Dementia and Geriatric Cognitive Disorders · 1998 · 182 citations · 25 references
Creutzfeldt-jakob DiseaseNeurological DisorderS-100 ProteinPathologyNeurochemical BiomarkersSocial SciencesNeurobiology Of DiseaseCerebrospinal FluidPrion DiseaseNeurologyNeuropathologyNeuroimmunologyNeuron-specific Enolase14-3-3 ProteinCsf ProteinsNeurodegenerative DiseasesNeuroscienceMultiple SclerosisMedicine
We explored simultaneously 14-3-3 protein, neuron-specific enolase (NSE), and one astroglial protein, S-100, recently proposed as Creutzfeld-Jakob disease (CJD) markers, in the cerebrospinal fluid (CSF) of 129 patients with suspected CJD. Cutoff values for NSE and S-100 were established at 25 and 2.5 ng/ml, respectively. The highest sensitivity was observed for S-100 (94.2%) followed by 14-3-3 (89.8%) and NSE (79.7%), while the highest specificity in CJD diagnosis was obtained with 14-3-3 protein (100%) as compared with NSE (91.5%) and S-100 (85.4%). No influence of sex, genotype at codon 129 of the prion protein gene, time between sampling, and death or disease duration has been found. Based on 90 cases initially referred as 'probable' or 'possible' CJD, with 14-3-3, NSE, or S-100 we could correctly discriminate between 'CJD' or 'non-CJD' categories in 94.4, 86.5, and 90% of the cases, respectively. When limited to 'possible CJD' cases, diagnosis based on one of the three CSF proteins was accurate in 98, 90.7 and 87.3%, respectively. In view of the fact that the CSF 14-3-3 protein test alone has the highest specificity and good sensitivity, it appears that there is no additional advantage at the moment to include NSE and/or S-100 protein in the exploration of clinically suspected CJD cases.
25
A new variant of Creutzfeldt-Jakob disease in the UK
Robert Will, James W. Ironside, Martin Zeidler et al. · The Lancet · 1996 · 2.7K citations
Creutzfeldt-jakob Disease, Neurological Disorder, New Variant +6
Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent
M. E. Bruce, Robert Will, James W. Ironside et al. · Nature · 1997 · 2K citations
Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease
Piero Parchi, Rudolph J. Castellani, Sabina Capellari et al. · Annals of Neurology · 1996 · 868 citations
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome
Karen Hsiao, Harry F. Baker, Tim Crow et al. · Nature · 1989 · 843 citations