Clinical Significance of Myelin Oligodendrocyte Glycoprotein Autoantibodies in Patients with Typical MS Lesions on MRI

Pietro Zara, Valentina Floris, Eoin P. Flanagan, A. Sebastian Lopez-Chiriboga, Brian G. Weinshenker, Paolo Solla, Elia Sechi

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Myelin-oligodendrocyte-glycoprotein (MOG)-IgG-positivity in patients with typical MS lesions on MRI may lead to diagnostic/therapeutic uncertainty. Objective and Methods: We reviewed reports of cases with MS phenotype on MRI and MOG-IgG-positivity published in Pubmed between 01/2012-06/2021. Results: Sixteen patients were included (median age [range], 37,5 [25-66] years; 60% female). Three patients initially tested negative for MOG-IgG. Disease course was: relapsing-remitting, 10; or progressive, 6. Intrathecal IgG-synthesis was common (79%). Low and high-efficacy MS-targeted agents prevented relapses in 30% and 100%, respectively. None of the patients showed resolution of MRI T2-lesions over time. Conclusions: MOG-IgG-positivity is unlikely to alter the expected treatment response and outcomes in patients with otherwise typical MS phenotype on MRI.

Original languageEnglish (US)
JournalMultiple Sclerosis Journal - Experimental, Translational and Clinical
Volume7
Issue number4
DOIs
StatePublished - 2021

Keywords

  • MOG-IgG
  • MOGAD
  • MS
  • NMOSD
  • false positive

ASJC Scopus subject areas

  • Clinical Neurology
  • Cellular and Molecular Neuroscience

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