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Volumetric Brain Loss Correlates With a Relapsing MOGAD Disease Course
Ariel Rechtman1, Livnat Brill1, Omri Zveik1
1Department of Neurology and Laboratory of Neuroimmunology and the Agnes-Ginges Center for Neurogenetics, Hadassah-Medical Center, Ein-Kerem, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Background:
Myelin oligodendrocyte glycoprotein antibody disorders (MOGAD) have evolved as a distinct group of inflammatory, demyelinating diseases of the CNS. MOGAD can present with a monophasic or relapsing disease course with distinct clinical manifestations.However, data on the disease course and disability outcomes of these patients are scarce. We aim to compare brain volumetric changes for MOGAD patients with different disease phenotypes and HCs.
Methods:
Brain magnetic resonance imaging (MRI) scans and clinical data were obtained for 22 MOGAD patients and 22 HCs. Volumetric brain information was determined using volBrain and MDbrain platforms.
Results:
We found decreased brain volume in MOGAD patients compared to HCs, as identified in volume of total brain, gray matter, white matter and deep gray matter (DGM) structures. In addition, we found significantly different volumetric changes between patients with relapsing and monophasic disease course, with significantly decreased volume of total brain and DGM, cerebellum and hippocampus in relapsing patients during the first year of diagnosis. A significant negative correlation was found between EDSS and volume of thalamus.
Conclusions:
Brain MRI analyses revealed volumetric differences between MOGAD patients and HCs, and between patients with different disease phenotypes. Decreased gray matter volume during the first year of diagnosis, especially in the cerebrum and hippocampus of MOGAD patients was associated with relapsing disease course.
Insights
Myelin oligodendrocyte glycoprotein antibody disorders (MOGAD) cause reduced brain volume in patients compared to healthy controls. Relapsing MOGAD shows greater volume loss, particularly in the first year, impacting disability outcomes.
Area of Science:
- Neuroimmunology
- Neuroimaging
- Demyelinating Diseases
Background:
- Myelin oligodendrocyte glycoprotein antibody disorders (MOGAD) are distinct inflammatory CNS demyelinating diseases.
- MOGAD presents with monophasic or relapsing courses, but disease progression data is limited.
- Understanding brain volumetric changes in MOGAD phenotypes is crucial for predicting outcomes.
Purpose of the Study:
- To compare brain volumetric changes in MOGAD patients versus healthy controls (HCs).
- To investigate differences in brain volume between relapsing and monophasic MOGAD phenotypes.
- To correlate brain volume with clinical disability (EDSS).
Main Methods:
- Acquired brain MRI scans and clinical data from 22 MOGAD patients and 22 HCs.
- Utilized volBrain and MDbrain platforms for volumetric brain analysis.
- Assessed total brain, gray matter, white matter, and deep gray matter volumes.
Main Results:
- MOGAD patients exhibited decreased total brain, gray matter, white matter, and deep gray matter volumes compared to HCs.
- Relapsing MOGAD patients showed significantly reduced total brain, deep gray matter, cerebellum, and hippocampus volumes within the first year.
- A negative correlation was observed between Expanded Disability Status Scale (EDSS) and thalamus volume.
Conclusions:
- Brain MRI reveals significant volumetric differences between MOGAD patients and HCs.
- Relapsing MOGAD is associated with decreased gray matter volume, particularly in the cerebrum and hippocampus, within the first year of diagnosis.
- Volumetric changes correlate with disease course and disability in MOGAD.
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