Bullido M J, Artiga M J, Recuero M, Sastre I, García M A, Aldudo J, Lendon C, Han S W, Morris J C, Frank A, Vázquez J, Goate A, Valdivieso F
Departamento de Biología Molecular and Centro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid, Cantoblanco, Spain.
Nat Genet. 1998 Jan;18(1):69-71. doi: 10.1038/ng0198-69.
The epsilon4 allele of the apolipoprotein E gene (APOE) has been associated with an increased risk of developing Alzheimer's disease (AD; refs 1,2). However, it is apparent that the APOEepsilon4 allele alone is neither necessary nor sufficient to cause the disease. We have recently found three new polymorphisms within the APOE transcriptional regulatory region (M.J.A. et al., manuscript submitted) and now establish an association between one of these polymorphisms (-491A/T) and dementia as observed in Alzheimer's disease, in two independent clinical populations. The results suggest that homozygosity of a common variant (-491A) is associated with increased risk for AD, and that this association is independent of APOEepsilon4 status. In vitro studies suggest that the -491A/T polymorphism may increase risk for AD by altering the level of ApoE protein expression.
载脂蛋白E基因(APOE)的ε4等位基因与患阿尔茨海默病(AD)的风险增加有关(参考文献1,2)。然而,很明显,仅APOEε4等位基因既不是引发该疾病的必要条件也不是充分条件。我们最近在APOE转录调控区域发现了三个新的多态性(M.J.A.等人,稿件待提交),现在在两个独立的临床群体中证实了其中一个多态性(-491A/T)与阿尔茨海默病中观察到的痴呆之间存在关联。结果表明,常见变体(-491A)的纯合性与AD风险增加有关,并且这种关联独立于APOEε4状态。体外研究表明,-491A/T多态性可能通过改变载脂蛋白E蛋白表达水平增加患AD的风险。