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中国南方汉族人群中基质金属蛋白酶-9多态性与缺血性中风风险的关联。

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

作者信息

Gao Ning, Guo Tie, Luo Han, Tu Guolong, Niu Fanglin, Yan Mengdan, Xia Ying

机构信息

Department of Neurosurgery, Affiliated Haikou Hospital of Xiangya Medical College in Central South University, Haikou, Hainan, 570208, China.

The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.

出版信息

BMC Neurol. 2019 Apr 16;19(1):67. doi: 10.1186/s12883-019-1285-7.

Abstract

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.

摘要

背景

中风是一种严重的心血管疾病,也是发展中国家和发达国家长期残疾的主要原因。由于基质金属蛋白酶-9(MMP-9)与许多心血管疾病的风险相关,我们在中国南方汉族人群中研究了MMP-9单核苷酸多态性(SNP)与缺血性中风(IS)风险之间的关系。

方法

本研究纳入250例中风患者和250例健康对照。使用Agena MassARRAY系统进行基因分型,并采用卡方检验和遗传模型评估MMP-9 SNP与IS风险之间的关联。通过对年龄进行校正的无条件逻辑回归计算比值比(OR)和95%置信区间(CI)。

结果

多态性rs3787268与IS风险增加相关。具体而言,在共显性模型中,基因型“G/A”与IS风险显著相关[比值比(OR)=1.62;95%置信区间(CI)=1.10 - 2.41;p = 0.035],而基于显性模型,基因型“G/A”和“A/A”可能增加IS风险(OR = 1.62;95% CI = 1.12 - 2.35;p = 0.0097)。该SNP在对数加性模型中也与IS风险显著相关(OR = 1.33;95% CI = 1.03 - 1.70;p = 0.026)。相反,单倍型“C/G”似乎降低了IS风险(OR = 0.71;95% CI = 0.54 - 0.95;p = 0.019)。

结论

我们的研究表明,MMP-9基因中的rs3787268位点可能增加中国南方汉族人群患IS的风险,从而为IS的发病机制提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55b/6469199/ce6738fc17de/12883_2019_1285_Fig1_HTML.jpg

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