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Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Simvastatin treatment improves endothelial function and increases fibrinolysis in patients with hypercholestrolemia
Gulay S Guven1, Enver Atalar, Bunyamin Yavuz
1Hacettepe University Faculty of Medicine, Department of Internal Medicine, Ankara, Turkey.
Insights
Simvastatin treatment significantly lowered cholesterol and decreased thrombin activatable fibrinolysis inhibitor (TAFI) levels in hyperlipidemic patients. This study also demonstrated simvastatin
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Biochemistry
Background:
- Statins offer cardiovascular benefits beyond lipid reduction.
- Thrombin activatable fibrinolysis inhibitor (TAFI) is a risk factor for thrombosis.
- Endothelial dysfunction predicts cardiovascular events.
Purpose of the Study:
- To evaluate simvastatin's impact on circulating TAFI levels.
- To assess simvastatin's effect on endothelial function in hypercholesterolemia.
- To explore non-lipid-related mechanisms of statin action.
Main Methods:
- 35 hyperlipidemic patients received 40 mg daily simvastatin for 8 weeks.
- Endothelial function assessed via brachial artery flow-mediated dilation (FMD).
- Plasma lipids, TAFI levels, and FMD measured pre- and post-treatment.
Main Results:
- Simvastatin significantly reduced total cholesterol, LDL, and triglycerides (p<0.05).
- Plasma TAFI levels decreased significantly post-treatment (p<0.001).
- Mean FMD improved significantly from 7.7% to 13.0% (p=0.001).
Conclusions:
- Decreased TAFI suggests simvastatin benefits fibrinolysis.
- Improved endothelial function indicates potential for reduced cardiovascular events.
- Simvastatin demonstrates pleiotropic effects in hyperlipidemic patients.
Objectives:
Statins reduce cardiovascular events by cholesterol-lowering as well as nonlipid-related actions. Thrombin activatable fibrinolysis inhibitor (TAFI) is a recently identified independent risk factor of thrombosis. Endothelial dysfunction is also a strong predictor of cardiovascular events. The aim of this study was to assess the effects of simvastatin treatment on circulating TAFI concentrations and endothelial function in patients with hypercholesterolemia.
Methods:
Thirty-five patients (19 female, mean age 48 +/- 7 years) with hyperlipidemia were recruited into the study. Simvastatin was administered, 40 mg daily, for eight weeks to all subjects. Study subjects did not receive any medication except for lipid-lowering therapy during the follow-up period. Endothelial function was evaluated by flow-mediated dilation (FMD) from the brachial artery of the patients. Plasma lipid parameters, TAFI levels and endothelial function were measured before and after simvastatin treatment.
Results:
Treatment with simvastatin showed a significant decrement in plasma total cholesterol, LDL cholesterol and triglyceride levels (p<0.05). Plasma TAFI levels were also significantly decreased after simvastatin treatment [median 17.0 (range 0.4-93.7) mcg/mL versus median 6.9 (range 0.8-63.0) mcg/mL, p<0.001]. Mean FMD was measured 7.7 +/- 2.5% at baseline and significantly improved after treatment (13.0 +/- 1.4%) (p=0.001).
Conclusion:
Our findings of decreased TAFI levels may reflect the beneficial effect of simvastatin treatment on fibrinolysis, and improved endothelial function may suggest the improved future cardiovascular events in hyperlipidemic patients.
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