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Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Effect of atorvastatin on low-density lipoprotein subpopulations and comparison between indicators of plasma
Marek Kucera1, Stanislav Oravec2, Eva Hirnerova2
12nd Medical Clinic, Faculty of Medicine, Comenius University Bratislava, Bratislava, Slovakia marekucera@gmail.com.
Insights
Atorvastatin treatment in hypercholesterolemia patients significantly reduced LDL-C and shifted small, dense LDL subfractions to larger, buoyant ones. This suggests atorvastatin improves atherogenic profiles beyond standard lipid reduction.
Area of Science:
- Cardiovascular Medicine
- Lipid Metabolism
- Pharmacology
Background:
- Statin therapy for hypercholesterolemia leaves residual cardiovascular risk.
- Lipoprotein subfractions offer deeper insights into atherogenicity.
- Small, dense LDL (sdLDL) particles are particularly atherogenic.
Purpose of the Study:
- To evaluate the effect of atorvastatin on LDL-C and lipoprotein subfractions in hypercholesterolemia patients.
- To assess changes in atherogenic index of plasma (AIP) and its correlation with LDL subfractions.
Main Methods:
- 40 hypercholesterolemia patients (no prior lipid-lowering treatment) received atorvastatin 40 mg/d for 3 months.
- Measurements included total cholesterol, LDL-C, triglycerides, sdLDL, apolipoprotein B (apoB), and AIP.
- Correlations between AIP, sdLDL, and apoB were analyzed.
Main Results:
- Atorvastatin significantly reduced total cholesterol, LDL-C, triglycerides, sdLDL, and apoB.
- A significant shift from small, dense LDL subfractions (3-7) to larger, buoyant LDL subfractions was observed.
- AIP showed a stronger correlation with sdLDL levels than with apoB levels.
Conclusions:
- Atorvastatin 40 mg/d effectively improves lipid profiles and favorably alters LDL subfraction distribution in hypercholesterolemia.
- The shift towards larger, buoyant LDL particles and changes in AIP suggest a reduced atherogenic potential.
- Lipoprotein subfraction analysis provides valuable information on the comprehensive effects of statin therapy.
Abstract:
Treatment with statins to achieve target low-density lipoprotein cholesterol (LDL-C) levels is still associated with residual risk. Lipoprotein subfraction evaluation can provide additional information regarding atherogenicity in these individuals. Patients (n = 40) with hypercholesterolemia (29 females, mean age 63 years), without previous hypolipemic treatment, were treated with atorvastatin 40 mg/d for 3 months. Atorvastatin significantly reduced total cholesterol (6.7 ± 1.0 vs 4.6 ± 1.3 mmol/L, P < .001), LDL-C (4.3 ± 1.0 vs 2.6 ± 0.9 mmol/L, P < .001), triglycerides (1.8 ± 0.9 vs 1.5 ± 1.00 mmol/L, P < .05), small-dense LDL (sdLDL) fraction 3 to 7 (0.22 ± 0.37 vs 0.09 ± 0.16 mmol/L, P < .001), and apolipoprotein B (apoB; 1.0 ± 0.2 vs 0.74 ± 0.2 g/L, P < .001). There was a negative correlation of atherogenic index of plasma (AIP) with buoyant LDL-1 and LDL-2 (r = -.35; P < .05) and positive with sdLDL-3 to sdLDL-7 (r = .52, P < .001). Administration of atorvastatin 40 mg/d in patients with hypercholesterolemia caused a shift in sdLDL subfractions to large, buoyant subfractions. The AIP better correlated with sdLDL than apoB levels.
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