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脑梗死中ACE基因多态性的Meta分析

Meta-analysis of the ACE gene polymorphism in cerebral infarction.

作者信息

Tao Hong-miao, Shao Bei, Chen Guo-zhong

机构信息

School of Medicine, Jinhua College of Profession and Technology, The People's Republic of China.

出版信息

Can J Neurol Sci. 2009 Jan;36(1):20-5. doi: 10.1017/s0317167100006259.

Abstract

BACKGROUND

The angiotensin-1 converting enzyme (ACE) gene is known to have two polymorphic alleles insertion/deletion (I/D). People with the DD genotype have been shown to be at greater risk of cerebral infarction, but only in some studies. Identification of cerebral infarction susceptibility genes and quantification of associated risks have been hampered by conflicting results from underpowered case-control studies. This meta-analysis was made to look specifically into the genetics of cerebral infarction among Han Chinese population.

METHODS

Genetic associations studies published from January 1, 1990 to December 30, 2007 were collected from databases of MEDLINE, EMBASE, CBM and CNKI. Data were extracted using standardised forms and pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated.

RESULTS

Twenty-nine original case-control studies of Han Chinese population, comprising 3654 patients with cerebral infarction and 3058 controls were included in the meta-analysis. Using the random effects model, the pooled ORs of ACE DD genotype VS ID+ II was 1.91 (95% CI 1.56 to 2.34, P<0.00001).

CONCLUSIONS

These data suggest that the ACE DD genotype may be a risk factor for cerebral infarction in Han Chinese population. A large scale case-control study is needed to clarify the functional effect of the polymorphism of the ACE I/D gene in the pathogenesis of cerebral infarction in Han Chinese population.

摘要

背景

已知血管紧张素转换酶(ACE)基因有两种多态性等位基因插入/缺失(I/D)。研究表明,DD基因型的人患脑梗死的风险更高,但仅在部分研究中如此。病例对照研究样本量不足导致结果相互矛盾,阻碍了脑梗死易感基因的鉴定及相关风险的量化。本荟萃分析旨在专门研究汉族人群脑梗死的遗传学情况。

方法

收集1990年1月1日至2007年12月30日发表的基因关联研究,来源于MEDLINE、EMBASE、CBM和CNKI数据库。使用标准化表格提取数据,并计算合并比值比(OR)及95%置信区间(CI)。

结果

荟萃分析纳入了29项针对汉族人群的原始病例对照研究,包括3654例脑梗死患者和3058例对照。采用随机效应模型,ACE基因DD基因型与ID + II基因型相比的合并OR为1.91(95%CI 1.56至2.34,P < 0.00001)。

结论

这些数据表明,ACE基因DD基因型可能是汉族人群脑梗死的一个危险因素。需要开展大规模病例对照研究,以阐明ACE基因I/D多态性在汉族人群脑梗死发病机制中的功能作用。

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