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Institute of Laboratory Medicine, Clinical Chemistry, and Molecular Diagnostics, Leipzig University Hospital, Leipzig, GERMANY
Address reprint requests to: Daniel Teupser M.D., Ph.D., Institute of Laboratory Medicine, Clinical Chemistry, and Molecular Diagnostics, Leipzig University Hospital, Liebigstrasse 27, 04103 Leipzig, GERMANY. E-mail: teupser{at}medizin.uni-leipzig.de
Objective: The purpose of this study was to investigate the dose-dependent effects of RRR-
-tocopherol supplementation in coronary heart disease (CHD) patients and healthy subjects on plasma
-tocopherol levels, plasma lipoprotein distribution, LDL oxidation, and inflammatory plasma markers.
Methods: 12 patients with coronary heart disease and 12 healthy subjects were supplemented with increasing dosages of RRR-
-tocopherol at 100, 200 and 400 mg/day for a period of 3 weeks per dose. Lipoproteins were separated by FPLC and ultracentrifugation.
-Tocopherol was measured by HPLC. Resistance of LDL to oxidation was determined by reading the absorption at 234 nm after CuCl2-induced oxidation. Clinical chemistry and inflammatory markers were measured on automated analysis systems.
Results: Plasma
-tocopherol concentrations at baseline were comparable between CHD-patients and healthy subjects (21.7 ± 4.7 µmol/L and 25.8 ± 7.6 µmol/L, respectively). CHD-patients showed a significant increase (59%) of plasma
-tocopherol concentrations to 34.6 ± 9.8 µmol/L at a dosage of 100 mg/day RRR-
-tocopherol, whereas healthy subjects showed a significant (54%) increase to 39.7 ± 6.1 µmol/L only with 400 mg/day RRR-
-tocopherol. In addition, CHD-patients showed a significantly increased enrichment of
-tocopherol in VLDL. Supplementation (200 mg/day) caused a significant decrease of the acute phase plasma proteins C-reactive protein (CRP) (65%) and fibrinogen (24%).
Conclusion: Our data demonstrate that CHD-patients require lower dosages of
-tocopherol supplementation than healthy subjects to exert biological effects on plasma lipoproteins and acute phase response.
Key words: coronary heart disease, alpha-tocopherol, vitamin E, C-reactive protein, fibrinogen
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