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Retinal Periphlebitis May Be a Marker for Subphenotype in Multiple Sclerosis
Reili Rebane1, Katrin Sonajalg1, Kaarel Kree2
1Department of Ophthalmology, East Tallinn Central Hospital, Tallinn, Estonia.
Abstract:
Retinal periphlebitis (RPP) is a long-known entity in patients with multiple sclerosis (MS) and has not been revisited in the context of recent developments in MS pathogenesis and heterogeneity. We present six cases of RPP in three female and three male MS patients. They all have relapsing-remitting MS and did not have or had minor ocular symptoms. It is important to perform a thorough retinal examination in patients with MS, as peripheral and sectorial lesions could be unseen. A better knowledge on the concomitant involvement of retinal veins contributes to the understanding of immunopathology, with potentially distinct autoantigenic targets. RPP might serve as a subphenotype marker that may influence treatment choices in MS. Further research is needed.
Insights
Retinal periphlebitis (RPP) in multiple sclerosis (MS) patients may indicate distinct immunopathology. Early retinal exams in MS patients are crucial for identifying RPP and potentially guiding treatment decisions.
Area of Science:
- Ophthalmology
- Neurology
- Immunology
Background:
- Retinal periphlebitis (RPP) is a known complication in multiple sclerosis (MS).
- Recent advances in MS pathogenesis and heterogeneity warrant a re-evaluation of RPP.
- RPP's role in MS has not been extensively studied in light of new developments.
Purpose of the Study:
- To investigate retinal periphlebitis (RPP) in contemporary multiple sclerosis (MS) patients.
- To explore the potential of RPP as a marker for MS subphenotypes.
- To understand the immunopathological implications of RPP in MS.
Main Methods:
- Case series presentation of six MS patients with RPP.
- Clinical evaluation including ophthalmological examinations.
- Analysis of RPP in the context of MS characteristics and potential immunopathology.
Main Results:
- Six cases of RPP were identified in relapsing-remitting MS patients (3 female, 3 male).
- Most patients had minimal or no ocular symptoms, highlighting the need for thorough retinal screening.
- RPP involvement suggests potential distinct autoantigenic targets in MS immunopathology.
Conclusions:
- Retinal periphlebitis may be an underdiagnosed sign in MS patients, even with minor ocular symptoms.
- RPP could serve as a valuable subphenotype marker in MS, potentially influencing therapeutic strategies.
- Further research is essential to elucidate the full impact and implications of RPP in MS.
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