Evolution of cerebrospinal fluid total α-synuclein in Parkinson's disease
Cerebrospinal fluid (CSF) total α-synuclein is considered a potential biomarker for Parkinson's disease (PD), but little is known about the evolution of this marker during the course of the disease. Our objective was to investigate whether CSF total α-synuclein concentrations change over time a...
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Published in | Parkinsonism & related disorders Vol. 49; pp. 4 - 8 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.04.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Cerebrospinal fluid (CSF) total α-synuclein is considered a potential biomarker for Parkinson's disease (PD), but little is known about the evolution of this marker during the course of the disease. Our objective was to investigate whether CSF total α-synuclein concentrations change over time and are associated with motor and cognitive function in PD.
CSF total α-synuclein concentrations were quantified in 56 longitudinally followed PD patients, 27 of whom provided CSF repeatedly 2 and/or 4 years later. Another 18 subjects were included as controls. The samples were analyzed using two independent, validated ELISA methods: our recently developed and validated in-house ELISA and a commercial kit from BioLegend.
CSF total α-synuclein levels did not distinguish PD patients from controls, displayed no substantial changes during a period of up to 4 years, and did not predict subsequent motor or cognitive decline. These findings were consistent for both analytical methods.
Our findings do not support the clinical utility of total α-synuclein as a single diagnostic or prognostic biomarker in PD.
•α-synuclein (α-syn) is considered a potential biomarker for PD.•Little is known about the evolution of this marker during the course of PD.•Our study covers the longest follow-up period so far and used 2 independent methods.•α-syn concentrations in PD were similar to controls and did not change over 4 years.•α-syn did not predict motor and cognitive decline. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1353-8020 1873-5126 1873-5126 |
DOI: | 10.1016/j.parkreldis.2018.01.018 |