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Local and Systemic Endothelial Damage in Patients with CEAP C2 Chronic Venous Insufficiency: Role of Mesoglycan
Angelo Santoliquido1,2, Claudia Carnuccio1, Luca Santoro1
1Angiology and Noninvasive Vascular Diagnostics Unit, Department of Cardiovascular Sciences, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Rome, Italy.
Abstract:
Chronic venous disease (CVD) involves complex pathophysiological mechanisms, particularly an imbalance between matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs), contributing to venous remodeling and varicosities. Elevated MMP-2 and MMP-9 levels are commonly found in tissues affected by venous ulcers. Inflammation plays a central role in CVD, with higher levels of pro-inflammatory markers present in varicose veins compared to healthy ones. Syndecans, key components of the endothelial glycocalyx, are involved in inflammatory responses. Alterations in the glycocalyx structure are associated with vascular damage in both venous and arterial diseases. This study aimed to investigate inflammatory changes in CVD patients, focusing on glycocalyx damage and the therapeutic role of mesoglycan, a glycosaminoglycan-based drug. A prospective, monocentric study included 23 patients with C2 clinical-etiological-anatomical-pathological (CEAP) CVD. Serum samples were collected before and after mesoglycan treatment. Results showed significantly elevated levels of VCAM-1, MMP-2, MMP-9, SDC-1, IL-6, and IL-8 in blood from varicose veins versus the systemic circulation. Patients received 50 mg of mesoglycan orally every 12 h for 90 days. After treatment, a notable reduction in inflammatory markers was observed. These results support the hypothesis that mesoglycan may alleviate both local and systemic inflammation, providing insights into new therapeutic strategies for CVD management.
Insights
Mesoglycan treatment reduced inflammation and glycocalyx damage in chronic venous disease (CVD) patients. This glycosaminoglycan therapy shows promise for managing CVD by targeting key inflammatory markers.
Area of Science:
- Vascular Biology
- Pharmacology
- Biochemistry
Background:
- Chronic venous disease (CVD) is linked to matrix metalloproteinase (MMP) and tissue inhibitor of metalloproteinase (TIMP) imbalance, venous remodeling, and inflammation.
- Elevated MMP-2, MMP-9, and pro-inflammatory markers are observed in varicose veins, with syndecan-1 (SDC-1) alterations indicating glycocalyx damage.
- Endothelial glycocalyx integrity is crucial for vascular health, and its damage is implicated in various vascular diseases.
Purpose of the Study:
- To investigate inflammatory changes and glycocalyx damage in patients with chronic venous disease (CVD).
- To evaluate the therapeutic efficacy of mesoglycan, a glycosaminoglycan, in managing CVD-related inflammation.
Main Methods:
- A prospective study involving 23 patients with C2 CEAP (Clinical-Etiological-Anatomical-Pathological) classification of CVD.
- Serum samples were analyzed for inflammatory markers (VCAM-1, MMP-2, MMP-9, SDC-1, IL-6, IL-8) before and after 90 days of mesoglycan treatment.
- Patients received 50 mg of mesoglycan orally twice daily.
Main Results:
- Significantly elevated levels of VCAM-1, MMP-2, MMP-9, SDC-1, IL-6, and IL-8 were detected in blood from varicose veins compared to systemic circulation.
- Mesoglycan treatment resulted in a significant reduction in these inflammatory markers.
- These findings suggest mesoglycan alleviates both local and systemic inflammation associated with CVD.
Conclusions:
- Mesoglycan demonstrates a therapeutic role in reducing inflammation and potentially mitigating glycocalyx damage in CVD patients.
- The study provides evidence for mesoglycan as a potential treatment strategy for managing chronic venous disease.
- Further research into mesoglycan's mechanisms in CVD is warranted.
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