Antioxidant Vitamin Concentrations and LDL Oxidation in Nephrotic Syndrome

Author:

Warwick G L1,Waller H12,Ferns G A A3

Affiliation:

1. Department of Nephrology, Leicester General Hospital, Leicester LE5 4PW

2. Division of Chemical Pathology, Glenfield General Hospital, Leicester

3. Department of Clinical Biochemistry, Royal Surrey County Hospital, Guildford, UK

Abstract

The increased risk of atherosclerosis in nephrotic syndrome is attributable in part to the associated hyperlipidaemia. The importance of oxidation of LDL in the atherogenic process has been recognized over the last 15 years. However, there are few data on the balance of antioxidant defences and lipoprotein oxidation in nephrotic syndrome. Plasma antioxidant vitamin concentrations and indices of LDL oxidation (LDL lipid hydroperoxide content and the susceptibility of LDL to oxidation) were measured in two groups of patients; group I comprised 29 nephrotic patients and group II comprised 25 patients with haematuria. Plasma ascorbate concentration was significantly lower in group I (the nephrotic group) compared with group II (median 13·3 versus 22·2 μmol/L; P < 0·001). Vitamin E concentrations were higher in group I but were not significantly different if corrected for total plasma cholesterol (6·12 versus 5·88 μmol/mmol; P = 0·33). However, these changes resulted in a low ascorbate:vitamin E ratio in group I (0·19 versus 0·87; P < 0·0001). Despite these changes in important antioxidant vitamin concentrations, we were unable to demonstrate any increased susceptibility to LDL oxidation in vitro or any difference in LDL lipid hydroperoxide content. These data suggest that there may be a relative defect of oxidant/antioxidant balance in nephrotic syndrome which could predispose to increased oxidative stress. However, measures of LDL oxidation were not significantly different between the two groups. LDL was protected from oxidation despite the severe hyperlipidaemia and the low circulating vitamin C concentrations.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

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