Department of Psychology, University of Southern California, Los Angeles, CA, USA.
Davis School of Gerontology, University of Southern California, Los Angeles, CA, USA.
Brain Imaging Behav. 2021 Oct;15(5):2572-2582. doi: 10.1007/s11682-021-00459-y. Epub 2021 Mar 1.
Neuropathological research suggests the tau pathology of Alzheimer's disease may originate in brainstem nuclei, yet it remains unknown whether tau-mediated degeneration of brainstem nuclei influences cognitive impairment in prodromal Alzheimer's disease. The present study examined cognitive domains impacted in prodromal Alzheimer's disease and brainstem substructure volume in cognitively normal older adults (n = 814) and those with mild cognitive impairment (n = 542). Subsamples of cognitively normal (n = 112) and mild cognitive impairment (n = 202) also had cerebrospinal fluid Alzheimer's disease biomarker characterization. Region-of-interest and voxel-level analyses related whole brainstem, midbrain, pons, and locus coeruleus volumes to cognition with multiple linear regression models corrected for age, sex, education, apolipoprotein-ε4 carrier status, and MRI magnet strength. Within mild cognitive impairment participants, smaller midbrain and locus coeruleus volumes were significantly related to poorer performance on tests of attention and executive function, and the relationship between locus coeruleus volume and executive abilities remained significant in the mild cognitive impairment subsample with biomarker-confirmed Alzheimer's disease. A brainstem-masked voxel-wise regression further demonstrated an association between locus coeruleus volume and executive abilities. Brainstem volumes were not significantly related to memory processes. Study findings implicate midbrain and locus coeruleus volume in attention and executive deficits in mild cognitive impairment. Together with prior neuropathological studies, our data suggest a link between Alzheimer's disease-related degeneration of brainstem nuclei and cognitive deficits in prodromal Alzheimer's disease.
神经病理学研究表明,阿尔茨海默病的 tau 病理学可能起源于脑干核,但tau 介导的脑干核变性是否会影响前驱期阿尔茨海默病的认知障碍仍不清楚。本研究检查了前驱期阿尔茨海默病受影响的认知领域和认知正常的老年人(n=814)和轻度认知障碍(n=542)的脑干亚结构体积。认知正常的亚组(n=112)和轻度认知障碍的亚组(n=202)也进行了脑脊液阿尔茨海默病生物标志物特征分析。使用多元线性回归模型,对全脑干、中脑、脑桥和蓝斑体积与认知进行了区域兴趣和体素水平分析,模型校正了年龄、性别、教育程度、载脂蛋白 E4 携带状态和 MRI 磁场强度。在轻度认知障碍参与者中,较小的中脑和蓝斑体积与注意力和执行功能测试的表现较差显著相关,在轻度认知障碍亚组中,蓝斑体积与执行能力的关系仍然显著,并且该亚组中存在经生物标志物证实的阿尔茨海默病。基于脑干部位的体素回归进一步表明蓝斑体积与执行能力之间存在关联。脑干体积与记忆过程无显著相关性。研究结果表明,中脑和蓝斑体积与轻度认知障碍的注意力和执行功能缺陷有关。结合先前的神经病理学研究,我们的数据表明,阿尔茨海默病相关的脑干核变性与前驱期阿尔茨海默病的认知缺陷之间存在联系。