The VITamin D and OmegA-3 TriaL (VITAL): Rationale and design of a large randomized controlled trial of vitamin D and marine omega-3 fatty acid supplements for the primary prevention of cancer and cardiovascular disease

被引:402
作者
Manson, JoAnn E. [1 ,2 ]
Bassuk, Shari S. [1 ]
Lee, I-Min [1 ,2 ]
Cook, Nancy R. [1 ,2 ]
Albert, Michelle A. [1 ,3 ]
Gordon, David [1 ]
Zaharris, Elaine [1 ]
MacFadyen, Jean G. [1 ]
Danielson, Eleanor [1 ]
Lin, Jennifer [1 ]
Zhang, Shumin M. [1 ]
Buring, Julie E. [1 ,2 ]
机构
[1] Harvard Univ, Div Prevent Med, Dept Med, Brigham & Womens Hosp,Med Sch, Boston, MA 02215 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Cardiovasc Med,Dept Med, Boston, MA 02115 USA
关键词
Cancer; Cardiovascular disease; Cholecalciferol; Primary prevention; Omega-3 fatty acids; Vitamin D; Randomized controlled trial; CORONARY-HEART-DISEASE; POLYUNSATURATED FATTY-ACIDS; FOOD FREQUENCY QUESTIONNAIRE; SERUM; 25-HYDROXYVITAMIN-D; COLORECTAL-CANCER; CALCIUM SUPPLEMENTATION; FISH CONSUMPTION; UNITED-STATES; MYOCARDIAL-INFARCTION; DIETARY QUESTIONNAIRE;
D O I
10.1016/j.cct.2011.09.009
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Data from laboratory studies, observational research, and/or secondary prevention trials suggest that vitamin D and marine omega-3 fatty acids may reduce risk for cancer or cardiovascular disease (CVD), but primary prevention trials with adequate dosing in general populations (i.e., unselected for disease risk) are lacking. The ongoing VITamin D and OmegA-3 TriaL (VITAL) is a large randomized, double-blind, placebo-controlled, 2x2 factorial trial of vitamin D (in the form of vitamin D-3 [cholecalciferol], 2000 IU/day) and marine omega-3 fatty acid (Omacor fish oil, eicosapentaenoic acid [EPA] + docosahexaenoic acid [DHA], 1 g/day) supplements in the primary prevention of cancer and CVD among a multi-ethnic population of 20,000 U.S. men aged >= 50 and women aged >= 55. The mean treatment period will be 5 years. Baseline blood samples will be collected in at least 16,000 participants, with follow-up blood collection in about 6000 participants. Yearly follow-up questionnaires will assess treatment compliance (plasma biomarker measures will also assess compliance in a random sample of participants), use of non-study drugs or supplements, occurrence of endpoints, and cancer and vascular risk factors. Self-reported endpoints will be confirmed by medical record review by physicians blinded to treatment assignment, and deaths will be ascertained through national registries and other sources. Ancillary studies will investigate whether these agents affect risk for diabetes and glucose intolerance; hypertension; cognitive decline; depression; osteoporosis and fracture; physical disability and falls; asthma and other respiratory diseases; infections; and rheumatoid arthritis, systemic lupus erythematosus, thyroid diseases, and other autoimmune disorders. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:159 / 171
页数:13
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