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Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis

BACKGROUND: The analysis of markers in the cerebrospinal fluid (CSF) is useful in the diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD). However, the time at which the study of these markers is most sensitive remains controversal. OBJECTIVE: To assess the influence of time of sampling on the va...

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Detalles Bibliográficos
Autores principales: Sanchez-Juan, P., Sánchez-Valle, R., Green, A., Ladogana, A., Cuadrado-Corrales, N., Mitrová, E., Stoeck, K., Sklaviadis, T., Kulczycki, J., Hess, K., Krasnianski, A., Equestre, M., Slivarichová, D., Saiz, A., Calero, M., Pocchiari, M., Knight, R., van Duijn, C. M., Zerr, I.
Formato: Texto
Lenguaje:English
Publicado: Steinkopff-Verlag 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779401/
https://www.ncbi.nlm.nih.gov/pubmed/17385081
http://dx.doi.org/10.1007/s00415-006-0472-9
Descripción
Sumario:BACKGROUND: The analysis of markers in the cerebrospinal fluid (CSF) is useful in the diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD). However, the time at which the study of these markers is most sensitive remains controversal. OBJECTIVE: To assess the influence of time of sampling on the value of CSF tests in the diagnosis of sCJD. METHOD: In the framework of a multinational European study, we studied the results of 14-3-3, S100b, neurone specific enolase (NSE) and tau protein in 833 CSF samples from sCJD patients at different stages of disease and in 66 sequentially repeated lumbar punctures (LP). RESULTS: 14-3-3 and tau protein tended to increase in sensitivity from onset (88%, 81%) to the advanced stage (91%, 90%). This was significant only in the methionine-valine (MV) heterozygous group of patients at codon 129. The absolute levels of S100b (p < 0.05), NSE and tau protein increased in the last stage of disease. High levels of tau protein, NSE and S100b were associated with shorter survival times (p < 0.01). Sixty-six sCJD patients underwent repeated LP. These sCJD patients were younger, had longer disease durations and were more frequently MV at codon 129 (p < 0.001) than the whole group. 14-3-3 sensitivity increased from 64% to 82% in the second LP (p = 0.025) and 88% sCJD patients had at least one positive result. CONCLUSIONS: Sensitivity and absolute levels of CJD markers increased with disease progression and were modulated by the codon 129 genotype. Early negative results should be inter-preted with caution, especially in young patients or those who are MV at codon 129.