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Dynamic Visual Tests to Identify and Quantify Visual Damage and Repair Following Demyelination in Optic Neuritis Patients
Published on: April 14, 2014
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Changes of retinal structure and visual function in patients with demyelinating transverse myelitis
Jang Ho Lee1, Yeji Moon2, Young Nam Kwon3
1Seoul National University College of Medicine, Seoul, Republic of Korea.
Summary
Patients with demyelinating transverse myelitis (TM) show retinal microstructural damage, particularly in aquaporin-4 IgG-positive neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS), but visual function remains preserved.
Area of Science:
- Neuro-ophthalmology
- Neuroimmunology
Background:
- Demyelinating diseases like aquaporin-4 IgG-positive neuromyelitis optica spectrum disorder (NMOSD), myelin oligodendrocyte glycoprotein-associated disease (MOGAD), and multiple sclerosis (MS) can affect the central nervous system.
- Transverse myelitis (TM) is a form of myelitis characterized by inflammation across the spinal cord, and its association with specific neuroimmunological diseases without optic neuritis (ON) warrants investigation into potential ocular structural changes.
Approach:
- This retrospective cross-sectional study analyzed 97 patients with demyelinating TM without ON, categorized into AQP4-IgG-positive NMOSD, MOGAD, and MS groups.
- Optical coherence tomography (OCT) was used to measure retinal nerve fiber layer (RNFL) and ganglion cell inner plexiform layer (GCIPL) thickness.
- Visual acuity and visual field tests assessed functional outcomes, with comparisons made to age-matched healthy controls.
Key Points:
- All TM patient groups exhibited reduced mean RNFL and GCIPL thickness compared to healthy controls, indicating retinal microstructural damage.
- While RNFL thickness reduction was consistent across TM groups, GCIPL thinning was significantly more pronounced in AQP4-IgG-positive NMOSD-TM and MS-TM patients compared to MOGAD-TM patients.
- Despite structural alterations, visual function, assessed by visual acuity and visual field tests, was generally well-preserved across all TM patient groups.
Conclusions:
- Demyelinating TM, irrespective of the underlying disease entity (NMOSD, MOGAD, MS), leads to distinct patterns of retinal microstructural damage.
- The observed retinal damage is more severe in AQP4-IgG-positive NMOSD and MS-TM compared to MOGAD-TM, particularly affecting the GCIPL.
- Current findings suggest that while retinal microstructural integrity is compromised in TM, this damage does not significantly impair visual function in the studied patient cohorts.
Keywords:
Aquaporin-4-IgG-positive neuromyelitis optica spectrum disorder (NMOSD)Multiple sclerosisMyelin oligodendrocyte glycoprotein-associated disease (MOGAD)Optic neuritisTransverse myelitis
