Enhanced expression of monocyte tissue factor in patients with liver cirrhosis

Gut. 1998 Sep;43(3):428-32. doi: 10.1136/gut.43.3.428.

Abstract

Background: Previous studies have shown that cirrhotic patients produce increased amounts of thrombin but the underlying mechanism is still unknown.

Aims: To analyse the relation between the rate of thrombin generation and monocyte expression of tissue factor (TF) in cirrhosis.

Patients: Thirty three cirrhotic patients classified as having low (n = 7), moderate (n = 17), or severe (n = 9) liver failure according to Child-Pugh criteria.

Methods: Prothrombin fragment F1 + 2, monocyte TF activity and antigen, and endotoxaemia were measured in all patients. Polymerase chain reaction (PCR) analysis of TF mRNA was performed in monocytes of five cirrhotic patients.

Results: Prothrombin fragment F1 + 2 was higher in cirrhotic patients than in controls (p < 0.0001). Monocytes from cirrhotic patients had higher TF activity and antigen than those from controls (p < 0.001) with a progressive increase from low to severe liver failure. Monocyte expression of TF was significantly correlated with plasma levels of F1 + 2 (TF activity: r = 0.98, p < 0.0001; TF antigen: r = 0.95, p < 0.0001) and with endotoxaemia (TF activity: r = 0.94, p < 0.0001; TF antigen: r = 0.91, p < 0.0001). PCR analysis of TF mRNA showed TF expression only in three patients with endotoxaemia (more than 15 pg/ml).

Conclusions: Cirrhotic patients have enhanced expression of TF which could be responsible for clotting activation, suggesting that endotoxaemia might play a pivotal role.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antigens / analysis
  • Blood Coagulation
  • Case-Control Studies
  • Cross-Sectional Studies
  • Endotoxemia / complications
  • Endotoxemia / immunology
  • Endotoxemia / metabolism
  • Female
  • Humans
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / immunology
  • Liver Cirrhosis / metabolism*
  • Male
  • Middle Aged
  • Monocytes / immunology
  • Monocytes / metabolism*
  • Peptide Fragments / metabolism
  • Polymerase Chain Reaction
  • Prothrombin / metabolism
  • RNA, Messenger / analysis
  • Regression Analysis
  • Thromboplastin / genetics
  • Thromboplastin / metabolism*

Substances

  • Antigens
  • Peptide Fragments
  • RNA, Messenger
  • prothrombin fragment 1.2
  • Prothrombin
  • Thromboplastin