Ryu Hye Guk, Youn Sung-Won, Kwon Oh Dae
Department of Biological Science, College of Natural Sciences, Daegu University, Daegu, South Korea.
Dement Geriatr Cogn Dis Extra. 2012 Jan;2(1):1-9. doi: 10.1159/000335494. Epub 2012 Jan 19.
The relationship between apolipoprotein E (ApoE) and onset of vascular dementia remains controversial. The aim of this study was to evaluate the relationship between ApoE polymorphism and the onset of subcortical vascular dementia (SVaD) compared to Alzheimer's disease (AD) and normal controls.
The study was comprised of 61 patients with SVaD (42 Binswanger type, 19 lacunar type) and 112 patients with AD (16 early-onset AD, 96 late-onset AD) as well as 284 age-, gender- and education-matched normal controls. The diagnosis of SVaD was based on modified NINDS-AIREN criteria, and the diagnosis of AD was based on NINCDS-ADRDA criteria. ApoE polymorphism was genotyped in all participants.
None of the three ApoE alleles was more prevalent in SVaD patients compared to normal controls, which was the case when both Binswanger and lacunar types were analyzed separately. ApoE ∊4 did not accelerate the onset of SVaD (OR 1.66, 95% CI: 0.8-3.4), in contrast to a significant relation with late-onset AD (OR 3.78, 95% CI: 2.2-6.5).
Our results suggest that ApoE polymorphism is not associated with the onset of SVaD and that the two subtypes of SVaD may share similar pathophysiologies.
载脂蛋白E(ApoE)与血管性痴呆发病之间的关系仍存在争议。本研究旨在评估ApoE基因多态性与皮质下血管性痴呆(SVaD)发病之间的关系,并与阿尔茨海默病(AD)及正常对照进行比较。
本研究纳入61例SVaD患者(42例宾斯旺格型,19例腔隙型)、112例AD患者(16例早发型AD,96例晚发型AD)以及284例年龄、性别和教育程度匹配的正常对照。SVaD的诊断基于改良的NINDS-AIREN标准,AD的诊断基于NINCDS-ADRDA标准。对所有参与者进行ApoE基因多态性基因分型。
与正常对照相比,SVaD患者中三种ApoE等位基因均无更高的流行率,分别分析宾斯旺格型和腔隙型时情况亦是如此。与晚发型AD存在显著关联(比值比3.78,95%可信区间:2.2 - 6.5)不同,ApoE ε4并未加速SVaD的发病(比值比1.66,95%可信区间:0.8 - 3.4)。
我们的结果表明,ApoE基因多态性与SVaD的发病无关,且SVaD的两种亚型可能具有相似的病理生理学机制。