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肾素-血管紧张素原系统基因多态性与特发性复发性流产的关联。

The association of renin-angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss.

作者信息

Heidari Mohammad Mehdi, Sheikholeslami Mozhgan, Yavari Mahdieh, Khatami Mehri, Seyedhassani Seyed Mohammad

机构信息

a Department of Biology, Faculty of Science, Yazd University , Yazd , Iran.

b Dr. Seyedhassani Medical Genetic Center , Yazd , Iran.

出版信息

Hum Fertil (Camb). 2019 Sep;22(3):164-170. doi: 10.1080/14647273.2017.1388545. Epub 2017 Oct 23.

Abstract

The most common complication of pregnancy is idiopathic recurrent pregnancy loss (RPL). To identify the contribution of gene polymorphisms to this condition, we evaluated the association between RPL and the angiotensinogen (), angiotensin receptor 1 () and Angiotensinogen converting enzyme (ACE). In this case-control study, the frequency of (rs4762 and rs699), (rs5186) and insertion/deletion (rs4340) polymorphisms in 202 idiopathic RPL women was compared with 210 women with no history of abortion, using tetra-primer ARMS-PCR. Polymorphisms were analysed by logistic regression analysis according to inheritance models. The CT genotype of rs4762, the CC genotype of rs699 and the AC genotype of rs5186 in a co-dominant inheritance model were associated with idiopathic RPL (OR = 1.63, 95% CI = 1.07-2.49 of CT versus CC; OR = 5.97, 95% CI = 1.28-27.82 of CC versus TT; and OR = 1.99, 95% CI = 1.22-3.07 of AC versus AA). The allele frequency of rs699 and rs5186 polymorphisms, but not rs4762 and rs4340 polymorphisms were significantly different between women with RPL patients and controls ( = 0.020,  = 0.003,  = 0.105 and  = 0.065, respectively). These results show that there is a significant relationship between (rs699) and (rs5186) polymorphisms and idiopathic RPL in the Iranian population.

摘要

妊娠最常见的并发症是特发性复发性流产(RPL)。为了确定基因多态性对这种情况的影响,我们评估了RPL与血管紧张素原()、血管紧张素受体1()和血管紧张素转换酶(ACE)之间的关联。在这项病例对照研究中,使用四引物扩增受阻突变系统聚合酶链反应(tetra - primer ARMS - PCR),比较了202例特发性RPL女性与210例无流产史女性中(rs4762和rs699)、(rs5186)和插入/缺失(rs4340)多态性的频率。根据遗传模型,通过逻辑回归分析对多态性进行分析。在共显性遗传模型中,rs4762的CT基因型、rs699的CC基因型和rs5186的AC基因型与特发性RPL相关(CT与CC相比,OR = 1.63,95%CI = 1.07 - 2.49;CC与TT相比,OR = 5.97,95%CI = 1.28 - 27.82;AC与AA相比,OR = 1.99,95%CI = 1.22 - 3.07)。RPL患者与对照组女性之间,rs699和rs5186多态性的等位基因频率存在显著差异,但rs4762和rs4340多态性无显著差异(分别为 = 0.020, = 0.003, = 0.105和 = 0.065)。这些结果表明,在伊朗人群中,(rs699)和(rs5186)多态性与特发性RPL之间存在显著关系。

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