Bailey Heather R, Sargent Jesse Q, Flores Shaney, Nowotny Petra, Goate Alison, Zacks Jeffrey M
a Department of Psychology , Washington University , St. Louis , MO , USA.
Neuropsychol Dev Cogn B Aging Neuropsychol Cogn. 2015;22(6):639-66. doi: 10.1080/13825585.2015.1020916. Epub 2015 Mar 10.
The apolipoprotein E (ApOE) ε4 allele is associated with neuropathological buildup of amyloid in the brain, and with lower performance on some laboratory measures of memory in some populations. In two studies, we tested whether ApOE genotype affects memory for everyday activities. In Study 1, participants aged 20-79 years old (n = 188) watched movies of actors engaged in daily activities and completed memory tests for the activities in the movies. In Study 2, cognitively healthy and demented older adults (n = 97) watched and remembered similar movies, and also underwent structural MRI scanning. All participants provided saliva samples for genetic analysis. In both samples we found that, in older adults, ApOE ε4 carriers demonstrated worse everyday memory performance than did ε4 noncarriers. In Study 2, ApOE ε4 carriers had smaller medial temporal lobes (MTL) volumes, and MTL volume mediated the relationship between ApOE genotype and everyday memory performance. These everyday memory tasks measure genetically determined cognitive decline that can occur prior to a clinical diagnosis of dementia. Further, these tasks are easily administered and may be a useful clinical tool in identifying ε4 carriers who may be at risk for MTL atrophy and further cognitive decline that is a common characteristic of the earliest stages of Alzheimer's disease.
载脂蛋白E(ApOE)ε4等位基因与大脑中淀粉样蛋白的神经病理堆积有关,并且在某些人群中,与一些记忆实验室指标的较低表现有关。在两项研究中,我们测试了ApOE基因型是否会影响对日常活动的记忆。在研究1中,20至79岁的参与者(n = 188)观看了演员进行日常活动的电影,并完成了对电影中活动的记忆测试。在研究2中,认知健康和患有痴呆症的老年人(n = 97)观看并记住了类似的电影,并且还接受了结构磁共振成像扫描。所有参与者都提供了唾液样本用于基因分析。在两个样本中我们都发现,在老年人中,ApOE ε4携带者的日常记忆表现比非ε4携带者更差。在研究2中,ApOE ε4携带者的内侧颞叶(MTL)体积较小,并且MTL体积介导了ApOE基因型与日常记忆表现之间的关系。这些日常记忆任务测量的是在临床诊断痴呆症之前可能发生的基因决定的认知衰退。此外,这些任务易于实施,可能是一种有用的临床工具,可用于识别可能有MTL萎缩风险以及进一步认知衰退风险的ε4携带者,而MTL萎缩和进一步认知衰退是阿尔茨海默病最早阶段的常见特征。