Aggarwal Neelum T, Wilson Robert S, Beck Todd L, Bienias Julia L, Berry-Kravis Elizabeth, Bennett David A
Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois 60612-3872, USA.
Neurocase. 2005 Feb;11(1):3-7. doi: 10.1080/13554790490903038.
Possession of one or more copies of the apolipoprotein E (APOE) epsilon4 allele is a known risk factor for Alzheimer's disease (AD), but it is uncertain whether the epsilon4 allele is associated with disease incidence among persons with mild cognitive impairment (MCI). We addressed this issue with data from the Religious Orders Study. Participants were 181 older Catholic clergy members who met criteria for MCI based on a uniform structured clinical evaluation; 56 (30.9%) had at least one epsilon4 allele. Clinical evaluations, which included clinical classification of dementia and AD, were repeated annually. During a mean of 5.7 years of observation, 79 persons (43.6%) developed AD. In a proportional hazards model that controlled for age, sex, and education, possession of an epsilon4 allele was associated with a 93% increase in the risk of developing Alzheimer's disease (95% CI; 1.02, 2.63). There was a marginally significant reduction in the effect of epsilon4 in older compared to younger participants (p=.053). The results suggest that possession of an epsilon4 allele does increase risk of AD in persons with MCI.
拥有一个或多个载脂蛋白E(APOE)ε4等位基因拷贝是已知的阿尔茨海默病(AD)风险因素,但ε4等位基因是否与轻度认知障碍(MCI)患者的疾病发病率相关尚不确定。我们利用宗教团体研究的数据解决了这个问题。参与者是181名年龄较大的天主教神职人员,他们基于统一的结构化临床评估符合MCI标准;56人(30.9%)至少有一个ε4等位基因。临床评估(包括痴呆和AD的临床分类)每年重复进行。在平均5.7年的观察期内,79人(43.6%)患上了AD。在控制了年龄、性别和教育程度的比例风险模型中,拥有ε4等位基因与患阿尔茨海默病的风险增加93%相关(95%CI;1.02,2.63)。与年轻参与者相比,老年参与者中ε4的影响略有显著降低(p = 0.053)。结果表明,拥有ε4等位基因确实会增加MCI患者患AD的风险。