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Recurrence of clinical events at the same anatomical location in patients with MOG antibody-associated disease

  • Jae Won Hyun
  • , Young Nam Kwon
  • , Hye Lim Lee
  • , Woo Kyo Jeong
  • , Hye Jung Lee
  • , Byoung Joon Kim
  • , Seung Woo Kim
  • , Ha Young Shin
  • , Hyun June Shin
  • , Sun Young Oh
  • , Min Young Lee
  • , Su Hyun Kim
  • , So Young Huh
  • , Woojun Kim
  • , Min Su Park
  • , Sun Young Kim
  • , Sung Min Kim
  • , Ho Jin Kim
    • National Cancer Center
    • National Cancer Center
    • Seoul National University
    • Korea University
    • Samsung Medical Center, Sungkyunkwan university
    • Yonsei University
    • Jeonbuk National University
    • Kosin University
    • Yeungnam University

    Research output: Contribution to journalArticlepeer-review

    5 Scopus citations

    Abstract

    Objectives: Likelihood of clinical events occurring within the same anatomical location in patients with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) was retrospectively investigated. Methods: A total of 236 clinical events in 90 patients with MOGAD from nine referral hospitals were analyzed via logistic regression, and odds ratios (ORs) were calculated. Anatomical lesion location was divided into four groups; optic nerve, spinal cord, cerebral hemisphere, and brainstem/cerebellum. Results: At all locations, there was an increased likelihood of a second attack occurring at the same location as the initial event (cerebral hemisphere OR = 22.14, brainstem/cerebellum OR = 18.4, spinal cord OR = 9.1, and optic nerve OR = 7.8). There was an increased likelihood of a third attack occurring at the same location as the initial event in the optic nerve (OR = 14.9), cerebral hemisphere (OR = 11.7), and spinal cord (OR = 6.7). There were positive trends toward a third clinical event occurring at the same location as the first and/or second events if the event was in the optic nerve (OR = 13.5), cerebral hemisphere (OR = 6.9), or spinal cord (OR = 5.7). Conclusions: The current study suggests that clinical relapses of MOGAD during early stage tend to recur at the same anatomical locations in the central nervous system.

    Original languageEnglish
    Pages (from-to)449-452
    Number of pages4
    JournalMultiple Sclerosis Journal
    Volume27
    Issue number3
    DOIs
    StatePublished - Mar 2021

    Bibliographical note

    Publisher Copyright:
    © The Author(s), 2020.

    Keywords

    • Myelin oligodendrocyte glycoprotein
    • diagnosis
    • dissemination
    • location
    • onset

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