Use of cerebrospinal fluid biomarkers in diagnosis of dementia across Europe

被引:56
作者
Hort, J. [1 ]
Bartos, A. [2 ,3 ]
Pirttila, T. [4 ]
Scheltens, P. [5 ]
机构
[1] Charles Univ Prague, Memory Disorders Clin, Dept Neurol, Fac Med 2,Univ Hosp Motol, Prague, Czech Republic
[2] Charles Univ Prague, Fac Med 3, Dept Neurol, Univ Hosp Kralovske Vinohrady, Prague, Czech Republic
[3] Prague Psychiat Ctr, Alzheimer Dis Ctr, Prague, Czech Republic
[4] Kuopio Univ Hosp, Dept Neurol, SF-70210 Kuopio, Finland
[5] Vrije Univ Amsterdam Med Ctr, Dept Neurol, Alzheimer Ctr, Amsterdam, Netherlands
关键词
Alzheimer's disease; beta-amyloid; biomarker; cerebrospinal fluid; phosphorylated tau; total tau; MILD COGNITIVE IMPAIRMENT; ALZHEIMERS-DISEASE; PHOSPHORYLATED TAU; CSF BIOMARKERS; PREDICTION; A-BETA-42; CRITERIA; ADULTS;
D O I
10.1111/j.1468-1331.2009.02753.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose: Cerebrospinal fluid (CSF) biomarkers have been reported to be useful in dementia diagnosis. Not much is known about their use in clinical practice in Europe. Methods: We analyzed data from a survey on the use of CSF biomarkers in the diagnosis of dementia across Europe using a questionnaire which was filled out by representatives of the 25 member countries of the European Federation of Neurological Societies (EFNS). Results: Cerebrospinal fluid beta-amyloid, total tau, and phosphorylated tau proteins are frequently evaluated in the majority of the countries (in 18 out of 23 countries). No major technical or ethical issues were found that would hamper the procedure's ability to become routine in early and differential diagnostics of Alzheimer's disease. Cut-off values for beta-amyloid (median 500, range 300-849 pg/ml), total tau (367; 195-450 pg/ml) and phosphorylated tau (60; 40-85 pg/ml) varied considerably amongst countries and even within every country. Conclusions: Cerebrospinal fluid analysis of beta-amyloid, tau, and phosphorylated tau is frequently used in Europe. However, the use of various cut off values seriously hampers comparability and yields a potential threat to an interpretation and balanced use in clinical practice. We recommend that each laboratory establishes normative data and that multi-centered studies should be organized to explore the reasons for any differences.
引用
收藏
页码:90 / 96
页数:7
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