14-3-3 testing in diagnosing Creutzfeldt-Jakob disease - A prospective study in 112 patients

被引:82
作者
Lemstra, AW [1 ]
van Meegen, MT
Vreyling, JP
Meijerink, PHS
Jansen, GH
Bulk, S
Baas, F
van Gool, WA
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Neurol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Utrecht, Med Ctr, Dept Pathol, Utrecht, Netherlands
关键词
D O I
10.1212/WNL.55.4.514
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To study the sensitivity and specificity of 14-3-3 testing in a prospective series of patients suspected of having Creutzfeldt-Jakob disease (CJD). Background: The 14-3-3 protein immunoassay on CSF has favorable test characteristics as a premortem diagnostic tool in CJD. However, the 14-3-3 protein is a normal cellular protein expressed in various tissues, and its presence in CSF reflects extensive destruction of brain tissue as in CJD, but also in ischemic stroke and meningoencephalitis. Methods: 14-3-3 was tested in the CSF of a prospective series of 110 consecutive patients suspected of having CJD. Results: The sensitivity was 97% and the specificity was 87% in this series. False-positive results were mainly caused by stroke and meningoencephalitis. Conclusion: The 14-3-3 protein is a highly sensitive and specific marker for CJD when used in the appropriate clinical context.
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页码:514 / 516
页数:3
相关论文
共 18 条
[11]  
MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939
[12]   Diffusion-weighted magnetic resonance imaging in probable Creutzfeldt-Jakob disease -: A clinical-anatomic correlation [J].
Na, DL ;
Suh, CK ;
Choi, SH ;
Moon, HS ;
Seo, DW ;
Kim, SE ;
Na, DG ;
Adair, JC .
ARCHIVES OF NEUROLOGY, 1999, 56 (08) :951-957
[13]   Frontotemporal lobar degeneration - A consensus on clinical diagnostic criteria [J].
Neary, D ;
Snowden, JS ;
Gustafson, L ;
Passant, U ;
Stuss, D ;
Black, S ;
Freedman, M ;
Kertesz, A ;
Robert, PH ;
Albert, M ;
Boone, K ;
Miller, BL ;
Cummings, J ;
Benson, DF .
NEUROLOGY, 1998, 51 (06) :1546-1554
[14]   VASCULAR DEMENTIA - DIAGNOSTIC-CRITERIA FOR RESEARCH STUDIES - REPORT OF THE NINDS-AIREN INTERNATIONAL WORKSHOP [J].
ROMAN, GC ;
TATEMICHI, TK ;
ERKINJUNTTI, T ;
CUMMINGS, JL ;
MASDEU, JC ;
GARCIA, JH ;
AMADUCCI, L ;
ORGOGOZO, JM ;
BRUN, A ;
HOFMAN, A ;
MOODY, DM ;
OBRIEN, MD ;
YAMAGUCHI, T ;
GRAFMAN, J ;
DRAYER, BP ;
BENNETT, DA ;
FISHER, M ;
OGATA, J ;
KOKMEN, E ;
BERMEJO, F ;
WOLF, PA ;
GORELICK, PB ;
BICK, KL ;
PAJEAU, AK ;
BELL, MA ;
DECARLI, C ;
CULEBRAS, A ;
KORCZYN, AD ;
BOGOUSSLAVSKY, J ;
HARTMANN, A ;
SCHEINBERG, P .
NEUROLOGY, 1993, 43 (02) :250-260
[15]   The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture [J].
Satoh, J ;
Kurohara, K ;
Yukitake, M ;
Kuroda, Y .
EUROPEAN NEUROLOGY, 1999, 41 (04) :216-225
[16]   MRI in sporadic Creutzfeldt-Jakob disease: Correlation with clinical and neuropathological data [J].
Urbach, H ;
Klisch, J ;
Wolf, HK ;
Brechtelsbauer, D ;
Gass, S ;
Solymosi, L .
NEURORADIOLOGY, 1998, 40 (02) :65-70
[17]   A RETROSPECTIVE STUDY OF CREUTZFELDT-JAKOB DISEASE IN ENGLAND AND WALES 1970-79 .1. CLINICAL-FEATURES [J].
WILL, RG ;
MATTHEWS, WB .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1984, 47 (02) :134-140
[18]   Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease [J].
Zerr, I ;
Bodemer, M ;
Gefeller, O ;
Otto, M ;
Poser, S ;
Wiltfang, J ;
Windl, O ;
Kretzschmar, HA ;
Weber, T .
ANNALS OF NEUROLOGY, 1998, 43 (01) :32-40