Perry R J, Hodges J R
University of Cambridge Neurology Unit, Addenbrooke's Hospital, Cambridge, UK.
Dement Geriatr Cogn Disord. 2000 Nov-Dec;11(6):342-9. doi: 10.1159/000017264.
Currently used criteria for the diagnosis of probable Alzheimer's disease requires the presence of cognitive deficit in addition to loss of episodic memory. The recent developments in drug treatments for Alzheimer's disease have highlighted the importance of early diagnosis and the need to characterise the cognitive profile of the earliest stages of the disease. We set out to examine the pattern of decline in terms of individual cognitive domains in non-demented subjects with clinically isolated progressive amnesia which we have termed questionable Alzheimer's disease. Twelve subjects who fulfill criteria for a clinical diagnosis of possible Alzheimer's disease by NINCDS-ADRDA criteria were compared to 20 age-matched controls in a longitudinal study. All subjects had MMSE scores of 24 or greater at entry to study. Individual profiles were measured by impairment in the cognitive domains of episodic memory, attention, semantic memory, visuospatial function and auditory verbal short-term (working) memory. Even after subjects were given this intensive neuropsychological battery, 8 of 12 subjects had episodic memory deficits only. Within 12 months just 3 patients were only amnesic and the other patients with pure amnesia at year 1 developed either semantic or attentional deficits. Impairment in both these cognitive domains preceded impairment in visuospatial function and auditory-verbal short-term memory. Our findings are consistent with the pattern of cognitive impairment in Alzheimer's disease increasing in accordance with neuropathological correlates of cognitive function with amnesia linked to the initial medial temporal pathology before the pattern of spread affects critical neural substrates for attention and semantic memory. Tests of selective attention and semantic memory appear to be the most sensitive markers of decline beyond the amnestic phase of early Alzheimer's disease.
目前用于诊断可能的阿尔茨海默病的标准,除了情景记忆丧失外,还需要存在认知缺陷。阿尔茨海默病药物治疗的最新进展凸显了早期诊断的重要性,以及刻画该疾病最早阶段认知特征的必要性。我们着手研究临床上孤立性进行性失忆的非痴呆受试者(我们称之为可疑阿尔茨海默病)在各个认知领域的衰退模式。在一项纵向研究中,将12名符合NINCDS - ADRDA标准临床诊断为可能阿尔茨海默病的受试者与20名年龄匹配的对照组进行比较。所有受试者在进入研究时的简易精神状态检查表(MMSE)得分均为24分或更高。通过情景记忆、注意力、语义记忆、视觉空间功能和听觉言语短期(工作)记忆等认知领域的损伤来测量个体特征。即使在对受试者进行了这种全面的神经心理学测试后,12名受试者中仍有8名仅存在情景记忆缺陷。在12个月内,只有3名患者仅患有失忆症,而在第1年患有单纯失忆症的其他患者出现了语义或注意力缺陷。这两个认知领域的损伤先于视觉空间功能和听觉言语短期记忆的损伤。我们的研究结果与阿尔茨海默病认知障碍模式一致,即认知障碍随着认知功能的神经病理学相关性增加,失忆与最初的内侧颞叶病理学相关,在扩散模式影响注意力和语义记忆的关键神经基质之前。选择性注意力和语义记忆测试似乎是早期阿尔茨海默病失忆阶段之后衰退的最敏感指标。