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载脂蛋白 E 基因调控区多态性-491T 等位基因与阿尔茨海默病的关联:一项在突尼斯人群中的研究。

Association between Alzheimer disease and the -491T allele of regulatory region polymorphism of Apolipoprotein E in a Tunisian population.

机构信息

Neurological Department, Charles Nicolle Hospital, Boulevard du 9 Avril, 1006, Tunis, Tunisia,

出版信息

Neurochem Res. 2014 Feb;39(2):244-7. doi: 10.1007/s11064-013-1213-y. Epub 2013 Dec 11.

DOI:10.1007/s11064-013-1213-y
PMID:24326531
Abstract

The apolipoprotein E (APOE) is a well-established risk factor for late-onset Alzheimer's disease (AD). Several studies have attempted to confirm the association between the polymorphism located at position -491 in the transcriptional regulatory region of the APOE gene and AD. We examined in 85 AD patients and 90 control subjects of a Tunisian population the potential involvement of this polymorphism as a risk factor for AD, either through an independent effect or through interaction with the existing APOE ε4 allele risk. The T allele frequency was significantly higher in the AD patients group (45.3 %) than in the controls group (32.78 %) and may possibly constitute a significant risk factor for AD. The APOE ε4 allele did not influence the distribution of the -491 polymorphism after stratification.

摘要

载脂蛋白 E(APOE)是晚发性阿尔茨海默病(AD)的一个既定的风险因素。多项研究试图证实位于 APOE 基因转录调控区的位置-491 处的多态性与 AD 之间的关联。我们在 85 名 AD 患者和 90 名来自突尼斯人群的对照者中研究了该多态性作为 AD 的风险因素的潜在作用,无论是通过独立效应还是通过与现有的 APOE ε4 等位基因风险的相互作用。在 AD 患者组(45.3%)中,T 等位基因频率明显高于对照组(32.78%),可能是 AD 的一个重要风险因素。在分层后,APOE ε4 等位基因并不影响-491 多态性的分布。

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本文引用的文献

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Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease.阿尔茨海默病中APOE调控区多态性的综合关联分析
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Apolipoprotein E -491 promoter polymorphism is an independent risk factor for Alzheimer's disease in the Chinese population.载脂蛋白E -491启动子多态性是中国人群中阿尔茨海默病的独立危险因素。
Neurosci Lett. 2003 Oct 16;350(1):25-8. doi: 10.1016/s0304-3940(03)00815-2.
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Effect of the APOE-491A/T promoter polymorphism on apolipoprotein E levels and risk of Alzheimer disease: The Rotterdam Study.APOE-491A/T启动子多态性对载脂蛋白E水平及阿尔茨海默病风险的影响:鹿特丹研究
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