Cited by 11Multiple Sclerosis Research StudiesOcular Diseases and Behçet’s SyndromePeripheral Neuropathies and Disorders

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Frequency of Asymptomatic Optic Nerve Enhancement in 203 Patients With MOG Antibody-Associated Disease

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Tajfirouz, Deena, Madhavan, Ajay, Pacheco Marrero, Johann M., Krecke, Karl N., Fautsch, Kalli J., Flanagan, Eoin P., Pittock, Sean J., Shah, Shailee, Bhatti, M. Tariq, Chen, John J.·2024·Neurology Neuroimmunology & Neuroinflammation

Abstract

BACKGROUND AND OBJECTIVES: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a distinct CNS demyelinating disease. The rate of asymptomatic optic nerve enhancement on MRI has not been explored in patients with MOGAD. An improved understanding of this would guide clinical practice and assessment of treatment efficacy. We aimed to determine the frequency of asymptomatic optic nerve enhancement in MOGAD. METHODS: This was a retrospective review of patients evaluated at Mayo Clinic with MOGAD between January 1, 2000, and August 1, 2021 (median follow-up 1.6 [range 1-19] years). MRI studies were reviewed by masked neuroradiologists. Scans performed within 30 days of ON attack were classified as attack scans. Images obtained for routine surveillance, before ON attack, or at the time of non-ON attack were classified as interattack scans. RESULTS: Five hundred sixty-six MRIs (203 unique patients, 53% female) were included. Interattack MRIs represented 341 (60%) of the scans (median 36 days post-ON [range -1,032 to 6,001]). Of the interattack scans, 43 of 341 (13%), 30 unique patients, showed optic nerve enhancement. The enhancement was located at prior sites of ON in 35 of 43 (81%). Among the 8 patients with enhancement in new optic nerve areas, 6 had acute disseminated encephalomyelitis without an eye examination at the time of the MRI and 2 had preceding ON without imaging. Long-term visual outcomes showed no significant difference between those with and without asymptomatic enhancement, with improved visual acuity in most patients. DISCUSSION: Asymptomatic optic nerve enhancement occurred in 13% of interattack MRIs, the majority in patients with prior ON and occurring at prior sites of optic nerve enhancement. New asymptomatic optic nerve enhancement in areas without prior ON was rare. These findings are important for understanding the natural history of MOGAD, the interpretation of symptoms or response to treatment, and the adjudication of attacks in clinical trials.

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Research works printed but not linked: 12

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Metadata

Authors
Tajfirouz, D., Madhavan, A., Pacheco Marrero, J. M., Krecke, K. N., Fautsch, K. J., Flanagan, E. P., Pittock, S. J., Shah, S., Bhatti, M. T., & Chen, J. J.
Affiliations
  • Mayo Clinic (US)
  • From the Department of Ophthalmology and Neurology (D.T.), Mayo Clinic; Department of Radiology (A.M., K.N.K.); Department of Ophthalmology (J.M.P.M., K.J.F.), Mayo Clinic; Department of Neurology (E.P.F.); Department of Neurology (S.J.P.), Center for MS and Autoimmune Neurology, Mayo Clinic, Rochester, MN; Department of Neurology (S.S.), Vanderbilt University Medical Center, Nashville, TN; The Permanente Medical Group, Department of Ophthalmology (M.T.B.), Kaiser Permanente-Northern California,...
Corresponding author
Chen, John J.
Venue
Neurology Neuroimmunology & Neuroinflammation
Published
2024-09
Volume
11
Issue
5
Pages
e200277-e200277
ISSN
2332-7812 (ISSN-L)
OpenAlex
W4400030333
Cited by
11
References
0
Citations by year
2026: 5 · 2025: 5 · 2024: 1
FWCI
3.34
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Neurology Neuroimmunology & Neuroinflammation (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
  • Health Sciences › Medicine › Ophthalmology › Ocular Diseases and Behçet’s Syndrome
  • Health Sciences › Medicine › Clinical Neurology › Peripheral Neuropathies and Disorders
Keywords
MOG antibody-associated disease, myelin oligodendrocyte glycoprotein, optic neuritis, demyelinating disease, acute disseminated encephalomyelitis, natural history (disease), visual outcome
MeSH terms
Adolescent, Adult, Aged, Aged, 80 and over, Autoantibodies, Child, Child, Preschool, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Optic Nerve, Retrospective Studies, Demyelinating Autoimmune Diseases, CNS, Young Adult, Asymptomatic Diseases, Myelin-Oligodendrocyte Glycoprotein

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