The Relationship Between MMP17 Variants and Ischemic Stroke Risk in the Population from Shaanxi Province in China.

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pharmacogenomics & Personalized Medicine Pub Date : 2023-01-01 DOI:10.2147/PGPM.S396076
Weiping Li, Yanqing Liu, Xiaoling Xu, Qi Zhang, Xiao Zhang, Jie Zhang, Xiaochen Niu, Shiyao Yang, Xiaobo Zhang, Wenzhen Shi, Gejuan Zhang, Mingze Chang, Ye Tian
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Abstract

Background: Ischemic stroke (IS) was a multifactorial disease, which was the main cause of death and adult disability. Genetic factors cannot be ignored.

Objective: The present study discussed the relationship between MMP17 variants and the susceptibility of IS.

Methods: Based on the Agena MassARRAY platform, we genotyped single nucleotide polymorphisms (SNPs) on the MMP17 gene in 1345 participants (670 controls and 675 cases). We used logistic regression analysis to analyze the association of MMP17 SNPs with the risk of IS in the Chinese population, with odds ratio (OR) and 95% confidence intervals (CIs). False-positive report probability (FPRP) detected false positives on the significant results. Besides, we detected the SNP-SNP interaction to predict IS risk by multi-factor dimensionality reduction (MDR) analysis.

Results: In the total analysis, MMP17 rs7975920 conferred an increased susceptibility to IS. After a stratified analysis by age and gender, the significant association between rs7975920 and IS risk was displayed in the subjects aged >55 years old and females. After stratified analysis by smoking and drinking, MMP17 rs6598163 was related to the risk of IS in smokers and rs7975920 was associated with the risk of IS in smokers and was in correlation with IS risk in drinkers.

Conclusion: In short, we first observed that MMP17 rs7975920 and rs6598163 were related to the risk of IS. The above results provided a theoretical basis for the elaboration of the role of MMP17 in IS in the Chinese population.

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陕西省人群MMP17变异与缺血性脑卒中风险的关系
背景:缺血性脑卒中是一种多因素疾病,是导致成人死亡和残疾的主要原因。遗传因素不容忽视。目的:探讨MMP17变异与IS易感性的关系。方法:基于Agena MassARRAY平台,对1345名参与者(对照组670人,病例675人)的MMP17基因单核苷酸多态性(snp)进行基因分型。我们采用logistic回归分析分析中国人群中MMP17 snp与IS风险的关系,采用比值比(OR)和95%置信区间(ci)。假阳性报告概率(FPRP)对显著结果检测假阳性。此外,我们通过多因素降维(MDR)分析检测SNP-SNP相互作用来预测IS风险。结果:在总分析中,MMP17 rs7975920增加了IS的易感性。根据年龄和性别进行分层分析后发现,rs7975920与IS风险在>55岁和女性受试者中存在显著相关性。通过吸烟和饮酒的分层分析,MMP17 rs6598163与吸烟者IS风险相关,rs7975920与吸烟者IS风险相关,与饮酒者IS风险相关。结论:总之,我们首先观察到MMP17 rs7975920和rs6598163与IS风险相关。以上结果为阐述MMP17在中国人群IS中的作用提供了理论基础。
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来源期刊
Pharmacogenomics & Personalized Medicine
Pharmacogenomics & Personalized Medicine Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
3.30
自引率
5.30%
发文量
110
审稿时长
16 weeks
期刊介绍: Pharmacogenomics and Personalized Medicine is an international, peer-reviewed, open-access journal characterizing the influence of genotype on pharmacology leading to the development of personalized treatment programs and individualized drug selection for improved safety, efficacy and sustainability. In particular, emphasis will be given to: Genomic and proteomic profiling Genetics and drug metabolism Targeted drug identification and discovery Optimizing drug selection & dosage based on patient''s genetic profile Drug related morbidity & mortality intervention Advanced disease screening and targeted therapeutic intervention Genetic based vaccine development Patient satisfaction and preference Health economic evaluations Practical and organizational issues in the development and implementation of personalized medicine programs.
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