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谷胱甘肽 S-转移酶基因多态性与男性特发性不育症风险的关系:系统评价和荟萃分析。

Glutathione S-transferases gene polymorphisms and risk of male idiopathic infertility: a systematic review and meta-analysis.

机构信息

Urologic Institute of PLA, Southwest Hospital, Third Military Medical University, 30 Gaotanyan Street, Shapingba District, Chongqing, 400038, China.

出版信息

Mol Biol Rep. 2013 Mar;40(3):2431-8. doi: 10.1007/s11033-012-2323-3. Epub 2012 Dec 14.

Abstract

The Glutathione S-transferases (GSTs) polymorphisms have been implicated in susceptibility to male idiopathic infertility, but study results are still controversial. To investigate the genetic associations between GSTs polymorphisms and risk of male idiopathic infertility, a systematic review and meta-analysis were performed. Meta-analysis was performed by pooling odds ratio (OR) with its corresponding 95 % confidence interval (95 % CI) form studies in electronic databases up to March 16, 2012. Glutathione S-transferase M 1 (GSTM1) null genotype, Glutathione S-transferase T 1 (GSTT1) null genotype, and dual null genotype of GSTM1/GSTT1 were analyzed independently. 14 eligible studies with a total of 1,845 idiopathic infertility males and 1,729 controls were included. There were 13 studies on GSTM1 polymorphism, 10 ones on GSTT1 polymorphism and 5 ones on GSTM1-GSTT1 interaction analysis. Meta-analyses of total relevant studies showed GSTM1 null genotype was significantly associated with an increased risk of male idiopathic infertility (OR = 1.40, 95 % CI 1.07-1.84, P OR = 0.015). The GSTM1-GSTT1 interaction analysis showed dual null genotype of GSTM1/GSTT1 was also significantly associated with increased risk of male idiopathic infertility (OR = 1.85, 95 % CI 1.07-3.21, P OR = 0.028). Subgroup analyses by ethnicity showed the associations above were still statistically significant in Caucasians (For GSTM1, OR = 1.51, 95 % CI 1.11-2.05, P OR = 0.009; For GSTM1/GSTT1, OR = 2.10, 95 % CI 1.51-2.91, P OR < 0.001). This meta-analysis suggests GSTM1 null genotype contributes to increased risk of male idiopathic infertility in Caucasians, and males with dual null genotype of GSTM1/GSTT1 are particularly susceptible to developing idiopathic infertility.

摘要

谷胱甘肽 S-转移酶(GSTs)多态性与男性特发性不育易感性有关,但研究结果仍存在争议。为了研究 GSTs 多态性与男性特发性不育风险之间的遗传关联,进行了系统评价和荟萃分析。通过合并电子数据库中截至 2012 年 3 月 16 日的研究的优势比(OR)及其相应的 95%置信区间(95%CI)进行荟萃分析。谷胱甘肽 S-转移酶 M1(GSTM1)缺失基因型、谷胱甘肽 S-转移酶 T1(GSTT1)缺失基因型和 GSTM1/GSTT1 双重缺失基因型分别进行分析。纳入了 14 项符合条件的研究,共有 1845 名特发性不育男性和 1729 名对照。其中 13 项研究涉及 GSTM1 多态性,10 项研究涉及 GSTT1 多态性,5 项研究涉及 GSTM1-GSTT1 相互作用分析。对所有相关研究的荟萃分析显示,GSTM1 缺失基因型与男性特发性不育的风险增加显著相关(OR=1.40,95%CI 1.07-1.84,P<0.001)。GSTM1-GSTT1 相互作用分析显示,GSTM1/GSTT1 双重缺失基因型也与男性特发性不育的风险增加显著相关(OR=1.85,95%CI 1.07-3.21,P=0.028)。按种族进行的亚组分析显示,上述关联在白种人中仍具有统计学意义(对于 GSTM1,OR=1.51,95%CI 1.11-2.05,P=0.009;对于 GSTM1/GSTT1,OR=2.10,95%CI 1.51-2.91,P<0.001)。这项荟萃分析表明,GSTM1 缺失基因型导致白种人男性特发性不育的风险增加,而 GSTM1/GSTT1 双重缺失基因型的男性尤其容易患上特发性不育。

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