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While unbiased proteomics of human cerebrospinal fluid (CSF) has been used successfully to identify biomarkers of amyotrophic lateral sclerosis (ALS), high-abundance proteins mask the presence of lower abundance proteins that may have diagnostic and prognostic value. However, developments in mass spectrometry (MS) proteomic data acquisition methods offer improved protein depth. In this study, MS with library-free data-independent acquisition (DIA) was used to compare the CSF proteome of people with ALS (n = 40), healthy (n = 15) and disease (n = 8) controls. Quantified protein groups were subsequently correlated with clinical variables. Univariate analysis identified 7 proteins, all significantly upregulated in ALS versus healthy controls, and 9 with altered abundance in ALS versus disease controls (FDR 

Original publication

DOI

10.1111/jnc.16030

Type

Journal article

Journal

J Neurochem

Publication Date

02/2024

Volume

168

Pages

115 - 127

Keywords

CSF, DIA, amyotrophic lateral sclerosis, biomarker, mass spectrometry, proteomics, Humans, Amyotrophic Lateral Sclerosis, Proteomics, Biomarkers, Prognosis, Mass Spectrometry