MRI findings and clinical manifestations in adult Mexican patients with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD)

Introduction: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an inflammatory demyelinating disorder of the central nervous system.The clinical and imaging characteristics of MOGAD in the Mexican population remain unknown.This study describes the clinical manifestations and magnetic resonance imaging (MRI) findings of the brain, optic nerve, and spinal cord in adult Mexican patients with MOGAD.Material and methods: This cross-sectional study included adult patients with suspected MOGAD who were evaluated at a national Mexican referral center.Demographic data, clinical manifestations, anti-MOG antibody status, and MRI findings of the brain, optic nerve, and spinal cord were reviewed.Descriptive statistics were calculated.Results: Twenty patients with MOGAD were included.All patients had a positive anti-MOG antibody.Decreased visual acuity and pain with eye movements were the most common clinical manifestations, occurring in 15 (75.0%) patients, while optic nerve abnormalities on MRI were identified in 16 (80.0%)patients.The predominant MRI findings were longitudinally extensive T2 hyperintensity involving the anterior or intraorbital optic nerve in 15 (75.0%) patients, bilateral involvement in 10 (50.0%) patients, and perineural enhancement in 6 (30.0%) patients.Brain lesions were observed in 5 (25.0%) of 20 patients, predominantly presenting as fluffy cortical and infratentorial T2/FLAIR hyperintensities.Spinal cord lesions were identified in 4 (20.0%)patients, mainly as short-segment cervical and thoracic lesions, with conus medullaris involvement in 2 (10.0%) patients.Conclusion: In patients with MOGAD, optic neuritis was the predominant clinical and imaging phenotype.Brain and spinal cord involvement was less frequent and exhibited characteristic MRI patterns.These findings represent the first description of the clinical and MRI features of MOGAD in a Mexican cohort and support the recognition of characteristic imaging patterns.

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Journal
Journal of the Mexican Federation of Radiology and Imaging
Published
2026-10-27
DOI
https://doi.org/10.24875/jmexfri.m26000133
Primary Topic
Multiple Sclerosis Research Studies
Type
article
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article

MRI findings and clinical manifestations in adult Mexican patients with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD)

Katherine Isamara Jacome-Portilla, Rebeca de J. Ramos-Sanchez
1 links
Journal of the Mexican Federation of Radiology and Imaging
Multiple Sclerosis Research Studies
article

MRI findings and clinical manifestations in adult Mexican patients with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD)

Katherine Isamara Jacome-Portilla, Rebeca de J. Ramos-Sanchez
article en

Abstract

Introduction: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an inflammatory demyelinating disorder of the central nervous system.The clinical and imaging characteristics of MOGAD in the Mexican population remain unknown.This study describes the clinical manifestations and magnetic resonance imaging (MRI) findings of the brain, optic nerve, and spinal cord in adult Mexican patients with MOGAD.Material and methods: This cross-sectional study included adult patients with suspected MOGAD who were evaluated at a national Mexican referral center.Demographic data, clinical manifestations, anti-MOG antibody status, and MRI findings of the brain, optic nerve, and spinal cord were reviewed.Descriptive statistics were calculated.Results: Twenty patients with MOGAD were included.All patients had a positive anti-MOG antibody.Decreased visual acuity and pain with eye movements were the most common clinical manifestations, occurring in 15 (75.0%) patients, while optic nerve abnormalities on MRI were identified in 16 (80.0%)patients.The predominant MRI findings were longitudinally extensive T2 hyperintensity involving the anterior or intraorbital optic nerve in 15 (75.0%) patients, bilateral involvement in 10 (50.0%) patients, and perineural enhancement in 6 (30.0%) patients.Brain lesions were observed in 5 (25.0%) of 20 patients, predominantly presenting as fluffy cortical and infratentorial T2/FLAIR hyperintensities.Spinal cord lesions were identified in 4 (20.0%)patients, mainly as short-segment cervical and thoracic lesions, with conus medullaris involvement in 2 (10.0%) patients.Conclusion: In patients with MOGAD, optic neuritis was the predominant clinical and imaging phenotype.Brain and spinal cord involvement was less frequent and exhibited characteristic MRI patterns.These findings represent the first description of the clinical and MRI features of MOGAD in a Mexican cohort and support the recognition of characteristic imaging patterns.

Journal of the Mexican Federation of Radiology and ImagingVol. 5(3)
Secretaria de Salud (MX), Instituto Nacional de Neurología y Neurocirugía (MX)
Good health and well-being
Openalex Percentile: Top 12%
Multiple Sclerosis Research Studies
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