Key result
Atorvastatin 20 mg/day significantly reduced total cholesterol, PAI-1, and prothrombin fragment 1 + 2 levels after 6 and 12 months of treatment in hypercholesterolemic patients.
Why the study?
Does atorvastatin 20 mg/day improve hemostatic parameters in hypercholesterolemic patients?
Observational (n=57)
Does atorvastatin 20 mg/day improve hemostatic parameters in hypercholesterolemic patients?
Atorvastatin therapy reduces hemostatic abnormalities such as elevated PAI-1 and F1 + 2 in hypercholesterolemic patients, suggesting an additional pleiotropic benefit.
May support pleiotropic hemostatic benefits; hypothesis-generating and should not change practice pending randomized confirmation.
This study assessed hemostatic effects of an HMC-CoA reductase inhibitor, atorvastatin, on different parameters in 32 hypercholesterolemic patients of both sexes. In the patients and in 25 control subjects, plasma levels of tissue-type plasminogen activator, plasminogen activator inhibitor (PAI-1), D-dimer, prothrombin fragment 1 + 2 (F1 + 2), total cholesterol, triglycerides and fibrinogen had been measured. All these parameters were evaluated in patients after 6 and 12 months of treatment with atorvastatin at a dosage of 20 mg/day. This treatment significantly lowered the total cholesterol level in all patients. Moreover, after 6 months of atorvastatin treatment, PAI-1 and F1 + 2, which were both increased at baseline, were significantly reduced. This reduction continued after 12 months. The present results show that a reduction of hemostatic abnormalities, which exist in hypercholesterolemia, may be another important effect of the atorvastatin therapy.
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Trifiletti et al. (2003) conducted an observational in Hypercholesterolemia (n=57). Atorvastatin vs. Control subjects / Baseline was evaluated on Plasma levels of tissue-type plasminogen activator, PAI-1, D-dimer, F1 + 2, total cholesterol, triglycerides and fibrinogen. Atorvastatin 20 mg/day significantly reduced total cholesterol, PAI-1, and prothrombin fragment 1 + 2 levels after 6 and 12 months of treatment in hypercholesterolemic patients.
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