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即使在考虑神经病理学因素之后,痴呆仍与内侧颞叶萎缩有关。

Dementia is associated with medial temporal atrophy even after accounting for neuropathologies.

作者信息

Woodworth Davis C, Sheikh-Bahaei Nasim, Scambray Kiana A, Phelan Michael J, Perez-Rosendahl Mari, Corrada María M, Kawas Claudia H, Sajjadi Seyed Ahmad

机构信息

Department of Neurology, University of California, Irvine, CA, USA.

Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA, USA.

出版信息

Brain Commun. 2022 Mar 7;4(2):fcac052. doi: 10.1093/braincomms/fcac052. eCollection 2022.

Abstract

Brain atrophy is associated with degenerative neuropathologies and the clinical status of dementia. Whether dementia is associated with atrophy independent of neuropathologies is not known. In this study, we examined the pattern of atrophy associated with dementia while accounting for the most common dementia-related neuropathologies. We used data from National Alzheimer's Coordinating Center ( = 129) and Alzheimer's Disease Neuroimaging Initiative ( = 47) participants with suitable 3D-Tw MRI and autopsy data. We determined dementia status at the visit closest to MRI. We examined the following dichotomized neuropathological variables: Alzheimer's disease neuropathology, hippocampal sclerosis, Lewy bodies, cerebral amyloid angiopathy and atherosclerosis. Voxel-based morphometry identified areas associated with dementia after accounting for neuropathologies. Identified regions of interest were further analysed. We used multiple linear regression models adjusted for neuropathologies and demographic variables. We also examined models with dementia and Clinical Dementia Rating sum of the boxes as the outcome and explored the potential mediating effect of medial temporal lobe structure volumes on the relationship between pathology and cognition. We found strong associations for dementia with volumes of the hippocampus, amygdala and parahippocampus (semi-partial correlations ≥ 0.28, < 0.0001 for all regions in National Alzheimer's Coordinating Center; semi-partial correlations ≥ 0.35, ≤ 0.01 for hippocampus and parahippocampus in Alzheimer's Disease Neuroimaging Initiative). Dementia status accounted for more unique variance in atrophy in these structures (∼8%) compared with neuropathological variables; the only exception was hippocampal sclerosis which accounted for more variance in hippocampal atrophy (10%). We also found that the volumes of the medial temporal lobe structures contributed towards explaining the variance in Clinical Dementia Rating sum of the boxes (ranging from 5% to 9%) independent of neuropathologies and partially mediated the association between Alzheimer's disease neuropathology and cognition. Even after accounting for the most common neuropathologies, dementia still had among the strongest associations with atrophy of medial temporal lobe structures. This suggests that atrophy of the medial temporal lobe is most related to the clinical status of dementia rather than Alzheimer's disease or other neuropathologies, with the potential exception of hippocampal sclerosis.

摘要

脑萎缩与退行性神经病理学及痴呆的临床状态相关。痴呆是否独立于神经病理学而与萎缩相关尚不清楚。在本研究中,我们在考虑最常见的痴呆相关神经病理学的同时,研究了与痴呆相关的萎缩模式。我们使用了来自国家阿尔茨海默病协调中心(n = 129)和阿尔茨海默病神经影像倡议组织(n = 47)的参与者的数据,这些参与者具有合适的三维双回波磁共振成像(3D-Tw MRI)和尸检数据。我们在最接近磁共振成像的访视时确定痴呆状态。我们检查了以下二分法神经病理学变量:阿尔茨海默病神经病理学、海马硬化、路易体、脑淀粉样血管病和动脉粥样硬化。基于体素的形态测量法在考虑神经病理学因素后确定了与痴呆相关的区域。对确定的感兴趣区域进行了进一步分析。我们使用了针对神经病理学和人口统计学变量进行调整的多元线性回归模型。我们还检查了以痴呆和临床痴呆评定量表总分作为结果的模型,并探讨了内侧颞叶结构体积对病理学与认知之间关系的潜在中介作用。我们发现痴呆与海马、杏仁核和海马旁回的体积有很强的相关性(国家阿尔茨海默病协调中心所有区域的半偏相关系数≥0.28,P < 0.0001;阿尔茨海默病神经影像倡议组织中海马和海马旁回的半偏相关系数≥0.35,P≤0.01)。与神经病理学变量相比,痴呆状态在这些结构的萎缩中占更多独特的方差(约8%);唯一的例外是海马硬化,其在海马萎缩中占更多方差(10%)。我们还发现,内侧颞叶结构的体积有助于解释临床痴呆评定量表总分的方差(范围从5%到9%),独立于神经病理学因素,并且部分介导了阿尔茨海默病神经病理学与认知之间的关联。即使在考虑了最常见的神经病理学因素之后,痴呆与内侧颞叶结构萎缩之间的关联仍然是最强的之一。这表明内侧颞叶萎缩与痴呆的临床状态最为相关,而不是与阿尔茨海默病或其他神经病理学相关,海马硬化可能是个例外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccdc/8952251/d289854d03b4/fcac052ga1.jpg

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