4.7 Article

Supplementation with a β-glucan tablet has no effect on hyperlipidemia: a randomized, placebo-controlled clinical trial

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 117, Issue 6, Pages 1232-1239

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajcnut.2023.04.012

Keywords

hyperlipidemia; dyslipidemia; lipids; cholesterol; cardiovascular disease; atherosclerosis; fibers; oats; beta-glucan; natural supplements

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This clinical trial aimed to evaluate the efficacy and safety of high-medium molecular weight β-glucan on serum low-density lipoprotein (LDL) cholesterol and other lipid subfractions in subjects with hyperlipidemia. The results showed that compared with the placebo group, the β-glucan group did not show significant changes in LDL cholesterol concentration or other lipid subfractions. This study is of importance for investigating the lipid-lowering effects of β-glucan.
Background: Clinical evidence has suggested that the oat-soluble fiber & beta;-glucan might have lipid-lowering effects.Objectives: The present clinical trial was conducted to evaluate the efficacy and safety of high-medium molecular weight & beta;-glucan on serum low-density lipoprotein (LDL) cholesterol and other lipid subfractions in subjects with hyperlipidemia.Methods: A randomized double-blinded trial was performed to assess the efficacy and safety of & beta;-glucan supplementation in reducing lipid levels. Subjects with LDL cholesterol levels of >3.37 mmol/L when treated or not with a statin were randomly assigned to receive 1 of 3 daily doses of a tableted formulation of & beta;-glucan (1.5, 3, or 6 g) or placebo. The primary efficacy end point was the change from baseline to 12 wk in LDL cholesterol. Secondary end points of lipid subfractions and safety were also assessed.Results: A total of 263 subjects were enrolled; 66 subjects were assigned to each of the 3 & beta;-glucan groups, and 65 subjects were assigned to the placebo group. The mean change from baseline to 12 wk in serum LDL cholesterol level was 0.08, 0.11, and -0.04 mmol/L in the 3 & beta;-glucan groups (P = 0.23, 0.18, and 0.72 compared with the placebo group, respectively) and -0.10 mmol/L in the placebo group. The changes in total cholesterol, small LDL cholesterol subclass particle concentration, non-high-density lipoprotein cholesterol, apolipoprotein B, very low-density lipoprotein cholesterol, and high-sensitivity C-reactive protein were also not significant in the & beta;-glucan groups when compared with the placebo group. Gastrointestinal adverse events were reported in 23.4%, 34.8%, and 66.7% of patients in the & beta;-glucan groups and in 36.9% of patients in the placebo group (P < 0.0001 for the overall comparison across the 4 groups).Conclusions: In subjects with LDL cholesterol levels of >3.37 mmol/L, a tablet formulation of & beta;-glucan was not effective in reducing LDL cholesterol concentration or other lipid subfractions when compared with a placebo. This trial was registered at clinicaltrials.gov as NCT03857256.

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