Similar effects of atorvastatin, simvastatin and pravastatin on thrombogenic and inflammatory parameters in patients

C Joukhadar1, N Klein, M Prinz

  • 1Department of Clinical Pharmacology, University of Vienna Medical School, Austria.

Thrombosis and Haemostasis
|February 24, 2001
PubMed

Insights

This study found that atorvastatin, simvastatin, and pravastatin similarly affected hemostatic and inflammatory markers in hypercholesterolemic patients over three months. These findings suggest that chemical and pharmacological differences between statins do not significantly impact these markers.

Area of Science:

  • Cardiovascular Pharmacology
  • Lipid Metabolism and Atherosclerosis
  • Hemostasis and Thrombosis Research

Background:

  • Statins offer cardiovascular benefits beyond lipid reduction, potentially through effects on thrombosis, inflammation, plaque stability, and endothelial function.
  • The specific impact of different statins on these non-lipid-lowering effects remains incompletely understood.

Purpose of the Study:

  • To compare the short-term effects of three distinct statins (atorvastatin, simvastatin, pravastatin) on hemostatic and inflammatory markers.
  • To determine if chemical and pharmacokinetic differences influence these non-lipid-lowering effects.

Main Methods:

  • A randomized, double-blind, controlled study involving 99 hypercholesterolemic patients.
  • Patients received nearly equieffective cholesterol-lowering doses of atorvastatin, simvastatin, or pravastatin for three months.
  • Measurements included plasma levels of von Willebrand factor antigen (vWf-Ag), fibrinogen, d-dimer, prothrombin fragment 1+2 (F1.2), and C-reactive protein (CRP).

Main Results:

  • All statins significantly reduced total plasma cholesterol by 22-29%.
  • No significant differences were observed in the effects of the three statins on F1.2, vWf-Ag, d-dimer, and CRP.
  • Simvastatin showed a more pronounced effect on fibrinogen compared to atorvastatin and pravastatin, though F1.2 and vWf-Ag were reduced across all statins when data were pooled.

Conclusions:

  • Short-term (3-month) treatment with atorvastatin, simvastatin, and pravastatin demonstrated similar effects on selected hemostatic and inflammatory plasma markers in hypercholesterolemic patients.
  • The chemical and pharmacological variations among these statins do not appear to exert a major influence on these specific markers.
Abstract

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