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Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment

Background. Oxidative stress is well documented in multiple sclerosis (MS) lesions, but its correspondence at peripheral level is still controversial. Objective. To evaluate peripheral oxidative stress markers in MS patients. Methods. We studied total blood levels of Coenzyme Q(10) (CoQ(10)), oxidiz...

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Autores principales: Gironi, Maira, Borgiani, Bruno, Mariani, Enrica, Cursano, Cristina, Mendozzi, Laura, Cavarretta, Rossella, Saresella, Marina, Clerici, Mario, Comi, Giancarlo, Rovaris, Marco, Furlan, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984797/
https://www.ncbi.nlm.nih.gov/pubmed/24741637
http://dx.doi.org/10.1155/2014/961863
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author Gironi, Maira
Borgiani, Bruno
Mariani, Enrica
Cursano, Cristina
Mendozzi, Laura
Cavarretta, Rossella
Saresella, Marina
Clerici, Mario
Comi, Giancarlo
Rovaris, Marco
Furlan, Roberto
author_facet Gironi, Maira
Borgiani, Bruno
Mariani, Enrica
Cursano, Cristina
Mendozzi, Laura
Cavarretta, Rossella
Saresella, Marina
Clerici, Mario
Comi, Giancarlo
Rovaris, Marco
Furlan, Roberto
author_sort Gironi, Maira
collection PubMed
description Background. Oxidative stress is well documented in multiple sclerosis (MS) lesions, but its correspondence at peripheral level is still controversial. Objective. To evaluate peripheral oxidative stress markers in MS patients. Methods. We studied total blood levels of Coenzyme Q(10) (CoQ(10)), oxidized and reduced forms of glutathione, malondialdehyde, reactive oxygen species (ROS), anti-oxidized-low-density lipoproteins (anti-oxLDL) antibodies, and antioxidant power (PAO) in 87 patients with different MS clinical phenotypes and in 77 controls. Results. CoQ(10) was lower whereas anti-oxLDL antibodies titer was higher in MS patients than in controls. The benign variant of MS displayed both higher CoQ(10) and higher anti-oxLDL than other MS clinical variants. Female patients had lower CoQ(10) and PAO and higher ROS than male patients. Differences were greater in younger patients with shorter disease duration. Surprisingly, there was no difference for these markers between treated and untreated patients. Conclusion. We found lower antioxidant agents and higher anti-oxLDL antibodies in MS, and the highest antibody titers occurred in the benign form. We suggest that natural anti-oxLDL antibodies can be protective against MS, saving blood brain barrier integrity. Our findings also suggest that milder MS is associated with a distinct oxidative stress pattern, which may provide a useful biomarker of disease prognosis.
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spelling pubmed-39847972014-04-16 Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment Gironi, Maira Borgiani, Bruno Mariani, Enrica Cursano, Cristina Mendozzi, Laura Cavarretta, Rossella Saresella, Marina Clerici, Mario Comi, Giancarlo Rovaris, Marco Furlan, Roberto J Immunol Res Research Article Background. Oxidative stress is well documented in multiple sclerosis (MS) lesions, but its correspondence at peripheral level is still controversial. Objective. To evaluate peripheral oxidative stress markers in MS patients. Methods. We studied total blood levels of Coenzyme Q(10) (CoQ(10)), oxidized and reduced forms of glutathione, malondialdehyde, reactive oxygen species (ROS), anti-oxidized-low-density lipoproteins (anti-oxLDL) antibodies, and antioxidant power (PAO) in 87 patients with different MS clinical phenotypes and in 77 controls. Results. CoQ(10) was lower whereas anti-oxLDL antibodies titer was higher in MS patients than in controls. The benign variant of MS displayed both higher CoQ(10) and higher anti-oxLDL than other MS clinical variants. Female patients had lower CoQ(10) and PAO and higher ROS than male patients. Differences were greater in younger patients with shorter disease duration. Surprisingly, there was no difference for these markers between treated and untreated patients. Conclusion. We found lower antioxidant agents and higher anti-oxLDL antibodies in MS, and the highest antibody titers occurred in the benign form. We suggest that natural anti-oxLDL antibodies can be protective against MS, saving blood brain barrier integrity. Our findings also suggest that milder MS is associated with a distinct oxidative stress pattern, which may provide a useful biomarker of disease prognosis. Hindawi Publishing Corporation 2014 2014-03-26 /pmc/articles/PMC3984797/ /pubmed/24741637 http://dx.doi.org/10.1155/2014/961863 Text en Copyright © 2014 Maira Gironi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gironi, Maira
Borgiani, Bruno
Mariani, Enrica
Cursano, Cristina
Mendozzi, Laura
Cavarretta, Rossella
Saresella, Marina
Clerici, Mario
Comi, Giancarlo
Rovaris, Marco
Furlan, Roberto
Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment
title Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment
title_full Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment
title_fullStr Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment
title_full_unstemmed Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment
title_short Oxidative Stress Is Differentially Present in Multiple Sclerosis Courses, Early Evident, and Unrelated to Treatment
title_sort oxidative stress is differentially present in multiple sclerosis courses, early evident, and unrelated to treatment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984797/
https://www.ncbi.nlm.nih.gov/pubmed/24741637
http://dx.doi.org/10.1155/2014/961863
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