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Updated: Jun 25, 2026

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Dose-dependent effect of rosuvastatin treatment on HDL-subfraction phenotype in patients with primary hyperlipidemia
Michael S Kostapanos1, Haralampos J Milionis, Theodosios D Filippatos
1Department of Internal Medicine, University of Ioannina, Ioannina, Greece.
Insights
Rosuvastatin increases high-density lipoprotein cholesterol by boosting the cholesterol in large high-density lipoprotein particles. This effect is dose-dependent, with higher doses yielding greater increases in beneficial cholesterol levels.
Area of Science:
- Cardiology
- Pharmacology
- Biochemistry
Background:
- The effect of rosuvastatin on high-density lipoprotein cholesterol (HDL-C) is known.
- Data on rosuvastatin's impact on HDL subfractions is limited.
Purpose of the Study:
- To investigate the effect of rosuvastatin on HDL subfraction phenotype.
- To determine if rosuvastatin alters HDL particle size and cholesterol content.
Main Methods:
- 150 participants without cardiovascular disease were randomized.
- Groups received lifestyle modification alone or with rosuvastatin (10 mg/d or 20 mg/d).
- HDL subfractions and cholesterol mass were measured at baseline and after 12 weeks.
Main Results:
- Rosuvastatin significantly increased HDL cholesterol in a dose-dependent manner.
- A dose-related increase in the cholesterol concentration of large HDL particles was observed.
- The increase in HDL cholesterol was attributed to increased cholesterol in larger HDL particles.
Conclusions:
- Rosuvastatin increases HDL cholesterol by increasing the cholesterol mass of large HDL particles.
- The effect is dose-dependent, highlighting the importance of dosage in HDL modification.
- Rosuvastatin may favorably alter HDL subfraction phenotype.
Abstract:
Although the raising effect of rosuvastatin on high-density lipoprotein cholesterol is well-established, there is a paucity of data regarding the effect of this statin on the high-density lipoprotein subfraction phenotype. A total of 150 participants without evidence of cardiovascular disease were randomized to therapeutic lifestyle modification (nonstatin-treated group) or to therapeutic lifestyle modification plus rosuvastatin at 10 mg/d (RSV10 group) or 20 mg/d (RSV20 group). We assessed the effect of rosuvastatin on the cholesterol mass of high-density lipoprotein subfractions at baseline as well as after 12 weeks post-treatment. Rosuvastatin treatment dose-dependently increased the high-density lipoprotein cholesterol (3.4% vs 5.3% in the RSV10 and RSV20 groups, respectively, P = .02). A dose-related rosuvastatin-induced increase in the cholesterol concentration of large high-density lipoprotein particles was also noted (by 11.4% in RSV10 group vs 22.0% in the RSV20 group, P = .01). Rosuvastatin treatment increases the high-density lipoprotein cholesterol by increasing the cholesterol mass only of the larger high-density lipoprotein particles in a dose-dependent manner.
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