Anti-NMDA receptor encephalitis concomitant with myelin oligodendrocyte glycoprotein antibody diseases: A

Li Du1,2,3, Huabing Wang1,2,3, Heng Zhou1,2,3

  • 1Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, 100070.

Medicine
|August 7, 2020
PubMed

Insights

Anti-N-methyl-D-aspartate receptor encephalitis (NMDARe) can co-occur with myelin oligodendrocyte glycoprotein antibody (MOG-ab) disease. Most patients with overlapping conditions show good outcomes with steroid treatment.

Area of Science:

  • Neuroimmunology
  • Neurology

Background:

  • Anti-N-methyl-D-aspartate receptor encephalitis (NMDARe) and myelin oligodendrocyte glycoprotein antibody (MOG-ab) disease are distinct autoimmune neurological disorders.
  • Coexistence of NMDARe and MOG-ab disease presents unique clinical challenges and diagnostic considerations.

Observation:

  • A study identified 32 patients with coexisting NMDARe and MOG-ab disease, with onset ages ranging from 3 to 48 years.
  • Over 74% of these patients experienced abnormal behavior or cognitive dysfunction during NMDARe episodes.
  • No tumor comorbidity was observed in the studied NMDARe patients with MOG-ab disease.

Findings:

  • High-dose steroids were the primary first-line immunotherapy in 84% of cases.
  • Mycophenolate mofetil (MMF) was used for relapse prevention in 28% of patients.
  • A significant 96% of patients achieved a good outcome following treatment.

Implications:

  • Steroids are confirmed as a common and effective first-line immunotherapy for overlapping NMDARe and MOG-ab disease.
  • The findings suggest a generally favorable prognosis for NMDARe patients who also have MOG-ab disease.
  • Further research may elucidate optimal treatment strategies for this specific patient cohort.

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