Hypercoagulability in end-stage liver disease: prevalence and its correlation with severity of liver disease and portal vein thrombosis

Clin Appl Thromb Hemost. 2012 Nov;18(6):594-8. doi: 10.1177/1076029612440034. Epub 2012 Apr 11.

Abstract

Contrary to well-recognized bleeding diathesis in chronic liver disease, thrombotic events can occur in these patients due to reduction or loss of synthesis of anticoagulant proteins. Forty-seven consecutive patients with end-stage liver disease (ESLD) were investigated for activity of protein C, protein S, antithrombin, and factor V Leiden mutation. Forty-two (89.4%) patients had low levels of at least 1 while 33 (70.2%) patients were deficient for all anticoagulant proteins studied. Forty-six (97.9%) patients were negative for factor V Leiden mutation. The deficiencies were more marked in hepatitis C virus-positive patients and patients with model for end-stage liver disease (MELD) score >15. Six (12.8%) patients had portal vein thrombosis (PVT), and all had diminished protein S activity. In conclusions, deficiency of anticoagulant proteins occur in early phase of chronic liver disease. The severity of deficiency is proportional to the severity of liver disease. Despite the high prevalence of hypercoagulability, the incidence of PVT is low. Further studies with larger cohort of patients are needed to support these conclusions and to study other associated factors.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Antithrombin Proteins / genetics
  • Antithrombin Proteins / metabolism
  • Budd-Chiari Syndrome / blood
  • Budd-Chiari Syndrome / complications
  • Budd-Chiari Syndrome / epidemiology*
  • Budd-Chiari Syndrome / genetics
  • End Stage Liver Disease / blood
  • End Stage Liver Disease / complications
  • End Stage Liver Disease / epidemiology*
  • Factor V / genetics
  • Factor V / metabolism
  • Female
  • Hepatitis C / blood
  • Hepatitis C / complications
  • Hepatitis C / epidemiology
  • Hepatitis C / genetics
  • Humans
  • Male
  • Middle Aged
  • Portal Vein*
  • Prevalence
  • Protein C / genetics
  • Protein C / metabolism
  • Protein S / genetics
  • Protein S / metabolism
  • Retrospective Studies
  • Severity of Illness Index
  • Thrombophilia / blood
  • Thrombophilia / complications
  • Thrombophilia / epidemiology*
  • Thrombophilia / genetics

Substances

  • Antithrombin Proteins
  • Protein C
  • Protein S
  • factor V Leiden
  • Factor V