Corder E H, Saunders A M, Risch N J, Strittmatter W J, Schmechel D E, Gaskell P C, Rimmler J B, Locke P A, Conneally P M, Schmader K E
Division of Neurology, Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University Medical Center, Durham, North Carolina 27710.
Nat Genet. 1994 Jun;7(2):180-4. doi: 10.1038/ng0694-180.
Gene dosage of the apolipoprotein E (APOE) epsilon 4 allele is a major risk factor for familial Alzheimer disease (AD) of late onset (after age 60). Here we studied a large series of 115 AD case subjects and 243 controls as well as 150 affected and 197 unaffected members of 66 AD families. Our data demonstrate a protective effect of the epsilon 2 allele, in addition to the dose effect of the epsilon 4 allele in sporadic AD. Although a substantial proportion (65%) of AD is attributable to the presence of epsilon 4 alleles, risk of AD is lowest in subjects with the epsilon 2/epsilon 3 genotype, with an additional 23% of AD attributable to the absence of an epsilon 2 allele. The opposite actions of the epsilon 2 and epsilon 4 alleles further support the direct involvement of APOE in the pathogenesis of AD.
载脂蛋白E(APOE)ε4等位基因的基因剂量是晚发型(60岁以后)家族性阿尔茨海默病(AD)的主要危险因素。在此,我们研究了一大组115例AD病例受试者和243例对照,以及66个AD家族中的150名患病成员和197名未患病成员。我们的数据表明,除了ε4等位基因在散发性AD中的剂量效应外,ε2等位基因具有保护作用。虽然相当一部分(65%)的AD归因于ε4等位基因的存在,但ε2/ε3基因型受试者的AD风险最低,另外23%的AD归因于不存在ε2等位基因。ε2和ε4等位基因的相反作用进一步支持了APOE直接参与AD的发病机制。