Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 900 Commonwealth Avenue East, Boston, MA 02215, United States.
Contemp Clin Trials. 2012 Jan;33(1):159-71. doi: 10.1016/j.cct.2011.09.009. Epub 2011 Oct 2.
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, 2 x 2 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], 1g/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.
来自实验室研究、观察性研究和/或二级预防试验的数据表明,维生素 D 和海洋ω-3 脂肪酸可能降低癌症或心血管疾病(CVD)的风险,但一般人群(即未选择疾病风险)中缺乏足够剂量的一级预防试验。正在进行的维生素 D 和欧米伽-3 试验(VITAL)是一项大型随机、双盲、安慰剂对照、2 x 2 析因试验,研究维生素 D(以维生素 D(3)[胆钙化醇]的形式,每天 2000IU)和海洋 ω-3 脂肪酸(Omacor 鱼油,二十碳五烯酸[EPA]+二十二碳六烯酸[DHA],每天 1 克)补充剂在多民族人群中的一级预防作用,该人群由 20000 名年龄≥50 岁的美国男性和年龄≥55 岁的女性组成。平均治疗期将为 5 年。将在至少 16000 名参与者中采集基线血液样本,并在约 6000 名参与者中采集随访血液样本。每年进行一次随访问卷调查,评估治疗依从性(血浆生物标志物测量也将在参与者的随机样本中评估依从性)、非研究药物或补充剂的使用、终点事件以及癌症和血管危险因素的发生情况。自我报告的终点事件将通过对治疗分配盲法的医生进行病历审查来确认,死亡情况将通过国家登记处和其他来源确定。辅助研究将调查这些药物是否会影响糖尿病和葡萄糖耐量异常、高血压、认知能力下降、抑郁、骨质疏松症和骨折、身体残疾和跌倒、哮喘和其他呼吸道疾病、感染以及类风湿关节炎、系统性红斑狼疮、甲状腺疾病和其他自身免疫性疾病的风险。