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Activation of coagulation system in dilated cardiomyopathy: comparison of patients with and without left ventricular
Ali Riza Erbay1, Hasan Turhan, Yuksel Aksoy
1Turkiye Yuksek Ihtisas Hospital Department of Cardiology, Ankara, Turkey.
Insights
Platelet activation, thrombin activation, and fibrinolysis are elevated in dilated cardiomyopathy (DCM) patients compared to controls. Left ventricular thrombus presence did not alter these coagulation markers in DCM.
Area of Science:
- Cardiology
- Hematology
- Biochemistry
Background:
- Dilated cardiomyopathy (DCM) is associated with increased risk of thromboembolic events.
- Understanding the prothrombotic state in DCM is crucial for risk stratification and management.
Purpose of the Study:
- To investigate plasma levels of molecular markers for platelet activity, thrombin activation, and fibrinolytic status in patients with DCM.
- To compare these markers between DCM patients with and without left ventricular (LV) thrombus and with healthy controls.
Main Methods:
- Sixty DCM patients (22 with LV thrombus, 38 without) and 23 healthy controls were included.
- Plasma levels of platelet markers (PF4, beta-TG), thrombin generation markers (FpA, TAT), and fibrinolysis markers (D-dimer, PAP) were measured.
- Comparisons were made between DCM patients and controls, and between DCM subgroups with and without LV thrombus.
Main Results:
- Patients with DCM exhibited significantly higher levels of platelet activity markers (PF4, beta-TG) compared to controls.
- Markers of thrombin activation (FpA, TAT) and fibrinolysis (D-dimer, PAP) were also significantly elevated in DCM patients versus controls.
- No significant differences in these coagulation markers were observed between DCM patients with and without LV thrombus.
Conclusions:
- Platelet activation, thrombin activation, and fibrinolytic activity are increased in patients with DCM.
- The presence of LV thrombus in DCM does not appear to be associated with distinct alterations in these specific coagulation markers.
Objectives:
We aimed to investigate plasma levels of molecular markers for platelet activity, thrombin activation and fibrinolytic status in patients with dilated cardiomyopathy (DCM) with and without left ventricular (LV) thrombus and to compare these markers between patients with DCM and control participants.
Materials And Methods:
The study population comprised 60 patients with DCM who met the inclusion criteria. Patients were divided into two groups: 22 patients with LV thrombus and 38 patients without LV thrombus. The age-matched control group consisted of 23 healthy participants (18 men and five women with a mean age of 49). Patients with DCM and healthy participants were compared with respect to platelet activity, thrombin activation and fibrinolytic status. These comparisons were also performed in patients with DCM with and without LV thrombus.
Results:
Platelet factor 4 (28.2+/-4.4 ng/ml compared with 20+/-3.1 ng/ml, P<0.01) and beta-thromboglobulin (40+/-2 ng/ml compared with 17+/-3 ng/ml) levels, reflecting platelet activity, were significantly higher in patients with DCM than in control participants. Fibrinopeptide A (6.94+/-0.69 ng/ml compared with 1.96+/-0.1 ng/ml, P<0.001) and thrombin-antithrombin III complex (5.26+/-2.60 ng/ml compared with 3.17+/-1.23 ng/ml, P<0.001) levels, as markers of fibrin generation, were also higher in patients with DCM than in normal participants. Plasma levels of D-dimer (118+/-16 ng/ml compared with 85+/-3 ng/ml, P<0.001) and plasmin-alpha2-plasmin inhibitor complex (0.8+/-1.1 microg/ml compared with 0.6+/-1.7 microg/ml, P<0.001) in patients with DCM significantly exceeded those in the normal participants. There were no statistically significant differences between patients with and without LV thrombus in DCM with respect to platelet activity, thrombin activation and fibrinolytic status.
Conclusion:
We have shown that platelet activation, thrombin activation and fibrinolytic activity are increased in patients with DCM compared to control participants. However, these markers reflecting coagulation activation in patients with LV thrombus are comparable to those in patients without LV thrombus.
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