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Treatment with Sulodexide Downregulates Biomarkers for Endothelial Dysfunction in Convalescent COVID-19 Patients
Alejandro J Gonzalez-Ochoa1,2, Gyozo Szolnoky3, Ana G Hernandez-Ibarra4
1Vascular Surgery Department, Centro Médico del Noroeste, San Luis Rio Colorado, Sonora, México.
Insights
Sulodexide reduced key endothelial dysfunction biomarkers like Thrombomodulin and von Willebrand Factor in convalescent COVID-19 patients. This suggests sulodexide may protect against long COVID-related vascular issues.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Infectious Diseases
Background:
- Persistent endothelial dysfunction biomarkers post-COVID-19 are linked to long-term cardiovascular risks, including long COVID syndrome.
- Sulodexide possesses vascular endothelial affinity and protective properties.
- Evaluating sulodexide's impact on endothelial dysfunction biomarkers in COVID-19 convalescence is crucial.
Purpose of the Study:
- To assess the efficacy of sulodexide in mitigating endothelial dysfunction markers during the COVID-19 convalescent phase.
- To investigate sulodexide's potential to reduce biomarkers associated with long-term cardiovascular complications after COVID-19.
Main Methods:
- A double-blind, randomized, placebo-controlled trial was conducted over 8 weeks.
- Adult patients in the early convalescent phase of COVID-19 received either sulodexide (250 LRU twice daily) or a placebo.
- Serum biomarker levels, with Thrombomodulin (TM) as the primary endpoint, were analyzed using repeated measures and post hoc tests.
Main Results:
- The sulodexide group showed significantly lower mean levels of Thrombomodulin (TM), von Willebrand Factor (vWF), and Interleukin-6 (IL-6) at week 8 compared to placebo.
- Sulodexide also led to reductions in D-dimer and C-reactive protein (CRP) levels.
- No significant differences were found for P-selectin, fibrinogen, VCAM-1, or ICAM-1.
Conclusions:
- Eight weeks of sulodexide treatment in convalescent COVID-19 patients reduced serum levels of TM, vWF, D-dimer, CRP, and IL-6.
- These findings indicate a potential protective role for sulodexide against post-COVID-19 thromboinflammation and endothelial damage.
- Sulodexide may offer a therapeutic strategy for managing long-term cardiovascular sequelae of COVID-19.
Introduction:
Persistent elevation of biomarkers associated with endothelial dysfunction in convalescent COVID-19 patients has been linked to an increased risk of long-term cardiovascular complications, including long COVID syndrome. Sulodexide, known for its vascular endothelial affinity, has demonstrated pleiotropic protective properties. This study aims to evaluate the impact of sulodexide on serum levels of endothelial dysfunction biomarkers in patients during the convalescent phase of COVID-19.
Methods:
We conducted a double-blind, single-center, randomized, placebo-controlled trial in Mexico, comparing sulodexide (250 LRU orally, twice daily) with placebo over 8 weeks in adult patients during early COVID-19 convalescence. Differences in serum biomarkers between the groups were analyzed using repeated measures and post hoc tests, with Thrombomodulin (TM) as the primary endpoint.
Results:
Among 206 analyzed patients (103 in each group), at week 8, the sulodexide group exhibited significantly lower mean levels of Thrombomodulin (TM) (25.2 ± 7.9 ng/mL vs 29.9 ± 14.7 ng/mL, P = .03), von Willebrand Factor (vWF) (232 ± 131 U/dL vs 266 ± 122 U/dL, P = .02) and Interleukin-6 (IL-6) (12.5 ± 13.2 pg/mL vs 16.2 ± 16.5 pg/mL, P = .03) compared to the placebo group. D-dimer and C reactive protein (CRP) in the sulodexide group were also lowered. No significant differences were observed for P-selectin, fibrinogen, VCAM-1, or ICAM-1 levels.
Conclusions:
Patients in the convalescent phase of COVID-19 who received sulodexide for eight weeks showed a reduction in TM, vWF, D-dimer, CRP, and IL-6 serum levels compared to placebo. These findings suggest a potential protective effect of sulodexide against thromboinflammation and endothelial damage.
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