Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

Inga Zerr, Kai Kallenberg(University of Göttingen), David Summers(Western General Hospital), Carlos Romero(Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia), A.L. Taratuto(Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia), Uta Heinemann(University of Göttingen), Maren Breithaupt(University of Göttingen), Daniela Varges(University of Göttingen), Bettina Meißner(University of Göttingen), Anna Ladogana(Istituto Superiore di Sanità), Maaike Schuur(Erasmus University Rotterdam), Stéphane Haı̈k(Inserm), Steven Collins(The University of Melbourne), Gerard H. Jansen(Public Health Agency of Canada), Gorazd B. Stokin(University of Ljubljana), José Pimentel(University of Lisbon), Ekkehard Hewer(University of Zurich), Donald A. Collie(Western General Hospital), P. Smith(Sisters of Mercy Health System), Hannah Roberts(The University of Melbourne), J.P. Brandel(Inserm), Cornelia M. van Duijn(Erasmus University Rotterdam), Maurizio Pocchiari(Istituto Superiore di Sanità), Christián Begué(Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia), Patrick Cras(University of Antwerp), Robert Will(Western General Hospital), Pascual Sánchez‐Juan(Biomedical Research Networking Center on Neurodegenerative Diseases)
Brain
September 22, 2009
Cited by 918Open Access
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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.


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