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Updated: Aug 26, 2025

Dynamic Visual Tests to Identify and Quantify Visual Damage and Repair Following Demyelination in Optic Neuritis Patients
Published on: April 14, 2014
Trans-Synaptic Degeneration Following Acute Optic Neuritis in Multiple Sclerosis
Olwen C Murphy1, Elias S Sotirchos1, Grigorios Kalaitzidis1
1Division of Neuroimmunology and Neurological Infections, Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.
Acute optic neuritis in multiple sclerosis causes accelerated brain atrophy, particularly in the occipital lobe and thalamus. This brain degeneration is linked to vision loss, indicating trans-synaptic degeneration
Area of Science:
- Neuroscience
- Ophthalmology
- Radiology
Background:
- Multiple sclerosis (MS) is a demyelinating disease affecting the central nervous system.
- Acute optic neuritis (AON) is a common initial presentation of MS.
- Understanding the long-term consequences of AON, including brain atrophy and visual outcomes, is crucial for patient management.
Purpose of the Study:
- To investigate longitudinal changes in brain volumetric measures and retinal layer thicknesses after AON in people with MS (PwMS).
- To explore the process of trans-synaptic degeneration following AON.
- To determine the clinical relevance of these changes on visual function.
Main Methods:
- Recruited 49 PwMS within 40 days of AON onset and 73 PwMS without recent AON.
- Utilized longitudinal optical coherence tomography and brain MRI for up to 5 years.
- Employed mixed-effects linear regression models to analyze data.
Main Results:
- Accelerated atrophy observed in occipital gray matter, calcarine gray matter, and thalamus in the AON cohort compared to the non-AON cohort.
- No significant differences in whole-brain, cortical gray matter, or T2 lesion accumulation rates between cohorts.
- Greater reduction in retinal ganglion cell+inner plexiform layer thickness post-AON correlated with faster whole-brain, white matter, and thalamic atrophy.
- Faster subcortical gray matter and thalamic atrophy linked to worse visual function outcomes.
Conclusions:
- Provided in-vivo evidence for anterograde trans-synaptic degeneration after AON in PwMS.
- Suggests that trans-synaptic degeneration following AON is associated with clinically relevant visual outcomes.
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