首页> 外文期刊>Journal of Gynecology and Obstetrics >Lack of association between ACE I/D and AGTR1 A1166C gene polymorphisms and preeclampsia in Turkish pregnant women of Trakya region
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Lack of association between ACE I/D and AGTR1 A1166C gene polymorphisms and preeclampsia in Turkish pregnant women of Trakya region

机译:Trakya地区土耳其孕妇中ACE I / D和AGTR1 A1166C基因多态性与先兆子痫之间缺乏关联

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The aim of this study was to investigate the distribution of Angiotensin Converting Enzyme Insertion/Deletion (ACE I/D) and the distribution of Angiotensin II Type 1 Receptor A1166C (AGTR1 A1166C) gene polymorphisms in preeclamptic pregnant women comparing to control pregnant women in Turkish subjects of Trakya Region. We aimed to determine whether these polymorphisms are genetic risk factor for preeclampsia. The study included 75 preeclamptic pregnant women and 75 control pregnant women, which were categorized according to The World Health Organization Detecting Pre-eclampsia: A Practical Guide. The ACE I/D gene polymorphism was investigated using Polymerase Chain Reaction (PCR) method. The AGTR1 A1166C gene polymorphism was identified using PCR and followed by Restriction Fragment Length Polymorphism (RFLP) methods. The ACE I/D genotype distribution in preeclamptic pregnant women DD=36.0%, ID=44.0% and II=20.0% did not significantly differ from those in control pregnant women DD=38.7%, ID=50.7% and II=10.6% (P=0.279). The AGTR1 A1166C genotype distribution in preeclamptic pregnant women AA=57.3%, AC=33.4% and CC=9.3% also did not significantly differ from those in control pregnant women AA=70.7, AC=24.0% and CC=5.3% (P=0.223). This case-control study show that ACE I/D and AGTR1 A1166C gene polymorphisms are not genetic risk factors for preeclampsia in this population in Turkish pregnant women of Trakya Region.
机译:这项研究的目的是调查先兆子痫孕妇与土耳其对照孕妇相比,血管紧张素转换酶插入/缺失(ACE I / D)的分布和血管紧张素II 1型受体A1166C(AGTR1 A1166C)基因多态性的分布特拉卡地区的主题。我们旨在确定这些多态性是否是先兆子痫的遗传危险因素。该研究包括75名先兆子痫孕妇和75名对照孕妇,根据《世界卫生组织检测先兆子痫:实用指南》进行了分类。使用聚合酶链反应(PCR)方法研究了ACE I / D基因多态性。使用PCR鉴定AGTR1 A1166C基因多态性,然后采用限制性片段长度多态性(RFLP)方法进行鉴定。子痫前期孕妇DD = 36.0%,ID = 44.0%和II = 20.0%的ACE I / D基因型分布与对照组孕妇DD = 38.7%,ID = 50.7%和II = 10.6%的差异无统计学意义( P = 0.279)。子痫前期孕妇中的AGTR1 A1166C基因型分布AA = 57.3%,AC = 33.4%和CC = 9.3%也与对照组孕妇的AA = 70.7,AC = 24.0%和CC = 5.3%差异无统计学意义(P = 0.223)。这项病例对照研究表明,在该人群中,ACE I / D和AGTR1 A1166C基因多态性并非先兆子痫的遗传危险因素。

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