From the Mesulam Center for Cognitive Neurology and Alzheimer's Disease (M.-M.M., C.C., E.H.B., Q.M., M.E.F., T.G., J.S., C.G., H.Z., S.W., E.J.R.), Department of Preventive Medicine (A.K., H.Z.), Department of Pathology (E.H.B., Q.M., M.E.F.), and Department of Psychiatry and Behavioral Sciences (T.G., S.W., E.J.R.), Northwestern University Feinberg School of Medicine, Chicago. IL.
Neurology. 2021 Feb 9;96(6):e916-e925. doi: 10.1212/WNL.0000000000011397. Epub 2021 Jan 13.
To determine whether memory is preserved longitudinally in primary progressive aphasia (PPA) associated with Alzheimer disease (AD) and to identify potential factors that maintain memory despite underlying neurofibrillary degeneration of mediotemporal memory areas.
Longitudinal memory assessment was done in 17 patients with PPA with autopsy or biomarker evidence of AD (PPA-AD) and 14 patients with amnestic dementia of the Alzheimer type with AD at autopsy (DAT-AD).
In PPA-AD, episodic memory, tested with nonverbal items, was preserved at the initial testing and showed no decline at retesting 2.35 ± 0.78 years later, at which time symptoms had been present for 6.26 ± 2.21 years. In contrast, language functions declined significantly during the same period. In DAT-AD, both verbal memory and language declined with equal severity. Although imaging showed asymmetric left-sided mediotemporal atrophy in PPA-AD, autopsy revealed bilateral hippocampo-entorhinal neurofibrillary degeneration at Braak stages V and VI. Compared to DAT-AD, however, the PPA-AD group had lower incidence of ε4 and of mediotemporal TAR DNA-binding protein 43 (TDP-43) pathology.
Memory preservation in PPA is not just an incidental finding at onset but a core feature that persists for years despite the hippocampo-entorhinal AD neuropathology that is as severe as that of DAT-AD. Asymmetry of mediotemporal atrophy and a lesser impact of ε4 and of TDP-43 on the integrity of memory circuitry may constitute some of the factors underlying this resilience. Our results also suggest that current controversies on memory in PPA-AD reflect inconsistencies in the diagnosis of logopenic PPA, the clinical variant most frequently associated with AD.
NCT00537004 and NCT03371706.
确定是否在与阿尔茨海默病(AD)相关的原发性进行性失语症(PPA)中纵向保留记忆,并确定尽管存在中颞叶记忆区的神经纤维变性,但仍能维持记忆的潜在因素。
对 17 例经尸检或生物标志物证实有 AD 的 PPA 患者(PPA-AD)和 14 例 AD 经尸检证实的遗忘型阿尔茨海默病性痴呆患者(DAT-AD)进行纵向记忆评估。
在 PPA-AD 中,用非言语项目测试的情景记忆在初始测试时保持不变,在 2.35 ± 0.78 年后的重新测试中没有下降,此时症状已经存在 6.26 ± 2.21 年。相比之下,语言功能在同一时期显著下降。在 DAT-AD 中,言语记忆和语言能力都以同样的严重程度下降。尽管影像学显示 PPA-AD 左侧中颞叶不对称性萎缩,但尸检显示双侧海马-内嗅皮质神经纤维缠结处于 Braak 阶段 V 和 VI。然而,与 DAT-AD 相比,PPA-AD 组 ε4 和中颞叶 TAR DNA 结合蛋白 43(TDP-43)病理的发生率较低。
PPA 中的记忆保留不仅仅是发病时的偶然发现,而是一种核心特征,尽管存在与 DAT-AD 一样严重的海马-内嗅皮质 AD 神经病理学,但可以持续多年。中颞叶萎缩的不对称性以及 ε4 和 TDP-43 对记忆回路完整性的影响较小,可能构成这种弹性的部分因素。我们的结果还表明,目前关于 PPA-AD 中记忆的争议反映了在诊断最常与 AD 相关的流利型 PPA 时存在不一致性。
临床试验.gov 标识符:NCT00537004 和 NCT03371706。