| Literature DB >> 29708756 |
Ilijana Begcevic1,2, Davor Brinc1,2,3, Lora Dukic4, Ana-Maria Simundic4, Iris Zavoreo5, Vanja Basic Kes5, Eduardo Martinez-Morillo6, Ihor Batruch2, Andrei P Drabovich1,3, Eleftherios P Diamandis1,2,3.
Abstract
Cerebrospinal fluid (CSF) is a promising clinical sample for identification of novel biomarkers for various neurological disorders. Considering its direct contact with brain tissue, CSF represents a valuable source of brain-related and brain-specific proteins. Multiple sclerosis is an inflammatory, demyelinating neurological disease affecting the central nervous system, and so far there are no diagnostic or prognostic disease specific biomarkers available in the clinic. The primary aim of the present study was to develop a targeted mass spectrometry assay for simultaneous quantification of 30 brain-related proteins in CSF and subsequently to demonstrate assay feasibility in neurological samples derived from multiple sclerosis patients. Our multiplex selected reaction monitoring assay had wide dynamic range (median fold range across peptides = 8.16 × 103) and high assay reproducibility (median across peptides CV = 4%). Candidate biomarkers were quantified in CSF samples from neurologically healthy individuals (n = 9) and patients diagnosed with clinically isolated syndrome (n = 29) or early multiple sclerosis (n = 15).Entities:
Keywords: biomarkers; cerebrospinal fluid; mass spectrometry; multiple sclerosis; selected reaction monitoring
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Year: 2018 PMID: 29708756 DOI: 10.1021/acs.jproteome.7b00768
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466