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Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population

BACKGROUND: Stroke is a serious cardiovascular disease and is also the leading cause of long-term disability in developing and developed countries. Because matrix metalloproteinase-9 (MMP-9) is associated with the risk of many cardiovascular diseases, we investigated the relationship between single...

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Autores principales: Gao, Ning, Guo, Tie, Luo, Han, Tu, Guolong, Niu, Fanglin, Yan, Mengdan, Xia, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469199/
https://www.ncbi.nlm.nih.gov/pubmed/30992065
http://dx.doi.org/10.1186/s12883-019-1285-7
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author Gao, Ning
Guo, Tie
Luo, Han
Tu, Guolong
Niu, Fanglin
Yan, Mengdan
Xia, Ying
author_facet Gao, Ning
Guo, Tie
Luo, Han
Tu, Guolong
Niu, Fanglin
Yan, Mengdan
Xia, Ying
author_sort Gao, Ning
collection PubMed
description BACKGROUND: Stroke is a serious cardiovascular disease and is also the leading cause of long-term disability in developing and developed countries. Because matrix metalloproteinase-9 (MMP-9) is associated with the risk of many cardiovascular diseases, we investigated the relationship between single nucleotide polymorphisms (SNPs) in MMP-9 and the risk of Ischemic stroke (IS) in a southern Chinese Han population. METHODS: This study included 250 stroke patients and 250 healthy controls. Genotyping was performed using the Agena MassARRAY system, and chi-squared tests and genetic models were used to evaluate the associations between MMP-9 SNPs and the risk of IS. Odds ratio (OR) and 95% confidence intervals (CIs) were calculated by unconditional logistic regression adjusted for age. RESULTS: Polymorphism rs3787268 was associated with increased the risk of IS. Specifically, the genotype “G/A” significantly correlated with IS risk in the co-dominant model [odds ratio (OR) = 1.62; 95% confidence interval (CI) = 1.10–2.41; p = 0.035)], while genotypes “G/A” and “A/A” may increase the risk of IS based on the dominant model (OR = 1.62; 95% CI = 1.12–2.35; p = 0.0097). This SNP was also significantly associated with IS risk in the log-additive model (OR = 1.33; 95% CI = 1.03–1.70; p = 0.026). Conversely, haplotype “C/G” appears to reduce the risk of IS (OR = 0.71; 95% CI = 0.54–0.95; p = 0.019). CONCLUSIONS: Our study showed that the rs3787268 locus in the MMP-9 gene may increase risk of IS in a southern Chinese Han population and thus provide insight into the IS pathogenesis.
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spelling pubmed-64691992019-04-23 Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population Gao, Ning Guo, Tie Luo, Han Tu, Guolong Niu, Fanglin Yan, Mengdan Xia, Ying BMC Neurol Research Article BACKGROUND: Stroke is a serious cardiovascular disease and is also the leading cause of long-term disability in developing and developed countries. Because matrix metalloproteinase-9 (MMP-9) is associated with the risk of many cardiovascular diseases, we investigated the relationship between single nucleotide polymorphisms (SNPs) in MMP-9 and the risk of Ischemic stroke (IS) in a southern Chinese Han population. METHODS: This study included 250 stroke patients and 250 healthy controls. Genotyping was performed using the Agena MassARRAY system, and chi-squared tests and genetic models were used to evaluate the associations between MMP-9 SNPs and the risk of IS. Odds ratio (OR) and 95% confidence intervals (CIs) were calculated by unconditional logistic regression adjusted for age. RESULTS: Polymorphism rs3787268 was associated with increased the risk of IS. Specifically, the genotype “G/A” significantly correlated with IS risk in the co-dominant model [odds ratio (OR) = 1.62; 95% confidence interval (CI) = 1.10–2.41; p = 0.035)], while genotypes “G/A” and “A/A” may increase the risk of IS based on the dominant model (OR = 1.62; 95% CI = 1.12–2.35; p = 0.0097). This SNP was also significantly associated with IS risk in the log-additive model (OR = 1.33; 95% CI = 1.03–1.70; p = 0.026). Conversely, haplotype “C/G” appears to reduce the risk of IS (OR = 0.71; 95% CI = 0.54–0.95; p = 0.019). CONCLUSIONS: Our study showed that the rs3787268 locus in the MMP-9 gene may increase risk of IS in a southern Chinese Han population and thus provide insight into the IS pathogenesis. BioMed Central 2019-04-16 /pmc/articles/PMC6469199/ /pubmed/30992065 http://dx.doi.org/10.1186/s12883-019-1285-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gao, Ning
Guo, Tie
Luo, Han
Tu, Guolong
Niu, Fanglin
Yan, Mengdan
Xia, Ying
Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population
title Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population
title_full Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population
title_fullStr Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population
title_full_unstemmed Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population
title_short Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population
title_sort association of the mmp-9 polymorphism and ischemic stroke risk in southern chinese han population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469199/
https://www.ncbi.nlm.nih.gov/pubmed/30992065
http://dx.doi.org/10.1186/s12883-019-1285-7
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