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临床前阿尔茨海默病的“终末期”神经原纤维缠结病理:事实还是虚构?

"End-stage" neurofibrillary tangle pathology in preclinical Alzheimer's disease: fact or fiction?

机构信息

Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY 40536-0230, USA.

出版信息

J Alzheimers Dis. 2011;25(3):445-53. doi: 10.3233/JAD-2011-101980.

Abstract

Among individuals who were cognitively intact before death, autopsies may reveal some Alzheimer's disease-type pathology. The presence of end-stage pathology in cognitively intact persons would support the hypothesis that pathological markers are epiphenomena. We assessed advanced neurofibrillary (Braak stages V and VI) pathology focusing on nondemented individuals. Data from the National Alzheimer's Coordinating Center database (n = 4,690 included initially) and from the Nun Study (n = 526 included initially) were analyzed, with antemortem information about global cognition and careful postmortem studies available from each case. Global cognition (final Mini-Mental State Examination scores (MMSE) and clinical 'dementia' status) was correlated with neuropathology, including the severity of neurofibrillary pathology (Braak stages and neurofibrillary tangle counts in cerebral neocortex). Analyses support three major findings: 1. Braak stage V cases and Braak VI cases are significantly different from each other in terms of associated antemortem cognition; 2. There is an appreciable range of pathology within the category of Braak stage VI based on tangle counts such that brains with the most neurofibrillary tangles in neocortex always had profound antemortem cognitive impairment; and 3. There was no nondemented case with final MMSE score of 30 within a year of life and Braak stage VI pathology. It may be inappropriate to combine Braak stages V and VI cases, particularly in patients with early cognitive dysfunction, since the two pathological stages appear to differ dramatically in terms of both pathological severity and antemortem cognitive status. There is no documented example of truly end-stage neurofibrillary pathology coexisting with intact cognition.

摘要

在死亡前认知正常的个体中,尸检可能会发现一些阿尔茨海默病类型的病理学改变。认知正常的个体存在终末期病理学改变,将支持病理性标志物是伴随现象的假说。我们评估了聚焦于认知正常个体的高级神经纤维(Braak 阶段 V 和 VI)病理学。分析了来自国家阿尔茨海默病协调中心数据库(最初纳入 4690 例)和修女研究(最初纳入 526 例)的数据,每个病例均有生前关于整体认知的信息和仔细的死后研究。整体认知(最终的简易精神状态检查评分(MMSE)和临床“痴呆”状态)与神经病理学相关,包括神经纤维病理学的严重程度(Braak 阶段和大脑新皮质中的神经原纤维缠结计数)。分析结果支持以下三个主要发现:1. Braak 阶段 V 病例和 Braak 阶段 VI 病例在与生前认知相关方面存在显著差异;2. 根据缠结计数,Braak 阶段 VI 类别内存在相当大的病理学范围,以至于新皮质中神经纤维缠结最多的大脑始终存在严重的生前认知障碍;3. 在一年内生命和 Braak 阶段 VI 病理学中,没有最终 MMSE 评分为 30 的认知正常病例。将 Braak 阶段 V 和 VI 病例合并在一起可能是不合适的,特别是在有早期认知功能障碍的患者中,因为这两个病理阶段在病理严重程度和生前认知状态方面似乎存在显著差异。没有记录到真正的终末期神经纤维病理学与认知正常共存的例子。

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