Wang J C, Kwon J M, Shah P, Morris J C, Goate A
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
Neurology. 2000 Dec 12;55(11):1644-9. doi: 10.1212/wnl.55.11.1644.
To verify the association between APOE gene promoter polymorphisms and the development of AD and to determine whether the effect of promoter polymorphisms on AD is independent of the APOE epsilon4 allele.
Three polymorphisms in the APOE promoter have been shown to modify APOE expression in vitro. Several studies have suggested that these polymorphisms may also modulate risk for AD, either independently or by modifying the effect of the APOE coding polymorphism.
The authors analyzed allele and genotype distributions for APOE and all three known APOE promoter polymorphisms (-491 A/T, -427 T/C, and -219 G/T) in a study group consisting of 237 subjects with AD and 274 age-matched controls. They then used log-linear and logistic regression analyses to test for possible interactions between APOE genotype and the promoter polymorphisms on risk of AD.
A strong association between the APOE epsilon 4 allele and AD was detected regardless of promoter polymorphism status. In addition, the -491 AA genotype appears to be an independent genetic risk factor for AD. The -427 T/C polymorphism and the -219 T/G polymorphism were not directly associated with AD.
验证载脂蛋白E(APOE)基因启动子多态性与阿尔茨海默病(AD)发病之间的关联,并确定启动子多态性对AD的影响是否独立于APOE ε4等位基因。
已证实在体外,APOE启动子的三种多态性可改变APOE的表达。几项研究表明,这些多态性可能还会独立地或通过改变APOE编码多态性的效应来调节AD的发病风险。
作者在一个由237名AD患者和274名年龄匹配的对照组成的研究组中,分析了APOE以及所有三种已知的APOE启动子多态性(-491 A/T、-427 T/C和-219 G/T)的等位基因和基因型分布。然后,他们使用对数线性和逻辑回归分析来检验APOE基因型与启动子多态性之间对AD发病风险可能存在的相互作用。
无论启动子多态性状态如何,均检测到APOE ε4等位基因与AD之间存在强关联。此外,-491 AA基因型似乎是AD的一个独立遗传危险因素。-427 T/C多态性和-219 T/G多态性与AD无直接关联。