Plasma Metabolomic Biomarker Panel To Distinguish Patients With Amyotrophic Lateral Sclerosis From Disease Mimics
Department
neurobiology
Document Type
Article
Abstract
Our objective was to identify plasma biomarkers of ALS that can aid in distinguishing patients with ALS from those with disease mimics. In this multi-center study, plasma samples were collected from 172 patients recently diagnosed with ALS, 50 healthy controls, and 73 neurological disease mimics. Samples were analyzed using metabolomics. Using all identified biochemicals detected in > 50% of all samples in the metabolomics analysis, samples were classified as ALS or mimic with 65% sensitivity and 81% specificity by LASSO analysis (AUC of 0.76). A subset panel of 32 candidate biomarkers classified these diagnosis groups with a specificity of 90%/sensitivity 58% (AUC of 0.81). Creatinine was lower in subjects with lower revised ALS Functional Rating Scale (ALSFRS-R) scores. In conclusion, ALS can be distinguished from neurological disease mimics by global biochemical profiling of plasma samples. Our analysis identified ALS versus mimics with relatively high sensitivity. We identified a subset of 32 metabolites that identify patients with ALS with a high specificity. Interestingly, lower creatinine correlates significantly with a lower ALSFRS-R score. Finally, molecules previously reported to be important in disease pathophysiology, such as urate, are included in our metabolite panel. © 2014 Informa Healthcare.
Publication Date
1-1-2014
Publication Title
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
ISSN
21678421
Volume
15
Issue
2019-05-06 00:00:00
First Page
362
Last Page
370
Digital Object Identifier (DOI)
10.3109/21678421.2014.908311
Recommended Citation
Lawton, Kay A.; Brown, Meredith V.; Alexander, Danny; Li, Zhen; Wulff, Jacob E.; Lawson, Robert; Jaffa, Matt; Milburn, Mike V.; Ryals, John A.; Bowser, Robert; Cudkowicz, Merit E.; and Berry, James D., "Plasma Metabolomic Biomarker Panel To Distinguish Patients With Amyotrophic Lateral Sclerosis From Disease Mimics" (2014). Translational Neuroscience. 29.
https://scholar.barrowneuro.org/neurobiology/29