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Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report

BACKGROUND AND PURPOSE: Aging in multiple sclerosis is associated with both disease- and age-dependent neurodegeneration. Serum metabolomic profiling of amino acids seems to be a promising method for searching for biomarkers of neurodegenerative disorders. The aim of this study was to determine the...

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Autores principales: Rzepiński, Łukasz, Kośliński, Piotr, Gackowski, Marcin, Koba, Marcin, Maciejek, Zdzisław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444553/
https://www.ncbi.nlm.nih.gov/pubmed/36062770
http://dx.doi.org/10.3988/jcn.2022.18.5.529
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author Rzepiński, Łukasz
Kośliński, Piotr
Gackowski, Marcin
Koba, Marcin
Maciejek, Zdzisław
author_facet Rzepiński, Łukasz
Kośliński, Piotr
Gackowski, Marcin
Koba, Marcin
Maciejek, Zdzisław
author_sort Rzepiński, Łukasz
collection PubMed
description BACKGROUND AND PURPOSE: Aging in multiple sclerosis is associated with both disease- and age-dependent neurodegeneration. Serum metabolomic profiling of amino acids seems to be a promising method for searching for biomarkers of neurodegenerative disorders. The aim of this study was to determine the profile of nonessential amino acids in the serum of elderly patients with secondary progressive multiple sclerosis (SPMS). METHODS: We used high-performance liquid chromatography to evaluate the serum concentrations of nonessential amino acids in subjects aged >65 years: six patients with SPMS and 20 control subjects (CS). RESULTS: The serine and alanine levels were significantly higher in SPMS patients than in CS, whereas the concentrations of aspartic acid, arginine, and cysteine were significantly lower in SPMS patients. These observations indicate that amino acids may be involved in SPMS neurodegeneration mechanisms. There were no significant differences in the serum concentrations of the other four amino acids investigated (glutamic acid, glycine, proline, and tyrosine) between patients with SPMS and CS. CONCLUSIONS: The preliminary results obtained in the study suggest that the metabolism of some amino acids is altered in patient with SPMS. We also conclude that amino acid profiling might be helpful in searching for putative biomarkers of central nervous system diseases. However, considering the multifactorial, heterogeneous, and complex nature of SPMS, further validation research involving larger study samples is required before applying these biomarkers in diagnostic practice.
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spelling pubmed-94445532022-09-13 Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report Rzepiński, Łukasz Kośliński, Piotr Gackowski, Marcin Koba, Marcin Maciejek, Zdzisław J Clin Neurol Original Article BACKGROUND AND PURPOSE: Aging in multiple sclerosis is associated with both disease- and age-dependent neurodegeneration. Serum metabolomic profiling of amino acids seems to be a promising method for searching for biomarkers of neurodegenerative disorders. The aim of this study was to determine the profile of nonessential amino acids in the serum of elderly patients with secondary progressive multiple sclerosis (SPMS). METHODS: We used high-performance liquid chromatography to evaluate the serum concentrations of nonessential amino acids in subjects aged >65 years: six patients with SPMS and 20 control subjects (CS). RESULTS: The serine and alanine levels were significantly higher in SPMS patients than in CS, whereas the concentrations of aspartic acid, arginine, and cysteine were significantly lower in SPMS patients. These observations indicate that amino acids may be involved in SPMS neurodegeneration mechanisms. There were no significant differences in the serum concentrations of the other four amino acids investigated (glutamic acid, glycine, proline, and tyrosine) between patients with SPMS and CS. CONCLUSIONS: The preliminary results obtained in the study suggest that the metabolism of some amino acids is altered in patient with SPMS. We also conclude that amino acid profiling might be helpful in searching for putative biomarkers of central nervous system diseases. However, considering the multifactorial, heterogeneous, and complex nature of SPMS, further validation research involving larger study samples is required before applying these biomarkers in diagnostic practice. Korean Neurological Association 2022-09 2022-05-20 /pmc/articles/PMC9444553/ /pubmed/36062770 http://dx.doi.org/10.3988/jcn.2022.18.5.529 Text en Copyright © 2022 Korean Neurological Association https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Rzepiński, Łukasz
Kośliński, Piotr
Gackowski, Marcin
Koba, Marcin
Maciejek, Zdzisław
Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report
title Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report
title_full Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report
title_fullStr Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report
title_full_unstemmed Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report
title_short Amino Acid Levels as Potential Biomarkers of Multiple Sclerosis in Elderly Patients: Preliminary Report
title_sort amino acid levels as potential biomarkers of multiple sclerosis in elderly patients: preliminary report
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444553/
https://www.ncbi.nlm.nih.gov/pubmed/36062770
http://dx.doi.org/10.3988/jcn.2022.18.5.529
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