Folic acid for the prevention of colorectal adenomas - A randomized clinical trial

被引:686
作者
Cole, Bernard F.
Baron, John A.
Sandler, Robert S.
Haile, Robert W.
Ahnen, Dennis J.
Bresalier, Robert S.
McKeown-Eyssen, Gail
Summers, Robert W.
Rothstein, Richard I.
Burke, Carol A.
Snover, Dale C.
Church, Timothy R.
Allen, John I.
Robertson, Douglas J.
Beck, Gerald J.
Bond, John H.
Byers, Tim
Mandel, Jack S.
Mott, Leila A.
Pearson, Loretta H.
Barry, Elizabeth L.
Rees, Judy R.
Marcon, Norman
Saibil, Fred
Ueland, Per Magne
Greenberg, E. Robert
机构
[1] Dartmouth Med Sch, Dept Community & Family Med, Hanover, NH USA
[2] Dartmouth Med Sch, Dept Med, Hanover, NH USA
[3] Univ N Carolina, Dept Med, Chapel Hill, NC USA
[4] Univ So Calif, Dept Prevent Med, Keck Sch Med, Los Angeles, CA 90089 USA
[5] Univ Colorado, Dept Med, Denver, CO 80202 USA
[6] Univ Colorado, Dept Prevent Med & Biometr, Denver, CO 80202 USA
[7] Univ Texas, MD Anderson Canc Ctr, Dept Gastrointestinal Med & Nutr, Houston, TX 77030 USA
[8] Univ Toronto, Dept Publ Hlth Sci & Nutr Sci, Toronto, ON, Canada
[9] Univ Toronto, Dept Med, Toronto, ON, Canada
[10] Univ Iowa, Carver Coll Med, Div Gastroenterol Hepatol, Iowa City, IA USA
[11] Cleveland Clin Fdn, Dept Gastroenterol, Cleveland, OH 44195 USA
[12] Cleveland Clin Fdn, Dept Quantitat Hlth Sci, Cleveland, OH 44195 USA
[13] Fairview Southdale Hosp, Dept Pathol, Edina, MN USA
[14] Univ Minnesota, Sch Publ Hlth, Div Environm Hlth Sci, Minneapolis, MN USA
[15] Minneapolis Vet Affairs Med Ctr, Dept Med, Minneapolis, MN USA
[16] Dept Vet Affairs Med Ctr, Gastroenterol Sect, White River Jct, VT USA
[17] Emory Univ, Rollins Sch Publ Hlth, Dept Epidemiol, Atlanta, GA 30322 USA
[18] Univ Bergen, Pharmacol Sect, Inst Med, Bergen, Norway
[19] Haukeland Hosp, N-5021 Bergen, Norway
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2007年 / 297卷 / 21期
关键词
D O I
10.1001/jama.297.21.2351
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Laboratory and epidemiological data suggest that folic acid may have an antineoplastic effect in the large intestine. Objective To assess the safety and efficacy of folic acid supplementation for preventing colorectal adenomas. Design, Setting, and Participants A double-blind, placebo-controlled, 2-factor, phase 3, randomized clinical trial conducted at 9 clinical centers between July 6, 1994, and October 1, 2004. Participants included 1021 men and women with a recent history of colorectal adenomas and no previous invasive large intestine carcinoma. Intervention Participants were randomly assigned in a 1: 1 ratio to receive 1 mg/d of folic acid ( n= 516) or placebo ( n= 505), and were separately randomized to receive aspirin ( 81 or 325 mg/d) or placebo. Follow-up consisted of 2 colonoscopic surveillance cycles ( the first interval was at 3 years and the second at 3 or 5 years later). Main Outcome Measures The primary outcome measure was occurrence of at least 1 colorectal adenoma. Secondary outcomes were the occurrence of advanced lesions (similar to 25% villous features, high-grade dysplasia, size similar to 1 cm, or invasive cancer) and adenoma multiplicity ( 0, 1-2, or similar to 3 adenomas). Results During the first 3 years, 987 participants ( 96.7%) underwent colonoscopic follow-up, and the incidence of at least 1 colorectal adenoma was 44.1% for folic acid ( n= 221) and 42.4% for placebo ( n= 206) ( unadjusted risk ratio [ RR], 1.04; 95% confidence interval [ CI], 0.90-1.20; P=. 58). Incidence of at least 1 advanced lesion was 11.4% for folic acid ( n= 57) and 8.6% for placebo ( n= 42) ( unadjusted RR, 1.32; 95% CI, 0.90-1.92; P=. 15). A total of 607 participants ( 59.5%) underwent a second follow-up, and the incidence of at least 1 colorectal adenoma was 41.9% for folic acid ( n= 127) and 37.2% for placebo ( n= 113) ( unadjusted RR, 1.13; 95% CI, 0.93-1.37; P=. 23); and incidence of at least 1 advanced lesion was 11.6% for folic acid ( n= 35) and 6.9% for placebo ( n= 21) ( unadjusted RR, 1.67; 95% CI, 1.00-2.80; P=. 05). Folic acid was associated with higher risks of having 3 or more adenomas and of noncolorectal cancers. There was no significant effect modification by sex, age, smoking, alcohol use, body mass index, baseline plasma folate, or aspirin allocation. Conclusions Folic acid at 1 mg/d does not reduce colorectal adenoma risk. Further research is needed to investigate the possibility that folic acid supplementation might increase the risk of colorectal neoplasia.
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页码:2351 / 2359
页数:9
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