A Randomized Trial of Selenium Supplementation and Risk of Type-2 Diabetes, As Assessed by Plasma Adiponectin
Overview
Authors
Affiliations
Background: Evidence that selenium affects the risk of type-2 diabetes is conflicting, with observational studies and a few randomized trials showing both lower and higher risk linked to the level of selenium intake and status. We investigated the effect of selenium supplementation on the risk of type-2 diabetes in a population of relatively low selenium status as part of the UK PRECISE (PREvention of Cancer by Intervention with SElenium) pilot study. Plasma adiponectin concentration, a recognised independent predictor of type-2 diabetes risk and known to be correlated with circulating selenoprotein P, was the biomarker chosen.
Methods: In a randomized, double-blind, placebo-controlled trial, five hundred and one elderly volunteers were randomly assigned to a six-month intervention with 100, 200 or 300 µg selenium/d as high-selenium or placebo yeast. Adiponectin concentration was measured by ELISA at baseline and after six months of treatment in 473 participants with one or both plasma samples available.
Results: Mean (SD) plasma selenium concentration was 88.5 ng/g (19.1) at baseline and increased significantly in the selenium-treatment groups. In baseline cross-sectional analyses, the fully adjusted geometric mean of plasma adiponectin was 14% lower (95% CI, 0-27%) in the highest than in the lowest quartile of plasma selenium (P for linear trend = 0.04). In analyses across randomized groups, however, selenium supplementation had no effect on adiponectin levels after six months of treatment (P = 0.96).
Conclusions: These findings are reassuring as they did not show a diabetogenic effect of a six-month supplementation with selenium in this sample of elderly individuals of relatively low selenium status.
Karami M, Almaghrabi S, Banasr O, Hussein K Biol Trace Elem Res. 2024; .
PMID: 39500832 DOI: 10.1007/s12011-024-04435-7.
Khademi Z, Pourreza S, Hamedi-Shahraki S, Amirkhizi F Biol Trace Elem Res. 2023; 202(8):3442-3448.
PMID: 37910262 DOI: 10.1007/s12011-023-03935-2.
Selenium status and its determinants in very old adults: insights from the Newcastle 85+ Study.
Perri G, Mathers J, Martin-Ruiz C, Parker C, Walsh J, Eastell R Br J Nutr. 2023; 131(5):901-910.
PMID: 37877251 PMC: 10864996. DOI: 10.1017/S0007114523002398.
Selenium as a predictor of metabolic syndrome in middle age women.
Schneider-Matyka D, Cybulska A, Szkup M, Pilarczyk B, Panczyk M, Tomza-Marciniak A Aging (Albany NY). 2023; 15(6):1734-1747.
PMID: 36947700 PMC: 10085601. DOI: 10.18632/aging.204590.
Scientific opinion on the tolerable upper intake level for selenium.
Turck D, Bohn T, Castenmiller J, de Henauw S, Hirsch-Ernst K, Knutsen H EFSA J. 2023; 21(1):e07704.
PMID: 36698500 PMC: 9854220. DOI: 10.2903/j.efsa.2023.7704.