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Updated: Jun 4, 2025

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Management of Hypercholesterolemia in Patients with Coronary Artery Disease: A Glimpse into the Future
Alessandro Sciahbasi1, Paola Russo2, Michela Zuccanti2
1Interventional Cardiology, Sandro Pertini Hospital, 00157 Rome, Italy.
Insights
Atherosclerosis causes major global deaths. This review covers current and future therapies targeting low-density lipoprotein cholesterol (LDL-C) and lipoprotein (a) to prevent cardiovascular and cerebrovascular diseases.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Biochemistry
Background:
- Atherosclerosis remains a leading global cause of mortality.
- Low-density lipoprotein cholesterol (LDL-C) and apolipoprotein B are key drivers of atherosclerotic plaque formation.
- Emerging biomarkers like lipoprotein (a) indicate increased risk for atherosclerotic cardiovascular disease (ASCVD).
Purpose of the Study:
- To review current FDA-approved therapies for lowering LDL-C, assessing their efficacy, safety, and indications.
- To explore emerging and investigational therapies for LDL-C reduction, including novel agents, gene editing, and immunotherapy.
- To highlight lipoprotein (a) as a future therapeutic target for ASCVD prevention.
Main Methods:
- Comprehensive literature review of approved and investigational lipid-lowering therapies.
- Analysis of clinical trial data on efficacy, tolerability, and safety profiles.
- Evaluation of the role of biomarkers such as LDL-C and lipoprotein (a) in ASCVD.
Main Results:
- Multiple drug classes effectively reduce LDL-C through diverse mechanisms.
- Ongoing research explores novel pharmacological and technological approaches for lipid management.
- Lipoprotein (a) is emerging as a critical target for future ASCVD therapies.
Conclusions:
- Current therapies offer significant benefits in managing LDL-C and reducing ASCVD risk.
- Future therapeutic strategies will likely incorporate novel agents targeting both LDL-C and lipoprotein (a).
- Advancements in gene editing and immunotherapy hold promise for innovative ASCVD treatments.
Abstract:
Cardio-cerebral vascular diseases due to atherosclerosis are still the leading cause of death worldwide. Low-density lipoprotein cholesterol (LDL-C) and apolipoprotein B have been identified as the primary factors responsible for the atherosclerotic process, with a causal effect. Many drugs aimed at reducing LDL-C levels are already on the market, acting in different ways in terms of mechanism of action, efficacy, and safety. Moreover, new lipid-lowering agents and new technologies in the fields of gene editing and immunotherapy are currently under investigation. A more recent biomarker associated with an increased risk of plaque generation, progression, and subsequent ASCVD is the lipoprotein (a) and, in the next few years, it will be the new target of pharmacological therapy. The aim of this review is to present the landscape of therapies already approved to reduce LDL-C levels, evaluating their efficacy, tolerability, and indications. Moreover, we take a glimpse into the future to evaluate experimental novel therapies to lower LDL-C levels that will be approved in the next few years or are under clinical evaluation.
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