What's new in NMOSD and MOGAD?

Rev Neurol (Paris). 2024 Nov;180(9):957-962. doi: 10.1016/j.neurol.2024.08.004. Epub 2024 Sep 14.

Abstract

In this mini-review, we focus on novelties in the field of neuromyelitis optica spectrum disorders (NMOSD) and myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD). We first describe the proposed criteria for MOGAD and evaluate their impact and potential limitations, with a highlight on the subgroups of patients tested MOG-antibody positive only in the cerebrospinal fluid. We then propose a brief state of the art on the current knowledge on the so-call "double seronegative" NMOSD group, regarding nosology, clinical, biological and imaging features and the unmet need in this field. The last part is dedicating to the present and future of acute treatment in NMSOD and MOGAD.

Keywords: Antibodies myelitis; Multiple sclerosis; Myelin oligodendrocyte glycoprotein; Neuromyelitis optica; Optic neuritis.

Publication types

  • Review

MeSH terms

  • Autoantibodies* / blood
  • Autoantibodies* / immunology
  • Humans
  • Myelin-Oligodendrocyte Glycoprotein* / immunology
  • Neuromyelitis Optica* / diagnosis
  • Neuromyelitis Optica* / immunology
  • Neuromyelitis Optica* / therapy

Substances

  • Myelin-Oligodendrocyte Glycoprotein
  • Autoantibodies
  • MOG protein, human