RETRACTED ARTICLE: The effect of zinc and vitamin E cosupplementation on metabolic status and its related gene expression in patients with gestational diabetes

Abstract

<b>Objective:</b> The aim of this study was to determine the effects of zinc and vitamin E cosupplementation on metabolic status and gene expression related to insulin and lipid metabolism in women with gestational diabetes mellitus (GDM).<b>Methods:</b> Fifty-four women, in the age range of 18-40 years, diagnosed with GDM were recruited for this randomized, double-blinded, placebo-controlled trial. Subjects were randomly allocated into two intervention groups to either taking 233 mg/day Zinc Gluconate plus 400-IU/day vitamin E supplements or placebo (<i>n</i> = 27 each group) for 6 weeks. Gene expression related to insulin and lipid metabolism was evaluated in peripheral blood mononuclear cells (PBMCs) of women with GDM using RT-PCR method.<b>Results:</b> Participants who received zinc plus vitamin E supplements had significantly lower serum insulin levels (<i>β</i> = -3.81; 95% CI, -5.90, -1.72; <i>p</i> = .001), homeostasis model of assessment-insulin resistance (<i>β</i> = -0.96; 95% CI, -1.54, -0.38; <i>p</i> = .002), serum total-cholesterol (<i>β</i> = -8.56; 95% CI, -16.69, -0.43; <i>p</i> = .03) and low density lipoprotein-cholesterol (LDL)-cholesterol (<i>β</i> = -8.72; 95% CI, -15.27, -2.16; <i>p</i> = .01), and higher quantitative insulin sensitivity check index (<i>β</i> = 0.01; 95% CI, 0.005, 0.02; <i>p</i> = .007) compared with the placebo. Moreover, zinc and vitamin E cosupplementation upregulated gene expression of peroxisome proliferator-activated receptor gamma (PPAR-γ; <i>p</i> = .03) and low-density lipoprotein receptor (LDLR; <i>p</i> = .04) compared with the placebo. Though, zinc and vitamin E combination did not affect other metabolic parameters.<b>Conclusions:</b> Overall, zinc and vitamin E cosupplementation for 6 weeks in women with GDM significantly improved insulin metabolism, lipid profile, and the gene expression levels of PPAR-γ and LDLR.