From the Departments of Neurological Sciences (R.S.W., J.Y., L.Y., S.E.L., A.W.C., J.A.S., D.A.B.), Behavioral Sciences (R.S.W., P.A.B.), and Pathology (J.A.S.), Rush University Medical Center, Rush Alzheimer's Disease Center, Chicago, IL.
Neurology. 2019 Feb 19;92(8):e831-e840. doi: 10.1212/WNL.0000000000006949. Epub 2019 Jan 23.
To assess whether neurodegenerative pathologies are differentially related to trajectories of change in different cognitive abilities.
At annual intervals for up to 21 years, 915 older participants in a longitudinal clinical-pathologic cohort study completed a battery of 15 tests from which previously established composite measures of episodic memory, semantic memory, working memory, and perceptual speed were derived. At death, they underwent a neuropathologic examination to quantify Alzheimer disease pathology, Lewy bodies, transactive response DNA-binding protein 43 (TDP-43) pathology, and hippocampal sclerosis plus multiple markers of cerebrovascular disease. Time-varying effect models were used to assess change over time in the relation of neuropathologic markers to cognitive trajectories.
Controlling for pathology, decline in perceptual speed was evident about 15 years before death; modest decline in semantic and working memory occurred later; and there was little change in episodic memory. Each neurodegenerative marker was associated with lower episodic memory function beginning about 10 to 16 years before death. As time before death decreased, Alzheimer disease pathology, Lewy bodies, and hippocampal sclerosis were associated with impairment in other cognitive domains but the association of TDP-43 pathology with cognition continued to be mainly confined to episodic memory.
The results suggest that episodic memory impairment is an early sign of multiple neurodegenerative conditions, which primarily differ in their associations with other cognitive systems.
评估神经退行性病变是否与不同认知能力变化轨迹存在差异关系。
在一项长达 21 年的纵向临床病理队列研究中,每年对 915 名年龄较大的参与者进行一次随访,他们完成了一整套 15 项测试,这些测试得出了先前建立的关于情景记忆、语义记忆、工作记忆和知觉速度的综合衡量标准。在死亡时,他们接受了神经病理学检查,以量化阿尔茨海默病病理、路易体、转导反应 DNA 结合蛋白 43(TDP-43)病理和海马硬化症及多种脑血管疾病标志物。采用时变效应模型评估神经病理标志物与认知轨迹随时间变化的关系。
控制病理学因素后,在死亡前约 15 年,知觉速度下降明显;语义记忆和工作记忆的衰退发生在稍后;情景记忆变化不大。每个神经退行性病变标志物与情景记忆功能下降有关,大约在死亡前 10 到 16 年开始。随着死亡前时间的减少,阿尔茨海默病病理、路易体和海马硬化症与其他认知领域的损伤有关,但 TDP-43 病理与认知的关联仍主要局限于情景记忆。
研究结果表明,情景记忆障碍是多种神经退行性疾病的早期迹象,这些疾病主要在与其他认知系统的关联方面存在差异。