Activation of coagulation system in dilated cardiomyopathy: Comparison of patients with and without left ventricular thrombus


Erbay A. R., Turhan H., AKSOY Y., Senen K., Yetkin E.

Coronary Artery Disease, cilt.15, sa.5, ss.265-268, 2004 (SCI-Expanded, Scopus) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 15 Sayı: 5
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1097/01.mca.0000135596.54871.6f
  • Dergi Adı: Coronary Artery Disease
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.265-268
  • Anahtar Kelimeler: Coagulation activation, Dilated cardiomyopathy
  • Trakya Üniversitesi Adresli: Evet

Özet

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 β-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-α2-plasmin inhibitor complex (0.8 ± 1.1 μg/ml compared with 0.6 ± 1.7 μg/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. © 2004 Lippincott Williams & Wilkins.