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The Journal of Clinical Endocrinology & Metabolism Vol. 87, No. 6 2940-2945
Copyright © 2002 by The Endocrine Society


Other Original Articles

Vitamin E Supplementation Reduces Plasma Vascular Cell Adhesion Molecule-1 and von Willebrand Factor Levels and Increases Nitric Oxide Concentrations in Hypercholesterolemic Patients

Giovambattista Desideri, Maria Contina Marinucci, Gianluca Tomassoni, Pier Giorgio Masci, Anna Santucci and Claudio Ferri

University of L’Aquila, Department of Internal Medicine and Public Health, 67100 Coppito-L’Aquila, Italy

Address all correspondence and requests for reprints to: Giovambattista Desideri, M.D., University of L’Aquila, Department of Internal Medicine and Public Health, Blocco 11, Via Vetoio, 67100 Coppito-L’Aquila, Italy. E-mail: . gbdesi{at}iol.it

Abstract

Up-regulation of vascular cell adhesion molecule-1 (VCAM-1) and reduced nitric oxide (NO) availability represent early characteristics of atherosclerosis. To evaluate whether the antioxidant vitamin E affected the circulating levels of soluble VCAM-1 (sVCAM-1) and the plasma metabolite of NO (nitrite+nitrate) in hypercholesterolemic patients, either vitamin E (either 400 IU or 800 IU/d for 8 wk) or placebo were randomly, double-blindly given to 36 hypercholesterolemic patients and 22 age- and sex-matched controls. At baseline hypercholesterolemic patients showed higher plasma sVCAM-1 (µg•liter-1) (591.2 ± 132.5 vs. 505.0 ± 65.6, P < 0.007) and lower NO metabolite (µM) levels (15.9 ± 3.4 vs. 29.2 ± 5.1, P < 0.0001) than controls. In hypercholesterolemic patients, 8 wk vitamin E (but not placebo) treatment significantly decreased circulating sVCAM-1 levels (400 IU: -148.9 ± 84.6, P < 0.009; 800 IU: -204.0 ± 75.7, P < 0.0001; placebo: -4.7 ± 22.6, NS), whereas it increased NO metabolite concentrations (400 IU: +4.0 ± 1.7, P < 0.02; 800 IU: +5.5 ± 0.8, P < 0.0001; placebo: +0.1 ± 1.1, NS) without affecting circulating low- density lipoprotein levels. Changes in both plasma sVCAM-1 and NO metabolite levels showed a trend to significantly correlate (r = -0.515, P = 0.010; and r = 0.435, P = 0.034, respectively) with changes in vitamin E concentrations induced by vitamin E supplementation. In conclusion, isolated hypercholesterolemia both increased circulating sVCAM-1 and reduced NO metabolite concentrations. Vitamin E supplementation counteracts these alterations, thus representing a potential tool for endothelial protection in hypercholesterolemic patients.




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