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
    ALPEROVITCH, A
    BROWN, P
    WEBER, T
    POCCHIARI, M
    HOFMAN, A
    WILL, R
    [J]. LANCET, 1994, 343 (8902) : 918 - 918
  • [2] TAU IN CEREBROSPINAL-FLUID - A POTENTIAL DIAGNOSTIC MARKER IN ALZHEIMERS-DISEASE
    ARAI, H
    TERAJIMA, M
    MIURA, L
    HIGUCHI, S
    MURAMATSU, T
    MACHIDA, N
    SEIKI, H
    TAKASE, S
    CLARK, CM
    LEE, VMY
    TROJANOWSKI, JQ
    SASAKI, H
    [J]. 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
    BROWN, P
    GIBBS, CJ
    RODGERSJOHNSON, P
    ASHER, DM
    SULIMA, MP
    BACOTE, A
    GOLDFARB, LG
    GAJDUSEK, DC
    [J]. ANNALS OF NEUROLOGY, 1994, 35 (05) : 513 - 529
  • [4] Hyperphosphorylated tau proteins differentiate corticobasal degeneration and Pick's disease
    BueeScherrer, V
    Hof, PR
    Buee, L
    Leveugle, B
    Vermersch, P
    Perl, DP
    Olanow, CW
    Delacourte, A
    [J]. ACTA NEUROPATHOLOGICA, 1996, 91 (04) : 351 - 359
  • [5] ALZHEIMERS-DISEASE AND CREUTZFELDT-JAKOB-DISEASE - OVERLAP OF PATHOGENIC MECHANISMS
    DEARMOND, SJ
    [J]. 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
    Hsich, G
    Kinney, K
    Gibbs, CJ
    Lee, KH
    Harrington, MG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (13) : 924 - 930
  • [7] INCREASED CEREBROSPINAL-FLUID TAU IN PATIENTS WITH ALZHEIMERS-DISEASE
    JENSEN, M
    BASUN, H
    LANNFELT, L
    [J]. NEUROSCIENCE LETTERS, 1995, 186 (2-3) : 189 - 191
  • [8] Diagnostic criteria for sporadic Creutzfeldt-Jakob disease
    Kretzschmar, HA
    Ironside, JW
    DeArmond, SJ
    Tateishi, J
    [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
    MASTERS, CL
    HARRIS, JO
    GAJDUSEK, DC
    GIBBS, CJ
    BERNOULLI, C
    ASHER, DM
    [J]. ANNALS OF NEUROLOGY, 1979, 5 (02) : 177 - 188
  • [10] OTO M, 1996, AKTUEL NEUROL, V23, P71