{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,17]],"date-time":"2026-10-17T02:06:45Z","timestamp":1792202805215,"version":"4.4.0"},"reference-count":29,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2020,10,15]],"date-time":"2020-10-15T00:00:00Z","timestamp":1602720000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Annals of Neurology"],"published-print":{"date-parts":[[2021,1]]},"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>The main objective was to compare clinical features, disease course, and myelin oligodendrocyte glycoprotein (MOG) antibody (Ab) dynamics between children and adults with MOG\u2010Ab\u2013associated disease (MOGAD).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>This retrospective multicentric, national study included 98 children and 268 adults with MOGAD between January 2014 and September 2019. Cox regression model for recurrent time\u2010to\u2010event data and Kaplan\u2013Meier curves for time to antibody negativity were performed for the objectives.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Isolated optic neuritis was the most frequent clinical presentation in both children (40.8%) and adults (55.9%,\n                      <jats:italic>p<\/jats:italic>\n                      = 0.013), and acute disseminated encephalomyelitis syndrome was more frequent in children (36.7% vs 5.6%,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001). Compared to adults, children displayed better recovery (Expanded Disability Status Scale \u2265\u20093.0 at last follow\u2010up reached only by 10 of 97 [10.3%] vs 66\/247 [26.7%],\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001). In the multivariate analysis, adults were at higher risk of relapse than children (hazard ratio = 1.41, 95% confidence interval [CI] =\u20091.12\u20131.78,\n                      <jats:italic>p<\/jats:italic>\n                      = 0.003). At 2\u2009years, 64.2% (95% CI = 40.9\u201386.5) of nonrelapsing children became MOG\u2010Ab negative compared to 14.1% (95% CI = 4.7\u201338.3) of relapsing children (log\u2010rank\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001), with no differences observed in adults (log\u2010rank\n                      <jats:italic>p<\/jats:italic>\n                      = 0.280).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interpretation<\/jats:title>\n                    <jats:p>MOGAD patients differ in the clinical presentation at onset, showing an age\u2010related shift in the clinical features across age groups. Compared to children, adults have a higher risk of relapse and worse functional recovery. Finally, children with monophasic disease become MOG\u2010Ab negative earlier than relapsing children, but this is not true in adults. Considering these differences, management and treatment guidelines should be considered independently in children and adults. ANN NEUROL 2021;89:30\u201341<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/ana.25909","type":"journal-article","created":{"date-parts":[[2020,9,21]],"date-time":"2020-09-21T23:56:41Z","timestamp":1600732601000},"page":"30-41","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":268,"title":["Clinical Features and Risk of Relapse in Children and Adults with Myelin Oligodendrocyte Glycoprotein Antibody\u2013Associated Disease"],"prefix":"10.1002","volume":"89","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2574-0721","authenticated-orcid":false,"given":"Alvaro","family":"Cobo\u2010Calvo","sequence":"first","affiliation":[{"name":"Department of Neurology, Multiple Sclerosis and Neuroinflammation, Pierre Wertheimer Neurological Hospital, Lyon Civil Hospices  Lyon France"},{"name":"Department of Neurology\u2010Neuroimmunology, Multiple Sclerosis Center Catalonia, Vall d'Hebron Institute of Research, Vall d'Hebron University Hospital, Autonomous University of Barcelona  Barcelona Spain"},{"name":"Lyon Neuroscience Research Center, U1028 INSERM, UMR5292 CNRS, FLUID Team  Lyon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anne","family":"Ruiz","sequence":"additional","affiliation":[{"name":"Lyon Neuroscience Research Center, U1028 INSERM, UMR5292 CNRS, FLUID Team  Lyon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5752-2331","authenticated-orcid":false,"given":"Fabien","family":"Rollot","sequence":"additional","affiliation":[{"name":"University of Lyon, Claude Bernard University Lyon 1, Lyon Civil Hospices, EDMUS Foundation, OFSEP, Lyon Neuroscience Research Center  Lyon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Georgina","family":"Arrambide","sequence":"additional","affiliation":[{"name":"Department of Neurology\u2010Neuroimmunology, Multiple Sclerosis Center Catalonia, Vall d'Hebron Institute of Research, Vall d'Hebron University Hospital, Autonomous University of Barcelona  Barcelona Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Romain","family":"Deschamps","sequence":"additional","affiliation":[{"name":"Department of Neurology Adolphe de Rothschild Hospital Foundation  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elisabeth","family":"Maillart","sequence":"additional","affiliation":[{"name":"Department of Neurology and Reference Center for Rare Inflammatory Diseases of the Brain and Bone Piti\u00e9\u2010Salp\u00eatri\u00e8re Hospital, Public Hospital Network of Paris  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Caroline","family":"Papeix","sequence":"additional","affiliation":[{"name":"Department of Neurology and Reference Center for Rare Inflammatory Diseases of the Brain and Bone Piti\u00e9\u2010Salp\u00eatri\u00e8re Hospital, Public Hospital Network of Paris  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bertrand","family":"Audoin","sequence":"additional","affiliation":[{"name":"Aix\u2010Marseille University, Public Assistance Hospitals of Marseille, Timone Hospital, Clinical Neuroscience Center, Neurology Department  Marseille France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anne Fabienne","family":"L\u00e9pine","sequence":"additional","affiliation":[{"name":"Pediatric Neurology Department Timone Hospital, Public Assistance Hospitals of Marseille  Marseille France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H\u00e9l\u00e8ne","family":"Maurey","sequence":"additional","affiliation":[{"name":"National Referral Center for Neuroinflammatory Diseases and Pediatric Neurology Department Public Hospital Network of Paris, Bic\u00eatre Hospital  Le Kremlin\u2010Bic\u00eatre France"},{"name":"Department of Neuropediatrics, University of Paris\u2010Sud  Le Kremlin\u2010Bic\u00eatre 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