Simultaneous measurement of thrombin and plasmin generation to assess the interplay between coagulation and fibrinolysis

• DOI: 10.1160/th13-04-0345
• Publication Date: 2013-08-30T10:02:15Z
• Authors: Tomoko Matsumoto; Midori Shima; Keiji Nogami
• Keywords: Feedback, Physiological; Hemostasis; Fibrinolysis; Thrombomodulin; Thrombin; Skin Diseases, Genetic; Plasminogen; Afibrinogenemia; Conjunctivitis; Hemophilia A; Thromboplastin; 03 medical and health sciences; 0302 clinical medicine; Tissue Plasminogen Activator; Humans; Blood Coagulation Tests; Factor V Deficiency; Fibrinolysin; Blood Coagulation; Factor X Deficiency; Protein C Inhibitor

summaryNormal haemostasis is maintained by a controlled balance between coagulation and fibrinolysis, involving thrombin and plasmin the respective key enzymes. Simultaneous evaluation of both enzymes facilitates, therefore, an overall understanding of normal and pathological haemostasis. Combined thrombin and plasmin generation (T/P-G) assays have been recently described, and we have adapted the technique to investigate the interplay between coagulation and fibrinolysis in patients with various haemostatic disorders. Our modified T/P-G was initiated by the addition of a mixture of optimised lower concentrations of tissue factor and tissue-type plasminogen activator. Thrombin generation (TG) and plasmin generation (PG) were monitored simultaneously using individual fluorescent substrates in separate microtitre wells. The relationship between coagulation and fibrinolysis was demonstrated by analysing the effects of thrombin inhibitors, activated protein C and thrombomodulin. The most evident impairments in TG were observed with plasma samples deficient of coagulation factors participating in the prothrombinase complex. Defects in PG were observed with deficiencies of factor (F)V, FX, fibrinogen, and plasminogen. TG appeared to be a prerequisite for the initiation of PG, and overall PG was governed by fibrinogen concentration. TG in patients with haemophilia A correlated with levels of FVIII activity, but there was no significant relationship between PG and FVIII:C, confirming that the abnormal haemostasis in haemophilia A results in a severe imbalance between coagulation and fibrinolysis. The findings demonstrate that global haemostasis depends on a sensitive balance between coagulation and fibrinolysis, and that the modified T/P-G assay could provide an enhanced understanding of haemorrhage and thrombosis in clinical practice.