Suppr超能文献

谷胱甘肽 S-转移酶多态性(GSTM1 和 GSTT1)与原发性开角型青光眼的关联:基于证据的荟萃分析。

Association of glutathione S-transferase polymorphisms (GSTM1 and GSTT1) with primary open-angle glaucoma: an evidence-based meta-analysis.

机构信息

Zhongshan Ophthalmic Center, State Key Laboratory of Ophthalmology, Sun Yat-sen University, Guangzhou, People's Republic of China.

出版信息

Gene. 2013 Sep 10;526(2):80-6. doi: 10.1016/j.gene.2013.05.032. Epub 2013 Jun 4.

Abstract

Studies investigating the associations between glutathione S-transferase (GST) genetic polymorphisms and primary open-angle glaucoma (POAG) have reported controversial results. Therefore, a meta-analysis was performed to clarify the effects of GSTM1 and GSTT1 polymorphisms on POAG risk. Published literatures from PubMed, EMBASE, ISI Web of Science and CBM databases were retrieved. All studies evaluating the association between GSTM1/GSTT1 polymorphisms and POAG were included. Pooled odds ratio (OR) and 95% confidence interval (CI) were calculated using fixed- or random-effects model. Eleven studies on GSTM1 (1339 cases and 1412 controls) and seven studies on GSTT1 (958 cases, 1003 controls) were included. Overall analysis showed that the association between GSTM1 and GSTT1 null genotype and POAG risk is not statistically significant. Subgroup analyses showed that the null genotype of GSTM1 increased the risk of POAG in Asians. In GSTM1-GSTT1 interaction analysis, individuals with dual null genotype were associated with a significantly increased risk of POAG when compared with the dual present genotype. In conclusion, the present meta-analysis suggested that GSTM1 null genotypes are associated with increased POAG risk in Asian populations but not in Caucasian and mixed populations. Dual null genotype of GSTM1/GSTT1 is associated with increased risk of POAG. Given the limited sample size, the finding on GST polymorphisms needs further investigation.

摘要

研究调查谷胱甘肽 S-转移酶 (GST) 基因多态性与原发性开角型青光眼 (POAG) 之间的关系的报告结果存在争议。因此,进行了荟萃分析以阐明 GSTM1 和 GSTT1 多态性对 POAG 风险的影响。从 PubMed、EMBASE、ISI Web of Science 和 CBM 数据库中检索到已发表的文献。纳入了所有评估 GSTM1/GSTT1 多态性与 POAG 之间关系的研究。使用固定或随机效应模型计算合并的比值比 (OR) 和 95%置信区间 (CI)。纳入了 11 项关于 GSTM1(1339 例病例和 1412 例对照)和 7 项关于 GSTT1(958 例病例,1003 例对照)的研究。总体分析表明,GSTM1 和 GSTT1 缺失基因型与 POAG 风险之间没有统计学意义的关联。亚组分析表明,GSTM1 缺失基因型增加了亚洲人群 POAG 的风险。在 GSTM1-GSTT1 相互作用分析中,与双现型相比,双缺失基因型的个体与 POAG 的风险显著增加相关。总之,本荟萃分析表明,GSTM1 缺失基因型与亚洲人群 POAG 风险增加相关,但与白人和混合人群无关。GSTM1/GSTT1 的双重缺失基因型与 POAG 的风险增加相关。鉴于样本量有限,关于 GST 多态性的发现需要进一步研究。

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