Obesity and heart failure-the role of GLP-1 receptor agonists

Gregor Simonis1, Ulrike Schatz2

  • 1Kardiologische Ambulanz und Herzkatheterlabor, MVZ Praxisklinik Herz und Gefäße, Forststraße 3, 01099, Dresden, Germany. gregor.simonis@praxisklinik-dresden.de.

Herz
|April 2, 2025
PubMed

Insights

Glucagon-like peptide‑1 (GLP-1) receptor agonists and tirzepatide show promise for managing obesity-driven heart failure with preserved ejection fraction (HFpEF). These therapies may improve symptoms and outcomes in patients with HFpEF, regardless of diabetes status.

Area of Science:

  • Cardiology
  • Endocrinology
  • Metabolic Diseases

Background:

  • Obesity is a significant driver of heart failure with preserved ejection fraction (HFpEF), causing various pathophysiological changes.
  • Standard treatments like diuretics, SGLT2 inhibitors, and mineralocorticoid antagonists may not fully alleviate symptoms in these patients.
  • Understanding novel therapeutic targets is crucial for improving HFpEF management.

Purpose of the Study:

  • To review current evidence on GLP-1 receptor agonists and tirzepatide in obesity-driven HFpEF.
  • To evaluate the efficacy of these agents in improving symptoms and clinical outcomes.
  • To assess their utility in patients with and without diabetes.

Main Methods:

  • Literature review of clinical studies and trials.
  • Analysis of data on patient symptoms and adverse events.
  • Examination of outcomes related to HFpEF in the context of obesity and diabetes.

Main Results:

  • GLP-1 receptor agonists and tirzepatide demonstrate potential benefits in managing HFpEF symptoms driven by obesity.
  • These agents may offer improved cardiovascular outcomes in affected patient populations.
  • Evidence suggests efficacy irrespective of comorbid diabetes status.

Conclusions:

  • GLP-1 receptor agonists and tirzepatide represent a promising therapeutic avenue for obesity-related HFpEF.
  • Further research is warranted to fully elucidate their long-term benefits and optimal use.
  • These agents could become valuable additions to the treatment of HFpEF in obese individuals.

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