4.1 Article

Lung VITAL: Rationale, design, and baseline characteristics of an ancillary study evaluating the effects of vitamin D and/or marine omega-3 fatty acid supplements on acute exacerbations of chronic respiratory disease, asthma control, pneumonia and lung function in adults

期刊

CONTEMPORARY CLINICAL TRIALS
卷 47, 期 -, 页码 185-195

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cct.2016.01.003

关键词

Vitamin D; Omega-3 fatty acids; Respiratory symptoms; COPD; Lung function; Randomized clinical trial

资金

  1. National Heart, Lung and Blood Institute [R01 HL101932]
  2. National Cancer Institute
  3. National Heart, Lung and Blood Institute
  4. Office of Dietary Supplements
  5. National Institute of Neurological Disorders and Stroke
  6. National Center for Complementary and Alternative Medicine
  7. [U01 CA13962]

向作者/读者索取更多资源

Laboratory and observational research studies suggest that vitamin D and marine omega-3 fatty acids may reduce risk for pneumonia, acute exacerbations of respiratory diseases including chronic obstructive lung disease (COPD) or asthma, and decline of lung function, but prevention trials with adequate dosing, adequate power, and adequate time to follow-up are lacking. The ongoing Lung VITAL study is taking advantage of a large clinical trial the VITamin D and OmegA-3 TriaL (VITAL) to conduct the first major evaluation of the influences of vitamin D and marine omega-3 fatty acid supplementation on pneumonia risk, respiratory exacerbation episodes, asthma control and lung function in adults. VITAL is a 5-year U.S.-wide randomized, double-blind, placebo controlled, 2 x 2 factorial trial of supplementation with vitamin D3 ([cholecalciferol], 2000 IU/day) and marine omega-3 FA (Omacor (R) fish oil, eicosapentaenoic acid [EPA] + docosahexaenoic acid [DHA], 1 g/day) for primary prevention of CVD and cancer among men and women, at baseline aged. >= 50 and >= 55, respectively, with 5107 African Americans. In a subset of 1973 participants from 11 urban U.S. centers, lung function is measured before and two years after randomization. Yearly follow-up questionnaires assess incident pneumonia in the entire randomized population, and exacerbations of respiratory disease, asthma control and dyspnea in a subpopulation of 4314 randomized participants enriched, as shown in presentation of baseline characteristics, for respiratory disease, respiratory symptoms, and history of cigarette smoking. Self-reported pneumonia hospitalization will be confirmed by medical record review, and exacerbations will be confirmed by Center for Medicare and Medicaid Services data review. (C) 2016 Elsevier Inc. All rights reserved.

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