Outcomes of immunosuppressive therapy discontinuation in patients with myelin oligodendrocyte glycoprotein antibody-associated disease

  • You Ri Kang
  • , Hyunjin Ju
  • , Ki Hoon Kim
  • , Seung Ho Choo
  • , Woohee Ju
  • , Sung Min Kim
  • , Sooyoung Kim
  • , Eunhee Sohn
  • , Tai Seung Nam
  • , Sun Young Oh
  • , Byeol A. Yoon
  • , Jong Kuk Kim
  • , Hyunjin Kim
  • , Eun Jae Lee
  • , Young Min Lim
  • , Young Nam Kwon
  • , Seung Woo Kim
  • , Ha Young Shin
  • , Jee Eun Kim
  • , In Soo Joo
  • Minsu Park, Hyung Soo Lee, Byung Jo Kim, Jin Woo Park, Suk Yoon Lee, Woojun Kim, Jae Won Hyun, Su Hyun Kim, Ju Hong Min, Ho Jin Kim*
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Research on the optimal duration of immunosuppressive therapy (IST) and the outcome upon its discontinuation in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) remains limited. Objective: To evaluate the outcomes following IST discontinuation in MOGAD. Methods: This multicenter retrospective study collected data from 333 MOGAD patients in Korea. Among 273 patients who received IST, 41 who discontinued IST were analyzed. Results: The median age at disease onset was 38.3 years (interquartile range (IQR), 27.6–53.1). Before IST withdrawal, 21 (51%) patients exhibited relapsing courses. Over a median follow-up of 23.5 months (IQR, 12.1–39.5) after discontinuation, 10 patients (24.4%) relapsed after a median of 8.2 months (IQR, 6.3–11.5). All relapses occurred in patients with a prior relapsing course (10/21, 47.6%); none with prior monophasic courses relapsed. Among 21 prior relapsing patients, relapse after discontinuation group had a shorter IST duration than non-relapse group (median, 9.4 vs 50.9 months, p = 0.036). None of the 41 patients had severe disability (Expanded Disability Status Scale (EDSS) score ⩾ 4.0 or Visual Functional System score ⩾ 5) at the last visit. Conclusion: IST discontinuation did not necessarily lead to relapse and could be considered with an individualized approach based on factors such as disease course and IST duration.

Original languageEnglish
Pages (from-to)1102-1109
Number of pages8
JournalMultiple Sclerosis Journal
Volume31
Issue number9
DOIs
Publication statusPublished - 2025 Aug
Externally publishedYes

Bibliographical note

Publisher Copyright:
© The Author(s), 2025

Keywords

  • Myelin oligodendrocyte glycoprotein antibody-associated disease
  • immunosuppression therapy
  • outcome
  • relapse
  • treatment discontinuation

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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