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阿尔茨海默病临床前情景记忆缺陷的稳定性。

Stability of the preclinical episodic memory deficit in Alzheimer's disease.

作者信息

Bäckman L, Small B J, Fratiglioni L

机构信息

Department of Psychology, Uppsala University, Uppsala, Sweden.

出版信息

Brain. 2001 Jan;124(Pt 1):96-102. doi: 10.1093/brain/124.1.96.

Abstract

We sought to determine the course of the preclinical episodic memory deficit in Alzheimer's disease. Using data from a population-based study, we compared persons who developed Alzheimer's disease n = 15) with persons who were non-demented n = 105) 6 and 3 years prior to the diagnosis of dementia. Participants were tested on tasks assessing episodic memory free recall and recognition of words) and short-term memory digit span). The incident Alzheimer's disease cases performed more poorly than their non-demented counterparts both 3 and 6 years before diagnosis on recall and recognition. There were no group differences in either forward or backward digit span. The selective impairment of episodic memory before the diagnosis of Alzheimer's disease is consistent with the view that early changes in the hippocampal complex play an important role in the memory deficit in preclinical Alzheimer's disease. On both preclinical measurement occasions, recall and recognition made independent contributions to group classification in logistic regression analyses. However, there was no evidence for accelerated decline of episodic memory in the incident Alzheimer's disease group from 6 to 3 years before diagnosis. These results indicate that Alzheimer's disease is characterized by a long preclinical period during which episodic memory deficits are detectable. The magnitude of these deficits appears to be quite stable, at least up to 3 years before diagnosis. This may reflect the fact that those biological events that eventually result in clinically diagnosed Alzheimer's disease e.g. the appearance of amyloid plaques and neurofibrillary tangles) accumulate at a relatively slow rate.

摘要

我们试图确定阿尔茨海默病临床前期情景记忆缺陷的病程。利用一项基于人群的研究数据,我们比较了在痴呆症诊断前6年和3年时患阿尔茨海默病的人(n = 15)与未患痴呆症的人(n = 105)。参与者接受了评估情景记忆(自由回忆和单词识别)和短期记忆(数字广度)的任务测试。在诊断前3年和6年,新发阿尔茨海默病病例在回忆和识别方面的表现均比未患痴呆症的对照者差。在顺背或倒背数字广度方面,两组没有差异。阿尔茨海默病诊断前情景记忆的选择性损害与海马复合体早期变化在临床前期阿尔茨海默病记忆缺陷中起重要作用的观点一致。在两次临床前期测量时,回忆和识别在逻辑回归分析中对组分类均有独立贡献。然而,没有证据表明新发阿尔茨海默病组在诊断前6年到3年期间情景记忆加速衰退。这些结果表明,阿尔茨海默病的特征是有一个漫长的临床前期,在此期间情景记忆缺陷是可检测到的。这些缺陷的程度似乎相当稳定,至少在诊断前3年是这样。这可能反映了最终导致临床诊断为阿尔茨海默病的那些生物学事件(例如淀粉样斑块和神经原纤维缠结的出现)以相对缓慢的速度积累这一事实。

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