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Updated: Aug 23, 2026

Rapid Point-of-Care Assay of Enoxaparin Anticoagulant Efficacy in Whole Blood
Published on: October 12, 2012
Pravastatin potentiates the anticoagulant effects of low molecular weight heparin
Jennifer E Zimmer1, Charles R Spillert, Sirisha Puppala
1Department of Surgery, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, G-502 Medical Sciences Building, 185 South Orange Avenue, Newark, NJ 07102-2757, USA.
Insights
Pravastatin sodium (PS) and low molecular weight heparin (LMWH) together significantly prolong blood clotting time. This synergistic antithrombotic effect suggests PS inhibits fibrin formation, supporting its non-lipid-lowering benefits.
Area of Science:
- Pharmacology
- Hematology
- Cardiovascular Medicine
Background:
- Statins reduce coronary events irrespective of LDL-C levels.
- The precise mechanism of pravastatin's non-lipid-lowering effects remains debated.
- Pravastatin has demonstrated in vitro prolongation of clotting time.
Purpose of the Study:
- To investigate the synergistic effect of pravastatin sodium (PS) and low molecular weight heparin (LMWH) on in vitro clotting time.
- To test the hypothesis that pravastatin exerts antithrombotic effects by inhibiting fibrin formation.
Main Methods:
- Human whole blood was treated with PS and dalteparin (a LMWH).
- Clotting time was measured using a Sonoclot Coagulation Analyzer.
- The analyzer is sensitive to early fibrin generation.
Main Results:
- Both PS and LMWH significantly prolonged clotting time individually compared to control.
- The combination of PS and LMWH resulted in a significantly greater prolongation of clotting time than either agent alone.
- All observed differences in clotting time were statistically significant (p<0.05).
Conclusions:
- The combination of PS and LMWH exhibits a synergistic effect on prolonging clotting time.
- This suggests pravastatin sodium inhibits the coagulation cascade and fibrin formation.
- These findings support an antithrombotic mechanism for pravastatin's beneficial effects.
Introduction:
Statins have been shown in randomized trials to reduce coronary events independent of baseline LDL-C level. In the case of pravastatin sodium (PS), there is conflicting evidence as to what is the actual mechanism of its non-lipid lowering beneficial effects. Because pravastatin has been found to prolong the clotting time in vitro, we conducted a study to determine if pravastatin plus low molecular weight heparin (LMWH) would result in a synergistic effect on the in vitro clotting time, thus supporting the hypothesis that pravastatin exerts antithrombotic effects through reduction of fibrin formation.
Materials And Methods:
Aliquots of PS were combined with dalteparin, a LMWH, in 500 microl of human whole blood. The clotting time in seconds was analyzed on a Sonoclot Coagulation Analyzer, a miniviscometer that is sensitive to early fibrin generation.
Results:
PS and LMWH, each resulted in a significant prolongation of the clotting time compared with control. The combination of PS and LMWH resulted in a significantly prolonged clotting time compared with either given alone. All values were significantly different from each other (p<0.05). Our results showed that the combination of PS and a LMWH prolongs the clotting time to a significantly greater degree when compared to either administered alone.
Conclusions:
The synergistic effect of PS and LMWH on prolongation of the clotting time suggests that PS exerts its effect by inhibition of the coagulation cascade and fibrin formation.
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