Abstract
α-Synuclein is the major component of Lewy bodies and a candidate biomarker for neurodegenerative diseases in which Lewy bodies are common, including Parkinson's disease and dementia with Lewy bodies. A large body of literature suggests that these disorders are characterized by reduced concentrations of α-synuclein in cerebrospinal fluid (CSF), with overlapping concentrations compared to healthy controls and variability across studies. Several reasons can account for this variability, including technical ones, such as inter-assay and inter-laboratory variation (reproducibility). We compared four immunochemical methods for the quantification of α-synuclein concentration in 50 unique CSF samples. All methods were designed to capture most of the existing α-synuclein forms in CSF (‘total’ α-synuclein). Each of the four methods showed high analytical precision, excellent correlation between laboratories (R 2 0.83–0.99), and good correlation with each other (R 2 0.64–0.93), although the slopes of the regression lines were different between the four immunoassays. The use of common reference CSF samples decreased the differences in α-synuclein concentration between detection methods and technologies. Pilot data on an immunoprecipitation mass spectrometry (IP-MS) method is also presented. Our results suggest that the four immunochemical methods and the IP-MS method measure similar forms of α-synuclein and that a common reference material would allow harmonization of results between immunoassays. (Figure presented.).
| Original language | English |
|---|---|
| Pages (from-to) | 126-138 |
| Number of pages | 13 |
| Journal | Journal of Neurochemistry |
| Volume | 149 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Apr 2019 |
Keywords
- biomarker
- cerebrospinal fluid
- enzyme-linked immunoabsorbent assay
- mass spectrometry
- round robin
- α-synuclein