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ACE 基因 rs4343 多态性增加孕妇子痫前期的发病风险。

ACE gene rs4343 polymorphism elevates the risk of preeclampsia in pregnant women.

机构信息

Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Neuroscience Research Center, Iran University of Medical Sciences, Tehran, Iran.

出版信息

J Hum Hypertens. 2018 Dec;32(12):825-830. doi: 10.1038/s41371-018-0096-4. Epub 2018 Aug 20.

DOI:10.1038/s41371-018-0096-4
PMID:30127488
Abstract

The multifactorial basis of preeclampsia (PE) implies that there are several genes and risk factors that are important in the development of the disease. Therefore, the exact etiology and pathogenesis of preeclampsia remains unclear. It is suggested that inappropriate regulation of the renin-angiotensin system (RAS) is a risk factor for hypertension during pregnancy. The angiotensin I-converting enzyme (ACE) serum level, a key component of the RAS, affects the blood pressure. It is hypothesized that the ACE gene polymorphisms contribute to preeclampsia development. In a case-control study containing 296 subjects (165 PE patients and 131 normotensive controls), we aimed to examine the association of the ACE gene I/D and rs4343 polymorphisms with preeclampsia in Iranian women. Genotyping for rs4343 and ACE I/D polymorphisms was performed by using TP-ARMS-PCR and conventional PCR, respectively. The rs4343 G allele frequency was higher in the case group (OR = 1.90, 95% CI, 1.37-2.65; P = 0.0001). Besides, a significant difference was detected for the genotype frequencies between the studied groups under dominant (OR = 3.94, 95% CI, 2.05-7.56; P  < 0.0001) and recessive (OR = 2.21, 95% CI, 1.22-4.01; P = 0.009) inheritance models. For the I/D polymorphism, no significant differences were detected in the genotype and allele frequencies or any of the inheritance models between PE patients and controls. To verify the current results and validate the significance of the studied genetic variations, additional studies in diverse ethnic populations are required.

摘要

子痫前期(PE)的多因素基础意味着有几个基因和风险因素在疾病的发展中很重要。因此,子痫前期的确切病因和发病机制仍不清楚。有研究表明,肾素-血管紧张素系统(RAS)的调节不当是妊娠高血压的一个危险因素。血管紧张素 I 转换酶(ACE)血清水平,RAS 的一个关键组成部分,影响血压。有人假设 ACE 基因多态性有助于子痫前期的发展。在一项包含 296 名受试者(165 名 PE 患者和 131 名血压正常对照者)的病例对照研究中,我们旨在研究伊朗妇女 ACE 基因 I/D 和 rs4343 多态性与子痫前期的关系。rs4343 和 ACE I/D 多态性的基因分型分别采用 TP-ARMS-PCR 和常规 PCR 进行。病例组 rs4343 G 等位基因频率较高(OR=1.90,95%CI,1.37-2.65;P=0.0001)。此外,在显性(OR=3.94,95%CI,2.05-7.56;P<0.0001)和隐性(OR=2.21,95%CI,1.22-4.01;P=0.009)遗传模式下,研究组之间基因型频率存在显著差异。对于 I/D 多态性,PE 患者和对照组之间在基因型和等位基因频率或任何遗传模式中均未检测到显著差异。为了验证目前的结果并验证所研究遗传变异的意义,需要在不同种族人群中进行更多的研究。

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