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Published on: December 2, 2014
Effects of low and high doses of atorvastatin on arterial compliance
Yesari Karter1, Asli Curgunlu, Nurver Ertürk
1Department of Internal Medicine, Cerrahpasa Medical Faculty, Istanbul University, Turkey.
Insights
High-dose atorvastatin significantly reduces LDL cholesterol but does not improve arterial compliance more than standard doses. This suggests aggressive dosing may not be necessary for patients with hyperlipidemia but no other atherosclerosis risk factors.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
Background:
- Endothelial dysfunction, characterized by reduced vascular distensibility, precedes morphological lesions in atherosclerosis.
- Hyperlipidemia is a primary risk factor for atherosclerosis development.
Purpose of the Study:
- To compare the effects of standard (20 mg/day) versus high (80 mg/day) doses of atorvastatin on lipid profiles and arterial compliance in patients with hyperlipidemia.
- To determine if higher atorvastatin doses offer superior improvements in arterial compliance.
Main Methods:
- A randomized, double-blind study involving 24 patients with LDL-C > 170 mg/dL and no other atherosclerosis risk factors.
- Patients received either 20 mg/day or 80 mg/day of atorvastatin for three months.
- Serum lipid fractions and arterial compliance (measured via distensibility and compliance coefficients using Doppler ultrasound) were assessed at baseline and post-treatment.
Main Results:
- Both atorvastatin doses significantly reduced total cholesterol, LDL-C, and triglycerides, and increased HDL-C.
- The high-dose group showed significantly greater reductions in total cholesterol, LDL-C, and triglycerides compared to the standard-dose group.
- Arterial distensibility and compliance coefficients increased significantly in both groups, with no significant difference between the standard and high-dose groups.
Conclusions:
- Higher doses of atorvastatin are more effective in lowering blood lipid levels than standard doses.
- Improvements in arterial compliance are not dose-dependent with atorvastatin.
- For patients with hyperlipidemia but no other risk factors, aggressive dosing of atorvastatin may not be necessary for improving vascular function.
Abstract:
At the beginning of atherosclerosis before evidence of morphological lesions or plaques, vascular distensibility or arterial compliance decreased gradually. This endothelial dysfunction is regarded as an early feature of atherosclerosis. In a randomized, double-blind study design, group 1 (12 patients; 7 males, 5 females) with serum LDL-C levels higher than 170 mg/dL and without any other risk factor for atherosclerosis received three months of 20 mg/day atorvastatin treatment while group 11 (8 males, 4 females) with the same characteristics received 80 mg/day. Baseline and posttreatment serum lipid fractions and arterial compliance were measured. Arterial compliance was measured noninvasively in the left common carotid artery with color Doppler ultrasound. Atorvastatin reduced total cholesterol (TC), LDL-C, and triglyceride levels by 32% (P < 0.001), 40.8% (P < 0.001), and 19% (P < 0.001), respectively, and increased HDL-C by 6.9%, (P = 0.002) in the first group. In the second group these reductions were 38.5% (P < 0.001), 46.2% (P < 0.001), and 26.78% (P < 0.001), respectively, and the increase in HDL was 7.8% (P = 0.03). It was observed that the decrease in serum TC, LDL-C and triglyceride levels were significantly higher in the second group than the first group. With atorvastatin, the distensibility coefficient (DC) and compliance coefficient (CC) increased from 18.7 +/- 3.4 to 21.3 +/- 2.9 10(-3) x kPa(-1) (P < 0.001) and from 0.69 +/- 0.05 to 0.77 +/- 0.03 mm2 x kPa(-1) (P < 0.001) in the first group while they changed from 18.3 +/- 3.6 to 21.9 +/- 3.0 10(-3) x kPa(-1) (P < 0.001) and from 0.70 +/- 0.04 to 0.81 +/- 0.01 mm2 x kPa(-1) (P < 0.001) respectively, in the second group. DC and CC increased in both groups, but the differences between the groups were not significant. High doses of atorvastatin reduce blood lipid levels more than conventional doses, however, the change in compliance is not dose-dependent. As endothelial dysfunction is regarded as an early feature of atherosclerosis, there would be no need to administer aggressive doses in a patient without any risk factors other than hyperlipidemia.
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