Folic acid and prevention of colorectal adenomas: A combined analysis of randomized clinical trials†
Jane C. Figueiredo
Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA
Search for more papers by this authorLeila A. Mott
Department of Community and Family Medicine, Dartmouth Medical School, Hanover, NH
Search for more papers by this authorEdward Giovannucci
Department of Epidemiology, Harvard School of Public Health, Boston, MA
Department of Nutrition, Harvard School of Public Health, Boston, MA
Search for more papers by this authorKana Wu
Department of Nutrition, Harvard School of Public Health, Boston, MA
Search for more papers by this authorBernard Cole
Department of Mathematics and Statistics, University of Vermont, Burlington, VT
Search for more papers by this authorMatthew J. Grainge
Division of Epidemiology and Public Health, University of Nottingham, University Hospital, Nottingham, United Kingdom
Search for more papers by this authorRichard F. Logan
Division of Epidemiology and Public Health, University of Nottingham, University Hospital, Nottingham, United Kingdom
Search for more papers by this authorCorresponding 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 authorJane C. Figueiredo
Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA
Search for more papers by this authorLeila A. Mott
Department of Community and Family Medicine, Dartmouth Medical School, Hanover, NH
Search for more papers by this authorEdward Giovannucci
Department of Epidemiology, Harvard School of Public Health, Boston, MA
Department of Nutrition, Harvard School of Public Health, Boston, MA
Search for more papers by this authorKana Wu
Department of Nutrition, Harvard School of Public Health, Boston, MA
Search for more papers by this authorBernard Cole
Department of Mathematics and Statistics, University of Vermont, Burlington, VT
Search for more papers by this authorMatthew J. Grainge
Division of Epidemiology and Public Health, University of Nottingham, University Hospital, Nottingham, United Kingdom
Search for more papers by this authorRichard F. Logan
Division of Epidemiology and Public Health, University of Nottingham, University Hospital, Nottingham, United Kingdom
Search for more papers by this authorCorresponding 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 authorDisclosure: 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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