首页> 外文期刊>EXCLI Journal >GENETIC POLYMORPHISMS OF GLUTATHIONE S-TRANSFERASE M1 (GSTM1) AND T1 (GSTT1) AND SUSCEPTIBILITY TO PRE- ECLAMPSIA: A CASE-CONTROL STUDY AND A META-ANALYSIS
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GENETIC POLYMORPHISMS OF GLUTATHIONE S-TRANSFERASE M1 (GSTM1) AND T1 (GSTT1) AND SUSCEPTIBILITY TO PRE- ECLAMPSIA: A CASE-CONTROL STUDY AND A META-ANALYSIS

机译:谷胱甘肽S-转移酶M1(GSTM1)和T1(GSTT1)的遗传多态性和易感性的研究:病例对照研究和Meta分析

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The objective of the present hospital-based case-control study was to assess the association between glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) genetic polymorphisms and susceptibility to pre-eclampsia (PE) in Shiraz (Fars province, southern Iran). A total of 200 healthy pregnant women and 151 pre-eclamptic women were included. The healthy control group was frequency matched with the age of the pre-eclamptic women. Control women had neither PE in current pregnancy nor history of pregnancies with PE previously. The genotypes of GSTT1 and GSTM1 polymorphisms were determined using a PCR-based method. Neither GSTM1 null genotype (OR=1.07, 95 % CI: 0.70-1.64, P=0.736) nor GSTT1 null genotype (OR=0.73, 95 % CI: 0.44-1.21, P=0.233) was associated with risk of PE. Association between combination genotypes and risk of PE was not significant. When family history was entered as a covariate in analysis, adjusted ORs revealed that neither GSTM1 nor GSTT1 polymor- phisms was associated with risk of PE. For meta-analysis, we identified 5 eligible studies, in- cluding 1217 subjects (515 patients, and 702 healthy controls) in relation to the study poly- morphisms and risk of PE. Our present meta-analysis indicated that there neither GSTM1 (OR=0.99, 95 % CI: 0.78-1.25, P=0.955) nor GSTT1 polymorphisms (OR=0.85, 95 % CI: 0.66-1.10, P=0.223) was associated with susceptibility to PE. Taken together it seems that the polymorphisms of GSTM1 and GSTT1 are not risk factors for PE. Further investigations ad- justing for confounding factors are needed to confirm the present findings.
机译:这项基于医院的病例对照研究旨在评估设拉子(伊朗南部法尔斯省)的谷胱甘肽S-转移酶M1(GSTM1)和T1(GSTT1)遗传多态性与子痫前期(PE)的易感性之间的关系。 )。总共包括200名健康孕妇和151名先兆子痫妇女。健康对照组的频率与先兆子痫妇女的年龄相匹配。对照女性在目前的怀孕中既没有PE,也没有以前怀孕的PE史。使用基于PCR的方法确定GSTT1和GSTM1多态性的基因型。 GSTM1无效基因型(OR = 1.07,95%CI:0.70-1.64,P = 0.736)和GSTT1无效基因型(OR = 0.73,95%CI:0.44-1.21,P = 0.233)与PE风险无关。组合基因型与PE风险之间的相关性不显着。当将家族史作为分析的协变量输入时,调整后的ORs显示GSTM1和GSTT1多态性均与PE的风险无关。对于荟萃分析,我们确定了5项合格研究,包括1217名受试者(515名患者和702名健康对照)与研究多态性和PE风险相关。我们目前的荟萃分析表明,GSTM1(OR = 0.99,95%CI:0.78-1.25,P = 0.955)和GSTT1多态性(OR = 0.85,95%CI:0.66-1.10,P = 0.223)均不相关对PE的敏感性。综上所述,GSTM1和GSTT1的多态性似乎不是PE的危险因素。需要对混杂因素进行进一步的研究以确认目前的发现。

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    《EXCLI Journal》 |2011年第2期|共8页
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  • 中图分类 临床医学;
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