Raykov Petar P, Daly Jessica, Fisher Simon E, Eising Else, Geerligs Linda, Bird Chris M
Medical Research Council Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.
School of Psychology, University of Sussex, Falmer, UK.
Brain Neurosci Adv. 2025 Jan 31;9:23982128251314577. doi: 10.1177/23982128251314577. eCollection 2025 Jan-Dec.
Apolipoprotein E ε4 is a major genetic risk factor for Alzheimer's disease, and some apolipoprotein E ε4 carriers show Alzheimer's disease-related neuropathology many years before cognitive changes are apparent. Therefore, studying healthy apolipoprotein E genotyped individuals offers an opportunity to investigate the earliest changes in brain measures that may signal the presence of disease-related processes. For example, subtle changes in functional magnetic resonance imaging functional connectivity, particularly within the default mode network, have been described when comparing healthy ε4 carriers to ε3 carriers. Similarly, very mild impairments of episodic memory have also been documented in healthy apolipoprotein E ε4 carriers. Here, we use a naturalistic activity (movie watching), and a marker of episodic memory encoding (transient changes in functional magnetic resonance imaging activity and functional connectivity around so-called 'event boundaries'), to investigate potential phenotype differences associated with the apolipoprotein E ε4 genotype in a large sample of healthy adults. Using Bayes factor analyses, we found strong evidence against existence of differences associated with apolipoprotein E allelic status. Similarly, we did not find apolipoprotein E-associated differences when we ran exploratory analyses examining: functional system segregation across the whole brain, and connectivity within the default mode network. We conclude that apolipoprotein E genotype has little or no effect on how ongoing experiences are processed in healthy adults. The mild phenotype differences observed in some studies may reflect early effects of Alzheimer's disease-related pathology in apolipoprotein E ε4 carriers.
载脂蛋白Eε4是阿尔茨海默病的主要遗传风险因素,一些载脂蛋白Eε4携带者在认知变化明显出现之前许多年就表现出与阿尔茨海默病相关的神经病理学特征。因此,研究健康的载脂蛋白E基因分型个体为调查大脑测量中可能预示疾病相关过程存在的最早变化提供了机会。例如,在将健康的ε4携带者与ε3携带者进行比较时,已经描述了功能磁共振成像功能连接的细微变化,特别是在默认模式网络内。同样,在健康的载脂蛋白Eε4携带者中也记录到了情节记忆的非常轻微的损伤。在这里,我们使用一种自然活动(观看电影)和一种情节记忆编码标记(在所谓的“事件边界”周围功能磁共振成像活动和功能连接的瞬时变化),来研究一大群健康成年人中与载脂蛋白Eε4基因型相关的潜在表型差异。使用贝叶斯因子分析,我们发现有力证据反对存在与载脂蛋白E等位基因状态相关的差异。同样,当我们进行探索性分析时,在检查全脑功能系统分离和默认模式网络内的连接性时,我们也没有发现与载脂蛋白E相关的差异。我们得出结论,载脂蛋白E基因型对健康成年人处理正在进行的经历的方式几乎没有影响。在一些研究中观察到的轻微表型差异可能反映了载脂蛋白Eε4携带者中阿尔茨海默病相关病理学的早期影响。