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精氨酸加压素(AVP)启动子多态性与子痫前期的关联。

Association of arginine vasopressin (AVP) promoter polymorphisms with preeclampsia.

机构信息

Research Center for Non-Communicable Diseases, Department of Advanced Medical Sciences and Technologies, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran.

Islamic Azad University, Arsanjan Branch, Arsanjan, Iran.

出版信息

Pregnancy Hypertens. 2019 Oct;18:122-125. doi: 10.1016/j.preghy.2019.09.017. Epub 2019 Oct 5.

Abstract

OBJECTIVES

Preeclampsia (PE) is a disease of pregnancy characterized by early onset of maternal hypertension and proteinuria. New findings indicate that arginine vasopressin (AVP) may be a contributing factor to ignite PE. The aim of this study was to identify if there is any correlation between arginine vasopressin promoter polymorphisms and PE.

STUDY DESIGN

Venous blood samples of 100 PE and 100 normal pregnant women were obtained for DNA extraction to identify the polymorphisms of AVP promoter by RFLP and nested-PCR techniques.

MAIN OUTCOME

rs3729965 polymorphism of PE women was detected to have significant correlation with body mass index (BMI) (P = 0.028).

RESULTS

Statistical analysis of three polymorphisms namely rs3729965, rs61138008 and rs3761249 of preeclamptic women (PEW) and none preeclamptic pregnant women (NPEW) revealed that rs3729965 genotypic distribution was significantly different between both groups (P = 0.04). Further analysis revealed that rs3729965 CT genotype of PEW had significant correlation to their BMI (P = 0.028).

CONCLUSION

Polymorphic variants located on the promoter region of AVP are associated with PE. Thus we hypothesize that allelic variation may have a role in increasing the risk of developing PE.

摘要

目的

子痫前期(PE)是一种妊娠疾病,其特征为孕妇高血压和蛋白尿的早期发作。新发现表明,精氨酸血管加压素(AVP)可能是引发 PE 的一个因素。本研究旨在确定 AVP 启动子多态性与 PE 是否存在相关性。

研究设计

采集 100 例 PE 患者和 100 例正常孕妇的静脉血样,用于提取 DNA,采用 RFLP 和巢式-PCR 技术鉴定 AVP 启动子的多态性。

主要结果

PE 女性的 rs3729965 多态性与体重指数(BMI)显著相关(P=0.028)。

结果

对 3 种多态性(rs3729965、rs61138008 和 rs3761249)在子痫前期患者(PEW)和非子痫前期孕妇(NPEW)中的统计分析表明,两组之间的 rs3729965 基因型分布存在显著差异(P=0.04)。进一步分析表明,PEW 的 rs3729965 CT 基因型与 BMI 显著相关(P=0.028)。

结论

位于 AVP 启动子区域的多态性变异与 PE 相关。因此,我们假设等位基因变异可能在增加发生 PE 的风险方面起作用。

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