The Use of Nitrosative Stress Molecules as Potential Diagnostic Biomarkers in Multiple Sclerosis
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Published:2024-01-08
Issue:2
Volume:25
Page:787
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ISSN:1422-0067
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Container-title:International Journal of Molecular Sciences
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language:en
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Short-container-title:IJMS
Author:
Räuber Saskia1ORCID, Förster Moritz12ORCID, Schüller Julia1, Willison Alice1ORCID, Golombeck Kristin S.1, Schroeter Christina B.1, Oeztuerk Menekse1, Jansen Robin1, Huntemann Niklas1ORCID, Nelke Christopher1, Korsen Melanie1, Fischer Katinka1, Kerkhoff Ruth12, Leven Yana1, Kirschner Patricia1, Kölsche Tristan1, Nikolov Petyo1, Mehsin Mohammed1, Marae Gelenar1, Kokott Alma1, Pul Duygu1, Schulten Julius1, Vogel Niklas1, Ingwersen Jens1, Ruck Tobias1ORCID, Pawlitzki Marc1, Meuth Sven G.1ORCID, Melzer Nico1ORCID, Kremer David13
Affiliation:
1. Department of Neurology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany 2. Department of Neurology, Kliniken Maria Hilf GmbH, Academic Teaching Hospital of the RWTH Aachen University Hospital, 41063 Moenchengladbach, Germany 3. Department of Neurology and Neurorehabilitation, Hospital Zum Heiligen Geist, Academic Teaching Hospital of the Heinrich Heine University Düsseldorf, 47906 Kempen, Germany
Abstract
Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) of still unclear etiology. In recent years, the search for biomarkers facilitating its diagnosis, prognosis, therapy response, and other parameters has gained increasing attention. In this regard, in a previous meta-analysis comprising 22 studies, we found that MS is associated with higher nitrite/nitrate (NOx) levels in the cerebrospinal fluid (CSF) compared to patients with non-inflammatory other neurological diseases (NIOND). However, many of the included studies did not distinguish between the different clinical subtypes of MS, included pre-treated patients, and inclusion criteria varied. As a follow-up to our meta-analysis, we therefore aimed to analyze the serum and CSF NOx levels in clinically well-defined cohorts of treatment-naïve MS patients compared to patients with somatic symptom disorder. To this end, we analyzed the serum and CSF levels of NOx in 117 patients (71 relapsing–remitting (RR) MS, 16 primary progressive (PP) MS, and 30 somatic symptom disorder). We found that RRMS and PPMS patients had higher serum NOx levels compared to somatic symptom disorder patients. This difference remained significant in the subgroup of MRZ-negative RRMS patients. In conclusion, the measurement of NOx in the serum might indeed be a valuable tool in supporting MS diagnosis.
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