Measurement of thirteen biological markers in CSF of patients with Alzheimer's disease and other dementias

被引:138
作者
Blasko, I
Lederer, W
Oberbauer, H
Walch, T
Kemmler, G
Hinterhuber, H
Marksteiner, J
Humpel, C
机构
[1] Innsbruck Med Univ, Dept Psychiat, Lab Expt Alzheimers Res, AT-6020 Innsbruck, Austria
[2] Innsbruck Med Univ, Dept Anaesthesiol & Crit Care Med, AT-6020 Innsbruck, Austria
关键词
cerebrospinal fluid beta-amyloid; total tau protein; phospho-tau181; nerve growth factor; monocyte chemoattractant protein 1;
D O I
10.1159/000089137
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Cerebrospinal fluid (CSF) biological markers may be of valuable help in the diagnosis of dementia. The aim of the present study was to evaluate CSF levels of 13 potential biomarkers in patients with Alzheimer's disease (AD), frontotemporal lobe dementia, alcohol dementia, major depression and control patients without any neuropsychiatric disease. The study was performed using beta-amyloid 1-42 (A beta 42), total tau and phosphorylated tau-181 (P-tau181) as core markers. The ratio P-tau181/A beta 42 could significantly distinguish AD patients from all other diagnostic subgroups. CSF levels of 5 growth factors (HGF, GDNF, VEGF, BDNF, FGF-2) and 3 cytokines/chemokines (TNF-alpha, TGF-beta(1), MIP-1 alpha) did not significantly differentiate between the studied groups. However, depending on the degree of neurodegeneration (as expressed by the ratio P-tau181/A beta 42), patients with AD displayed significantly increased CSF levels of nerve growth factor (NGF) as compared to healthy controls. CSF levels of monocyte chemoattractant protein 1 (MCP-1) were found to be significantly increased with age in all groups but did not distinguish AD patients from healthy controls. The results confirmed the suitability of the ratio P-tau181/A beta 42 for the diagnosis of AD, while CSF levels of NGF and MCP-1 are less specific and reliable for AD. It is suggested that the increase in NGF depends on the extent of neurodegeneration of the AD type and the increase in MCP-1 on age. Copyright (C) 2006 S. Karger AG, Basel.
引用
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页码:9 / 15
页数:7
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