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Decreased Cerebrospinal Fluid Antioxidative Capacity Is Related to Disease Severity and Progression in Early Multiple Sclerosis.
Voortman, Margarete M; Damulina, Anna; Pirpamer, Lukas; Pinter, Daniela; Pichler, Alexander; Enzinger, Christian; Ropele, Stefan; Bachmaier, Gerhard; Archelos, Juan-Jose; Marsche, Gunther; Khalil, Michael.
Affiliation
  • Voortman MM; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Damulina A; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Pirpamer L; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Pinter D; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Pichler A; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Enzinger C; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Ropele S; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Bachmaier G; Institute for Medical Informatics, Statistics and Documentation, Medical University of Graz, 8036 Graz, Austria.
  • Archelos JJ; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
  • Marsche G; Division of Pharmacology, Otto Loewi Research Center, Medical University of Graz, 8036 Graz, Austria.
  • Khalil M; Department of Neurology, Medical University of Graz, 8036 Graz, Austria.
Biomolecules ; 11(9)2021 08 25.
Article in En | MEDLINE | ID: mdl-34572477
Background: Oxidative stress-induced neuronal damage in multiple sclerosis (MS) results from an imbalance between toxic free radicals and counteracting antioxidants, i.e., antioxidative capacity (AOC). The relation of AOC to outcome measures in MS still remains inconclusive. We aimed to compare AOC in cerebrospinal fluid (CSF) and serum between early MS and controls and assess its correlation with clinical/radiological measures. Methods: We determined AOC (ability of CSF and serum of patients to inhibit 2,2'-azobis(2-amidinopropane) dihydrochloride-induced oxidation of dihydrorhodamine) in clinically isolated syndrome (CIS)/early relapsing-remitting MS (RRMS) (n = 55/11) and non-inflammatory neurological controls (n = 67). MS patients underwent clinical follow-up (median, 4.5; IQR, 5.2 years) and brain MRI at 3 T (baseline/follow-up n = 47/34; median time interval, 3.5; IQR, 2.1 years) to determine subclinical disease activity. Results: CSF AOC was differently regulated among CIS, RRMS and controls (p = 0.031) and lower in RRMS vs. CIS (p = 0.020). Lower CSF AOC correlated with physical disability (r = -0.365, p = 0.004) and risk for future relapses (exp(ß) = 0.929, p = 0.033). No correlations with MRI metrics were found. Conclusion: Decreased CSF AOC was associated with increased disability and clinical disease activity in MS. While our finding cannot prove causation, they should prompt further investigations into the role of AOC in the evolution of MS.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Severity of Illness Index / Disease Progression / Multiple Sclerosis / Antioxidants Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Biomolecules Year: 2021 Document type: Article Affiliation country: Austria Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Severity of Illness Index / Disease Progression / Multiple Sclerosis / Antioxidants Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Biomolecules Year: 2021 Document type: Article Affiliation country: Austria Country of publication: Switzerland