Wilson Robert S, Boyle Patricia A, Yu Lei, Barnes Lisa L, Sytsma Joel, Buchman Aron S, Bennett David A, Schneider Julie A
From Rush Alzheimer's Disease Center and Departments of Neurological Sciences (R.S.W., L.Y., L.L.B., A.S.B., D.A.B., J.A.S.), Behavioral Sciences (R.S.W., P.A.B., L.L.B.), and Pathology (J.A.S.), Rush University Medical Center, Chicago, IL.
Neurology. 2015 Sep 15;85(11):984-91. doi: 10.1212/WNL.0000000000001935. Epub 2015 Aug 26.
To characterize the natural history and neuropathologic basis of unawareness of memory loss in late-life dementia.
Analyses are based on 2,092 older persons from 3 longitudinal clinical-pathologic cohort studies who had no memory or cognitive impairment at baseline. Annual evaluations included clinical classification of dementia plus self-rating and performance testing of memory. At death, there was a uniform neuropathologic examination to quantify 7 dementia-related pathologies.
In the full group, memory ratings were modestly correlated with memory performance (intercepts r = 0.26, p < 0.001; slopes r = 0.23, p < 001) and so we regressed each person's memory performance on their memory ratings, and the residuals provided longitudinal indicators of memory awareness. In a subset of 239 persons who developed dementia, episodic memory awareness was stable until a mean of 2.6 years before dementia onset (95% credible interval -2.7, -1.6); thereafter, memory awareness declined rapidly (mean annual change -0.32, 95% credible interval -0.37, -0.28). Older age at baseline was associated with later onset of memory unawareness. In a subset of 385 persons who died and underwent neuropathologic examination, transactive response DNA-binding protein 43 (TDP-43) pathology, tau tangles, and gross cerebral infarcts were related to decline in memory awareness. In the absence of these pathologies, no decline in memory awareness was evident. Results were similar in subgroups with and without dementia.
Awareness of memory impairment typically begins to decline about 2-3 years before dementia onset and is associated with postmortem evidence of TDP-43 pathology, tangles, and gross cerebral infarcts.
描述老年痴呆症患者记忆丧失无意识状态的自然病程及神经病理学基础。
分析基于3项纵向临床病理队列研究中的2092名老年人,这些老年人在基线时无记忆或认知障碍。年度评估包括痴呆症的临床分类以及记忆的自评和表现测试。死亡时,进行统一的神经病理学检查以量化7种与痴呆症相关的病理学特征。
在整个研究组中,记忆评分与记忆表现呈适度相关(截距r = 0.26,p < 0.001;斜率r = 0.23,p < 0.001),因此我们将每个人的记忆表现对其记忆评分进行回归分析,残差提供了记忆意识的纵向指标。在239名患痴呆症的亚组中,情景记忆意识在痴呆症发病前平均2.6年保持稳定(95%可信区间-2.7,-1.6);此后,记忆意识迅速下降(平均每年变化-0.32,95%可信区间-0.37,-0.28)。基线时年龄较大与记忆无意识状态的发病较晚有关。在385名死亡并接受神经病理学检查的亚组中,反应性DNA结合蛋白43(TDP-43)病理学、tau缠结和大面积脑梗死与记忆意识下降有关。在没有这些病理学特征的情况下,记忆意识没有明显下降。在有和没有痴呆症的亚组中结果相似。
记忆障碍的意识通常在痴呆症发病前约2 - 3年开始下降,并且与死后TDP-43病理学、缠结和大面积脑梗死的证据有关。