a history of adenomas randomized to either 0.5 or 1.0 mg/day of folic acid or placebo and who had a follow-up endoscopy 6 to 42 months after randomization [mean = 30.6 (standard deviation = 8.1) months]. We used random-effects meta-analysis to estimate risk ratios (RRs) and 95% confidence intervals (CIs). The RR comparing folic acid versus placebo was 0.98 (95% CI = 0.82–1.17) for all adenomas and 1.06 (95% CI = 0.81–1.39) for advanced lesions. Folic acid was associated with a nonsignificant decreased risk of any adenoma among subjects in the lowest quartile of baseline plasma folate (≤11 nmol/L) and no effect among individuals in the highest quartile (>29 nmol/L, p for trend = 0.17). There was a nonsignificant trend of decreasing risk of any adenoma associated with folic acid supplements with increasing alcohol intake. During the early follow-up reported here, more deaths occurred in the placebo group than in the folic acid group (1.7% vs. 0.5%, p = 0.002). In conclusion, after up to 3.5 years of folic acid use, there is no clear decrease or increase in the occurrence of new adenomas in patients with a history of adenoma.

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