Corder E H, Saunders A M, Strittmatter W J, Schmechel D E, Gaskell P C, Rimmler J B, Locke P A, Conneally P M, Schmader K E, Tanzi R E
Division of Neurology, Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University Medical Center, Durham, NC, USA.
Neurology. 1995 Jul;45(7):1323-8. doi: 10.1212/wnl.45.7.1323.
The apolipoprotein E (APOE) epsilon 4 allele carries an increased risk of a patient developing Alzheimer's disease (AD) while the epsilon 2 allele carries a decreased risk. We compared survival from the onset of AD in subjects with different numbers of epsilon 4 alleles and evaluated changes in genotypic frequencies with age. Two subject groups were investigated: unrelated AD case and control subjects, and affected and unaffected members from 74 multiplex AD families. In both subject groups, survival from onset decreased with increasing onset age, was longer in women, and was unrelated to epsilon 4 gene dose. The epsilon 2/epsilon 3 genotype became more common with age (p = 0.004). The epsilon 4 allele decreased in frequency with age in all patient groups but, unexpectedly, remained unchanged in control subjects. We conclude that the progression of AD is not strongly related to epsilon 4 gene dose, that the higher prevalence of AD in women may involve the longer survival of affected women, and that AD and death are competing risks involving APOE that change over time.
载脂蛋白E(APOE)ε4等位基因会增加患者患阿尔茨海默病(AD)的风险,而ε2等位基因则会降低这种风险。我们比较了携带不同数量ε4等位基因的受试者从AD发病开始的生存期,并评估了基因型频率随年龄的变化。研究了两个受试者组:无亲缘关系的AD病例和对照受试者,以及来自74个多病例AD家族的患病和未患病成员。在这两个受试者组中,从发病开始的生存期随着发病年龄的增加而缩短,女性的生存期更长,并且与ε4基因剂量无关。ε2/ε3基因型随年龄增长变得更为常见(p = 0.004)。在所有患者组中,ε4等位基因的频率随年龄下降,但出乎意料的是,在对照受试者中保持不变。我们得出结论,AD的进展与ε4基因剂量没有密切关系,女性中AD患病率较高可能与患病女性生存期较长有关,并且AD和死亡是涉及APOE的相互竞争风险,它们会随时间变化。