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伊朗东南部血管紧张素转换酶内含子16插入/缺失及血管紧张素II 1型受体A1166C基因多态性与子痫前期的相关性

Association of angiotensin-converting enzyme intron 16 insertion/deletion and angiotensin II type 1 receptor A1166C gene polymorphisms with preeclampsia in South East of Iran.

作者信息

Salimi Saeedeh, Mokhtari Mojgan, Yaghmaei Minoo, Jamshidi Mohammad, Naghavi Anoosh

机构信息

Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.

出版信息

J Biomed Biotechnol. 2011;2011:941515. doi: 10.1155/2011/941515. Epub 2011 Jul 26.

Abstract

Some evidence suggests that a variety of genetic factors contributed in pathogenesis of the preeclampsia. The aim of this study was to assess the association between the angiotensin-converting enzyme (ACE) I/D and angiotensin II type1 receptor A1166C polymorphisms with preeclampsia. This study was performed in 125 preeclamptic pregnant women and 132 controls. The I/D Polymorphism of the ACE gene was assessed by polymerase chain reaction and the A1166C Polymorphism of the AT1R gene was determined by restriction fragment length polymorphism. The genotype and allele frequencies of I/D polymorphism differed between two groups. The risk of preeclampsia was 3.2-fold in pregnant women with D allele (OR, 3.2 [95% CI, 1.1 to 3.8]; P = 0.01). The distribution of the AT1R gene A1166C polymorphism was similar in affected and control groups. Our results supported that presence of the I/D polymorphism of ACE gene is a marker for the increased risk of preeclampsia.

摘要

一些证据表明,多种遗传因素参与了先兆子痫的发病机制。本研究的目的是评估血管紧张素转换酶(ACE)I/D多态性和血管紧张素II 1型受体A1166C多态性与先兆子痫之间的关联。本研究纳入了125例先兆子痫孕妇和132例对照。采用聚合酶链反应评估ACE基因的I/D多态性,通过限制性片段长度多态性确定AT1R基因的A1166C多态性。两组之间I/D多态性的基因型和等位基因频率存在差异。携带D等位基因的孕妇发生先兆子痫的风险是对照组的3.2倍(比值比,3.2 [95%可信区间,1.1至3.8];P = 0.01)。AT1R基因A1166C多态性在病例组和对照组中的分布相似。我们的结果支持ACE基因I/D多态性的存在是先兆子痫风险增加的一个标志物。

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