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Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis

INTRODUCTION: Studies on the relation between aldosterone synthase -344 T/C polymorphism and diabetic nephropathy showed controversial conclusions. This meta-analysis aimed to systematically summarize the association between aldosterone synthase (CYP11B2) gene polymorphism and diabetic nephropathy r...

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Autores principales: Xu, Haiyan, Wang, Xu, Liu, Mingming, Shao, Xin, He, Xueyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843876/
https://www.ncbi.nlm.nih.gov/pubmed/27009287
http://dx.doi.org/10.1177/1470320316633896
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author Xu, Haiyan
Wang, Xu
Liu, Mingming
Shao, Xin
He, Xueyuan
author_facet Xu, Haiyan
Wang, Xu
Liu, Mingming
Shao, Xin
He, Xueyuan
author_sort Xu, Haiyan
collection PubMed
description INTRODUCTION: Studies on the relation between aldosterone synthase -344 T/C polymorphism and diabetic nephropathy showed controversial conclusions. This meta-analysis aimed to systematically summarize the association between aldosterone synthase (CYP11B2) gene polymorphism and diabetic nephropathy risk. METHODS: Embase, PubMed, ScienceDirect, Web of Science, Wanfang Data, VIP Database, China Knowledge Resource Integrated Database and SinoMed have been searched. A total of five studies including 825 cases and 910 controls were included. RESULTS: In overall analysis, significant increased risk was found in recessive comparison (OR = 1.27, 95% CI 1.05–1.55), homozygote comparison (OR = 1.39, 95% CI 1.04–1.88) and allele comparison (OR = 1.20, 95% CI = 1.05–1.39). No significant association was detected in dominant comparison (OR = 1.27, 95% CI 0.97–1.66) and heterozygote comparison (OR = 1.17, 95% CI 0.88–1.56). In subgroup analysis, significant increased risk existed in Asian population in allele comparison (OR = 1.45, 95% CI = 1.17–1.79), dominant comparison (OR = 1.78, 95% CI 1.11–2.87), homozygote comparison (OR = 2.11, 95% CI 1.29–3.47), recessive comparison (OR = 1.54, 95% CI 1.17–2.03), except for heterozygote comparison (OR = 1.44, 95% CI 0.87–2.38). CONCLUSIONS: Our meta-analysis indicates that aldosterone synthase (CYP11B2) gene polymorphism may contribute to diabetic nephropathy development, especially in Asian group, with the T allele acting as a risk factor.
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spelling pubmed-58438762018-03-20 Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis Xu, Haiyan Wang, Xu Liu, Mingming Shao, Xin He, Xueyuan J Renin Angiotensin Aldosterone Syst Original Article INTRODUCTION: Studies on the relation between aldosterone synthase -344 T/C polymorphism and diabetic nephropathy showed controversial conclusions. This meta-analysis aimed to systematically summarize the association between aldosterone synthase (CYP11B2) gene polymorphism and diabetic nephropathy risk. METHODS: Embase, PubMed, ScienceDirect, Web of Science, Wanfang Data, VIP Database, China Knowledge Resource Integrated Database and SinoMed have been searched. A total of five studies including 825 cases and 910 controls were included. RESULTS: In overall analysis, significant increased risk was found in recessive comparison (OR = 1.27, 95% CI 1.05–1.55), homozygote comparison (OR = 1.39, 95% CI 1.04–1.88) and allele comparison (OR = 1.20, 95% CI = 1.05–1.39). No significant association was detected in dominant comparison (OR = 1.27, 95% CI 0.97–1.66) and heterozygote comparison (OR = 1.17, 95% CI 0.88–1.56). In subgroup analysis, significant increased risk existed in Asian population in allele comparison (OR = 1.45, 95% CI = 1.17–1.79), dominant comparison (OR = 1.78, 95% CI 1.11–2.87), homozygote comparison (OR = 2.11, 95% CI 1.29–3.47), recessive comparison (OR = 1.54, 95% CI 1.17–2.03), except for heterozygote comparison (OR = 1.44, 95% CI 0.87–2.38). CONCLUSIONS: Our meta-analysis indicates that aldosterone synthase (CYP11B2) gene polymorphism may contribute to diabetic nephropathy development, especially in Asian group, with the T allele acting as a risk factor. SAGE Publications 2016-03-08 /pmc/articles/PMC5843876/ /pubmed/27009287 http://dx.doi.org/10.1177/1470320316633896 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Xu, Haiyan
Wang, Xu
Liu, Mingming
Shao, Xin
He, Xueyuan
Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis
title Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis
title_full Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis
title_fullStr Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis
title_full_unstemmed Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis
title_short Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis
title_sort association of aldosterone synthase (cyp11b2) -344 t/c polymorphism with diabetic nephropathy: a meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843876/
https://www.ncbi.nlm.nih.gov/pubmed/27009287
http://dx.doi.org/10.1177/1470320316633896
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