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Prognostic factors of first-onset optic neuritis based on diagnostic criteria and antibody status: a multicentre analysis of 427 eyes

Authors
Min, Young GiMoon, YejiKwon, Young NamLee, Byung JooPark, Kyung-AhHan, Jae YongHan, JinuLee, Haeng-JinBaek, Seol-HeeKim, Byung-JoKim, Jun-SoonPark, Kyung SeokKim, Nam-HeeKim, MarthaNam, Tai-SeungOh, Seong-IlJung, Jae HoSung, Jung-JoonJang, Myoung-JinKim, Seong-JoonKim, Sung-Min
Issue Date
Feb-2024
Publisher
BMJ Publishing Group
Keywords
OPHTHALMOLOGY; NEUROIMMUNOLOGY; CLINICAL NEUROLOGY
Citation
Journal of Neurology, Neurosurgery and Psychiatry
Indexed
SCIE
SCOPUS
Journal Title
Journal of Neurology, Neurosurgery and Psychiatry
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/65822
DOI
10.1136/jnnp-2023-333133
ISSN
0022-3050
1468-330X
Abstract
Background Optic neuritis (ON) prognosis is influenced by various factors including attack severity, underlying aetiologies, treatments and consequences of previous episodes. This study, conducted on a large cohort of first ON episodes, aimed to identify unique prognostic factors for each ON subtype, while excluding any potential influence from pre-existing sequelae. Methods Patients experiencing their first ON episodes, with complete aquaporin-4 (AQP4) and myelin oligodendrocyte glycoprotein (MOG) antibody testing, and clinical data for applying multiple sclerosis (MS) diagnostic criteria, were enrolled. 427 eyes from 355 patients from 10 hospitals were categorised into four subgroups: neuromyelitis optica with AQP4 IgG (NMOSD-ON), MOG antibody-associated disease (MOGAD-ON), ON in MS (MS-ON) or idiopathic ON (ION). Prognostic factors linked to complete recovery (regaining 20/20 visual acuity (VA)) or moderate recovery (regaining 20/40 VA) were assessed through multivariable Cox regression analysis. Results VA at nadir emerged as a robust prognostic factor for both complete and moderate recovery, spanning all ON subtypes. Early intravenous methylprednisolone (IVMP) was associated with enhanced complete recovery in NMOSD-ON and MOGAD-ON, but not in MS-ON or ION. Interestingly, in NMOSD-ON, even a slight IVMP delay in IVMP by >3 days had a significant negative impact, whereas a moderate delay up to 7-9 days was permissible in MOGAD-ON. Female sex predicted poor recovery in MOGAD-ON, while older age hindered moderate recovery in NMOSD-ON and ION. Conclusion This comprehensive multicentre analysis on first-onset ON unveils subtype-specific prognostic factors. These insights will assist tailored treatment strategies and patient counselling for ON.
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Kim, Byung-Jo
Anam Hospital (Department of Neurology, Anam Hospital)
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