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Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

Several molecular subtypes of sporadic Creutzfeldt–Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype. In recent years, a series of publications have demonstrat...

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Autores principales: Zerr, I., Kallenberg, K., Summers, D. M., Romero, C., Taratuto, A., Heinemann, U., Breithaupt, M., Varges, D., Meissner, B., Ladogana, A., Schuur, M., Haik, S., Collins, S. J., Jansen, Gerard H., Stokin, G. B., Pimentel, J., Hewer, E., Collie, D., Smith, P., Roberts, H., Brandel, J. P., van Duijn, C., Pocchiari, M., Begue, C., Cras, P., Will, R. G., Sanchez-Juan, P.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759336/
https://www.ncbi.nlm.nih.gov/pubmed/19773352
http://dx.doi.org/10.1093/brain/awp191
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author Zerr, I.
Kallenberg, K.
Summers, D. M.
Romero, C.
Taratuto, A.
Heinemann, U.
Breithaupt, M.
Varges, D.
Meissner, B.
Ladogana, A.
Schuur, M.
Haik, S.
Collins, S. J.
Jansen, Gerard H.
Stokin, G. B.
Pimentel, J.
Hewer, E.
Collie, D.
Smith, P.
Roberts, H.
Brandel, J. P.
van Duijn, C.
Pocchiari, M.
Begue, C.
Cras, P.
Will, R. G.
Sanchez-Juan, P.
author_facet Zerr, I.
Kallenberg, K.
Summers, D. M.
Romero, C.
Taratuto, A.
Heinemann, U.
Breithaupt, M.
Varges, D.
Meissner, B.
Ladogana, A.
Schuur, M.
Haik, S.
Collins, S. J.
Jansen, Gerard H.
Stokin, G. B.
Pimentel, J.
Hewer, E.
Collie, D.
Smith, P.
Roberts, H.
Brandel, J. P.
van Duijn, C.
Pocchiari, M.
Begue, C.
Cras, P.
Will, R. G.
Sanchez-Juan, P.
author_sort Zerr, I.
collection PubMed
description Several molecular subtypes of sporadic Creutzfeldt–Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype. In recent years, a series of publications have demonstrated a potentially important role for magnetic resonance imaging in the pre-mortem diagnosis of sporadic Creutzfeldt–Jakob disease. Magnetic resonance imaging signal alterations correlate with distinct sporadic Creutzfeldt–Jakob disease molecular subtypes and thus might contribute to the earlier identification of the whole spectrum of sporadic Creutzfeldt–Jakob disease cases. This multi-centre international study aimed to provide a rationale for the amendment of the clinical diagnostic criteria for sporadic Creutzfeldt–Jakob disease. Patients with sporadic Creutzfeldt–Jakob disease and fluid attenuated inversion recovery or diffusion-weight imaging were recruited from 12 countries. Patients referred as ‘suspected sporadic Creutzfeldt–Jakob disease’ but with an alternative diagnosis after thorough follow up, were analysed as controls. All magnetic resonance imaging scans were assessed for signal changes according to a standard protocol encompassing seven cortical regions, basal ganglia, thalamus and cerebellum. Magnetic resonance imaging scans were evaluated in 436 sporadic Creutzfeldt–Jakob disease patients and 141 controls. The pattern of high signal intensity with the best sensitivity and specificity in the differential diagnosis of sporadic Creutzfeldt–Jakob disease was identified. The optimum diagnostic accuracy in the differential diagnosis of rapid progressive dementia was obtained when either at least two cortical regions (temporal, parietal or occipital) or both caudate nucleus and putamen displayed a high signal in fluid attenuated inversion recovery or diffusion-weight imaging magnetic resonance imaging. Based on our analyses, magnetic resonance imaging was positive in 83% of cases. In all definite cases, the amended criteria would cover the vast majority of suspected cases, being positive in 98%. Cerebral cortical signal increase and high signal in caudate nucleus and putamen on fluid attenuated inversion recovery or diffusion-weight imaging magnetic resonance imaging are useful in the diagnosis of sporadic Creutzfeldt–Jakob disease. We propose an amendment to the clinical diagnostic criteria for sporadic Creutzfeldt–Jakob disease to include findings from magnetic resonance imaging scans.
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spelling pubmed-27593362009-10-09 Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease Zerr, I. Kallenberg, K. Summers, D. M. Romero, C. Taratuto, A. Heinemann, U. Breithaupt, M. Varges, D. Meissner, B. Ladogana, A. Schuur, M. Haik, S. Collins, S. J. Jansen, Gerard H. Stokin, G. B. Pimentel, J. Hewer, E. Collie, D. Smith, P. Roberts, H. Brandel, J. P. van Duijn, C. Pocchiari, M. Begue, C. Cras, P. Will, R. G. Sanchez-Juan, P. Brain Original Articles Several molecular subtypes of sporadic Creutzfeldt–Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype. In recent years, a series of publications have demonstrated a potentially important role for magnetic resonance imaging in the pre-mortem diagnosis of sporadic Creutzfeldt–Jakob disease. Magnetic resonance imaging signal alterations correlate with distinct sporadic Creutzfeldt–Jakob disease molecular subtypes and thus might contribute to the earlier identification of the whole spectrum of sporadic Creutzfeldt–Jakob disease cases. This multi-centre international study aimed to provide a rationale for the amendment of the clinical diagnostic criteria for sporadic Creutzfeldt–Jakob disease. Patients with sporadic Creutzfeldt–Jakob disease and fluid attenuated inversion recovery or diffusion-weight imaging were recruited from 12 countries. Patients referred as ‘suspected sporadic Creutzfeldt–Jakob disease’ but with an alternative diagnosis after thorough follow up, were analysed as controls. All magnetic resonance imaging scans were assessed for signal changes according to a standard protocol encompassing seven cortical regions, basal ganglia, thalamus and cerebellum. Magnetic resonance imaging scans were evaluated in 436 sporadic Creutzfeldt–Jakob disease patients and 141 controls. The pattern of high signal intensity with the best sensitivity and specificity in the differential diagnosis of sporadic Creutzfeldt–Jakob disease was identified. The optimum diagnostic accuracy in the differential diagnosis of rapid progressive dementia was obtained when either at least two cortical regions (temporal, parietal or occipital) or both caudate nucleus and putamen displayed a high signal in fluid attenuated inversion recovery or diffusion-weight imaging magnetic resonance imaging. Based on our analyses, magnetic resonance imaging was positive in 83% of cases. In all definite cases, the amended criteria would cover the vast majority of suspected cases, being positive in 98%. Cerebral cortical signal increase and high signal in caudate nucleus and putamen on fluid attenuated inversion recovery or diffusion-weight imaging magnetic resonance imaging are useful in the diagnosis of sporadic Creutzfeldt–Jakob disease. We propose an amendment to the clinical diagnostic criteria for sporadic Creutzfeldt–Jakob disease to include findings from magnetic resonance imaging scans. Oxford University Press 2009-10 2009-09-22 /pmc/articles/PMC2759336/ /pubmed/19773352 http://dx.doi.org/10.1093/brain/awp191 Text en © The Author(s) 2009. Published by Oxford University Press on behalf of Brain. http://creativecommons.org/licenses/by-nc/2.5/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zerr, I.
Kallenberg, K.
Summers, D. M.
Romero, C.
Taratuto, A.
Heinemann, U.
Breithaupt, M.
Varges, D.
Meissner, B.
Ladogana, A.
Schuur, M.
Haik, S.
Collins, S. J.
Jansen, Gerard H.
Stokin, G. B.
Pimentel, J.
Hewer, E.
Collie, D.
Smith, P.
Roberts, H.
Brandel, J. P.
van Duijn, C.
Pocchiari, M.
Begue, C.
Cras, P.
Will, R. G.
Sanchez-Juan, P.
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
title Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
title_full Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
title_fullStr Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
title_full_unstemmed Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
title_short Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
title_sort updated clinical diagnostic criteria for sporadic creutzfeldt-jakob disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759336/
https://www.ncbi.nlm.nih.gov/pubmed/19773352
http://dx.doi.org/10.1093/brain/awp191
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