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Updated: May 13, 2026

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
New therapeutic principles in dyslipidaemia: focus on LDL and Lp(a) lowering drugs
Giuseppe Danilo Norata1, Christie M Ballantyne, Alberico Luigi Catapano
1Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via Balzaretti 9, 20133 Milan, Italy. danilo.norata@unimi.it
Insights
Many patients struggle to reach cholesterol goals with statins alone. New therapies targeting atherogenic lipoproteins offer improved cardiovascular risk reduction for high-risk individuals.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Genetics
Background:
- Dyslipidemias are significant contributors to cardiovascular risk.
- Statins are effective but many patients do not achieve target lipid levels (LDL-C, non-HDL-C, apoB) even at maximal doses.
- Novel therapeutic targets and agents are needed to address unmet needs in lipid management.
Purpose of the Study:
- To review current therapeutic strategies for dyslipidemias.
- To discuss emerging pharmacological targets and agents for lowering atherogenic lipoproteins.
- To emphasize the importance of further low-density lipoprotein-cholesterol (LDL-C) reduction in high-risk patients.
Main Methods:
- Review of current literature on dyslipidemia management.
- Analysis of novel drug development targeting lipoprotein metabolism.
- Discussion of genetic insights into lipid regulation.
Main Results:
- Statins are a cornerstone therapy, but add-on treatments are often necessary.
- Emerging therapies include proprotein convertase subtilisin/kexin type-9 (PCSK9) inhibitors and modulators of apoB-containing lipoprotein production.
- Lipoprotein(a) is an emerging target requiring further investigation.
Conclusions:
- Achieving recommended lipid goals remains a challenge for many patients.
- Advancements in understanding lipid metabolism have led to novel therapeutic agents.
- Continued LDL-C lowering is crucial for managing cardiovascular risk in high-risk populations.
Abstract:
Dyslipidaemias play a key role in determining cardiovascular risk; the discovery of statins has contributed a very effective approach. However, many patients do not achieve, at the maximal tolerated dose, the recommended goals for low-density lipoprotein-cholesterol (LDL-C), non-high-density lipoprotein-cholesterol, and apolipoprotein B (apoB). Available agents combined with statins can provide additional LDL-C reduction, and agents in development will increase therapeutic options impacting also other atherogenic lipoprotein classes. In fact, genetic insights into mechanisms underlying regulation of LDL-C levels has expanded potential targets of drug therapy and led to the development of novel agents. Among them are modulators of apoB containing lipoproteins production and proprotein convertase subtilisin/kexin type-9 inhibitors. Alternative targets such as lipoprotein(a) also require attention; however, until we have a better understanding of these issues, further LDL-C lowering in high and very high-risk patients will represent the most sound clinical approach.
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