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组织学诊断为阿尔茨海默病的脑脊液中乙酰胆碱酯酶的异常分子形式。

Anomalous molecular form of acetylcholinesterase in cerebrospinal fluid in histologically diagnosed Alzheimer's disease.

作者信息

Navaratnam D S, Priddle J D, McDonald B, Esiri M M, Robinson J R, Smith A D

机构信息

University Department of Pharmacology, Oxford, UK.

出版信息

Lancet. 1991 Feb 23;337(8739):447-50. doi: 10.1016/0140-6736(91)93391-l.

Abstract

The possibility that the different molecular forms of acetylcholinesterase (AChE) in cerebrospinal fluid (CSF) which can be revealed by isoelectric focusing may reflect changes in AChE in pathologically affected neurons in Alzheimer's disease was tested in a retrospective study. CSF samples obtained at necropsy from 33 patients with clinically diagnosed dementia, 9 with possible dementia, and 19 without a diagnosis of dementia were examined by isoelectric focusing. An additional band indicating an anomalous molecular form of AChE was present in CSF from 19 of 23 patients with a histological diagnosis of Alzheimer's disease and no other central nervous system disorder but in none of the 19 non-demented patients (without a histological diagnosis of Alzheimer's disease). The band was also present in 2 of 8 patients with histologically defined Alzheimer's disease plus other neurological disorders and in 4 of 8 patients with possible dementia who did not meet histopathological criteria for Alzheimer's disease. The absence of the anomalous form of AChE from the CSF of non-demented patients and its presence in the CSF of the majority of patients with Alzheimer's disease has implications for our understanding of the biological basis of the disease and might form the basis of an antemortem diagnostic test.

摘要

在一项回顾性研究中,对脑脊液(CSF)中可通过等电聚焦显示的不同分子形式的乙酰胆碱酯酶(AChE)是否可能反映阿尔茨海默病中病理受影响神经元中AChE的变化进行了测试。通过等电聚焦检查了33例临床诊断为痴呆的患者、9例可能患有痴呆的患者以及19例未诊断为痴呆的患者尸检时获得的脑脊液样本。在23例经组织学诊断为阿尔茨海默病且无其他中枢神经系统疾病的患者中,有19例患者的脑脊液中出现了一条额外的带,表明存在AChE的异常分子形式,而19例非痴呆患者(无阿尔茨海默病组织学诊断)中均未出现。在8例经组织学定义为阿尔茨海默病加其他神经系统疾病的患者中,有2例出现了这条带,在8例可能患有痴呆但不符合阿尔茨海默病组织病理学标准的患者中,有4例出现了这条带。非痴呆患者脑脊液中不存在AChE的异常形式,而大多数阿尔茨海默病患者脑脊液中存在该形式,这对我们理解该疾病的生物学基础具有启示意义,并且可能构成生前诊断测试的基础。

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