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Principal results of the VITamin D and OmegA-3 TriaL (VITAL) and updated meta-analyses of relevant vitamin D trials

Manson JE, Bassuk SS, Buring JE, VITAL Research Group

The Journal of steroid biochemistry and molecular biology · 116 citas

Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Eventos clínicos como enfermedad o muerte

Quién lo pagó

Financiación
Financiación independiente
Gobierno
National Institutes of Health
Gobierno
National Heart, Lung, and Blood Institute
Gobierno
National Cancer Institute
Gobierno
National Center for Complementary and Integrative Health
Gobierno
NCI NIH HHS
Subvenciones
National Cancer Institute (U01CA138962); National Cancer Institute (R01CA138962)

Según 5 financiadores declarados.

Publicación

Publicado
2019-11-13 · J Steroid Biochem Mol Biol · vol. 198 · pág. 105522
Editorial
Elsevier BV
Citado
159 citas · más que el 97% de estudios similares · 6.1× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
96 trabajos
Acceso
Acceso abierto (copia en repositorio)
Áreas de investigación
Vitamin D Research Studies · Nutritional Studies and Diet · Antioxidant Activity and Oxidative Stress
Palabras clave
vitamin D supplementation, vitamin D3, omega-3 fatty acids, marine fatty acids, cancer incidence, cancer mortality, cardiovascular disease, major adverse cardiovascular events, all-cause mortality, primary prevention, older adults, African Americans, VITAL trial
MeSH
humans, neoplasms, cardiovascular diseases, cholecalciferol, fatty acids, omega-3, vitamins, placebo effect, aged, middle aged, female, male

3 autores

  • JoAnn E. Manson🇺🇸 · autor de correspondenciaBrigham and Women's Hospital; Harvard University
  • Shari S. Bassuk🇺🇸Brigham and Women's Hospital; Harvard University
  • Julie E. Buring🇺🇸Brigham and Women's Hospital; Harvard University

Resumen

El texto original del estudio, en el idioma en que se publicó.

Whether supplemental vitamin D reduces risk of cancer or cardiovascular disease (CVD) is relatively unexplored in randomized trial settings. The VITamin D and OmegA-3 TriaL (VITAL) was a nationwide, randomized, placebo-controlled, 2 × 2 factorial trial of daily vitamin D3 (2000 IU) and marine omega-3 fatty acids (1 g) in the primary prevention of cancer and CVD among 25,871 U.S. men aged ≥50 and women aged ≥55, including 5106 African Americans. Median treatment duration was 5.3 years. Vitamin D did not significantly reduce the primary endpoint of total invasive cancer incidence (hazard ratio [HR] = 0.96 [95% confidence interval 0.88-1.06]) but showed a promising signal for reduction in total cancer mortality (HR = 0.83 [0.67-1.02]), especially in analyses that accounted for latency by excluding the first year (HR = 0.79 [0.63-0.99]) or first 2 years (HR = 0.75 [0.59-0.96]) of follow-up. Vitamin D did not significantly reduce the co-primary endpoint of major CVD events (HR = 0.97 [0.85-1.12]), other cardiovascular endpoints, or all-cause mortality (HR = 0.99 [0.87-1.12]). Updated meta-analyses that include VITAL and other recent vitamin D trials indicate a significant reduction in cancer mortality but not in cancer incidence or CVD endpoints. Additional research is needed to determine which individuals may be most likely to derive a net benefit from vitamin D supplementation. (VITAL clinicaltrials.gov identifier: NCT01169259).

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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