Related Experiment Video
Updated: Oct 7, 2026

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
The effect of fluvastatin on fibrinolytic factors in patients with hypercholesterolemia
1Division of Cardiology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Insights
Fluvastatin therapy improved cardiovascular health by reducing LDL cholesterol and enhancing the fibrinolytic system. This suggests statins offer benefits beyond lipid-lowering, potentially explaining their cardiovascular protective effects.
Area of Science:
- Cardiovascular Pharmacology
- Lipid Metabolism
- Hemostasis and Thrombosis
Background:
- HMG-CoA reductase inhibitors (statins) demonstrate cardiovascular benefits beyond cholesterol reduction.
- The role of statins in modulating fibrinolytic factors remains unclear due to inconsistent clinical findings.
- Understanding these effects is crucial for a comprehensive view of statin-mediated cardiovascular protection.
Purpose of the Study:
- To investigate the impact of fluvastatin on key fibrinolytic factors in hypercholesterolemic patients.
- To assess whether fluvastatin's effects on fibrinolysis contribute to its cardiovascular benefits.
Main Methods:
- A study cohort of 23 hypercholesterolemic outpatients was selected based on LDL cholesterol levels and cardiovascular risk factors.
- Patients received fluvastatin (40 mg/day) for 8 weeks following a 6-week dietary intervention.
- Blood samples were analyzed at baseline and post-treatment for lipid profiles, tissue plasminogen activator (t-PA), plasminogen activator inhibitor-1 (PAI-1), fibrinogen, and D-dimer.
Main Results:
- Fluvastatin significantly reduced total cholesterol (11%) and LDL cholesterol (22%).
- A significant decrease in D-dimer levels was observed post-therapy.
- Trends indicated reductions in t-PA, PAI-1, and fibrinogen, suggesting an improved fibrinolytic profile.
Conclusions:
- Fluvastatin therapy positively impacts the fibrinolytic system in hypercholesterolemic individuals.
- These findings suggest that statins may confer cardiovascular benefits through mechanisms independent of lipid-lowering.
- The modulation of fibrinolytic factors could partially explain the observed cardiovascular advantages of HMG-CoA reductase inhibitors.
Abstract:
Several studies have shown cardiovascular benefit in treating hypercholesterolemia with HMG-CoA reductase inhibitor. However, in addition to the lowering of cholesterol, the beneficial effects of this inhibitor reflect other pharmacological activities. Whether these beneficial effects are partly mediated by changes in fibrinolytic factors remains to be proven, since clinical studies on the effects of HMG-CoA reductase inhibitors on fibrinolytic factors have not yielded consistent results. The purpose of this study was to evaluate the effects of fluvastatin on fibrinolytic factors in hypercholesterolemic patients. After 6 weeks on a low-fat, low-cholesterol diet, 23 outpatients known to have primary hypercholesterolemia with low density lipoprotein cholesterol (LDL-C) > or = 130 mg/dl with at least 2 risk factors or fasting LDL-C > or = 160 mg/dl were selected for the study. Venous blood samples were collected at baseline and at 8 weeks after fluvastatin therapy (40 mg/day) to measure of tissue plasminogen activator (t-PA), plasminogen activators inhibitor-1 (PAI-1), fibrinogen, D-dimer and lipid profile. After 8 weeks of therapy, fluvastatin reduced serum cholesterol by 11% (261.9 mg/dl vs 233.2 mg/dl, P < 0.01) and LDL-C by 22% (191.9 mg/dl vs 149.3 mg/dl, P < 0.01). D-dimer was significantly decreased (0.38 ng/L vs 0.28 ng/L, P = 0.02) and tPA, PAI-1 and fibrinogen tended to decrease after therapy. Fluvastatin therapy improved fibrinolytic profile; the result of this study may in part explain the benefit of HMG-CoA reductase inhibitor on cardiovascular system other than lipid lowering.
Related Concept Videos
Lipid-Lowering Drugs: Statins and Miscellaneous Agents
Clot Retraction and Fibrinolysis
Atherosclerosis III: Management
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Venous Thrombosis III: Interprofessional Care
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
