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载脂蛋白 E 启动子多态性与阿尔茨海默病风险:荟萃分析证据。

Apolipoprotein E promoter polymorphisms and risk of Alzheimer's disease: evidence from meta-analysis.

机构信息

Department of Neurology & Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

J Alzheimers Dis. 2010;19(4):1283-94. doi: 10.3233/JAD-2010-1329.

Abstract

Apolipoprotein E (APOE) promoter polymorphisms have long been linked to Alzheimer disease (AD) susceptibility, although the established data remains controversial. Using meta-analysis, our study aimed to clarify the nature of the genetic risks contributed by the three polymorphisms for developing AD. Medline, Embase, and Alzgene search identified 40 studies with 9,662 cases and 9.696 controls. Both -491A/T polymorphism (AA vs AT + TT: OR = 1.49, 95% CI=1.29-1.72) and -219T/G polymorphism (TT vs TG + GG: OR=1.30, 95% CI=1.10-1.55) showed a significant association with AD susceptibility; however, significant association was not identified in the analysis for -427T/C polymorphism (TT vs TC + CC: OR =1.03, 95% CI= 0.82-1.30). Among the APOE epsilon 4} carriers, the -491A homozygotes were at higher risk to develop AD compared with the -491T carriers (OR=1.42, 95% CI =1.15-1.76). For subjects carrying the -491AA genotype, the presence of the APOE epsilon4 allele increased the risk of AD 4.37-fold (95% CI=3.43-5.56). Subgroup analysis restricted to the late-onset or the Caucasian individuals revealed a similar association as that identified without restriction regarding -491A/T polymorphism. Our results confirm a significant but modest association between APOE promoter -491A/T and -219T/G polymorphisms and AD susceptibility.

摘要

载脂蛋白 E (APOE) 启动子多态性与阿尔茨海默病 (AD) 的易感性密切相关,尽管已有的数据仍存在争议。本研究采用荟萃分析,旨在阐明三种多态性对 AD 发病的遗传风险的性质。通过 Medline、Embase 和 Alzgene 搜索,共确定了 40 项研究,包含 9662 例病例和 9696 例对照。-491A/T 多态性(AA 与 AT+TT:OR=1.49,95%CI=1.29-1.72)和-219T/G 多态性(TT 与 TG+GG:OR=1.30,95%CI=1.10-1.55)与 AD 易感性显著相关;然而,-427T/C 多态性(TT 与 TC+CC:OR=1.03,95%CI=0.82-1.30)的分析中未发现显著相关性。在 APOE epsilon 4 携带者中,与-491T 携带者相比,-491A 纯合子发生 AD 的风险更高(OR=1.42,95%CI=1.15-1.76)。对于携带-491AA 基因型的个体,APOE epsilon4 等位基因的存在使 AD 的发病风险增加了 4.37 倍(95%CI=3.43-5.56)。仅针对晚发性或白种人进行的亚组分析显示,-491A/T 多态性与 AD 易感性之间存在类似的关联。我们的研究结果证实了 APOE 启动子-491A/T 和-219T/G 多态性与 AD 易感性之间存在显著但适度的关联。

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