Vitamin E Supplementation Reduces Cardiovascular Events in a Subgroup of Middle-Aged Individuals With Both Type 2 Diabetes Mellitus and the Haptoglobin 2-2 Genotype

Author:

Milman Uzi1,Blum Shany1,Shapira Chen1,Aronson Doron1,Miller-Lotan Rachel1,Anbinder Yefim1,Alshiek Junia1,Bennett Lawrence1,Kostenko Maria1,Landau Michele1,Keidar Shlomo1,Levy Yishai1,Khemlin Alexander1,Radan Arman1,Levy Andrew P.1

Affiliation:

1. From Clalit Health Services (U.M., C.S., L.B., M.K., A.K., A.R.), Haifa and Western Galilee, Israel; Technion Faculty of Medicine (S.B., R.M.L., Y.A., J.A., A.P.L.), Technion-Israel Institute of Technology, Haifa, Israel; Cardiology Department (D.A.), Rambam Medical Center, Haifa, Israel; Internal Medicine (S.K., Y.L.), Rambam Medical Center, Haifa, Israel; and PharmaBrains Israel (M.L.), Tel Aviv, Israel.

Abstract

Objective— Clinical trials of vitamin E have failed to demonstrate a decrease in cardiovascular events. However, these studies did not address possible benefit to subgroups with increased oxidative stress. Haptoglobin (Hp), a major antioxidant protein, is a determinant of cardiovascular events in patients with Type 2 diabetes mellitus (DM). The Hp gene is polymorphic with 2 common alleles, 1 and 2. The Hp 2 allelic protein product provides inferior antioxidant protection compared with the Hp 1 allelic product. We sought to test the hypothesis that vitamin E could reduce cardiovascular events in DM individuals with the Hp 2-2 genotype, a subgroup that comprises 2% to 3% of the general population. Methods and Results— 1434 DM individuals ≥55 years of age with the Hp 2-2 genotype were randomized to vitamin E (400 U/d) or placebo. The primary composite outcome was myocardial infarction, stroke, and cardiovascular death. At the first evaluation of events, 18 months after initiating the study, the primary outcome was significantly reduced in individuals receiving vitamin E (2.2%) compared with placebo (4.7%; P =0.01) and led to early termination of the study. Conclusions— Vitamin E supplementation appears to reduce cardiovascular events in individuals with DM and the Hp 2-2 genotype (ClinicalTrials.gov NCT00220831).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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