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Published on: November 10, 2017
Effects of statins on high-density lipoproteins: a potential contribution to cardiovascular benefit
Fergus McTaggart1, Peter Jones
1Clinical Development, AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire SK10 4TG, UK. mctaggarts@aol.com
Insights
Statins modestly increase high-density lipoprotein cholesterol (HDL-C) and apolipoprotein A-I (apo A-I), potentially offering cardiovascular benefits beyond lowering low-density lipoproteins (LDL). Further research is needed to confirm these independent effects.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
Background:
- Statins are primary agents for lowering low-density lipoprotein cholesterol (LDL).
- Their impact on high-density lipoproteins (HDL) and associated cardiovascular benefits requires systematic evaluation.
Purpose of the Study:
- To systematically review clinical trial data on statin effects on HDL.
- To assess if HDL changes contribute to cardiovascular benefits independently of LDL reduction.
Main Methods:
- A systematic review of PubMed-published clinical trials for atorvastatin, pravastatin, rosuvastatin, and simvastatin.
- Selection of 103 trials based on predefined criteria.
Main Results:
- Statins significantly increase HDL-cholesterol (HDL-C) and apolipoprotein A-I (apo A-I) compared to placebo.
- Increases are more pronounced in patients with low baseline HDL-C and high triglycerides.
- Evidence suggests statin-induced HDL changes may independently reduce atherosclerosis progression and cardiovascular disease risk.
Conclusions:
- Statins induce modest increases in HDL-C and apo A-I, likely via reduced cholesteryl ester transfer protein (CETP) activity.
- These HDL modifications may offer independent cardiovascular protection, warranting further investigation.
Purpose:
The objective was to systematically review clinical trial data on the effects of statins on high-density lipoproteins (HDL) and to examine the possibility that this provides cardiovascular benefits in addition to those derived from reductions in low-density lipoproteins (LDL).
Methods:
The PubMed database was searched for publications describing clinical trials of atorvastatin, pravastatin, rosuvastatin, and simvastatin. On the basis of predefined criteria, 103 were selected for review.
Results:
Compared with placebo, statins raise HDL, measured as HDL-cholesterol (HDL-C) and apolipoprotein A-I (apo A-I); these elevations are maintained in the long-term. In hypercholesterolemia, HDL-C is raised by approximately 4% to 10%. The percentage changes are greater in patients with low baseline levels, including those with the common combination of high triglycerides (TG) and low HDL-C. These effects do not appear to be dose-related although there is evidence that, with the exception of atorvastatin, the changes in HDL-C are proportional to reductions in apo B-containing lipoproteins. The most likely explanation is a reduced rate of cholesteryl ester transfer protein (CETP)-mediated flow of cholesterol from HDL. There is some evidence that the statin effects on HDL reduce progression of atherosclerosis and risk of cardiovascular disease independently of reductions in LDL.
Conclusion:
Statins cause modest increases in HDL-C and apo A-I probably mediated by reductions in CETP activity. It is plausible that such changes independently contribute to the cardiovascular benefits of the statin class but more studies are needed to further explore this possibility.
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