Atorvastatin reduces thrombin generation after percutaneous coronary intervention independent of soluble tissue factor

Thromb Res. 2005;115(6):469-74. doi: 10.1016/j.thromres.2004.09.017. Epub 2004 Oct 27.

Abstract

Introduction: Statins were previously shown to suppress cellular tissue factor (TF) in vitro. Here, we investigated the effect of atorvastatin on the TF-pathway and thrombin generation after coronary angioplasty and stenting in vivo.

Materials and methods: A cohort of 30 patients with coronary artery disease (CAD) was randomised to treatment with either none (n=10), 10 mg (n=10) or 80 mg (n=10) atorvastatin per day for the postinterventional period of 6 months starting the day before percutaneous coronary intervention (PCI). Fasting blood samples were collected on admission and after 6 weeks and 6 months of statin therapy to determine sTF, free tissue factor pathway inhibitor (TFPI) and prothrombin fragment F1.2 by immunoassay.

Results: Soluble TF (sTF) significantly correlated with thrombin generation as measured by prothrombin fragment F1.2 at baseline. This correlation was lost 6 weeks and 6 months after initiation of statin therapy. In vivo, F1.2 was significantly lowered after 6 months of statin therapy by both, low dose (0 vs. 10 mg: 1.3+/-0.3 vs. 0.7+/-0.2 ng/ml; P<0.05) and high dose (0 vs. 80 mg: 1.2+/-0.3 vs. 0.6+/-0.2 ng/ml; P=0.01) atorvastatin compared to control. However, sTF and free TFPI did not change significantly with atorvastatin therapy when compared to baseline or control.

Conclusions: Our results demonstrate reduced in vivo generation of thrombin six months after percutaneous coronary intervention and statin therapy independent of sTF and free TFPI.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Angioplasty, Balloon, Coronary*
  • Anticoagulants / pharmacology*
  • Anticoagulants / therapeutic use
  • Atorvastatin
  • Cohort Studies
  • Coronary Disease / drug therapy
  • Dose-Response Relationship, Drug
  • Female
  • Follow-Up Studies
  • Heptanoic Acids / pharmacology*
  • Heptanoic Acids / therapeutic use
  • Humans
  • Lipids / blood
  • Lipoproteins / blood
  • Lipoproteins / drug effects
  • Male
  • Middle Aged
  • Prothrombin / metabolism
  • Pyrroles / pharmacology*
  • Pyrroles / therapeutic use
  • Thrombin / biosynthesis*
  • Thrombin / drug effects
  • Thromboplastin / drug effects
  • Thromboplastin / metabolism*
  • Treatment Outcome

Substances

  • Anticoagulants
  • Heptanoic Acids
  • Lipids
  • Lipoproteins
  • Pyrroles
  • lipoprotein-associated coagulation inhibitor
  • Prothrombin
  • Thromboplastin
  • Atorvastatin
  • Thrombin