Genetic and acquired thrombotic factors in chronic hepatitis C

Am J Gastroenterol. 2004 Mar;99(3):527-31. doi: 10.1111/j.1572-0241.2004.04092.x.

Abstract

Objectives: During the progression of chronic liver disease towards cirrhosis, morphological studies have shown a close association between parenchymal remodeling and obliterative lesions of intrahepatic small portal and hepatic veins. These lesions are highly suggestive of intrahepatic thrombotic events, which may have a key role in the pathogenesis of hepatic fibrosis. The aim of the study was to investigate thrombotic risk factors in chronic hepatitis C patients with different extent of liver fibrosis.

Methods: The following thrombotic factors were evaluated in 68 hepatitis C patients with prothrombin activity >/= 80% (34 consecutive patients with extensive fibrosis and/or cirrhosis compared with 34 consecutive patients without extensive fibrosis and/or cirrhosis): factor V Leiden, G20210A prothrombin mutation, antithrombin, protein C and S deficiencies, hyperhomocysteinemia, elevated factor VIII level, and lupus anticoagulant.

Results: Three thrombotic risk factors were significantly more frequent in patients with extensive fibrosis and/or cirrhosis than in those without extensive fibrosis: protein C deficiency present in 14 patients (41%) as compared with three patients (9%), p= 0.004; elevated factor VIII level present in 19 patients (56%) as compared with six patients (18%), p= 0.002; and hyperhomocysteinemia present in 10 patients (29%) as compared with two patients (6%), p= 0.023. The association of two or three prothrombotic factors was present in 19 patients (56%) with extensive fibrosis and/or cirrhosis as compared with one patient (3%) without extensive fibrosis and/or cirrhosis, p < 0.001.

Conclusion: Multiple thrombotic risk factors coexist frequently in patients with extensive fibrosis and early stage of cirrhosis. Their association with local inflammation could favor thrombotic events in the liver micro-circulatory bed.

MeSH terms

  • Adult
  • Aged
  • Antithrombins / analysis
  • Factor VIII / analysis
  • Female
  • Hepatitis C, Chronic / blood
  • Hepatitis C, Chronic / etiology
  • Hepatitis C, Chronic / genetics*
  • Homocysteine / blood
  • Humans
  • Male
  • Middle Aged
  • Protein C / analysis
  • Protein S / analysis
  • Risk Factors
  • Thrombosis / blood
  • Thrombosis / complications
  • Thrombosis / genetics*

Substances

  • Antithrombins
  • Protein C
  • Protein S
  • Homocysteine
  • Factor VIII