CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

Standard

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease. / Sanchez-Juan, P; Green, A; Ladogana, A; Cuadrado-Corrales, N; Sáanchez-Valle, R; Mitrováa, E; Stoeck, Katharina; Sklaviadis, T; Kulczycki, J; Hess, K; Bodemer, M; Slivarichová, D; Saiz, A; Calero, M; Ingrosso, L; Knight, R; Janssens, A C J W; van Duijn, C M; Zerr, I.

in: NEUROLOGY, Jahrgang 67, Nr. 4, 4, 2006, S. 637-643.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Sanchez-Juan, P, Green, A, Ladogana, A, Cuadrado-Corrales, N, Sáanchez-Valle, R, Mitrováa, E, Stoeck, K, Sklaviadis, T, Kulczycki, J, Hess, K, Bodemer, M, Slivarichová, D, Saiz, A, Calero, M, Ingrosso, L, Knight, R, Janssens, ACJW, van Duijn, CM & Zerr, I 2006, 'CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.', NEUROLOGY, Jg. 67, Nr. 4, 4, S. 637-643. <http://www.ncbi.nlm.nih.gov/pubmed/16924018?dopt=Citation>

APA

Sanchez-Juan, P., Green, A., Ladogana, A., Cuadrado-Corrales, N., Sáanchez-Valle, R., Mitrováa, E., Stoeck, K., Sklaviadis, T., Kulczycki, J., Hess, K., Bodemer, M., Slivarichová, D., Saiz, A., Calero, M., Ingrosso, L., Knight, R., Janssens, A. C. J. W., van Duijn, C. M., & Zerr, I. (2006). CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease. NEUROLOGY, 67(4), 637-643. [4]. http://www.ncbi.nlm.nih.gov/pubmed/16924018?dopt=Citation

Vancouver

Sanchez-Juan P, Green A, Ladogana A, Cuadrado-Corrales N, Sáanchez-Valle R, Mitrováa E et al. CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease. NEUROLOGY. 2006;67(4):637-643. 4.

Bibtex

@article{891422f53c474e9985ae0f84e2dd430f,
title = "CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.",
abstract = "OBJECTIVES: To analyze the diagnostic sensitivity and specificity of various brain-derived proteins (14-3-3, Tau, neuron specific enolase [NSE], and S100b) in the CSF of patients with Creutzfeldt-Jakob disease (CJD) and to analyze biologic factors that modify these parameters. METHODS: CSF was tested for 14-3-3, Tau, NSE, and S100b in 1,859 patients with sporadic, genetic, iatrogenic, and variant CJD, and in 1,117 controls. RESULTS: The highest sensitivity was achieved for 14-3-3 and Tau in sporadic CJD (85% and 86%), and a combined determination of 14-3-3 and Tau, S100b, or NSE increased the sensitivity to over 93%. A multivariate analysis showed that the sensitivity of all tests was highest in patients with the shortest disease duration, age at onset >40 years, and homozygosity at codon 129 of the prion protein gene. In a group of patients with repeated lumbar punctures, a second test also increased the diagnostic sensitivity. CONCLUSIONS: The detection of elevated levels of brain-derived proteins in the CSF in patients with suspected Creutzfeldt-Jakob disease is a valuable diagnostic test. A second lumbar puncture may be of value in patients with atypical clinical course in whom the first test was negative.",
author = "P Sanchez-Juan and A Green and A Ladogana and N Cuadrado-Corrales and R S{\'a}anchez-Valle and E Mitrov{\'a}a and Katharina Stoeck and T Sklaviadis and J Kulczycki and K Hess and M Bodemer and D Slivarichov{\'a} and A Saiz and M Calero and L Ingrosso and R Knight and Janssens, {A C J W} and {van Duijn}, {C M} and I Zerr",
year = "2006",
language = "Deutsch",
volume = "67",
pages = "637--643",
journal = "NEUROLOGY",
issn = "0028-3878",
publisher = "Lippincott Williams and Wilkins",
number = "4",

}

RIS

TY - JOUR

T1 - CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

AU - Sanchez-Juan, P

AU - Green, A

AU - Ladogana, A

AU - Cuadrado-Corrales, N

AU - Sáanchez-Valle, R

AU - Mitrováa, E

AU - Stoeck, Katharina

AU - Sklaviadis, T

AU - Kulczycki, J

AU - Hess, K

AU - Bodemer, M

AU - Slivarichová, D

AU - Saiz, A

AU - Calero, M

AU - Ingrosso, L

AU - Knight, R

AU - Janssens, A C J W

AU - van Duijn, C M

AU - Zerr, I

PY - 2006

Y1 - 2006

N2 - OBJECTIVES: To analyze the diagnostic sensitivity and specificity of various brain-derived proteins (14-3-3, Tau, neuron specific enolase [NSE], and S100b) in the CSF of patients with Creutzfeldt-Jakob disease (CJD) and to analyze biologic factors that modify these parameters. METHODS: CSF was tested for 14-3-3, Tau, NSE, and S100b in 1,859 patients with sporadic, genetic, iatrogenic, and variant CJD, and in 1,117 controls. RESULTS: The highest sensitivity was achieved for 14-3-3 and Tau in sporadic CJD (85% and 86%), and a combined determination of 14-3-3 and Tau, S100b, or NSE increased the sensitivity to over 93%. A multivariate analysis showed that the sensitivity of all tests was highest in patients with the shortest disease duration, age at onset >40 years, and homozygosity at codon 129 of the prion protein gene. In a group of patients with repeated lumbar punctures, a second test also increased the diagnostic sensitivity. CONCLUSIONS: The detection of elevated levels of brain-derived proteins in the CSF in patients with suspected Creutzfeldt-Jakob disease is a valuable diagnostic test. A second lumbar puncture may be of value in patients with atypical clinical course in whom the first test was negative.

AB - OBJECTIVES: To analyze the diagnostic sensitivity and specificity of various brain-derived proteins (14-3-3, Tau, neuron specific enolase [NSE], and S100b) in the CSF of patients with Creutzfeldt-Jakob disease (CJD) and to analyze biologic factors that modify these parameters. METHODS: CSF was tested for 14-3-3, Tau, NSE, and S100b in 1,859 patients with sporadic, genetic, iatrogenic, and variant CJD, and in 1,117 controls. RESULTS: The highest sensitivity was achieved for 14-3-3 and Tau in sporadic CJD (85% and 86%), and a combined determination of 14-3-3 and Tau, S100b, or NSE increased the sensitivity to over 93%. A multivariate analysis showed that the sensitivity of all tests was highest in patients with the shortest disease duration, age at onset >40 years, and homozygosity at codon 129 of the prion protein gene. In a group of patients with repeated lumbar punctures, a second test also increased the diagnostic sensitivity. CONCLUSIONS: The detection of elevated levels of brain-derived proteins in the CSF in patients with suspected Creutzfeldt-Jakob disease is a valuable diagnostic test. A second lumbar puncture may be of value in patients with atypical clinical course in whom the first test was negative.

M3 - SCORING: Zeitschriftenaufsatz

VL - 67

SP - 637

EP - 643

JO - NEUROLOGY

JF - NEUROLOGY

SN - 0028-3878

IS - 4

M1 - 4

ER -