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Establishing a Swine Model of Post-myocardial Infarction Heart Failure for Stem Cell Treatment
Published on: May 25, 2020
Emerging therapies for heart failure
Amy E Rudolph1, Ellen G McMahon
1Cardiovascular & Metabolic Diseases, Pharmacia Corporation T1G, 800 North Lindbergh Blvd, St. Louis, Missouri 63167, USA.
Insights
Despite advancements, heart failure (HF) mortality remains high. Future treatments focusing on myocardial remodeling, cell, and gene therapy offer hope for improved outcomes.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Heart failure (HF) continues to have high mortality rates despite current treatments.
- Existing therapies include diuretics, digitalis, beta-blockers, and renin-angiotensin-aldosterone system inhibitors.
- Over 300,000 deaths annually in the US are linked to HF.
Purpose of the Study:
- To review current and emerging therapeutic strategies for heart failure.
- To highlight the potential of novel molecular targets and disease-modifying approaches.
- To emphasize the importance of targeting myocardial remodeling for improved HF outcomes.
Main Methods:
- Review of existing literature on heart failure treatments.
- Evaluation of preclinical and clinical data for novel therapeutic targets.
- Discussion of future directions including cell transplantation and gene therapy.
Main Results:
- Current HF treatments, while extensive, have not significantly reduced mortality.
- Several novel molecular targets are under investigation, including vasopeptidase, endothelin-1, arginine vasopressin, aldosterone, TNF-alpha, and matrix metalloproteinase inhibitors.
- Promising future strategies involve cell transplantation, gene therapy, and agents that attenuate myocardial remodeling.
Conclusions:
- Despite current therapeutic options, heart failure mortality remains a significant clinical challenge.
- Emerging molecular targets and advanced therapies like cell and gene therapy show promise.
- Attenuating myocardial remodeling is a key strategy for future heart failure treatment and improved survival.
Abstract:
Although multiple advancements have been made in the treatment of heart failure (HF), mortality rates remain alarmingly high. The accepted arsenal of therapeutics includes a diuretic, digitalis, a beta-blocking agent and an inhibitor of the renin-angiotensin-aldosterone system. Despite the employment of a vast array of agents, nearly 300,000 patients in the US die annually with HF as a primary or contributory cause of death. Additional molecular targets are being evaluated in preclinical and clinical settings including vasopeptidase inhibitors, endothelin-1 receptor antagonists, arginine vasopressin antagonists, selective aldosterone blockers, TNF-alpha blockers and matrix metalloproteinase inhibitors. Although these approaches hold promise as viable therapeutics, a thorough evaluation of clinical benefit from these agents requires additional trials. Future disease-modifying approaches will also undoubtedly include cell transplantation and gene therapy. It is likely that notable advances in HF treatment will come from agents that attenuate myocardial remodelling. Indeed, maintenance or improvement of cardiac structure can attenuate HF development and improve mortality.
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