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Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
The dawn of a new era of targeted lipid-lowering therapies
Lale Tokgözoğlu1, Peter Libby2
1Department of Cardiology, Hacettepe University Faculty of Medicine, Sıhhiye, Ankara 06100, Turkey.
Abstract:
Lipid risk factors for cardiovascular disease depend in part on lifestyle, but optimum control of lipids often demands additional measures. Low-density lipoprotein (LDL) doubtless contributes causally to atherosclerosis. Recent human genetic findings have substantiated a number of novel targets for lipid-lowering therapy including apolipoprotein C-III, angiopoietin-like protein 3 and 4, apolipoprotein V, and ATP citrate lyase. These discoveries coupled with advances in biotechnology development afford new avenues for management of LDL and other aspects of lipid risk. Beyond LDL, new treatments targeting triglyceride-rich lipoproteins and lipoprotein(a) have become available and have entered clinical development. Biological and RNA-directed agents have joined traditional small-molecule approaches, which themselves have undergone considerable refinement. Innovative targeting strategies have increased efficacy of some of these novel interventions and markedly improved their tolerability. Gene-editing approaches have appeared on the horizon of lipid management. This article reviews this progress offering insight into novel biological and therapeutic discoveries, and places them into a practical patient care perspective.
Insights
Novel therapies targeting lipid risk factors for cardiovascular disease are emerging, including new drugs for low-density lipoprotein (LDL) and other lipids. Advances in biotechnology offer improved management strategies for atherosclerosis and overall cardiovascular health.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Genetics
Background:
- Lifestyle modifications are crucial but often insufficient for optimal lipid control in cardiovascular disease.
- Low-density lipoprotein (LDL) is a confirmed causal factor in atherosclerosis development.
Purpose of the Study:
- To review recent advancements in lipid-lowering therapies and novel therapeutic targets.
- To discuss emerging strategies for managing LDL, triglyceride-rich lipoproteins, and lipoprotein(a).
Main Methods:
- Review of recent human genetic findings identifying novel lipid-lowering targets.
- Analysis of advancements in biotechnology for drug development.
- Examination of new biological, RNA-directed, and small-molecule agents.
- Assessment of innovative targeting strategies and gene-editing approaches.
Main Results:
- Identification of novel therapeutic targets such as apolipoprotein C-III, angiopoietin-like proteins 3 and 4, apolipoprotein V, and ATP citrate lyase.
- Development of new treatments for triglyceride-rich lipoproteins and lipoprotein(a).
- Improved efficacy and tolerability of novel lipid-lowering interventions.
- Emergence of gene-editing as a future therapeutic avenue.
Conclusions:
- Recent discoveries in genetics and biotechnology are revolutionizing lipid management for cardiovascular disease.
- A diverse array of novel therapeutic agents and strategies are enhancing the control of lipid risk factors.
- These advancements offer promising new avenues for practical patient care and improved cardiovascular outcomes.
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