The Effect of Simvastatin Therapy on the Expression of Procoagulant and Inflammatory Markers in Heart Failure

Heart failure is a significant public health problem in the United States. There are more than five million heart failure patients in America and this number grows by over 550,000 new cases each year.1 Heart failure is the primary diagnosis for nearly one million hospital admissions each year and another two million patients are admitted with a secondary diagnosis of heart failure, making it the single largest expense for Medicare.1 Furthermore, heart failure causes or contributes to more than 300,000 deaths each year and, in spite of advances in treatment, 70-80% of patients with heart failure will die within 8 years.1, 2 Therefore, heart failure is one of, if not the most important socioeconomic health problems of the 21st century.

Heart failure patients are at increased risks for thromboembolic events. Autopsy results from heart failure patients report a 50% to 60% incidence of thromboembolic events.3-5 Besides known thromboembolic risk factors associated with the heart failure state (such as blood stasis in a poorly contracting left ventricle, endothelial dysfunction and neuroendocrine activation), elevated TF expression may also contribute to enhanced thromboembolic risk. Recent evidence from our laboratory shows that functional TF procoagulant activity (TF-PCA) in monocytes is increased significantly by 2.8-fold in heart failure patients (n=48) compared to healthy controls (n=25) (p=0.03) (Figure 1), while the natural inhibitor tissue factor pathway inhibitor (TFPI) showed no significant difference.6 The heart failure subjects were subsequently followed to death, transplant, or clinical event (i.e. heart failure hospitalization, arrhythmia, acute coronary event, thromboembolic event, death or cardiac transplant). When TF-PCA values were divided at the median, the upper 50-percentile demonstrated a trend toward increased mortality (p=0.06) with a significant increase in clinical events (p=0.04) compared to the lower 50-percentile (Figure 2).

Elevated TF expression is believed to play an integral role in intravascular coagulation seen in coronary artery disease.7-9 Human atherosclerotic plaques are highly thrombogenic, and exhibit high levels of TF antigen and functional TF procoagulant activity.10-15 In addition, TF antigen is higher in plaques from patients with myocardial infarction and unstable angina than in those with stable angina.15 Recent evidence also shows that local TF inhibition by TFPI decreases the thrombogenicity of disrupted human atherosclerotic plaques.16 These data support that increased TF expression may mediate an increased risk of thromboembolic events.

Simvastatin, an antilipidemic agent of the HMG-CoA reductase inhibitor type, has been shown to decrease monocyte TF expression in vitro and ex vivo.17-20 In monocytes collected from both healthy volunteers and hyperlipidemic patients and stimulated with LPS (a potent inducer of TF) in vitro, simvastatin inhibits monocyte TF expression in a dose-dependent manner.17 In an in vivo model, hyperlipidemic patients receiving simvastatin exhibited a significant decrease in TF-Ag and TF-PCA from baseline (mean reduction 68% and 61%, respectively), while these TF parameters remained unchanged in the placebo group (p=0.0002).18 Whether simvastatin also decreases TF expression in heart failure is unknown.

Clinical studies of simvastatin and other statins have mostly been confined to their lipid-lowering effects. However, evidence also suggests that they improve outcomes in heart failure. In a post-hoc analysis of the Scandinavian Simvastatin Survival Study (4S), simvastatin 20-40 mg daily in patients with coronary heart disease significantly reduced the occurrence of heart failure (relative risk reduction 21.7%, p<0.015) and heart failure mortality (relative risk reduction 37%, p=0.014).21 Simvastatin also showed a non-significant trend in decreasing heart failure hospitalizations. An analysis of data from the PRAISE trial showed a 62% decrease in the risk of death in patients treated with statins, independent of their on-treatment cholesterol levels.22 The OMPTIMAAL trial also showed an improvement in survival of heart failure patients with statin therapy.23 In a cohort study by Horwich et al, statin use was associated with a reduction in the risk of heart transplant or death, again without regard to cholesterol levels.24 These results suggest that treatment with HMG-CoA reductase inhibitors have a beneficial effect, beyond that which would be expected from their ability to alter plasma lipid levels.