Abstract
Objective: The purpose of this study was to investigate the dose-dependent effects of RRR-α-tocopherol supplementation in coronary heart disease (CHD) patients and healthy subjects on plasma α-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-α-tocopherol at 100, 200 and 400 mg/day for a period of 3 weeks per dose. Lipoproteins were separated by FPLC and ultracentrifugation. α-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 α-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 α-tocopherol concentrations to 34.6 ± 9.8 μmol/L at a dosage of 100 mg/day RRR-α-tocopherol, whereas healthy subjects showed a significant (54%) increase to 39.7 ± 6.1 μmol/L only with 400 mg/day RRR-α-tocopherol. In addition, CHD-patients showed a significantly increased enrichment of α-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 α-tocopherol supplementation than healthy subjects to exert biological effects on plasma lipoproteins and acute phase response.
We thank Ulrike Haas, Wolfgang Wilfert, Julian Jöris and Martin Nerlich for expert technical assistance. We thank Dr. Wolfgang von Scheidt for recruiting the CHD-patients.
Notes
This study was supported by a grant from Bayer Vital GmbH & Co KG, Germany.