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Retinal periphlebitis is associated with multiple sclerosis severity
Santiago Ortiz-Pérez1, Elena H Martínez-Lapiscina, Iñigo Gabilondo
1Center of Neuroimmunology, Department of Neurology, Institute of Biomedical Research August Pi Sunyer, Hospital Clinic of Barcelona, Spain.
Objectives:
To assess the association of primary retinal inflammation, namely retinal periphlebitis (RP) and microcystic macular edema, with clinical, brain, and retinal imaging biomarkers of multiple sclerosis (MS) severity.
Methods:
One hundred patients with MS underwent a neurologic and ophthalmic examination, MRI, and optical coherence tomography. Disability was assessed using the Expanded Disability Status Scale at baseline and after a 1-year follow-up. The normalized brain volume, the normal-appearing gray matter volume, and T1 lesion volume were assessed at baseline as radiologic biomarkers of disease severity. Retinal nerve fiber layer thickness and macular volume at baseline were used as surrogate markers of axonal damage. We used general linear models adjusted for sex, age, disease duration, and MS treatment to compared adjusted means of these parameters among patients with RP and patients without primary retinal inflammation.
Results:
Five patients showed RP, 2 showed microcystic macular edema, and the retina was normal in the remaining 93. Patients with RP had a tendency toward a higher adjusted-mean Expanded Disability Status Scale score at baseline and disability progression after a 1-year follow-up compared with patients without primary retinal inflammation. These patients also had a higher adjusted-mean T1 lesion volume (adjusted differences: 10.4, 95% confidence interval [CI]: 0.6 to 20.2; p = 0.038) and lower T1 brain volume (adjusted differences: -68, 95% CI: -139 to 2; p = 0.059). Patients with RP had a lower adjusted-mean retinal nerve fiber layer thickness (adjusted differences: -13.4, 95% CI: -24.4 to -2.3; p = 0.018) and a trend toward lower macular volume.
Conclusions:
These results support the role of RP as a biomarker of MS severity.
Insights
Retinal periphlebitis (RP) is linked to increased multiple sclerosis (MS) severity. Patients with RP showed greater disability, higher brain lesion volume, and reduced retinal nerve fiber layer thickness, supporting RP as an MS severity biomarker.
Area of Science:
- Neuroimmunology
- Ophthalmology
- Radiology
Background:
- Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system.
- Assessing MS severity relies on clinical, imaging, and functional biomarkers.
- Primary retinal inflammation, such as retinal periphlebitis (RP), may offer insights into MS pathology.
Purpose of the Study:
- To investigate the association between primary retinal inflammation (retinal periphlebitis and microcystic macular edema) and biomarkers of multiple sclerosis severity.
- To correlate retinal findings with clinical disability, brain MRI metrics, and retinal structural changes.
Main Methods:
- A cohort of 100 MS patients underwent comprehensive ophthalmic and neurologic examinations, MRI, and optical coherence tomography.
- Disability was measured using the Expanded Disability Status Scale (EDSS) at baseline and 1-year follow-up.
- Brain imaging assessed normalized brain volume, gray matter volume, and T1 lesion volume; retinal imaging measured nerve fiber layer thickness and macular volume.
Main Results:
- Five patients exhibited RP, two had microcystic macular edema, and 93 had normal retinas.
- Patients with RP showed a trend towards higher baseline EDSS scores and disability progression.
- RP was associated with significantly higher T1 lesion volume (p=0.038) and lower retinal nerve fiber layer thickness (p=0.018).
Conclusions:
- Retinal periphlebitis (RP) is a potential biomarker for multiple sclerosis severity.
- RP is associated with increased disability, greater brain lesion burden, and axonal damage in MS patients.
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