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Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals

BACKGROUND: Contribution of cardiovascular disease related genetic risk factors for stroke are not clearly defined. We performed a genetic association study to assess the association of 56 previously characterized gene variants in 34 candidate genes from cardiovascular disease related biological pat...

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Autores principales: Ou, Wenjing, Liu, Xin, Shen, Yue, Li, Jiana, He, Lingbin, Yuan, Yuan, Tan, Xuerui, Liu, Lisheng, Zhao, Jingbo, Wang, Xingyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140791/
https://www.ncbi.nlm.nih.gov/pubmed/25144711
http://dx.doi.org/10.1371/journal.pone.0105516
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author Ou, Wenjing
Liu, Xin
Shen, Yue
Li, Jiana
He, Lingbin
Yuan, Yuan
Tan, Xuerui
Liu, Lisheng
Zhao, Jingbo
Wang, Xingyu
author_facet Ou, Wenjing
Liu, Xin
Shen, Yue
Li, Jiana
He, Lingbin
Yuan, Yuan
Tan, Xuerui
Liu, Lisheng
Zhao, Jingbo
Wang, Xingyu
author_sort Ou, Wenjing
collection PubMed
description BACKGROUND: Contribution of cardiovascular disease related genetic risk factors for stroke are not clearly defined. We performed a genetic association study to assess the association of 56 previously characterized gene variants in 34 candidate genes from cardiovascular disease related biological pathways with ischemic stroke and cerebral hemorrhage in a Chinese population. METHODS: There were 1280 stroke patients (1101 with ischemic stroke and 179 with cerebral hemorrhage) and 1380 controls in the study. The genotypes for 56 polymorphisms of 34 candidate genes were determined by the immobilized probe approach and the associations of gene polymorphisms with ischemic stroke and cerebral hemorrhage were performed by logistic regression under an allelic model. RESULTS: After adjusting for age, sex, BMI and hypertension status by logistic regression analysis, we found that NPPA rs5063 was significantly associated with both ischemic stroke (odds ratio [OR] 0.69; 95% confidence interval [CI], 0.52 to 0.90; P = 0.006) and cerebral hemorrhage(OR = 0.39; 95%CI, 0.19 to 0.78; P = 0.007). In addition, MTHFR rs1801133 also was associated with cerebral hemorrhage (OR = 1.48; 95%CI, 1.16 to1.89; P = 0.001) but not with ischemic stroke (OR = 1.08; 95%CI, 0.96 to1.22; P = 0.210). After false discovery rate (FDR) correction, the association of NPPA rs5063 and MTHFR rs1801133 with cerebral hemorrhage remained significant. CONCLUSIONS: The NPPA rs5063 is associated with reduced risk for cerebral hemorrhage and MTHFR rs1801133 is associated with increased risk of cerebral hemorrhage in a Chinese population.
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spelling pubmed-41407912014-08-25 Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals Ou, Wenjing Liu, Xin Shen, Yue Li, Jiana He, Lingbin Yuan, Yuan Tan, Xuerui Liu, Lisheng Zhao, Jingbo Wang, Xingyu PLoS One Research Article BACKGROUND: Contribution of cardiovascular disease related genetic risk factors for stroke are not clearly defined. We performed a genetic association study to assess the association of 56 previously characterized gene variants in 34 candidate genes from cardiovascular disease related biological pathways with ischemic stroke and cerebral hemorrhage in a Chinese population. METHODS: There were 1280 stroke patients (1101 with ischemic stroke and 179 with cerebral hemorrhage) and 1380 controls in the study. The genotypes for 56 polymorphisms of 34 candidate genes were determined by the immobilized probe approach and the associations of gene polymorphisms with ischemic stroke and cerebral hemorrhage were performed by logistic regression under an allelic model. RESULTS: After adjusting for age, sex, BMI and hypertension status by logistic regression analysis, we found that NPPA rs5063 was significantly associated with both ischemic stroke (odds ratio [OR] 0.69; 95% confidence interval [CI], 0.52 to 0.90; P = 0.006) and cerebral hemorrhage(OR = 0.39; 95%CI, 0.19 to 0.78; P = 0.007). In addition, MTHFR rs1801133 also was associated with cerebral hemorrhage (OR = 1.48; 95%CI, 1.16 to1.89; P = 0.001) but not with ischemic stroke (OR = 1.08; 95%CI, 0.96 to1.22; P = 0.210). After false discovery rate (FDR) correction, the association of NPPA rs5063 and MTHFR rs1801133 with cerebral hemorrhage remained significant. CONCLUSIONS: The NPPA rs5063 is associated with reduced risk for cerebral hemorrhage and MTHFR rs1801133 is associated with increased risk of cerebral hemorrhage in a Chinese population. Public Library of Science 2014-08-21 /pmc/articles/PMC4140791/ /pubmed/25144711 http://dx.doi.org/10.1371/journal.pone.0105516 Text en © 2014 Ou et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ou, Wenjing
Liu, Xin
Shen, Yue
Li, Jiana
He, Lingbin
Yuan, Yuan
Tan, Xuerui
Liu, Lisheng
Zhao, Jingbo
Wang, Xingyu
Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals
title Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals
title_full Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals
title_fullStr Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals
title_full_unstemmed Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals
title_short Association of CVD Candidate Gene Polymorphisms with Ischemic Stroke and Cerebral Hemorrhage in Chinese Individuals
title_sort association of cvd candidate gene polymorphisms with ischemic stroke and cerebral hemorrhage in chinese individuals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140791/
https://www.ncbi.nlm.nih.gov/pubmed/25144711
http://dx.doi.org/10.1371/journal.pone.0105516
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