Thromb Haemost 2013; 110(04): 761-768
DOI: 10.1160/TH13-04-0345
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

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

Tomoko Matsumoto
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
,
Keiji Nogami
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
,
Midori Shima
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
› Institutsangaben
Financial Support: This work was partly supported by grants for MEXT KAKENHI 24591558 and Baxter Coagulation Research Fund 2012.
Weitere Informationen

Publikationsverlauf

Received: 27. April 2013

Accepted after minor revision: 11. Juli 2013

Publikationsdatum:
01. Dezember 2017 (online)

summary

Normal 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.

 
  • References

  • 1 Sorensen B, Johansen P, Christiansen K. et al. Whole blood coagulation thrombelastographic profiles employing minimal tissue factor activation. J Thromb Haemost 2003; 1: 551-558.
  • 2 Hemker HC, Wielder S, Kessels H. et al. Continuous registration of thrombin generation in plasma, its use for the determination of the thrombin potential. Thromb Haemost 1993; 70: 617-624.
  • 3 Hemker HC, Giesen PL, Ramjee M. et al. The thrombogram: monitoring thrombin generation in platelet rich plasma. Thromb Haemost 2000; 83: 589-591.
  • 4 Wagenvoord RJ, Hendrix HH, Kai H. et al. A chromogenic test to determine the procoagulant phospholipids in platelet-rich plasma and whole blood. Thromb Haemost 1994; 72: 582-587.
  • 5 van Hylckama Vlieg A, Christiansen SC, Luddington R. et al. Elevated endogenous thrombin potential is associated with an increased risk of a first deep venous thrombosis but not with the risk of recurrence. Br J Haematol 2007; 138: 769-774.
  • 6 Hron G, Kollars M, Binder BR. et al. Identification of patients at low risk for recurrent venous thromboembolism by measuring thrombin generation. J Am Med Assoc 2006; 296: 397-402.
  • 7 Dargaud Y, Beguin S, Lienhart A. et al. Evaluation of thrombin generating capacity in plasma from patients with haemophilia A and B. Thromb Haemost 2005; 93: 475-480.
  • 8 Matsumoto T, Nogami K, Ogiwara K. et al. A putative inhibitory mechanism in the tenase complex responsible for loss of coagulation function in acquired haemophilia A patients with anti-C2 autoantibodies. Thromb Haemost 2012; 107: 288-301.
  • 9 Butenas S, van’t Veer C, Mann KG. “Normal” thrombin generation. Blood 1999; 94: 2169-2178.
  • 10 Goldenberg NA, Hathaway WE, Jacobson L. et al. A new global assay of coagulation and fibrinolysis. Thromb Res 2005; 116: 345-356.
  • 11 Simpson ML, Goldenber NA, Jacobson LJ. et al. Simultaneous thrombin and plasmin generation capacities in normal and abnormal states of coagulation and fibrinolysis in children and adults. Thromb Res 2011; 127: 317-332.
  • 12 Van Geffen M, Loof A, Lap P. et al. A novel haemostasis assay for the simultaneous measurement of coagulation and fibrinolysis. Hematology 2011; 16: 327-336.
  • 13 Mimms LT, Zampighi G, Nozaki Y. et al. Phospholipid vesicle formation and transmembrane protein incorporation using octyl glucoside. Biochemistry 1981; 20: 833-840.
  • 14 Hemker HC, Willems GM, Beguin S. A computer assisted methods to obtain the prothrombin activation velocity in whole plasma independent of thrombin decay process. Thromb Haemost 1986; 56: 9-17.
  • 15 Leurs J, Nerme V, Sim Y. et al. Carboxypeptidase U (TAFIa) prevents lysis from proceeding into the propagation phase through a threshold-dependent mechanism. J Thromb Haemost 2004; 2: 416-423.
  • 16 Matsumoto T, Shima M, Takeyama M. et al. The measurement of low levels of factor VIII or factor IX in haemophilia A and haemophilia B plasma by clot waveform analysis and thrombin generation assay. J Thromb Haemost 2006; 4: 377-384.
  • 17 Matsumoto T, Nogami K, Ogiwara K. et al. A modified thrombin generation test for investigating very low levels of factor VIII activity in haemophilia A. Int J Hematol 2009; 90: 576-582.
  • 18 Wagenvoord RJ, Deinum J, Elg M. et al. The paradoxical stimulation by a reversible thrombin inhibitor of thrombin generation in plasma measured with thrombinography is caused by alpha(2)-macroglobulin-thrombin. J Thromb Haemost 2010; 8: 1281-1289.
  • 19 Broze Jr. GJ, Higuchi DA. Coagulation-dependent inhibition of fibrinolysis: role of carboxypeptidase-U and premature lysis of from haemophilic plasma. Blood 1996; 88: 3815-3823.
  • 20 Mosnier LO, Lisman T, van den Berg HM. et al. The defective down regulation of fibrinolysis in haemophilia A can be restored by increasing the TAFI plasma concentration. Thromb Haemost 2001; 86: 1035-1039.