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Updated: Aug 11, 2026

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Emerging non-statin LDL-lowering therapies for dyslipidemia and atherosclerosis
1Division of Cardiology and Atherosclerosis Research Center, Cedars-Sinai Medical Center and The David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Insights
Elevated low-density lipoprotein cholesterol (LDL-C) is a key risk factor for cardiovascular disease. While statins are effective, non-statin therapies offer additional LDL-C reduction for patients needing better outcomes.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
Background:
- Elevated low-density lipoprotein cholesterol (LDL-C) is a significant risk factor for atherothrombotic arterial disease.
- Statins (HMG-CoA reductase inhibitors) effectively lower LDL-C and reduce cardiovascular events, leading to broad treatment recommendations.
Purpose of the Study:
- To explore the utility of non-statin therapies for LDL-C reduction.
- To identify alternative or supplementary treatments for patients with suboptimal statin response or intolerance.
Main Methods:
- Review of existing literature on non-statin LDL-C lowering mechanisms.
- Analysis of therapeutic targets beyond HMG-CoA reductase.
Main Results:
- Statins achieve only a 20%-40% reduction in cardiovascular events.
- Non-statin therapies offer diverse mechanisms for LDL-C management.
Conclusions:
- Non-statin therapies are valuable for patients requiring additional LDL-C reduction.
- These therapies are crucial for individuals intolerant to or inadequately responsive to statins alone.
Abstract:
Elevated low-density lipoprotein cholesterol is an important risk factor for atherothrombotic arterial disease. HMG-CoA reductase inhibitors, or statins, are very effective in lowering cholesterol levels, and several trials using statins have shown reductions in mortality and cardiovascular events, leading to the recent recommendations that all patients with known vascular disease, or who are at high risk for vascular disease, should be considered candidates for statin therapy. Yet statins reduce cardiovascular events by only about 20%-40%. Nonstatin therapies (either as monotherapy or in addition to statins) to reduce LDL cholesterol by mechanisms that do not involve inhibition of HMG-CoA reductase are likely to be useful for patients in need of LDL reduction; particularly those who either cannot take statins or respond only partially or not at all to statins alone. These therapies include cholesterol absorption inhibitors, Acyl-CoA cholesterol acyl transferase inhibitors, farnesoid X receptor antagonists, sterol-regulating binding protein cleavage activating protein, and microsomal triglyceride transfer protein.
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