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Quantitative Analysis of Cellular Composition in Advanced Atherosclerotic Lesions of Smooth Muscle Cell Lineage-Tracing Mice
Published on: February 20, 2019
Inflammation and beyond: new directions and emerging drugs for treating atherosclerosis
Marie-Jeanne Bertrand1, Jean-Claude Tardif1
1a Montreal Heart Institute, Department of medicine , Université de Montréal , Montreal , Canada.
Insights
Cardiovascular disease (CVD) remains a leading cause of death. Novel anti-inflammatory drugs and pharmacogenomics show promise for managing residual risk in atherosclerosis, despite current therapies.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Immunology
Background:
- Cardiovascular (CV) atherosclerotic disease is a primary global cause of death.
- Inflammation drives plaque rupture and acute coronary syndromes.
- Despite statin therapy, residual CV risk persists in many patients.
Purpose of the Study:
- To review current and emerging therapies for atherosclerosis.
- To explore novel anti-inflammatory drug targets.
- To discuss the role of pharmacogenomics in future lipid management.
Main Methods:
- Review of contemporary therapies for CV prevention.
- Analysis of ongoing Phase II and III trials for novel anti-inflammatory agents.
- Examination of PCSK9 inhibitors and pharmacogenomic approaches.
Main Results:
- Statins are effective lipid-lowering drugs for CV prevention.
- Novel anti-inflammatory drugs targeting pathways like IL-1 and TNF-α are under investigation.
- PCSK9 inhibitors reduce LDL-C; long-term effects are pending.
- Pharmacogenomics may personalize lipid therapies and reduce drug development failures.
Conclusions:
- Novel anti-inflammatory therapies offer potential for residual CV risk but require large trial validation.
- Pharmacogenomics presents a promising strategy for optimizing lipid management and drug development.
- Addressing inflammation and residual risk is crucial for improving CV outcomes.
Introduction:
Cardiovascular (CV) atherosclerotic disease remains the leading cause of morbidity and mortality worldwide, despite the advances in contemporary therapies. Inflammation is an important process in atherosclerosis, leading to plaque rupture and acute coronary syndrome. Although statin therapy has substantially reduced CV events in primary and secondary prevention, many treated patients will have recurrent adverse CV events despite the standard of care. Thus, drug development aiming to target inflammatory pathways seems a promising avenue for novel therapies in atherosclerosis. Areas covered: Statins have been extensively studied and are the most effective lipid-lowering drugs available for CV prevention. Novel anti-inflammatory drugs are being tested in Phase II and III trials, targeting pathways like interleukin-1, leukotrienes, TNF-α, P-selectin, CCL2-CCR2 and MAP Kinase. Expert opinion: Novel anti-inflammatory therapies seem promising additions to address the residual CV risk present despite the current standard of care, but large clinical trials have not yet shown beneficial effects on clinical events. PCSK9 inhibitors have been shown to substantially reduce LDL-C, however their long-term safety and effects on CV risk are currently being investigated. Pharmacogenomics holds great potential in future lipid trials, enabling the identification of patients who will respond with greater benefits and smaller risk to therapies and to decrease failure rates in drug development, as genotype-dependent effects of the CETP inhibitor dalcetrapib were shown in the dal-OUTCOMES and dal-PLAQUE-2 trials.
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