Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

被引:265
作者
Otto, M
Wiltfang, J
Tumani, H
Zerr, I
Lantsch, M
Kornhuber, J
Weber, T
Kretzschmar, HA
Poser, S
机构
[1] UNIV GOTTINGEN, DEPT PSYCHIAT, D-37075 GOTTINGEN, GERMANY
[2] UNIV GOTTINGEN, DEPT NEUROPATHOL, D-37075 GOTTINGEN, GERMANY
[3] MARIEN HOSP, DEPT NEUROL, D-22087 HAMBURG, GERMANY
关键词
Creutzfeldt-Jakob disease; tau-protein; cerebrospinal fluid; ELISA; dementia; Alzheimer's disease;
D O I
10.1016/S0304-3940(97)00215-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Creutzfeldt-Jakob disease (CJD) is a rare, fatal, neurodegenerative disease caused by a transmissible agent designated as proteinaceous infectious agent (prion). Searching for biochemical markers of CJD, we analysed cerebrospinal fluid (CSF) samples of 53 patients for tau-protein using an enzyme linked immunoassay (ELISA). In a group of 21 patients with definite CJD seen in the German case control study for CJD, tau-protein concentrations in CSF were significantly higher than in two control-groups of patients with other diseases (median 13153 pg/ml, range 1533-27648 pg/ml; P = 0.0001). One control group comprised 19 patients who were seen in the same study and were diagnosed as having other dementing diseases (tau concentration: median 558 pg/ml, range 233-1769 pg/ml). The second control group comprised 13 patients from our hospital with no dementing disease (tau concentration: median 296 pg/ml, range 109-640 pg/ml). We conclude that determination of tau protein levels in CSF is a useful marker for laboratory diagnosis of CJD. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:210 / 212
页数:3
相关论文
共 21 条
[1]   INCIDENCE OF CREUTZFELDT-JAKOB-DISEASE IN EUROPE IN 1993 [J].
ALPEROVITCH, A ;
BROWN, P ;
WEBER, T ;
POCCHIARI, M ;
HOFMAN, A ;
WILL, R .
LANCET, 1994, 343 (8902) :918-918
[2]   TAU IN CEREBROSPINAL-FLUID - A POTENTIAL DIAGNOSTIC MARKER IN ALZHEIMERS-DISEASE [J].
ARAI, H ;
TERAJIMA, M ;
MIURA, L ;
HIGUCHI, S ;
MURAMATSU, T ;
MACHIDA, N ;
SEIKI, H ;
TAKASE, S ;
CLARK, CM ;
LEE, VMY ;
TROJANOWSKI, JQ ;
SASAKI, H .
ANNALS OF NEUROLOGY, 1995, 38 (04) :649-652
[3]   HUMAN SPONGIFORM ENCEPHALOPATHY - THE NATIONAL-INSTITUTES-OF-HEALTH SERIES OF 300 CASES OF EXPERIMENTALLY TRANSMITTED DISEASE [J].
BROWN, P ;
GIBBS, CJ ;
RODGERSJOHNSON, P ;
ASHER, DM ;
SULIMA, MP ;
BACOTE, A ;
GOLDFARB, LG ;
GAJDUSEK, DC .
ANNALS OF NEUROLOGY, 1994, 35 (05) :513-529
[4]   Hyperphosphorylated tau proteins differentiate corticobasal degeneration and Pick's disease [J].
BueeScherrer, V ;
Hof, PR ;
Buee, L ;
Leveugle, B ;
Vermersch, P ;
Perl, DP ;
Olanow, CW ;
Delacourte, A .
ACTA NEUROPATHOLOGICA, 1996, 91 (04) :351-359
[5]   ALZHEIMERS-DISEASE AND CREUTZFELDT-JAKOB-DISEASE - OVERLAP OF PATHOGENIC MECHANISMS [J].
DEARMOND, SJ .
CURRENT OPINION IN NEUROLOGY, 1993, 6 (06) :872-881
[6]   The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies [J].
Hsich, G ;
Kinney, K ;
Gibbs, CJ ;
Lee, KH ;
Harrington, MG .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (13) :924-930
[7]   INCREASED CEREBROSPINAL-FLUID TAU IN PATIENTS WITH ALZHEIMERS-DISEASE [J].
JENSEN, M ;
BASUN, H ;
LANNFELT, L .
NEUROSCIENCE LETTERS, 1995, 186 (2-3) :189-191
[8]   Diagnostic criteria for sporadic Creutzfeldt-Jakob disease [J].
Kretzschmar, HA ;
Ironside, JW ;
DeArmond, SJ ;
Tateishi, J .
ARCHIVES OF NEUROLOGY, 1996, 53 (09) :913-920
[9]   CREUTZFELDT-JAKOB DISEASE - PATTERNS OF WORLDWIDE OCCURRENCE AND THE SIGNIFICANCE OF FAMILIAL AND SPORADIC CLUSTERING [J].
MASTERS, CL ;
HARRIS, JO ;
GAJDUSEK, DC ;
GIBBS, CJ ;
BERNOULLI, C ;
ASHER, DM .
ANNALS OF NEUROLOGY, 1979, 5 (02) :177-188
[10]  
OTO M, 1996, AKTUEL NEUROL, V23, P71