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Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study

Pregnancy-induced hypertension (PIH, including preeclampsia [PE] and gestational hypertension [GH]) and cardiovascular diseases (CVDs) have some metabolic changes and risk factors in common. Many studies have reported associations between single nucleotide polymorphisms (SNPs) of renin–angiotensin–a...

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Autores principales: Li, Xun, Tan, Hongzhuan, Zhou, Shujin, Hu, Shimin, Zhang, Tianyi, Li, Yangfen, Dou, Qianru, Lai, Zhiwei, Chen, Fenglei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133626/
https://www.ncbi.nlm.nih.gov/pubmed/27910864
http://dx.doi.org/10.1038/srep38030
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author Li, Xun
Tan, Hongzhuan
Zhou, Shujin
Hu, Shimin
Zhang, Tianyi
Li, Yangfen
Dou, Qianru
Lai, Zhiwei
Chen, Fenglei
author_facet Li, Xun
Tan, Hongzhuan
Zhou, Shujin
Hu, Shimin
Zhang, Tianyi
Li, Yangfen
Dou, Qianru
Lai, Zhiwei
Chen, Fenglei
author_sort Li, Xun
collection PubMed
description Pregnancy-induced hypertension (PIH, including preeclampsia [PE] and gestational hypertension [GH]) and cardiovascular diseases (CVDs) have some metabolic changes and risk factors in common. Many studies have reported associations between single nucleotide polymorphisms (SNPs) of renin–angiotensin–aldosterone system (RAAS) genes and CVDs (particularly hypertension), and their findings have provided candidate SNPs for research on genetic correlates of PIH. We explored the association between hypertension-related RAAS SNPs and PIH in a Chinese population. A total of 130 cases with PE, 67 cases with GH, and 316 controls were recruited. Six candidate SNPs of the RAAS system were selected. Multiple logistic regression analysis adjusting for maternal age, fetal sex, and gestational diabetes mellitus showed significant associations between angiotensinogen (AGT) rs3789678 T/C and GH (p = 0.0088) and between angiotensin II receptor type 1 (AGTR1) rs275645 G/A and PE (p = 0.0082). The study population was further stratified by maternal age (<30 and ≥30 years), and stratified and crossover analyses were conducted to determine genetic associations in different age groups. Our findings suggest that the impacts of different SNPs might be affected by maternal age; however, the effect of this potential gene–age interaction on PIH needs further exploration.
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spelling pubmed-51336262017-01-27 Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study Li, Xun Tan, Hongzhuan Zhou, Shujin Hu, Shimin Zhang, Tianyi Li, Yangfen Dou, Qianru Lai, Zhiwei Chen, Fenglei Sci Rep Article Pregnancy-induced hypertension (PIH, including preeclampsia [PE] and gestational hypertension [GH]) and cardiovascular diseases (CVDs) have some metabolic changes and risk factors in common. Many studies have reported associations between single nucleotide polymorphisms (SNPs) of renin–angiotensin–aldosterone system (RAAS) genes and CVDs (particularly hypertension), and their findings have provided candidate SNPs for research on genetic correlates of PIH. We explored the association between hypertension-related RAAS SNPs and PIH in a Chinese population. A total of 130 cases with PE, 67 cases with GH, and 316 controls were recruited. Six candidate SNPs of the RAAS system were selected. Multiple logistic regression analysis adjusting for maternal age, fetal sex, and gestational diabetes mellitus showed significant associations between angiotensinogen (AGT) rs3789678 T/C and GH (p = 0.0088) and between angiotensin II receptor type 1 (AGTR1) rs275645 G/A and PE (p = 0.0082). The study population was further stratified by maternal age (<30 and ≥30 years), and stratified and crossover analyses were conducted to determine genetic associations in different age groups. Our findings suggest that the impacts of different SNPs might be affected by maternal age; however, the effect of this potential gene–age interaction on PIH needs further exploration. Nature Publishing Group 2016-12-02 /pmc/articles/PMC5133626/ /pubmed/27910864 http://dx.doi.org/10.1038/srep38030 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Li, Xun
Tan, Hongzhuan
Zhou, Shujin
Hu, Shimin
Zhang, Tianyi
Li, Yangfen
Dou, Qianru
Lai, Zhiwei
Chen, Fenglei
Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study
title Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study
title_full Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study
title_fullStr Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study
title_full_unstemmed Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study
title_short Renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: A case–control gene-association study
title_sort renin–angiotensin–aldosterone system gene polymorphisms in gestational hypertension and preeclampsia: a case–control gene-association study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133626/
https://www.ncbi.nlm.nih.gov/pubmed/27910864
http://dx.doi.org/10.1038/srep38030
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