Affiliations: National TSE Reference Center at Department of Neurology, Georg-August University, Göttingen, Germany
Correspondence:
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Corresponding author: Dr. Inga Zerr, Georg-August-Universität, Neurologische Klinik und Poliklinik, Robert-Koch-Str. 40, 37075 Göttingen, Germany. E-mail: epicjd@med.uni-goettingen.de.
Abstract: We performed a study on levels of the total prion protein (PrP) in humans affected by different neurological diseases and assessed the influence of several factors such as age, gender, and disease severity on the cerebrospinal fluid PrP levels. PrP-ELISA technique was used to analyze cerebrospinal fluid (CSF) samples. 293 CSF samples of patients with Creutzfeldt-Jakob-disease (CJD), Alzheimer's disease, dementia with Lewy-bodies, Parkinson's disease, multiple sclerosis, cerebral ischemia, generalized epileptic seizures, and meningitis and encephalitis in comparison to controls were analyzed. We found a significant reduction of CSF PrP levels in patients suffering from all neurodegenerative disorders analyzed. This group exhibited mean PrP values of 164 ng/ml while non-neurodegenerative disorder patients and healthy controls showed PrP levels of 208 ng/ml and 226 ng/ml, respectively. CSF levels correlated with disease severity in CJD, Alzheimer's disease, and dementia with Lewy-bodies. The finding of decreased PrP levels in the CSF of patients not only with CJD but also in other neurodegenerative disorders is intriguing. Age-, gender-, and genetic-specific factors might be involved in the PrPc regulation.
Keywords: Alzheimer's disease, amyloid-β, cerebrospinal fluid, Creutzfeldt-Jakob-disease, dementia, dementia with Lewy-bodies, disease severity, prion protein, tau
