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中国陕西省人群中基因变异与缺血性中风风险的关系

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

作者信息

Li Weiping, Liu Yanqing, Xu Xiaoling, Zhang Qi, Zhang Xiao, Zhang Jie, Niu Xiaochen, Yang Shiyao, Zhang Xiaobo, Shi Wenzhen, Zhang Gejuan, Chang Mingze, Tian Ye

机构信息

Xi'an Key Laboratory of Cardiovascular and Cerebrovascular Diseases, Xi'an No.3 Hospital, The Affiliated Hospital of Northwest University, School of Life Sciences and Medicine, Northwest University, Xi'an, Shaanxi Province, People's Republic of China.

出版信息

Pharmgenomics Pers Med. 2023 Jan 30;16:59-66. doi: 10.2147/PGPM.S396076. eCollection 2023.

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 variants and the susceptibility of IS.

METHODS

Based on the Agena MassARRAY platform, we genotyped single nucleotide polymorphisms (SNPs) on the gene in 1345 participants (670 controls and 675 cases). We used logistic regression analysis to analyze the association of 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, 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, 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 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.

摘要

背景

缺血性中风(IS)是一种多因素疾病,是死亡和成人残疾的主要原因。遗传因素不容忽视。

目的

本研究探讨[基因名称]变异与IS易感性之间的关系。

方法

基于Agena MassARRAY平台,我们对1345名参与者(670名对照和675例病例)的[基因名称]上的单核苷酸多态性(SNP)进行基因分型。我们使用逻辑回归分析来分析中国人群中[基因名称]SNP与IS风险的关联,计算比值比(OR)和95%置信区间(CI)。假阳性报告概率(FPRP)用于检测显著结果中的假阳性。此外,我们通过多因素降维(MDR)分析检测SNP-SNP相互作用以预测IS风险。

结果

在总体分析中,rs7975920使IS易感性增加。按年龄和性别进行分层分析后,rs7975920与IS风险之间的显著关联在年龄>55岁的受试者和女性中表现出来。按吸烟和饮酒进行分层分析后,rs6598163与吸烟者的IS风险相关,rs7975920与吸烟者的IS风险相关且与饮酒者的IS风险相关。

结论

简而言之,我们首次观察到rs7975920和rs6598163与IS风险相关。上述结果为阐述MMP17在中国人群IS中的作用提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b7/9889100/b68a9ef6d119/PGPM-16-59-g0001.jpg

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