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首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women.
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Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women.

机译:亚甲基四氢叶酸还原酶C677T和谷胱甘肽S转移酶P1 A313G与Maya-Mestizo妇女先兆子痫的风险降低有关。

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Preeclampsia, a common complication of pregnancy, is characterized by elevated blood pressure and proteinuria developing after 20 weeks' gestational age. Susceptibility to this syndrome is believed to have a genetic component. The aim of this study was to investigate whether or not the 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T and glutathione S-transferase P1 (GSTP1) A313G polymorphisms are associated with preeclampsia in Maya-Mestizo women. A case-control study was performed, in which 125 preeclamptic patients and 274 healthy controls were genotyped for the MTHFR C677T and GSTP1 A313G polymorphisms by real-time PCR allelic discrimination. Allele and genotype frequencies were compared using the chi2 tests. The MTHFR 677T allele and the 677TT genotype were significantly more frequent in the controls, suggesting an association with a decreased risk of preeclampsia (p = 0.017 and p = 0.007, respectively). Similarly, GSTP1 313GG/GC genotypes and the G allele were more frequent in controls, showing a significant association with reduced risk of preeclampsia (p = 0.008 and p = 0.013, respectively). Our results suggest, for the first time, that the MTHFR 677T and GSTP1 313G polymorphisms confer a significantly decreased risk of developing preeclampsia in the Mexican Maya-Mestizo population.
机译:子痫前症是妊娠的常见并发症,其特征是在胎龄20周后血压升高和蛋白尿增多。据信这种综合征的易感性具有遗传成分。这项研究的目的是调查5,10-亚甲基四氢叶酸还原酶(MTHFR)C677T和谷胱甘肽S-转移酶P1(GSTP1)A313G多态性是否与先兆子痫妇女相关。进行了一项病例对照研究,其中通过实时PCR等位基因鉴别对MTHFR C677T和GSTP1 A313G多态性对125名先兆子痫患者和274名健康对照进行了基因分型。使用chi2测试比较了等位基因和基因型频率。 MTHFR 677T等位基因和677TT基因型在对照组中更为频繁,提示先兆子痫的风险降低(分别为p = 0.017和p = 0.007)。同样,GSTP1 313GG / GC基因型和G等位基因在对照组中更为频繁,显示出与先兆子痫风险降低显着相关(分别为p = 0.008和p = 0.013)。我们的结果首次表明,MTHFR 677T和GSTP1 313G多态性使墨西哥玛雅-梅斯蒂佐人群发生先兆子痫的风险大大降低。

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