Randomised controlled trial of the effect of long-term selenium supplementation on plasma cholesterol in an elderly Danish population

Br J Nutr. 2015 Dec 14;114(11):1807-18. doi: 10.1017/S0007114515003499. Epub 2015 Sep 30.

Abstract

Although cross-sectional studies have shown a positive association between Se and cholesterol concentrations, a recent randomised controlled trial in 501 elderly UK individuals of relatively low-Se status found that Se supplementation for 6 months lowered total plasma cholesterol. The Danish PRECISE (PREvention of Cancer by Intervention with Selenium) pilot study (ClinicalTrials.gov ID: NCT01819649) was a 5-year randomised, double-blinded, placebo-controlled trial with four groups (allocation ratio 1:1:1:1). Men and women aged 60-74 years (n 491) were randomised to 100 (n 124), 200 (n 122) or 300 (n 119) μg Se-enriched yeast or matching placebo-yeast tablets (n 126) daily for 5 years. A total of 468 participants continued the study for 6 months and 361 participants, equally distributed across treatment groups, continued for 5 years. Plasma samples were analysed for total and HDL-cholesterol and for total Se concentrations at baseline, 6 months and 5 years. The effect of different doses of Se supplementation on plasma lipid and Se concentrations was estimated by using linear mixed models. Plasma Se concentration increased significantly and dose-dependently in the intervention groups after 6 months and 5 years. Total cholesterol decreased significantly both in the intervention groups and in the placebo group after 6 months and 5 years, with small and nonsignificant differences in changes in plasma concentration of total cholesterol, HDL-cholesterol, non-HDL-cholesterol and total:HDL-cholesterol ratio between intervention and placebo groups. The effect of long-term supplementation with Se on plasma cholesterol concentrations or its sub-fractions did not differ significantly from placebo in this elderly population.

Keywords: CVD; Cholesterol; Lipids; PRECISE PREvention of Cancer by Intervention with Selenium; Randomised controlled trials; Selenium; Selenium supplementation; TFA trans-fatty acids.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anticholesteremic Agents / administration & dosage
  • Anticholesteremic Agents / adverse effects
  • Anticholesteremic Agents / blood
  • Anticholesteremic Agents / therapeutic use*
  • Cardiovascular Diseases / etiology
  • Cardiovascular Diseases / prevention & control*
  • Cholesterol / blood*
  • Cross-Sectional Studies
  • Deficiency Diseases / blood
  • Deficiency Diseases / diet therapy*
  • Deficiency Diseases / physiopathology
  • Denmark / epidemiology
  • Dietary Supplements* / adverse effects
  • Double-Blind Method
  • Elder Nutritional Physiological Phenomena*
  • Feasibility Studies
  • Female
  • Humans
  • Intention to Treat Analysis
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Patient Dropouts
  • Risk Factors
  • Selenium / adverse effects
  • Selenium / blood
  • Selenium / deficiency
  • Selenium / therapeutic use*
  • Time Factors
  • Yeast, Dried / adverse effects
  • Yeast, Dried / chemistry

Substances

  • Anticholesteremic Agents
  • Cholesterol
  • Selenium

Associated data

  • ClinicalTrials.gov/NCT01819649