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.

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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