Delimiting MOGAD as a disease entity using translational imaging

The first formal consensus diagnostic criteria for myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) were recently proposed. Yet, the distinction of MOGAD-defining characteristics from characteristics of its important differential diagnoses such as multiple sclerosis (MS) and a...

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Main Authors: Frederike Cosima Oertel, Maria Hastermann, Friedemann Paul
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2023.1216477/full
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author Frederike Cosima Oertel
Frederike Cosima Oertel
Frederike Cosima Oertel
Maria Hastermann
Maria Hastermann
Friedemann Paul
Friedemann Paul
Friedemann Paul
author_facet Frederike Cosima Oertel
Frederike Cosima Oertel
Frederike Cosima Oertel
Maria Hastermann
Maria Hastermann
Friedemann Paul
Friedemann Paul
Friedemann Paul
author_sort Frederike Cosima Oertel
collection DOAJ
description The first formal consensus diagnostic criteria for myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) were recently proposed. Yet, the distinction of MOGAD-defining characteristics from characteristics of its important differential diagnoses such as multiple sclerosis (MS) and aquaporin-4 antibody seropositive neuromyelitis optica spectrum disorder (NMOSD) is still obstructed. In preclinical research, MOG antibody-based animal models were used for decades to derive knowledge about MS. In clinical research, people with MOGAD have been combined into cohorts with other diagnoses. Thus, it remains unclear to which extent the generated knowledge is specifically applicable to MOGAD. Translational research can contribute to identifying MOGAD characteristic features by establishing imaging methods and outcome parameters on proven pathophysiological grounds. This article reviews suitable animal models for translational MOGAD research and the current state and prospect of translational imaging in MOGAD.
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spelling doaj.art-676e278f17474b62bc121a6d3b26c0612024-03-08T11:12:14ZengFrontiers Media S.A.Frontiers in Neurology1664-22952023-12-011410.3389/fneur.2023.12164771216477Delimiting MOGAD as a disease entity using translational imagingFrederike Cosima Oertel0Frederike Cosima Oertel1Frederike Cosima Oertel2Maria Hastermann3Maria Hastermann4Friedemann Paul5Friedemann Paul6Friedemann Paul7Experimental and Clinical Research Center, Max-Delbrück-Centrum für Molekulare Medizin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyNeuroscience Clinical Research Center, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyDepartment of Neurology, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyExperimental and Clinical Research Center, Max-Delbrück-Centrum für Molekulare Medizin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyNeuroscience Clinical Research Center, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyExperimental and Clinical Research Center, Max-Delbrück-Centrum für Molekulare Medizin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyNeuroscience Clinical Research Center, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyDepartment of Neurology, Freie Universität Berlin and Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Berlin, GermanyThe first formal consensus diagnostic criteria for myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) were recently proposed. Yet, the distinction of MOGAD-defining characteristics from characteristics of its important differential diagnoses such as multiple sclerosis (MS) and aquaporin-4 antibody seropositive neuromyelitis optica spectrum disorder (NMOSD) is still obstructed. In preclinical research, MOG antibody-based animal models were used for decades to derive knowledge about MS. In clinical research, people with MOGAD have been combined into cohorts with other diagnoses. Thus, it remains unclear to which extent the generated knowledge is specifically applicable to MOGAD. Translational research can contribute to identifying MOGAD characteristic features by establishing imaging methods and outcome parameters on proven pathophysiological grounds. This article reviews suitable animal models for translational MOGAD research and the current state and prospect of translational imaging in MOGAD.https://www.frontiersin.org/articles/10.3389/fneur.2023.1216477/fullmyelin oligodendrocyte glycoprotein associated diseaseimagingtranslational researchEAEanimal models
spellingShingle Frederike Cosima Oertel
Frederike Cosima Oertel
Frederike Cosima Oertel
Maria Hastermann
Maria Hastermann
Friedemann Paul
Friedemann Paul
Friedemann Paul
Delimiting MOGAD as a disease entity using translational imaging
Frontiers in Neurology
myelin oligodendrocyte glycoprotein associated disease
imaging
translational research
EAE
animal models
title Delimiting MOGAD as a disease entity using translational imaging
title_full Delimiting MOGAD as a disease entity using translational imaging
title_fullStr Delimiting MOGAD as a disease entity using translational imaging
title_full_unstemmed Delimiting MOGAD as a disease entity using translational imaging
title_short Delimiting MOGAD as a disease entity using translational imaging
title_sort delimiting mogad as a disease entity using translational imaging
topic myelin oligodendrocyte glycoprotein associated disease
imaging
translational research
EAE
animal models
url https://www.frontiersin.org/articles/10.3389/fneur.2023.1216477/full
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