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Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study

OBJECTIVE: To address the frequency of myelin oligodendrocyte glycoprotein (MOG) antibody (Ab) in an unselected large cohort of adults with MS. METHODS: This is a cross-sectional study in 2 MS expert centers (Lyon and Strasbourg University Hospitals, France) between December 1, 2017, and June 31, 20...

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Autores principales: Cobo-Calvo, Álvaro, d'Indy, Hyacintha, Ruiz, Anne, Collongues, Nicolas, Kremer, Laurent, Durand-Dubief, Françoise, Rollot, Fabien, Casey, Romain, Vukusic, Sandra, De Seze, Jérôme, Marignier, Romain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943364/
https://www.ncbi.nlm.nih.gov/pubmed/31836640
http://dx.doi.org/10.1212/NXI.0000000000000649
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author Cobo-Calvo, Álvaro
d'Indy, Hyacintha
Ruiz, Anne
Collongues, Nicolas
Kremer, Laurent
Durand-Dubief, Françoise
Rollot, Fabien
Casey, Romain
Vukusic, Sandra
De Seze, Jérôme
Marignier, Romain
author_facet Cobo-Calvo, Álvaro
d'Indy, Hyacintha
Ruiz, Anne
Collongues, Nicolas
Kremer, Laurent
Durand-Dubief, Françoise
Rollot, Fabien
Casey, Romain
Vukusic, Sandra
De Seze, Jérôme
Marignier, Romain
author_sort Cobo-Calvo, Álvaro
collection PubMed
description OBJECTIVE: To address the frequency of myelin oligodendrocyte glycoprotein (MOG) antibody (Ab) in an unselected large cohort of adults with MS. METHODS: This is a cross-sectional study in 2 MS expert centers (Lyon and Strasbourg University Hospitals, France) between December 1, 2017, and June 31, 2018. Patients aged ≥18 years with a definite diagnosis of MS according to 2010 McDonald criteria were tested for MOG-Ab by using a cell-based assay (CBA) in Lyon and subsequently included. Positive samples were tested by investigators blinded to the first result with a second assay in a different laboratory (Barcelona, Spain) by using the same plasmid and secondary Ab. RESULTS: Serum samples from 685 consecutive patients with MS were analyzed for MOG-Ab. Median disease duration at sampling was 11.5 (interquartile range, 5.8–17.7) years, and 72% were women. Two (0.3%) patients resulted to be MOG-Ab-positive. The 2 patients were women aged 42 and 38 at disease onset and were diagnosed with secondary and primary progressive forms of MS, respectively. This positive result was confirmed by the CBA in Barcelona. CONCLUSION: Our findings indicate that MOG-Ab are exceptional in MS phenotype, suggesting that the MOG-Ab testing should not be performed in typical MS presentation.
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spelling pubmed-69433642020-02-10 Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study Cobo-Calvo, Álvaro d'Indy, Hyacintha Ruiz, Anne Collongues, Nicolas Kremer, Laurent Durand-Dubief, Françoise Rollot, Fabien Casey, Romain Vukusic, Sandra De Seze, Jérôme Marignier, Romain Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To address the frequency of myelin oligodendrocyte glycoprotein (MOG) antibody (Ab) in an unselected large cohort of adults with MS. METHODS: This is a cross-sectional study in 2 MS expert centers (Lyon and Strasbourg University Hospitals, France) between December 1, 2017, and June 31, 2018. Patients aged ≥18 years with a definite diagnosis of MS according to 2010 McDonald criteria were tested for MOG-Ab by using a cell-based assay (CBA) in Lyon and subsequently included. Positive samples were tested by investigators blinded to the first result with a second assay in a different laboratory (Barcelona, Spain) by using the same plasmid and secondary Ab. RESULTS: Serum samples from 685 consecutive patients with MS were analyzed for MOG-Ab. Median disease duration at sampling was 11.5 (interquartile range, 5.8–17.7) years, and 72% were women. Two (0.3%) patients resulted to be MOG-Ab-positive. The 2 patients were women aged 42 and 38 at disease onset and were diagnosed with secondary and primary progressive forms of MS, respectively. This positive result was confirmed by the CBA in Barcelona. CONCLUSION: Our findings indicate that MOG-Ab are exceptional in MS phenotype, suggesting that the MOG-Ab testing should not be performed in typical MS presentation. Lippincott Williams & Wilkins 2019-12-13 /pmc/articles/PMC6943364/ /pubmed/31836640 http://dx.doi.org/10.1212/NXI.0000000000000649 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Cobo-Calvo, Álvaro
d'Indy, Hyacintha
Ruiz, Anne
Collongues, Nicolas
Kremer, Laurent
Durand-Dubief, Françoise
Rollot, Fabien
Casey, Romain
Vukusic, Sandra
De Seze, Jérôme
Marignier, Romain
Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study
title Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study
title_full Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study
title_fullStr Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study
title_full_unstemmed Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study
title_short Frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: A multicenter cross-sectional study
title_sort frequency of myelin oligodendrocyte glycoprotein antibody in multiple sclerosis: a multicenter cross-sectional study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943364/
https://www.ncbi.nlm.nih.gov/pubmed/31836640
http://dx.doi.org/10.1212/NXI.0000000000000649
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