Overlapping demyelinating syndromes and anti-NMDA receptor encephalitis

dc.contributor.authorTitulaer, Maarten J.
dc.contributor.authorHöftberger, Romana
dc.contributor.authorIizuka, Takahiro
dc.contributor.authorLeypoldt, Frank
dc.contributor.authorMcCracken, Lindsey
dc.contributor.authorCellucci, Tania
dc.contributor.authorBenson, Leslie A.
dc.contributor.authorShu, Huidy
dc.contributor.authorIrioka, Takashi
dc.contributor.authorHirano, Makito
dc.contributor.authorSingh, Gagandeep
dc.contributor.authorCobo Calvo, Álvaro
dc.contributor.authorKaida, Kenichi
dc.contributor.authorMorales, Pamela S.
dc.contributor.authorWirtz, Paul W.
dc.contributor.authorYamamoto, Tomotaka
dc.contributor.authorReindl, Markus
dc.contributor.authorRosenfeld, Myrna R.
dc.contributor.authorGraus Ribas, Francesc
dc.contributor.authorSaiz Hinarejos, Albert
dc.contributor.authorDalmau Obrador, Josep
dc.date.accessioned2018-11-08T15:10:34Z
dc.date.available2018-11-08T15:10:34Z
dc.date.issued2014-02-11
dc.date.updated2018-11-08T15:10:34Z
dc.description.abstractObjective: To report the clinical, radiological, and immunological association of demyelinating disorders with anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis. Methods: Clinical and radiological analysis was done of a cohort of 691 patients with anti-NMDAR encephalitis. Determination of antibodies to NMDAR, aquaporin-4 (AQP4), and myelin oligodendrocyte glycoprotein (MOG) was performed using brain immunohistochemistry and cell-based assays. Results: Twenty-three of 691 patients with anti-NMDAR encephalitis had prominent magnetic resonance imaging (MRI) and/or clinical features of demyelination. Group 1 included 12 patients in whom anti-NMDAR encephalitis was preceded or followed by independent episodes of neuromyelitis optica (NMO) spectrum disorder (5 cases, 4 anti-AQP4 positive) or brainstem or multifocal demyelinating syndromes (7 cases, all anti-MOG positive). Group 2 included 11 patients in whom anti-NMDAR encephalitis occurred simultaneously with MRI and symptoms compatible with demyelination (5 AQ4 positive, 2 MOG positive). Group 3 (136 controls) included 50 randomly selected patients with typical anti-NMDAR encephalitis, 56 with NMO, and 30 with multiple sclerosis; NMDAR antibodies were detected only in the 50 anti-NMDAR patients, MOG antibodies in 3 of 50 anti-NMDAR and 1 of 56 NMO patients, and AQP4 antibodies in 48 of 56 NMO and 1 of 50 anti-NMDAR patients (p < 0.0001 for all comparisons with Groups 1 and 2). Most patients improved with immunotherapy, but compared with anti-NMDAR encephalitis the demyelinating episodes required more intensive therapy and resulted in more residual deficits. Only 1 of 23 NMDAR patients with signs of demyelination had ovarian teratoma compared with 18 of 50 anti-NMDAR controls (p = 0.011). Interpretation: Patients with anti-NMDAR encephalitis may develop concurrent or separate episodes of demyelinating disorders, and conversely patients with NMO or demyelinating disorders with atypical symptoms (eg, dyskinesias, psychosis) may have anti-NMDAR encephalitis.
dc.format.extent18 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec654289
dc.identifier.issn0364-5134
dc.identifier.pmid24700511
dc.identifier.urihttps://hdl.handle.net/2445/125927
dc.language.isoeng
dc.publisherWiley-Liss
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1002/ana.24117
dc.relation.ispartofAnnals of Neurology, 2014, vol. 75, num. 3, p. 411-428
dc.relation.urihttps://doi.org/10.1002/ana.24117
dc.rights(c) American Neurological Association, 2014
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationEncefalitis
dc.subject.classificationReceptors cel·lulars
dc.subject.otherEncephalitis
dc.subject.otherCell receptors
dc.titleOverlapping demyelinating syndromes and anti-NMDA receptor encephalitis
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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