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Thrombin-activatable fibrinolysis inhibitor deficiency in cirrhosis is not associated with increased plasma fibrinolysis.

AbstractBACKGROUND AND AIMS:
The bleeding tendency of patients suffering from cirrhosis is in part ascribed to accelerated fibrinolysis. In this study, the role of the recently discovered inhibitor of fibrinolysis, thrombin-activatable fibrinolysis inhibitor (TAFI) in cirrhosis was examined.
METHODS:
In 64 patients with cirrhosis of varying severity, TAFI antigen levels were measured by enzyme-linked immunosorbent assay and compared with TAFI levels in control subjects. Furthermore, a plasma-based fibrinolysis assay was performed in the presence and absence of a specific inhibitor of activated TAFI.
RESULTS:
TAFI levels were decreased in cirrhosis. Mean TAFI levels were 66% in Child's A, 55% in Child's B, 47% in Child's C cirrhosis, and 26% in acute liver failure. Decreased TAFI antigen levels were highly correlated with antithrombin and alpha(2)-antiplasmin activity levels. Clot lysis times and clot lysis ratio (defined as ratio between clot lysis time in the absence and presence of a specific inhibitor of activated TAFI) of cirrhotics were not significantly different from healthy controls.
CONCLUSIONS:
Despite decreased levels of TAFI and other components of the fibrinolytic system, no evidence of increased plasma fibrinolytic potential in cirrhosis is observed using the plasma-based assay of this study. The reduction of antifibrinolytic factors in cirrhosis is compensated by the concomitant reduction in profibrinolytics.
AuthorsT Lisman, F W Leebeek, L O Mosnier, B N Bouma, J C Meijers, H L Janssen, H K Nieuwenhuis, P G De Groot
JournalGastroenterology (Gastroenterology) Vol. 121 Issue 1 Pg. 131-9 (Jul 2001) ISSN: 0016-5085 [Print] United States
PMID11438502 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens
  • Antithrombins
  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D
  • Carboxypeptidases
  • Carboxypeptidase B2
Topics
  • Antigens (blood)
  • Antithrombins (metabolism, pharmacology)
  • Blood Coagulation (drug effects)
  • Carboxypeptidase B2
  • Carboxypeptidases (deficiency, pharmacology)
  • Fibrin Fibrinogen Degradation Products (metabolism)
  • Fibrinolysis (drug effects)
  • Humans
  • Liver Cirrhosis (blood, classification, immunology)
  • Time Factors

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