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Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Combination therapy in cholesterol reduction: focus on ezetimibe and statins
Liliana Grigore1, Giuseppe Danilo Norata, Alberico L Catapano
1Department of Pharmacological Sciences, University of Milan, Milan, Italy.
Insights
High-dose statins often fail to lower LDL cholesterol to goal. Combining ezetimibe with statins offers a dual approach, effectively reducing LDL cholesterol by inhibiting both production and absorption.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Metabolic Disorders
Background:
- HMG CoA reductase inhibitors (statins) are primary lipid-lowering agents but frequently fail to achieve guideline-recommended LDL-C goals in hypercholesterolemia patients.
- A significant therapeutic gap exists between target and achieved LDL-C levels, with many patients not reaching goals even after 6 months of statin therapy.
Purpose of the Study:
- To evaluate the efficacy of dual inhibition of cholesterol production and absorption for managing hypercholesterolemia.
- To highlight the complementary mechanisms of statins and ezetimibe in lowering LDL-C.
Main Methods:
- Review of the roles of the liver and intestine in cholesterol homeostasis.
- Analysis of clinical data on the co-administration of ezetimibe with statins versus statins alone.
Main Results:
- Co-administering ezetimibe with statins provides greater LDL-C reductions compared to statins alone.
- Ezetimibe can be safely combined with any statin dose, enhancing lipid-lowering therapy.
Conclusions:
- Dual inhibition targeting both cholesterol production (liver) and absorption (intestine) is a more effective strategy for lowering LDL-C.
- Ezetimibe co-administration with statins represents a clinically relevant approach to bridge the therapeutic gap in hypercholesterolemia management.
Abstract:
Although widely used in lipid lowering therapy, HMG CoA reductase inhibitors (even when administered at high doses) are frequently insufficient to achieve guideline-recommended LDL-C goals for many patients with hypercholesterolemia in everyday clinical practice. Many patients do not achieve LDL-C goal on the initial dose of statin and the majority of these patients does not reach their goal after 6 months. As a consequence, a wide therapeutic gap exists between target LDL-C levels and those typically achieved in clinical practice. A recent and more effective therapeutic hypocholesterolemic strategy is to treat the two main sources of cholesterol simultaneously (production of cholesterol, mainly in the liver, and absorption of cholesterol in the intestine) with a complementary mechanism of action, by co-administering ezetimibe, a novel agent inhibiting cholesterol absorption, with a statin, which inhibits cholesterol production in the liver. Ezetimibe can be effectively and safely co-administered with any dose of any statin and, compared with the single inhibition of cholesterol production, afforded by statins alone, provides consistently greater reductions in LDL-C through dual inhibition of both cholesterol production and absorption. We summarize the pivotal role of both the liver and intestine in the overall balance of cholesterol in the body and describe the clinical impact and relevance of using ezetimibe either alone or co-administered with statins in controlling elevated levels of plasma LDL cholesterol.
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