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The real-world applicability of the 2023 international myelin oligodendrocyte glycoprotein antibody-associated disease criteria in a Latin American cohort

  • Edgar Carnero Contentti(corresponding author)
    ,
  • Claudia Pestchanker
    ,
  • Ethel Ciampi
    ,
  • ,
  • Cesar Caparo Zamalloa
    ,
  • Vanesa Daccach Marques
*Corresponding author for this work
  • Ciudad Autónoma de Buenos Aires
    ,
  • Dr. Ramón Carrillo Central Hospital
    ,
  • Hospital Sótero del Río
    ,
  • ,
  • docencia y atención especializada en epilepsia
    ,
  • Basic Research Center in Dementia and Central Nervous System Demyelinating Diseases
Research Output:
Contribution to journal
Article
Research
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Research
Peer-review

Original language

English

Article number

e16445

Journal (Volume, Issue Number)

European Journal of Neurology (Volume 31, Issue 12)

Publication milestones

  • Published - 12/2024

Publication status

Published - 12/2024

ISSN

1351-5101

Publication IDs

  • Scopus: 85204238058
  • PubMed: 39287067

Abstract

Background and Purpose: The diagnostic criteria for myelin oligodendrocyte glycoprotein antibody (MOG-IgG)-associated disease (MOGAD) were published in 2023. We aimed to determine the performance of the new criteria in Latin American (LATAM) patients compared with the 2018 criteria and explore the significance of MOG–IgG titers in diagnosis. Methods: We retrospectively reviewed the medical records of LATAM (Argentina, Chile, Brazil, Peru, Ecuador, and Colombia) adult patients with one clinical MOGAD event and MOG-IgG positivity confirmed by cell-based assay. Both 2018 and 2023 MOGAD criteria were applied, calculating diagnostic performance indicators. Results: Among 171 patients (predominantly females, mean age at first attack = 34.1 years, mean disease duration = 4.5 years), 98.2% patients met the 2018 criteria, and of those who did not fulfill diagnostic criteria (n = 3), all tested positive for MOG-IgG (one low-positive and two without reported titer). Additionally, 144 (84.2%) patients met the 2023 criteria, of whom 57 (39.5%) had MOG-IgG+ titer information (19 clearly positive and 38 low-positive), whereas 87 (60.5%) patients had no MOG-IgG titer. All 144 patients met diagnostic supporting criteria. The remaining 27 patients did not meet the 2023 MOGAD criteria due to low MOG-IgG (n = 12) or lack of titer antibody access (n = 15), associated with the absence of supporting criteria. The 2023 MOGAD criteria showed a sensitivity of 86% (95% confidence interval = 0.80–0.91) and specificity of 100% compared to the 2018 criteria. Conclusions: These findings support the diagnostic utility of the 2023 MOGAD criteria in an LATAM cohort in real-world practice, despite limited access to MOG-IgG titration.

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