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载脂蛋白 E 基因多态性与中国血管性痴呆的关系:荟萃分析。

Apolipoprotein E gene polymorphism in a Chinese population with vascular dementia: a meta-analysis.

机构信息

Department of Neurology, The First Affiliated Hospital, Guangxi Medical University, No. 22 Shuang Yong Lu, Nanning, China.

出版信息

Dement Geriatr Cogn Disord. 2012;33(2-3):96-103. doi: 10.1159/000337025. Epub 2012 Mar 20.

DOI:10.1159/000337025
PMID:22433749
Abstract

BACKGROUND

Apolipoprotein E (ApoE) gene has been reported to be associated with the development of vascular dementia (VD); however, results from observational studies are conflicting.

METHODS

We surveyed all case-control studies on ApoE gene and VD patients with comprehensive search and review of the references. A meta-analysis was performed to demonstrate the association of ApoE gene with VD by random effects models. The association was assessed by odds ratio (OR) with 95% confidence intervals (CI).

RESULTS

A total of 18 studies including 935 patients and 1,686 controls were eligible and abstracted. ApoE ε3/4 and ε4/4 genotype, as well as ε4 allele (OR = 1.95, 95% CI: 1.52-2.49; OR = 3.47, 95% CI: 1.85-6.51 and OR = 2.12, 95% CI: 1.64-2.74, respectively) were associated with an increased risk of VD, while ApoE ε3/3 genotype and ε3 allele (OR = 0.65, 95% CI: 0.53-0.79 and OR = 0.65, 95% CI: 0.53-0.80, respectively) trended to protect against VD. There was no significant difference in ApoE ε2 allele frequency, ε2/2, ε2/3 or ε2/4 genotype between VD and controls (OR = 0.85, 95% CI: 0.61-1.17; OR = 0.89, 95% CI: 0.39-2.01; OR = 0.82, 95% CI: 0.61-1.09 and OR = 1.03, 95% CI: 0.57-1.84, respectively).

CONCLUSIONS

Our results support a genetic association between ApoE polymorphism and VD in the Chinese population.

摘要

背景

载脂蛋白 E(ApoE)基因已被报道与血管性痴呆(VD)的发生有关;然而,观察性研究的结果存在冲突。

方法

我们全面检索了有关 ApoE 基因与 VD 患者的病例对照研究,并对参考文献进行了综述。采用随机效应模型进行荟萃分析,以显示 ApoE 基因与 VD 的关联。采用比值比(OR)及其 95%置信区间(CI)评估关联。

结果

共纳入 18 项研究,包括 935 例患者和 1686 例对照。ApoE ε3/4 和 ε4/4 基因型以及 ε4 等位基因(OR=1.95,95%CI:1.52-2.49;OR=3.47,95%CI:1.85-6.51 和 OR=2.12,95%CI:1.64-2.74)与 VD 风险增加相关,而 ApoE ε3/3 基因型和 ε3 等位基因(OR=0.65,95%CI:0.53-0.79 和 OR=0.65,95%CI:0.53-0.80)则趋势上保护 VD。VD 患者与对照组之间 ApoE ε2 等位基因频率、ε2/2、ε2/3 或 ε2/4 基因型无显著差异(OR=0.85,95%CI:0.61-1.17;OR=0.89,95%CI:0.39-2.01;OR=0.82,95%CI:0.61-1.09 和 OR=1.03,95%CI:0.57-1.84)。

结论

我们的研究结果支持 ApoE 多态性与中国人群 VD 之间存在遗传关联。

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