Effects of glucagon-like peptide-1 receptor agonists on patients with heart failure: a meta-analysis of randomized

Shota Obata1, Yoshihisa Miyamoto2, Leandro Slipczuk3

  • 1Department of Medicine, Mount Sinai Beth Israel, New York, New York, USA.

Abstract

Insights

Glucagon-like peptide-1 receptor agonists (GLP-1RAs) reduce major adverse cardiovascular events (MACE) in type 2 diabetes patients with heart failure. However, GLP-1RAs did not significantly alter heart failure admission rates in this population.

Area of Science:

  • Cardiology
  • Endocrinology
  • Pharmacology

Background:

  • Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are established to reduce cardiovascular events in type 2 diabetes mellitus (T2DM).
  • Subgroup analyses of prior trials suggest these benefits may not extend to patients with pre-existing heart failure.
  • This study specifically investigates GLP-1RA efficacy in T2DM patients with a history of heart failure.

Approach:

  • A systematic literature search of PubMed and EMBASE was conducted through March 2022.
  • Included randomized controlled trials (RCTs) comparing GLP-1RAs with placebo in T2DM patients with heart failure history.
  • A random-effects model meta-analysis was performed to assess major adverse cardiovascular events (MACE) and heart failure admissions.

Key Points:

  • The meta-analysis included 7 RCTs with 8,965 patients.
  • GLP-1RAs significantly reduced MACE (HR 0.88, P=0.039) in T2DM patients with prior heart failure.
  • No significant difference was observed in heart failure admission rates (HR 1.03, P=0.67).

Conclusions:

  • GLP-1RAs demonstrate a significant benefit in reducing MACE for T2DM patients who have a history of heart failure.
  • The risk of heart failure admissions was not significantly impacted by GLP-1RA treatment in this cohort.
  • Further research may be warranted to elucidate the mechanisms behind these differential effects.

Related Concept Videos

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
481
Heart Failure V: Medical Management01:30

Heart Failure V: Medical Management

Medical Management of Acute Decompensated Heart Failure (ADHF)The primary goals of therapy for patients hospitalized with acute decompensated heart failure (ADHF) include:Relieving symptomsOptimizing volume statusSupporting oxygenation and ventilationMaintaining cardiac output (CO) and end-organ perfusionIdentifying and addressing the cause of ADHFPreventing complicationsProviding patient education on factors precipitating HF exacerbationPlanning for dischargeOngoing monitoring and assessment...
19
Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
383
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
23
Heart Failure Drugs: β-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
412
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
667