A Comparison of Apelin Rs56204867 and Apelin Receptor Rs11544374 Gene Polymorphisms and Their Association with Risk of Preeclampsia in Southeast Iran.

IF 1.6 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Maryam Juybar, Mansour Shahraki, Marzieh Ghasemi, Abolfazl Payandeh, Shaghayegh Saljooghi, Mohsen Saravani
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引用次数: 0

Abstract

Background: Pre-eclampsia (PE) is a severe pregnancy condition with genetic and environmental factors affecting the placental function and vascular changes. Genetic variants in the apelinergic system may influence preeclampsia risk and birth outcomes. Therefore, this study aimed to compare apelin (APLN) rs56204867 and apelin receptor (APLNR) rs11544374 gene polymorphisms and to investigate their association with mothers' body mass index and infant's birth weight among women with preeclampsia and control group in southeast Iran.

Methods: A total of 123 PE patients and 125 age- and gender-matched control subjects were enrolled in the study. The PCR-RFLP method was employed to genotype the APLN rs56204867 and APLNR rs11544374 gene polymorphisms.

Results: There was no significant association between the genotypes of the rs11544374 variant and the PE risk. The incidence of the AG genotype of the rs54204867 variant in the control group was considerably greater than in the PE group. Also, a significant relationship was found between the body mass profile of patients with PE and the APLN rs54204867 gene polymorphism.

Conclusions: It was observed that the APLN rs54204867 gene polymorphism could affect the PE risk. No significant difference was found between the PE group and the control group in terms of the genotypes of the APLNR rs11544374 variant. It was not statistically significant between mothers' BMI and rs11544374 of the APLNR gene, whereas an obvious link was observed between mothers' BMI and rs54204867 of the APLN gene.

伊朗东南部Apelin Rs56204867和Apelin受体Rs11544374基因多态性及其与子痫前期风险的关系
背景:子痫前期(pre -子痫,PE)是一种严重的妊娠疾病,遗传和环境因素影响胎盘功能和血管改变。apelinergic系统的遗传变异可能影响子痫前期风险和出生结果。因此,本研究旨在比较伊朗东南部先兆子痫妇女和对照组中apelin (APLN) rss56204867和apelin受体(APLNR) rs11544374基因多态性,并探讨其与母亲体重指数和婴儿出生体重的关系。方法:共纳入123例PE患者和125例年龄和性别匹配的对照组。采用PCR-RFLP方法对APLN rss56204867和APLNR rs11544374基因多态性进行基因分型。结果:rs11544374基因型与PE风险无显著相关性。rs54204867变异AG基因型在对照组的发生率明显高于PE组。此外,PE患者的体重谱与APLN rs54204867基因多态性之间存在显著关系。结论:观察到APLN rs54204867基因多态性可能影响PE的发生。在APLNR rs11544374变异的基因型方面,PE组与对照组无显著差异。母亲的BMI与APLNR基因rs11544374之间无统计学意义,而母亲的BMI与APLN基因rss54204867之间有明显联系。
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来源期刊
Reports of Biochemistry and Molecular Biology
Reports of Biochemistry and Molecular Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
2.80
自引率
23.50%
发文量
60
审稿时长
10 weeks
期刊介绍: The Reports of Biochemistry & Molecular Biology (RBMB) is the official journal of the Varastegan Institute for Medical Sciences and is dedicated to furthering international exchange of medical and biomedical science experience and opinion and a platform for worldwide dissemination. The RBMB is a medical journal that gives special emphasis to biochemical research and molecular biology studies. The Journal invites original and review articles, short communications, reports on experiments and clinical cases, and case reports containing new insights into any aspect of biochemistry and molecular biology that are not published or being considered for publication elsewhere. Publications are accepted in the form of reports of original research, brief communications, case reports, structured reviews, editorials, commentaries, views and perspectives, letters to authors, book reviews, resources, news, and event agenda.
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