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Mechanisms of GLP-1 Receptor Agonists in HFpEF: Exploring Weight-Dependent and Independent Drivers of Therapeutic Benefit.

Mechanisms of GLP-1 Receptor Agonists in HFpEF: Exploring Weight-Dependent and Independent Drivers of Therapeutic Benefit.

期刊: Circulation 日期: 2026-05-01 PMID: 41878820 DOI: 10.1161/CIRCHEARTFAILURE.125.013279 浏览: 50
作者: Thomas J, Dagan M, Wang B, Gutman S, Kaye DM
J, T., M, D., B, W., S, G., & DM, K. (2026). Mechanisms of GLP-1 Receptor Agonists in HFpEF: Exploring Weight-Dependent and Independent Drivers of Therapeutic Benefit.. Circulation. https://doi.org/10.1161/CIRCHEARTFAILURE.125.013279
J T, M D, B W, S G, DM K. Mechanisms of GLP-1 Receptor Agonists in HFpEF: Exploring Weight-Dependent and Independent Drivers of Therapeutic Benefit.. Circulation. 2026; doi: 10.1161/CIRCHEARTFAILURE.125.013279
J T, M D, B W, et al. Mechanisms of GLP-1 Receptor Agonists in HFpEF: Exploring Weight-Dependent and Independent Drivers of Therapeutic Benefit.[J]. Circulation. 2026. DOI: 10.1161/CIRCHEARTFAILURE.125.013279.
@article{j2026,
  author = {Thomas J and Dagan M and Wang B and Gutman S and Kaye DM},
  title = {Mechanisms of GLP-1 Receptor Agonists in HFpEF: Exploring Weight-Dependent and Independent Drivers of Therapeutic Benefit.},
  journal = {Circulation},
  year = {2026},
  doi = {10.1161/CIRCHEARTFAILURE.125.013279},
  note = {PMID: 41878820},
}
TY  - JOUR
AU  - Thomas J
AU  - Dagan M
AU  - Wang B
AU  - Gutman S
AU  - Kaye DM
TI  - Mechanisms of GLP-1 Receptor Agonists in HFpEF: Exploring Weight-Dependent and Independent Drivers of Therapeutic Benefit.
T2  - Circulation
PY  - 2026
DO  - 10.1161/CIRCHEARTFAILURE.125.013279
AN  - PMID:41878820
ER  - 

摘要

Heart failure with preserved ejection fraction is a complex and increasingly prevalent condition often associated with metabolic comorbidities such as obesity, diabetes, and hypertension. Although its burden is substantial, therapeutic progress has lagged compared with heart failure with reduced ejection fraction. GLP-1RAs (glucagon-like peptide-1 receptor agonists), initially developed for glycemic control in type 2 diabetes, have emerged as promising therapeutic agents for the obese/cardiometabolic heart failure with preserved ejection fraction phenotype. Recent trials, including STEP-HFpEF and SUMMIT, have demonstrated improvements in symptoms, quality of life, and reductions in heart failure events. Beyond inducing substantial weight loss, GLP-1RAs exert a range of metabolic, cardiovascular, and anti-inflammatory effects. In this review, we summarize weight-dependent and weight-independent actions of GLP-1RAs and outline how these mechanisms may influence cardiovascular physiology, myocardial remodeling, cardiac metabolism, renal sodium handling, and systemic inflammation in heart failure with preserved ejection fraction.

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