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Published on: August 21, 2017
Microcystic inner nuclear layer abnormalities and neuromyelitis optica
Jeffrey M Gelfand1, Bruce A Cree, Rachel Nolan
1Multiple Sclerosis Center, Department of Neurology, University of California, San Francisco, San Francisco, CA 94158, USA. jeffrey.gelfand@ucsf.edu
Microcystic inner nuclear layer abnormalities were found in 20% of neuromyelitis optica (NMO) patients, exclusively in eyes with prior optic neuritis. Further research is needed to understand this retinal pathology in NMO.
Area of Science:
- Ophthalmology
- Neuroscience
- Immunology
Background:
- Microcystic abnormalities in the inner nuclear layer of the retina are observed in multiple sclerosis patients, particularly those with a history of optic neuritis.
- Acute optic neuritis is a key feature of neuromyelitis optica (NMO).
- Microcystic inner nuclear layer abnormalities have not been previously studied in NMO.
Purpose of the Study:
- To investigate the occurrence of microcystic inner nuclear layer abnormalities in patients diagnosed with NMO.
Main Methods:
- An observational, retrospective study was conducted at a university-based specialty clinic.
- Twenty-five patients meeting NMO diagnostic criteria or NMO spectrum disorder criteria were included.
- Spectral-domain optical coherence tomography (SD-OCT) was used to identify microcystic pathology in the inner nuclear layer.
Main Results:
- Microcystic changes were detected in 5 of 25 NMO patients (20%), affecting 7 eyes.
- These microcystic abnormalities were exclusively found in eyes with a history of symptomatic optic neuritis (100% of affected eyes).
- No significant differences in age, sex, or aquaporin 4-IgG antibody status were observed between NMO patients with and without microcystic changes.
Conclusions:
- Microcystic inner nuclear layer pathology is present in a subset of NMO patients, specifically in eyes previously affected by optic neuritis.
- The exact cause of this retinal finding in NMO requires further investigation.
- Additional research is necessary to determine if this pathology contributes to long-term visual impairment in NMO patients post-optic neuritis.
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