Suppr超能文献

中风患者的对氧磷酶基因多态性与血脂谱

The paraoxonase gene polymorphism in stroke patients and lipid profile.

作者信息

Shin B-S, Oh S-Y, Kim Y-S, Kim K-W

机构信息

Department of Neurology, Chonbuk National University Hospital and Medical School, Keumamdong, Jeonju, Chonbuk, Republic of Korea.

出版信息

Acta Neurol Scand. 2008 Apr;117(4):237-43. doi: 10.1111/j.1600-0404.2007.00929.x. Epub 2007 Sep 14.

Abstract

OBJECTIVES

The paraoxonase (PON) gene can reduce the risk of developing atherosclerosis. We investigated the associations between PON polymorphisms and ischemic stroke. We also investigated the associations between PON polymorphisms and lipid profile in stroke patients.

METHODS

A total of 350 patients with ischemic stroke and 242 control subjects in Korean population were genotyped for the PON1M55 L, PON1Q192R, PON2A148 G and PON2S311C polymorphisms using melting point analysis with LightCycler real-time polymerase chain reaction (PCR) technology.

RESULTS

There were no significant differences in genotype and allele distribution of the PON polymorphisms between the ischemic stroke patients and control subjects. The concentration of total homocysteine was significantly different in the PON1M55 L polymorphism (P = 0.047), and the apolipoprotein (Apo)B concentration was significantly different in the PON1Q192R polymorphism (P = 0.02) in stroke patients. The concentrations of low-density lipoprotein (LDL) cholesterol and ApoB were significantly different between the PON2A148 G (P = 0.011, P = 0.000, respectively) and PON2S311C polymorphisms (P = 0.046, P = 0.003, respectively) in stroke patients.

CONCLUSIONS

This study did not provide association between PON gene polymorphisms and ischemic stroke. However, it confirmed that the PON1L55 L allele is associated with plasma concentration of total homocysteine and that the PON2G148 G and PON2S311S allele is associated with plasma concentrations of LDL cholesterol and ApoB.

摘要

目的

对氧磷酶(PON)基因可降低动脉粥样硬化的发病风险。我们研究了PON基因多态性与缺血性卒中之间的关联。我们还研究了卒中患者中PON基因多态性与血脂谱之间的关联。

方法

采用LightCycler实时聚合酶链反应(PCR)技术通过熔点分析对韩国人群中总共350例缺血性卒中患者和对照对象进行PON1M55L、PON1Q192R、PON2A148G和PON2S311C基因多态性的基因分型。

结果

缺血性卒中患者与对照对象之间PON基因多态性的基因型和等位基因分布无显著差异。在卒中患者中,总同型半胱氨酸浓度在PON1M55L基因多态性中存在显著差异(P = 0.047),载脂蛋白(Apo)B浓度在PON1Q192R基因多态性中存在显著差异(P = 0.02)。在卒中患者中,低密度脂蛋白(LDL)胆固醇浓度和ApoB浓度在PON2A148G(分别为P = 0.011、P = 0.000)和PON2S311C基因多态性(分别为P = 0.046、P = 0.003)之间存在显著差异。

结论

本研究未发现PON基因多态性与缺血性卒中之间存在关联。然而,研究证实PON1L55L等位基因与总同型半胱氨酸的血浆浓度相关,而PON2G148G和PON2S311S等位基因与LDL胆固醇和ApoB的血浆浓度相关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验