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Author Spotlight: Investigating HR-Dependent Cardiac Function in Mouse Models Through a Novel Atrial-Pacing Approach
Published on: July 21, 2023
The Heart Failure Knights
Chiara Mozzini1, Mauro Pagani1
1Department of Medicine, ASST Mantova, C. Poma Hospital, Mantova, Italy.
Insights
New heart failure (HF) treatments focus on four drug classes and novel agents. Vericiguat shows promise, while myosin activators and inhibitors are under investigation for improved HF outcomes.
Area of Science:
- Cardiology
- Pharmacology
- Translational Medicine
Background:
- The 2021 European Society of Cardiology guidelines shifted from sequential to a four-pillar approach for heart failure (HF) management in reduced ejection fraction HF (HFrEF).
- Recent clinical trials have introduced novel therapeutic agents beyond the established four pillars.
Purpose of the Study:
- To review emerging molecular therapies for HFrEF, examining their efficacy and potential as future treatments.
- To highlight new agents like vericiguat, omecamtiv mecarbil, aficamten, and mavacamten.
Main Methods:
- Review of recent clinical trial data and guideline updates for HFrEF.
- Analysis of novel drug classes targeting different mechanisms in heart failure.
Main Results:
- Vericiguat, a soluble guanylate cyclase stimulator, demonstrated efficacy in hospitalized HFrEF patients.
- Omecamtiv mecarbil (cardiac myosin activator) reduced HF events and cardiovascular death.
- Aficamten and mavacamten (cardiac myosin inhibitors) improved functional capacity in hypertrophic cardiomyopathy by reducing hypercontractility.
Conclusions:
- Novel agents like vericiguat, omecamtiv mecarbil, aficamten, and mavacamten represent promising advancements in HFrEF treatment.
- These emerging therapies offer new strategies to improve outcomes for patients with heart failure.
Abstract:
The 2021 European Society of Cardiology guidelines for the diagnosis and treatment of acute and chronic heart failure (HF) have abandoned the sequential approach for optimal drug therapy and proposed four drug classes, the so-called 4 "pillars" (angiotensin-converting enzyme inhibitors; angiotensin receptor-neprilysin inhibitors; beta-blockers; mineralocorticoid receptor antagonists and sodium-glucose co-transporter 2 inhibitors) to be initiated and titrated in all patients with reduced ejection fraction HF (HFrEF). In addition, new molecules have been considered, derived from recently reported advances from trials in HFrEF. In this review, Authors examine in particular these new molecules, as further "knights" for HF. In particular, vericiguat, a novel oral soluble guanylate cyclase stimulator, has proved effective in patients with HFrEF who had recently been hospitalized or had received intravenous diuretic therapy. The selective cardiac myosin activator omecamtiv mecarbil and the cardiac myosin inhibitors aficamten and mavacamten are under investigation. Cardiac myosin stimulator, omecamtiv mecarbil, has shown efficacy in HFrEF, lowering HF related events or cardiovascular death, while the 2 inhibitors, mavacamten and aficamten have been shown to reduce hypercontractility and left ventricular outflow obstruction improving functional capacity in randomized trials targeting hypertrophic cardiomyopathy. These agents are the prototypes of active pipelines promising to deliver an array of molecules against HF in the near future.
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