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Keywords {🔍}

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Topics {✒️}

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Schema {🗺️}

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         headline:Anti-MOG antibodies are present in a subgroup of patients with a neuromyelitis optica phenotype
         description:Antibodies against myelin oligodendrocyte glycoprotein (MOG) have been identified in a subgroup of pediatric patients with inflammatory demyelinating disease of the central nervous system (CNS) and in some patients with neuromyelitis optica spectrum disorder (NMOSD). The aim of this study was to examine the frequency, clinical features, and long-term disease course of patients with anti-MOG antibodies in a European cohort of NMO/NMOSD. Sera from 48 patients with NMO/NMOSD and 48 patients with relapsing-remitting multiple sclerosis (RR-MS) were tested for anti-aquaporin-4 (AQP4) and anti-MOG antibodies with a cell-based assay. Anti-MOG antibodies were found in 4/17 patients with AQP4-seronegative NMO/NMOSD, but in none of the AQP4-seropositive NMO/NMOSD (n = 31) or RR-MS patients (n = 48). MOG-seropositive patients tended towards younger disease onset with a higher percentage of patients with pediatric (<18 years) disease onset (MOG+, AQP4+, MOG−/AQP4−: 2/4, 3/31, 0/13). MOG-seropositive patients presented more often with positive oligoclonal bands (OCBs) (3/3, 5/29, 1/13) and brain magnetic resonance imaging (MRI) lesions during disease course (2/4, 5/31, 1/13). Notably, the mean time to the second attack affecting a different CNS region was longer in the anti-MOG antibody-positive group (11.3, 3.2, 3.4 years). MOG-seropositive patients show a diverse clinical phenotype with clinical features resembling both NMO (attacks mainly confined to the spinal cord and optic nerves) and MS with an opticospinal presentation (positive OCBs, brain lesions). Anti-MOG antibodies can serve as a diagnostic and maybe prognostic tool in patients with an AQP4-seronegative NMO phenotype and should be tested in those patients.
         datePublished:2015-03-08T00:00:00Z
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            Neuromyelitis optica
            Neuromyelitis optica spectrum disorder
            Anti-aquaporin-4 antibodies
            Anti-MOG antibodies
            Inflammatory demyelinating CNS disease
            Neurosciences
            Neurology
            Neurobiology
            Immunology
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      headline:Anti-MOG antibodies are present in a subgroup of patients with a neuromyelitis optica phenotype
      description:Antibodies against myelin oligodendrocyte glycoprotein (MOG) have been identified in a subgroup of pediatric patients with inflammatory demyelinating disease of the central nervous system (CNS) and in some patients with neuromyelitis optica spectrum disorder (NMOSD). The aim of this study was to examine the frequency, clinical features, and long-term disease course of patients with anti-MOG antibodies in a European cohort of NMO/NMOSD. Sera from 48 patients with NMO/NMOSD and 48 patients with relapsing-remitting multiple sclerosis (RR-MS) were tested for anti-aquaporin-4 (AQP4) and anti-MOG antibodies with a cell-based assay. Anti-MOG antibodies were found in 4/17 patients with AQP4-seronegative NMO/NMOSD, but in none of the AQP4-seropositive NMO/NMOSD (n = 31) or RR-MS patients (n = 48). MOG-seropositive patients tended towards younger disease onset with a higher percentage of patients with pediatric (<18 years) disease onset (MOG+, AQP4+, MOG−/AQP4−: 2/4, 3/31, 0/13). MOG-seropositive patients presented more often with positive oligoclonal bands (OCBs) (3/3, 5/29, 1/13) and brain magnetic resonance imaging (MRI) lesions during disease course (2/4, 5/31, 1/13). Notably, the mean time to the second attack affecting a different CNS region was longer in the anti-MOG antibody-positive group (11.3, 3.2, 3.4 years). MOG-seropositive patients show a diverse clinical phenotype with clinical features resembling both NMO (attacks mainly confined to the spinal cord and optic nerves) and MS with an opticospinal presentation (positive OCBs, brain lesions). Anti-MOG antibodies can serve as a diagnostic and maybe prognostic tool in patients with an AQP4-seronegative NMO phenotype and should be tested in those patients.
      datePublished:2015-03-08T00:00:00Z
      dateModified:2015-03-08T00:00:00Z
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      pageEnd:7
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      keywords:
         Neuromyelitis optica
         Neuromyelitis optica spectrum disorder
         Anti-aquaporin-4 antibodies
         Anti-MOG antibodies
         Inflammatory demyelinating CNS disease
         Neurosciences
         Neurology
         Neurobiology
         Immunology
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      name:Department of Neurology, Hôpital de Hautepierre, University Hospital Strasbourg, Strasbourg, France
      name:Institute of Clinical Neuroimmunology, University Hospital Grosshadern, Munich, Germany
      name:Department of Neurology, Hôpital de Hautepierre, University Hospital Strasbourg, Strasbourg, France
      name:Department of Neurology, Hôpital de Hautepierre, University Hospital Strasbourg, Strasbourg, France
      name:Department of Neurology, University Hospital Basel, Basel, Switzerland
      name:Department of Biomedicine, University of Basel, Basel, Switzerland
      name:Department of Neurology, University Hospital Basel, Basel, Switzerland
      name:Department of Biomedicine, University of Basel, Basel, Switzerland
      name:Department of Neurology, University Hospital Basel, Basel, Switzerland
      name:Department of Biomedicine, University of Basel, Basel, Switzerland
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      name:Department of Neurology, University Hospital Basel, Basel, Switzerland
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