Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.

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Serval ID
serval:BIB_F7E292891E81
Type
Article: article from journal or magazin.
Collection
Publications
Title
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
Journal
Brain
Author(s)
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 G.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.
ISSN
1460-2156 (Electronic)
ISSN-L
0006-8950
Publication state
Published
Issued date
10/2009
Peer-reviewed
Oui
Volume
132
Number
Pt 10
Pages
2659-2668
Language
english
Notes
Publication types: Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
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.
Keywords
14-3-3 Proteins/analysis, Adult, Aged, Aged, 80 and over, Anti-Inflammatory Agents/therapeutic use, Biomarkers/analysis, Cerebral Cortex/pathology, Codon/genetics, Creutzfeldt-Jakob Syndrome/cerebrospinal fluid, Creutzfeldt-Jakob Syndrome/diagnosis, Creutzfeldt-Jakob Syndrome/genetics, Electroencephalography, False Positive Reactions, Female, Genotype, Humans, International Cooperation, Magnetic Resonance Imaging, Male, Middle Aged, Reference Standards
Pubmed
Web of science
Open Access
Yes
Create date
31/08/2020 13:02
Last modification date
10/11/2020 7:26
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