14-3-3 testing in diagnosing Creutzfeldt–Jakob disease
- 22 August 2000
- journal article
- clinical trial
- Published by Wolters Kluwer Health in Neurology
- Vol. 55 (4) , 514-516
- https://doi.org/10.1212/wnl.55.4.514
Abstract
Objective: To study the sensitivity and specificity of 14-3-3 testing in a prospective series of patients suspected of having Creutzfeldt-Jakob disease (CJD). Background: The 14-3-3 protein immunoassay on CSF has favorable test characteristics as a premortem diagnostic tool in CJD. However, the 14-3-3 protein is a normal cellular protein expressed in various tissues, and its presence in CSF reflects extensive destruction of brain tissue as in CJD, but also in ischemic stroke and meningoencephalitis. Methods: 14-3-3 was tested in the CSF of a prospective series of 110 consecutive patients suspected of having CJD. Results: The sensitivity was 97% and the specificity was 87% in this series. False-positive results were mainly caused by stroke and meningoencephalitis. Conclusion: The 14-3-3 protein is a highly sensitive and specific marker for CJD when used in the appropriate clinical context.Keywords
This publication has 19 references indexed in Scilit:
- Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samplesThe Lancet, 1999
- Creutzfeldt–Jakob Disease and Related Transmissible Spongiform EncephalopathiesNew England Journal of Medicine, 1998
- Detection of 14‐3‐3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt‐Jakob diseaseAnnals of Neurology, 1998
- The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform EncephalopathiesNew England Journal of Medicine, 1996
- Diagnostic Criteria for Sporadic Creutzfeldt-Jakob DiseaseArchives of Neurology, 1996
- Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted diseaseAnnals of Neurology, 1994
- 14-3-3 proteins: a highly conserved, widespread family of eukaryotic proteinsTrends in Biochemical Sciences, 1992
- Creutzfeldt‐Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified casesAnnals of Neurology, 1986
- Clinical diagnosis of Alzheimer's diseaseNeurology, 1984
- A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical features.Journal of Neurology, Neurosurgery & Psychiatry, 1984