Follow-up investigations of tau protein and S-100B levels in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
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vor 19 Jahren
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. Copyright (C) 2005 S. Karger AG, Basel.
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. Copyright (C) 2005 S. Karger AG, Basel.
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