Suppr超能文献

中国汉族人群中谷胱甘肽S-转移酶T1和M1基因多态性与缺血性中风风险的关联

Association of glutathione S-transferase T1 and M1 gene polymorphisms with ischemic stroke risk in the Chinese Han population.

作者信息

Wang Rui, Wang Yan, Wang Junhong, Yang Kun

机构信息

Department of Neurology, Affiliated Hospital of Qingdao University Medical College, Qingdao 266003, Shandong Province, China.

Central Laboratory, Affiliated Hospital of Qingdao University Medical College, Qingdao 266003, Shandong Province, China.

出版信息

Neural Regen Res. 2012 Jun 25;7(18):1420-7. doi: 10.3969/j.issn.1673-5374.2012.18.009.

Abstract

Atherosclerosis plays an important role in ischemic stroke, and oxidative stress participates in the entire process of atherosclerosis. Glutathione S-transferase (GST) acting with other antioxidant enzymes can eliminate reactive oxygen species and protect cells against oxidative damage. To assess the association of glutathione S-transferase (GSTT1 and GSTM1) gene polymorphisms with ischemic stroke in the Chinese Han population, the present study selected 315 patients with ischemic stroke and 210 healthy controls for comparison. GSTT1 and GSTM1 genotypes were determined using polymerase chain reactions, electrophoresis and imaging analysis. No obvious evidence of GSTT1-null, GSTM1-null and GSTT1/GSTM1-double null genotype distribution differences was found between case and control groups or between genders. Subgroup analysis showed that the risk of stroke was increased when hypertension was accompanied by GSTT1-null (odds ratio (OR) = 2.996, P < 0.001) and GSTM1-null (OR = 3.680, P < 0.001) genotypes; diabetes mellitus was accompanied by GSTT1-null (OR = 1.860, P = 0.031) and GSTM1-null (OR = 2.444, P = 0.002) genotypes, and smokers showed a GSTT1-null genotype (OR = 2.276, P = 0.003). GSTT1- and GSTM1-null genotypes may interact synergistically with hypertension, diabetes mellitus and smoking to increase the incidence risk of ischemic stroke.

摘要

动脉粥样硬化在缺血性卒中中起重要作用,氧化应激参与动脉粥样硬化的全过程。谷胱甘肽S-转移酶(GST)与其他抗氧化酶共同作用可清除活性氧,保护细胞免受氧化损伤。为评估谷胱甘肽S-转移酶(GSTT1和GSTM1)基因多态性与中国汉族人群缺血性卒中的关联,本研究选取315例缺血性卒中患者和210例健康对照进行比较。采用聚合酶链反应、电泳及成像分析确定GSTT1和GSTM1基因型。病例组与对照组之间或不同性别之间未发现GSTT1缺失、GSTM1缺失及GSTT1/GSTM1双缺失基因型分布有明显差异。亚组分析显示,高血压伴有GSTT1缺失(比值比(OR)=2.996,P<0.001)和GSTM1缺失(OR=3.680,P<0.001)基因型时,卒中风险增加;糖尿病伴有GSTT1缺失(OR=1.860,P=0.031)和GSTM1缺失(OR=2.444,P=0.002)基因型时,卒中风险增加,吸烟者表现为GSTT1缺失基因型(OR=2.276,P=0.003)。GSTT1和GSTM1缺失基因型可能与高血压、糖尿病和吸烟协同作用,增加缺血性卒中的发病风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d6/4308794/ba3d1ea5bc0f/NRR-7-1420-g002.jpg

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