NR APIE
AU Huang,N.; Marie,S.K.; Livramento,J.A.; Chammas,R.; Nitrini,R.
TI 14-3-3 protein in the CSF of patients with rapidly progressive dementia
QU Neurology 2003 Aug 12; 61(3): 354-7
PT clinical trial; journal article
AB BACKGROUND: The presence of 14-3-3 protein in the CSF has been described to have high sensitivity and specificity for Creutzfeldt-Jakob disease (CJD). OBJECTIVE: To relate 14-3-3 protein in the CSF with the clinical diagnoses of diseases causing rapidly progressive dementia. METHODS: The authors studied 46 patients with rapidly progressive dementia that was classified into three diagnostic groups: definitive or probable CJD, possible CJD, and other diagnoses. The definitive or probable CJD group comprised 17 patients (3 definitive sporadic, 1 probable iatrogenic, 3 familial, and 10 probable sporadic CJD cases), the possible CJD group was composed of 7 patients, and the group with other diagnoses had 22 patients. Detection of the 14-3-3 protein was done by the immunoblotting method. RESULTS: In the definitive or probable CJD group, the test for 14-3-3 protein in CSF was positive in 14 (82%) cases, whereas 3 patients (1 probable sporadic and 2 familial cases) had negative results. CSF was positive for 14-3-3 protein in three of seven cases with possible CJD (42%). In the group with other diagnoses, three individuals had false-positive results (13%). Their diagnoses were definitive Alzheimer's disease, hypercalcemia, and multiple intracerebral hemorrhages. CONCLUSIONS: The detection of 14-3-3 protein in CSF is a useful in vivo diagnostic test for CJD and, when used in the appropriate clinical context, shows a good correlation to CJD. The presence of the 14-3-3 protein in the CSF reinforces the CJD clinical diagnosis but may not be able to differentiate CJD from other causes of rapidly progressive dementia in everyday clinical practice.
MH Aged; Comparative Study; Creutzfeldt-Jakob Syndrome/cerebrospinal fluid/diagnosis; Dementia/*cerebrospinal fluid/classification/*diagnosis; Diagnosis, Differential; Disease Progression; False Negative Reactions; False Positive Reactions; Female; Human; Male; Middle Aged; Predictive Value of Tests; Sensitivity and Specificity; Tyrosine 3-Monooxygenase/*cerebrospinal fluid
AD Laboratory of Neurological Investigation, Cognitive and Behavioral Neurology Unit, Department of Neurology, University of Sao Paulo School of Medicine, Brazil. nancy@lim15.fm.usp.br
SP englisch
PO USA