Wang Yan-Li, Sun Mengfan, Wang Fang-Ze, Wang Xiaohong, Jia Ziyan, Zhang Yuan, Li Runzhi, Jiang Jiwei, Wang Linlin, Li Wenyi, Sun Yongan, Chen Jinglong, Zhang Cuicui, Shi Baolin, Liu Jianjian, Liu Xiangrong, Xu Jun
Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Front Aging Neurosci. 2022 Jun 30;14:928925. doi: 10.3389/fnagi.2022.928925. eCollection 2022.
The ε4 allele of the apolipoprotein E (APOE) gene is a strong genetic risk factor for aging-related cognitive decline. However, the causal connection between ε4 alleles and cognition is not well understood. The objective of this study was to identify the roles of cerebral blood flow (CBF) in cognitive-related brain areas in mediating the associations of APOE with cognition.
The multiple linear regression analyses were conducted on 369 subjects (mean age of 68.8 years; 62.9% of women; 29.3% of APOE ε4 allele carriers). Causal mediation analyses with 5,000 bootstrapped iterations were conducted to explore the mediation effects.
APOE ε4 allele was negatively associated with cognition ( < 0.05) and CBF in the amygdala, hippocampus, middle temporal gyrus, posterior cingulate, and precuneus (all < 0.05). The effect of the APOE genotype on cognition was partly mediated by the above CBF (all < 0.05).
CBF partially mediates the potential links between APOE genotype and cognition. Overall, the APOE ε4 allele may lead to a dysregulation of the vascular structure and function with reduced cerebral perfusion, which in turn leads to cognitive impairment.
载脂蛋白E(APOE)基因的ε4等位基因是与衰老相关的认知衰退的一个强大遗传风险因素。然而,ε4等位基因与认知之间的因果联系尚未完全明确。本研究的目的是确定脑血流量(CBF)在认知相关脑区中介导APOE与认知关联中的作用。
对369名受试者(平均年龄68.8岁;62.9%为女性;29.3%为APOE ε4等位基因携带者)进行多元线性回归分析。进行5000次自抽样迭代的因果中介分析以探究中介效应。
APOE ε4等位基因与认知呈负相关(<0.05),且与杏仁核、海马体、颞中回、后扣带回和楔前叶的CBF呈负相关(均<0.05)。APOE基因型对认知的影响部分由上述CBF介导(均<0.05)。
CBF部分介导了APOE基因型与认知之间的潜在联系。总体而言,APOE ε4等位基因可能导致血管结构和功能失调,脑灌注减少,进而导致认知障碍。