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血管紧张素转换酶插入/缺失基因多态性与出血性脑卒中风险的关系:53 项研究的系统评价和 Meta 分析。

Association between Angiotensin Converting Enzyme Insertion/Deletion gene polymorphism with the risk of Hemorrhagic Stroke: A systematic review and Meta-Analysis of 53 studies.

机构信息

Department of Neurology, All India Institute of Medical Sciences, New Delhi 110029, India.

Department of Neurology, All India Institute of Medical Sciences, New Delhi 110029, India.

出版信息

Gene. 2021 Jul 20;790:145696. doi: 10.1016/j.gene.2021.145696. Epub 2021 May 6.

DOI:10.1016/j.gene.2021.145696
PMID:33964377
Abstract

BACKGROUND AND AIMS

Hemorrhagic stroke (HS) results in significant mortality and disability worldwide. Angiotensin Converting Enzyme (ACE) is responsible for blood pressure regulation and vascular homeostasis. Our objective was to conduct a comprehensive meta-analysis for ascertaining the association of ACE I/D polymorphism with HS since a number of studies depicted inconclusive evidence.

METHODS

Literature search was performed till July 10, 2020 in PubMed, EMBASE, Cochrane, Chinese National Knowledge Information and Google Scholar databases with keywords: ('Angiotensin Converting Enzyme' OR 'ACE') AND ('Single Nucleotide polymorphisms' OR 'SNP') AND ('Hemorrhagic stroke or 'HS'). Pooled Odds Ratio (OR) and 95% Confidence Interval (CI) were determined for gene-disease association using either fixed (when I < 50%) or random effect (when I > 50%) models. Risk of bias in studies was assessed using funnel plots and sensitivity analyses. Statistical analysis was performed using STATA version 13.0 software.

RESULTS

A total of 53 studies having 5186 HS and 7347 healthy control subjects were included in our meta-analysis. Pooled analyses showed that ACE I/D gene polymorphism had significant association with risk of HS in overall study population [(dominant model: OR = 1.29, 95% CI = 1.12-1.50 & recessive model: OR = 1.79, 95% CI = 1.46-2.20)]. Population subgroup analyses further revealed significant relationship of ACE I/D polymorphism with ICH in Asians (recessive: OR 1.97, 95% CI = 1.57-2.47) but not in Caucasians (recessive: OR 1.02, 95% CI = 0.76-1.36).

CONCLUSION

This meta-analysis suggests that ACE I/D polymorphism may lead to risk of HS and can be a potential biomarker for HS susceptibility especially in Asian population.

摘要

背景与目的

出血性脑卒中(HS)在全球范围内导致了较高的死亡率和残疾率。血管紧张素转换酶(ACE)负责血压调节和血管稳态。我们的目的是进行一项全面的荟萃分析,以确定 ACE I/D 多态性与 HS 之间的关联,因为有许多研究结果并不一致。

方法

我们在 PubMed、EMBASE、Cochrane、中国国家知识基础设施和 Google Scholar 数据库中,使用关键词“(血管紧张素转换酶'或'ACE')和'单核苷酸多态性'或'SNP')和(出血性脑卒中或'HS')”,对截止到 2020 年 7 月 10 日的文献进行了检索。使用固定效应(当 I<50%)或随机效应模型(当 I>50%),计算基因-疾病关联的合并优势比(OR)和 95%置信区间(CI)。使用漏斗图和敏感性分析评估研究中的偏倚风险。使用 STATA 版本 13.0 软件进行统计分析。

结果

共有 53 项研究纳入了 5186 例 HS 患者和 7347 例健康对照者。荟萃分析显示,ACE I/D 基因多态性与总体研究人群 HS 风险显著相关[(显性模型:OR=1.29,95%CI=1.12-1.50;隐性模型:OR=1.79,95%CI=1.46-2.20)]。人群亚组分析进一步显示,ACE I/D 多态性与亚洲人群的 ICH 存在显著相关性(隐性:OR 1.97,95%CI=1.57-2.47),但与高加索人群无关(隐性:OR 1.02,95%CI=0.76-1.36)。

结论

这项荟萃分析表明,ACE I/D 多态性可能导致 HS 发病风险增加,并且可能是 HS 易感性的潜在生物标志物,尤其是在亚洲人群中。

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