Skip to main content
Journal cover image

Pulmonary artery pressure trajectories in heart failure patients treated with GLP-1 receptor agonists.

Publication ,  Journal Article
Jiang, H; Wattanachayakul, P; Kittipibul, V; Nicolsen, E; McVeigh, T; Kamneva, O; Fudim, M
Published in: ESC Heart Fail
August 2025

AIMS: Data support favourable haemodynamic benefits of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) on improving cardiac structural abnormalities and function in patients with heart failure (HF). However, the direct haemodynamic effects of GLP-1 RAs remain inadequately characterized. We aim to investigate temporal trends of pulmonary artery pressure (PAP) in HF patients receiving GLP-1 RAs. METHODS AND RESULTS: In this single-centre retrospective cohort study, we identified HF patients with a CardioMEMS device who received semaglutide or tirzepatide for at least 6 months during the monitoring period. Patients who were already on GLP-1 RAs prior to device implantation were excluded. The relationship between weight change and PAPs was assessed using Pearson correlation. A total of nine patients were included (54 years, BMI 41.4 kg/m2, 67% men, 44% with EF < 40%, 89% diabetes, 89% semaglutide). Median dose of semaglutide (or equivalent) at 6 months was 0.9 (range 0.25-1) mg/week. Body weight significantly decreased from 123.6 to 117.2 kg (P = 0.047), while guideline-directed medical therapy (GDMT) and loop diuretic uses and dosages remained unchanged. Significant reductions were observed in systolic PAP (38.9 to 34.0 mmHg, P = 0.045), diastolic PAP (20.0 to 17.8 mmHg, P = 0.019) and mean PAP (27.3 to 24.3 mmHg, P = 0.018). There was a significant correlation between weight loss and reductions in systolic PAP (r = 0.69, P = 0.04) and mean PAP (r = 0.72, P = 0.029). CONCLUSIONS: GLP1-RA use in HF patients was significantly associated with reductions in body weight and PAPs at 6 months, despite no changes in GDMT and loop diuretic doses.

Duke Scholars

Published In

ESC Heart Fail

DOI

EISSN

2055-5822

Publication Date

August 2025

Volume

12

Issue

4

Start / End Page

2578 / 2582

Location

England

Related Subject Headings

  • Retrospective Studies
  • Pulmonary Artery
  • Middle Aged
  • Male
  • Hypoglycemic Agents
  • Humans
  • Heart Failure
  • Glucagon-Like Peptides
  • Glucagon-Like Peptide-1 Receptor Agonists
  • Glucagon-Like Peptide 1
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Jiang, H., Wattanachayakul, P., Kittipibul, V., Nicolsen, E., McVeigh, T., Kamneva, O., & Fudim, M. (2025). Pulmonary artery pressure trajectories in heart failure patients treated with GLP-1 receptor agonists. ESC Heart Fail, 12(4), 2578–2582. https://doi.org/10.1002/ehf2.15308
Jiang, Haoran, Phuuwadith Wattanachayakul, Veraprapas Kittipibul, Erika Nicolsen, Todd McVeigh, Oksana Kamneva, and Marat Fudim. “Pulmonary artery pressure trajectories in heart failure patients treated with GLP-1 receptor agonists.ESC Heart Fail 12, no. 4 (August 2025): 2578–82. https://doi.org/10.1002/ehf2.15308.
Jiang H, Wattanachayakul P, Kittipibul V, Nicolsen E, McVeigh T, Kamneva O, et al. Pulmonary artery pressure trajectories in heart failure patients treated with GLP-1 receptor agonists. ESC Heart Fail. 2025 Aug;12(4):2578–82.
Jiang, Haoran, et al. “Pulmonary artery pressure trajectories in heart failure patients treated with GLP-1 receptor agonists.ESC Heart Fail, vol. 12, no. 4, Aug. 2025, pp. 2578–82. Pubmed, doi:10.1002/ehf2.15308.
Jiang H, Wattanachayakul P, Kittipibul V, Nicolsen E, McVeigh T, Kamneva O, Fudim M. Pulmonary artery pressure trajectories in heart failure patients treated with GLP-1 receptor agonists. ESC Heart Fail. 2025 Aug;12(4):2578–2582.
Journal cover image

Published In

ESC Heart Fail

DOI

EISSN

2055-5822

Publication Date

August 2025

Volume

12

Issue

4

Start / End Page

2578 / 2582

Location

England

Related Subject Headings

  • Retrospective Studies
  • Pulmonary Artery
  • Middle Aged
  • Male
  • Hypoglycemic Agents
  • Humans
  • Heart Failure
  • Glucagon-Like Peptides
  • Glucagon-Like Peptide-1 Receptor Agonists
  • Glucagon-Like Peptide 1