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Genetic polymorphisms of glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) and susceptibility to pre-eclampsia

机译:谷胱甘肽S-转移酶M1(GSTM1)和T1(GSTT1)的遗传多态性和子痫前期易感性

摘要

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 genotypesof GSTT1 and GSTM1 polymorphisms were determined using a PCR-based method. NeitherGSTM1 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 polymorphisms was associated with risk of PE. For meta-analysis, we identified 5 eligible studies, including 1217 subjects (515 patients, and 702 healthy controls) in relation to the study polymorphisms 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 adjusting 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的目的是评估设拉子(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)的易感性之间的关联)。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)或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OR显示GSTM1和GSTT1多态性均与PE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的易感性。总而言之,似乎GSTM1和GSTT1的多态性不是PE的危险因素。需要进一步的研究来调整混杂因素,以确认目前的发现。

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