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Retinal microvascular differences between multiple sclerosis and neuromyelitis optica spectrum disorder: a
Ruishan Liu1, Lingyao Kong1, Le Cao1
1Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.
Distinct retinal microvascular patterns in multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) were identified using OCT angiography. These OCTA-based models accurately differentiate MS from NMOSD and correlate with disability.
Area of Science:
- Ophthalmology
- Neurology
- Medical Imaging
Background:
- Retinal microvascular changes in multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) are not fully understood.
- Specific patterns and extent of microvascular alterations require detailed investigation for differential diagnosis.
Purpose of the Study:
- To compare retinal microvascular and structural alterations between MS and NMOSD.
- To develop logistic regression and machine learning models for differentiating MS from NMOSD using combined retinal metrics.
Main Methods:
- Swept-source optical coherence tomography (OCT) and OCT angiography (OCTA) were performed on patients with MS or NMOSD.
- Quantified OCTA metrics (vascular density, perfusion) and structural OCT metrics (RNFL, GCIPL thickness) were analyzed.
- Logistic regression and machine learning models were developed for disease classification.
Main Results:
- Significant differences in superficial vascular complex (SVC) metrics were observed between MS and NMOSD, varying with optic neuritis (ON) history.
- MS showed more severe microvascular loss in non-ON eyes, while NMOSD had steeper SVC decline in ON eyes.
- Machine learning models, particularly support vector machine, achieved high accuracy (84.5%) and AUC (0.912) in differentiating the diseases.
Conclusions:
- Distinct retinal microvascular patterns identified by OCTA can differentiate NMOSD from MS.
- These patterns correlate with disability severity and ON history.
- OCTA-based models offer accurate, non-invasive tools for differential diagnosis, with microvascular integrity as a key biomarker.
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