| Literature DB >> 30136097 |
Matthias Schmitz1, Anna Villar-Piqué2, Franc Llorens3,4,5, Karin Gmitterová6,7, Peter Hermann7, Daniela Varges7, Saima Zafar7, Paul Lingor7, Hugo Vanderstichele8, Leentje Demeyer8, Erik Stoops8, John Q Trojanowski9, Virginia M-Y Lee9, Inga Zerr7.
Abstract
High levels of total α-synuclein (t-α-synuclein) in the cerebrospinal fluid (CSF) were reported in sporadic Creutzfeldt-Jakob disease (sCJD). The potential use of t-α-synuclein in the discrimination of Lewy body dementias (i.e., Parkinson's disease dementia (PDD) and dementia with Lewy bodies (DLB)) is still under investigation. In addition, phospho-serine-129 α-synuclein (p-α-synuclein) has been described to be slightly increased in the CSF of synucleinopathies. Here, we analyzed t-α-synuclein and p-α-synuclein concentrations and their ratio in the context of differential diagnosis of neurodegenerative diseases. We quantified the levels of CSF t-α-synuclein and p-α-synuclein in a cohort of samples composed of neurological controls (NC), sCJD, PDD, and DLB by means of newly developed specific enzyme-linked immunosorbent assays. T-α-synuclein and p-α-synuclein were specifically elevated in sCJD compared to other disease groups. The area under the curve (AUC) values for t-α-synuclein were higher for the discrimination of sCJD from dementias associated to Lewy bodies as compared to the use of p-α-synuclein. A combination of both markers even increased the diagnostic accuracy. An inverse correlation was observed in CSF between t-α-synuclein and p-α-synuclein, especially in the DLB group, indicating a disease-relevant association between both markers. In conclusion, our data confirm t-α-synuclein and p-α-synuclein as robust biomarkers for sCJD and indicate the potential use of colorimetric t-α-synuclein ELISAs for differential diagnosis of dementia types.Entities:
Keywords: Cerebrospinal fluid; Creutzfeldt–Jakob disease; Dementia with Lewy bodies; Parkinson’s disease; Phospho-serine-129 α-synuclein; T-α-synuclein
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Year: 2018 PMID: 30136097 DOI: 10.1007/s12035-018-1313-4
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590