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Published on: December 9, 2015
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Serum endocan levels in multiple sclerosis relapse and remission
1Department of Neurology, Dicle University Medical School, Diyarbakır, Turkey. esrefakil@gmail.com.
European Review for Medical and Pharmacological Sciences
|June 22, 2021
Summary
Serum endocan levels are elevated in relapsing-remitting multiple sclerosis (RRMS) patients, particularly during relapse. This suggests endocan may serve as a useful marker for endothelial injury and disease activity in MS.
Area of Science:
- Neuroimmunology
- Biomarker Discovery
- Inflammatory Diseases
Background:
- Endocan is recognized as a marker for inflammatory conditions, vascular injury, and tumor progression.
- Understanding novel biomarkers for multiple sclerosis (MS) is crucial for disease management.
Purpose of the Study:
- To compare serum endocan, C-reactive protein (CRP), and neutrophil-lymphocyte ratio (NLR) levels in relapsing-remitting multiple sclerosis (RRMS) patients during remission and relapse.
- To evaluate the relationship between these markers and clinical parameters like disease duration, relapse frequency, and disability scores.
Main Methods:
- Serum samples were collected from 53 RRMS remission patients, 30 RRMS relapse/post-relapse patients, and 44 healthy controls.
- Endocan, CRP, and NLR levels were measured and compared across groups.
- Correlations with disease duration, relapse frequency, EDSS, treatment, and MRI lesion burden were analyzed.
Main Results:
- Serum endocan, CRP, and NLR levels were significantly higher in RRMS patients compared to controls (p < 0.05).
- Serum endocan was significantly elevated in the RRMS relapse group versus post-relapse and control groups (p < 0.05).
- No significant correlations were found between endocan, CRP, NLR and disease duration, EDSS, relapse frequency, or MRI lesion burden (p > 0.05).
Conclusions:
- Elevated serum endocan in MS patients indicates endothelial injury secondary to inflammation.
- Endocan shows potential as a moderately reliable indicator of MS relapse.

