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Published on: March 29, 2024
Effects of liraglutide on hemodynamic parameters in patients with heart failure
Jin Ying Zhang1, Xin Yun Wang1, Xiang Wang1
1Department of Emergency, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Insights
Liraglutide, a glucagon-like peptide-1 analogue, significantly improved cardiac output and stroke volume in heart failure patients. This suggests potential benefits for left ventricular function in heart failure management.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Glucagon-like peptide-1 (GLP-1) analogues have shown promise in improving cardiac function, particularly after acute myocardial infarction.
- Heart failure (HF) remains a significant clinical challenge with limited therapeutic options for improving hemodynamic parameters.
- Investigating novel therapeutic targets like GLP-1 receptor agonists is crucial for advancing HF treatment.
Purpose of the Study:
- To evaluate the efficacy of liraglutide, a GLP-1 analogue, in improving hemodynamic parameters in patients diagnosed with heart failure.
- To assess the impact of liraglutide on cardiac output, stroke volume, and left ventricular contractile function.
- To explore potential anti-inflammatory and anti-oxidative effects of liraglutide in the context of heart failure.
Main Methods:
- A randomized controlled trial involving 52 heart failure patients, allocated 1:1 to receive either liraglutide or a placebo for 7 days.
- Hemodynamic measurements were performed using advanced techniques, including transpulmonary thermodilution and arterial pulse contour analysis.
- Changes in cardiac output, stroke volume, and left ventricular contractile index were primary and secondary endpoints.
Main Results:
- Liraglutide treatment resulted in a statistically significant increase in cardiac output (+1.1 L/min) compared to placebo (P < 0.001).
- Stroke volume was significantly elevated in the liraglutide group (+14.6 ml) versus the control group (P < 0.001).
- A trend towards improved left ventricular contractile index was observed with liraglutide, alongside favorable changes in inflammation and oxidative stress markers.
Conclusions:
- Short-term treatment with liraglutide demonstrates significant improvements in key hemodynamic parameters in patients with heart failure.
- GLP-1 analogues, such as liraglutide, may represent a novel therapeutic strategy for enhancing left ventricular function in heart failure.
- Larger, invasive trials are warranted to confirm these findings and establish the long-term clinical utility of liraglutide in heart failure management.
Abstract:
Glucagon-like peptide-1 analogues improve left ventricular function in patients with acute myocardial infarction. This study aimed to evaluate the effects of liraglutide on hemodynamic parameters in patients with heart failure. A total of 78 patients with heart failure were enrolled in this study between August 2014 and November 2015. Of these, 52 patients were randomized 1:1 to receive either liraglutide or placebo for 7 days. Hemodynamic measurements were made using transpulmonary thermodilution and arterial pulse contour analysis. At 7 days, the difference in change of the primary endpoint of cardiac output between the liraglutide group and control group was +1.1 1/min (95% CI +0.1 to +2.2; P < 0.001). Stroke volume was significantly higher in the liraglutide group compared with the control group (difference: +14.6 ml; P < 0.001). The difference in an increase in the left ventricular contractile index after 7 days of treatment was +210.7 mmHg/s (liraglutide versus control, 95% CI-92.1 to +501.5; P < 0.001). Liraglutide causes favorable changes in markers of inflammation and oxidative stress. Glucagon-like peptide-1 may be associated with improvement in left ventricular function in patients with heart failure. These findings need to be confirmed by larger invasive trials.
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