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Single LDL apheresis improves serum remnant-like particle-cholesterol, C-reactive protein, and malondialdehyde-modified-low-density lipoprotein concentrations in Japanese hypercholesterolemic subjects

Background: Single low-density lipoprotein (LDL)-apheresis may affect serum remnant-like particle-cholesterol (RLP-C), C-reactive protein (CRP) and malondialdehyde-modified (MDA)-LDL concentrations. Subjects and methods: Six subjects with hypercholesterolemia (five men, one woman) were involved in t...

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Published in:Clinica chimica acta 2002-07, Vol.321 (1), p.107-112
Main Authors: Kobayashi, Junji, Katsube, Susumu, Shimoda, Mayumi, Furuhashi, Kenji, Kitano, Shouichi, Masuda, Mizue, Maruyama, Tokiko, Shinomiya, Masaki
Format: Article
Language:English
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Summary:Background: Single low-density lipoprotein (LDL)-apheresis may affect serum remnant-like particle-cholesterol (RLP-C), C-reactive protein (CRP) and malondialdehyde-modified (MDA)-LDL concentrations. Subjects and methods: Six subjects with hypercholesterolemia (five men, one woman) were involved in this study. Mean age and body mass index of the study subjects were 58±3.1 years and 23.6±2.07 kg/m 2, respectively. Five of the subjects were diagnosed as heterozygous familial hypercholesterolemia (FH) because of having both marked hypercholesterolemia and Achilles tendon xanthomas. LDL apheresis was introduced and continued using a dextran sulfate cellulose adsorption column technique every 2 weeks. Serum RLP-C was measured using an immunoaffinity mixed gel containing anti-apolipoprotein A-I and anti-apolipoprotein B monoclonal antibody. Serum CRP was measured by latex-enhanced assay. Serum MDA-LDL was measured using monoclonal antibody against MDA-LDL (ML25). Results: Combined treatment in the steady state pre-treatment yielded a total, LDL- and HDL-cholesterol, and TG concentrations of 5.39±0.81, 3.82±1.03, 1.24±0.29 and 0.92±0.43 mmol/l, respectively, and a post-treatment total, LDL- and HDL-cholesterol and TG concentrations of 2.79±0.37 (−48%, p
ISSN:0009-8981
1873-3492
DOI:10.1016/S0009-8981(02)00103-1