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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
Serum sPECAM-1 and sVCAM-1 levels are associated with conversion to multiple sclerosis in patients with optic
Alicja Kalinowska-Łyszczarz1, Sławomir Michalak2, Mikołaj A Pawlak3
1Division of Neurochemistry and Neuropathology, Department of Neurology, Poznan University of Medical Sciences, 49, Przybyszewskiego st., 60-355 Poznan, Poland.
Abstract:
Platelet-Endothelial-Cell-Adhesion-Molecule-1 (PECAM-1) and Human-Vascular-CAM-1 (VCAM-1) are adhesion molecules involved in leukocyte-endothelial interaction. In our study serum levels of sPECAM-1 and sVCAM-1 were measured (ELISA) in twenty-nine patients during their first monosymptomatic optic neuritis (ON) episode. Anti-aquaporin-4-antibodies (AQP4-IgG) were detected with the cell-based assay. Patients were followed for seven years, during which 16/24 AQP4-IgG (-) patients developed MS and 2/5 AQP4-IgG (+) patients developed NMO. Patients who developed MS had significantly lower sPECAM-1 and sVCAM-1 than those who did not. Serum sPECAM-1 and sVCAM-1 may turn out to be useful biomarkers correlated with the risk of progression to MS after first ON incident.
Insights
Lower levels of soluble Platelet-Endothelial-Cell-Adhesion-Molecule-1 (sPECAM-1) and soluble Vascular-Cell-Adhesion-Molecule-1 (sVCAM-1) may predict multiple sclerosis (MS) development after optic neuritis. These biomarkers could aid in assessing MS progression risk.
Area of Science:
- Neuroimmunology
- Immunology
- Neurology
Background:
- Leukocyte-endothelial interactions are crucial in inflammatory diseases.
- Platelet-Endothelial-Cell-Adhesion-Molecule-1 (PECAM-1) and Vascular-Cell-Adhesion-Molecule-1 (VCAM-1) are key adhesion molecules in these interactions.
- Optic neuritis (ON) is an initial demyelinating event, and predicting conversion to multiple sclerosis (MS) is clinically important.
Purpose of the Study:
- To investigate the association between serum levels of soluble PECAM-1 (sPECAM-1) and VCAM-1 (sVCAM-1) and the risk of developing MS after a first monosymptomatic ON episode.
- To explore the role of anti-aquaporin-4-antibodies (AQP4-IgG) in disease course and outcomes.
Main Methods:
- Serum sPECAM-1 and sVCAM-1 levels were quantified using ELISA in 29 patients with first ON.
- Anti-aquaporin-4-antibodies (AQP4-IgG) were detected via cell-based assay.
- Patients were followed for seven years to monitor conversion to MS or Neuromyelitis Optica (NMO).
Main Results:
- Patients who developed MS (16/24 AQP4-IgG negative) had significantly lower baseline sPECAM-1 and sVCAM-1 levels compared to those who did not develop MS.
- A minority of AQP4-IgG positive patients developed NMO (2/5).
Conclusions:
- Serum sPECAM-1 and sVCAM-1 may serve as potential biomarkers for predicting MS development following an initial ON episode.
- These adhesion molecules' levels correlate with the risk of progression to MS.
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