Follow-Up Investigations of Tau Protein and S-100B Levels in Cerebrospinal Fluid of Patients with Creutzfeldt-Jakob Disease

Autor: Mirko Bibl, Sigrid Poser, Jens Wiltfang, Walter J. Schulz-Schaeffer, Lukas Cepek, Barbara Ciesielczyk, Markus Otto, Birgitt Wiese, Hans A. Kretzschmar, Petra Steinacker, Inga Zerr, Brit Mollenhauer
Jazyk: angličtina
Rok vydání: 2013
Předmět:
Male
Pathology
animal diseases
Disease
Creutzfeldt-Jakob Syndrome
0302 clinical medicine
Degenerative disease
Cerebrospinal fluid
Neoplasms
Aged
80 and over

0303 health sciences
biology
S100 Proteins
Neurodegenerative Diseases
Middle Aged
3. Good health
Psychiatry and Mental health
Encephalitis
Female
Adult
medicine.medical_specialty
Cognitive Neuroscience
Medizinische Fakultät -ohne weitere Spezifikation
Tau protein
tau Proteins
S100 Calcium Binding Protein beta Subunit
Central nervous system disease
Diagnosis
Differential

03 medical and health sciences
Alzheimer Disease
mental disorders
medicine
Dementia
Humans
Nerve Growth Factors
ddc:610
030304 developmental biology
Aged
Uremia
Epilepsy
business.industry
medicine.disease
nervous system diseases
Hepatic Encephalopathy
biology.protein
Geriatrics and Gerontology
business
030217 neurology & neurosurgery
Biomarkers
Follow-Up Studies
Popis: Background: S-100B and tau protein have a high differential diagnostic potential for the diagnosis of Creutzfeldt-Jakob disease (CJD). So far there has been only limited information available about the dynamics of these parameters in the cerebrospinal fluid (CSF). However, there is a special interest in finding biochemical markers to monitor disease progression for differential diagnosis and treatment. Patients and Methods: We analyzed CSF of 45 patients with CJD and of 45 patients with other neurological diseases for tau protein and S-100B in a follow-up setting. All diagnoses of CJD were later neuropathologically verified. A ratio between tau protein differences and the time between lumbar puncture was calculated. The same was done for S-100B. Results: Tau protein levels of 34 cases were above the cut-off level for CJD (>1,300 pg/ml) in the first CSF sample. In 7 of 11 patients with lower tau levels in the first CSF sample, tau levels rose. The above-mentioned ratio was significantly higher in the CJD group than in the group with other neurological diseases. Similar results were obtained for S-100B. Conclusion: We conclude that follow-up investigations and calculation of ratios is a useful tool in the differential diagnosis of CJD. Variations in this pattern were observed in single cases.
Databáze: OpenAIRE