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In Vitro Thrombosis Test for Ventricular Assist Devices
Published on: March 21, 2025
Increased thrombogenesity in patients with cyanotic congenital heart disease
Hidemi Kajimoto1, Makoto Nakazawa, Kagari Murasaki
1Department of Pediatric Cardiology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan.
Insights
Platelet activation is present in cyanotic congenital heart disease (CCHD) patients, indicated by elevated P-selectin. This platelet activation may contribute to thromboembolic events in CCHD.
Area of Science:
- Cardiology
- Hematology
- Thrombosis Research
Background:
- Mechanisms of thromboembolism in cyanotic congenital heart disease (CCHD) remain unclear.
- P-selectin indicates platelet activation; thrombomodulin reflects endothelial anticoagulant activity.
- This study investigates platelet activation in CCHD patients.
Purpose of the Study:
- To evaluate the presence and extent of platelet activation in patients with CCHD.
- To assess markers of endothelial anticoagulant activity in CCHD.
- To explore the relationship between platelet activation and thromboembolic events in CCHD.
Main Methods:
- Examined P-selectin (platelet activation marker), plasma thrombomodulin, protein C activity (endothelial markers), and thrombin-antithrombin complex III (TAT) in 35 CCHD patients and controls.
- Measured P-selectin on platelets and plasma levels of thrombomodulin, protein C, and TAT.
- Compared marker levels between CCHD patients and healthy controls.
Main Results:
- CCHD patients showed significantly lower plasma thrombomodulin and protein C activity compared to controls.
- Levels of plasma TAT and platelet P-selectin were significantly higher in CCHD patients.
- Elevated platelet P-selectin was observed in CCHD patients who experienced thromboembolic events (p=0.02).
Conclusions:
- Platelet activation is evident in patients with CCHD.
- This platelet activation may play a significant role in the occurrence of thromboembolic events in CCHD.
- Findings suggest potential therapeutic targets for preventing thromboembolism in CCHD.
Background:
The basic mechanisms of thromboembolism in cyanotic congenital heart disease (CCHD) have not been well clarified. P-selectin on the platelets reflects platelet activation. Thrombomodulin is a critical cofactor for thrombin-mediated activation of protein C and reflects the anticoagulant activity of the endothelium. The present study was performed to evaluate whether platelet activation exists in patients with CCHD.
Methods And Results:
Platelet P-selectin as a marker of platelet activation, plasma thrombomodulin level and protein C activity as markers of anticoagulant activity of the endothelium and thrombin - antithrombin complex III (TAT) were examined in 35 patients with CCHD. Plasma thrombomodulin level (1.1+/-0.9 vs 2.2+/-0.3 FU/ml) and protein C activity (71.1+/-29.8 vs 117.8+/-24.8%) were significantly lower in patients with CCHD as compared with the control subjects. The levels of plasma TAT (255+/-811 vs 1.9+/-0.9 ng/ml) and P-selectin on platelets (6.3 +/-4.5 vs 3.3+/-0.3 mean fluorescence intensity) were significantly higher in the patients with CCHD than in the controls. Four of the CCHD patients who experienced thromboembolic events had elevated levels of platelet P-selectin (p=0.02) compared with CCHD patients without thromboembolic events.
Conclusion:
Platelet activation exists in patients with CCHD and it may play an important role in the thromboembolic events in CCHD.
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