Literature DB >> 19274593

An association study between catalase -262C>T gene polymorphism, sodium-lithium countertransport activity, insulin resistance, blood lipid parameters and their response to atorvastatin, in Greek dyslipidaemic patients and normolipidaemic controls.

Maria Kosmidou1, Apostolos I Hatzitolios, Dimitra Molyva, Nikolaos Raikos, Christos Savopoulos, Niki Daferera, Vassileios Kokkas, Antonis Goulas.   

Abstract

This study attempted to examine the effect of a functional catalase gene polymorphism, CAT -262C>T, on sodium-lithium countertransport (Na-Li CT) activity, insulin resistance determined as the homeostasis model assessment index (HOMA-IR), blood lipid parameters (cholesterol, triglycerides, low density lipoprotein cholesterol, high density lipoprotein cholesterol, apolipoprotein B, apolipoprotein A-I) and their response to atorvastatin, in previously characterized Greek dyslipidaemic patients and normolipidaemic controls. Putative associations were examined by running univariate analyses with a general linear model, using age, sex, smoking and hypertension as covariates. While no statistically significant associations were detected between the CAT -262C>T polymorphism and either baseline values or their modulation by atorvastatin in the patient group, HOMA-IR values were significantly (p=0.028) lower among CAT -262CC controls compared to their T allele carrier counterparts. A trend towards higher plasma triglyceride values among CAT -262CC genotypes was also detected, in both dyslipidaemic patients and normolipidaemic controls.

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Year:  2009        PMID: 19274593     DOI: 10.1080/10715760902783293

Source DB:  PubMed          Journal:  Free Radic Res        ISSN: 1029-2470


  5 in total

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4.  Atorvastatin treatment modulates the interaction between leptin and adiponectin, and the clinical parameters in patients with type II diabetes.

Authors:  Sayer I Al-Azzam; Asem M Alkhateeb; Karem H Alzoubi; Raya N Alzayadeen; Mera A Ababneh; Omar F Khabour
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  5 in total

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