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

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  • Additional Information
    • Contributors:
      Hôpital neurologique et neurochirurgical Pierre Wertheimer CHU - HCL; Hospices Civils de Lyon (HCL); Centre de Référence des Maladies Inflammatoires Rares du Cerveau et de la Moelle (MIRCEM); Centre de recherche en neurosciences de Lyon - Lyon Neuroscience Research Center (CRNL); Université Claude Bernard Lyon 1 (UCBL); Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); Biopathologie de la Myéline, Neuroprotection et Stratégies Thérapeutiques (BMNST); Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM); Centre Hospitalier Universitaire Strasbourg (CHU Strasbourg); Les Hôpitaux Universitaires de Strasbourg (HUS); Fédération de Médecine Translationnelle de Strasbourg (FMTS); Université de Strasbourg (UNISTRA); CIC Strasbourg (Centre d’Investigation Clinique Plurithématique (CIC - P) ); Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Nouvel Hôpital Civil de Strasbourg; Les Hôpitaux Universitaires de Strasbourg (HUS)-Les Hôpitaux Universitaires de Strasbourg (HUS)-Hôpital de Hautepierre Strasbourg; ANR-10-COHO-0002,OFSEP,Observatoire Français de la Sclérose en Plaques(2010)
    • Publication Information:
      HAL CCSD
      American Academy of neurology
    • Publication Date:
      2020
    • Collection:
      Université Jean Monnet – Saint-Etienne: HAL
    • Abstract:
      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.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/31836640; hal-03791044; https://hal.science/hal-03791044; https://hal.science/hal-03791044/document; https://hal.science/hal-03791044/file/islandora_148707.pdf; PUBMED: 31836640; PUBMEDCENTRAL: PMC6943364
    • Accession Number:
      10.1212/NXI.0000000000000649
    • Online Access:
      https://doi.org/10.1212/NXI.0000000000000649
      https://hal.science/hal-03791044
      https://hal.science/hal-03791044/document
      https://hal.science/hal-03791044/file/islandora_148707.pdf
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • Accession Number:
      edsbas.DD6E685A