(HFpEF) is associated with various comorbidities, including obesity, diabetes mellitus, and hypertension.
plays a significant role in the pathophysiology of HFpEF.
GLP-1 receptor agonists may improve endothelial function in HFpEF patients.
Semaglutide and liraglutide have shown cardioprotective effects, including reducing inflammation and preventing atherosclerosis.
Clinical trials, including the STEP-HFpEF trial, indicate positive outcomes in reducing symptoms and physical limitations for HFpEF patients treated with GLP-1 receptor agonists.
Further research is required to clarify the mechanisms of action of GLP-1 receptor agonists and assess their long-term safety and efficacy in HFpEF populations.
Simplified
(HFpEF) is a prevalent and complex condition with limited effective treatments. is a significant component of HFpEF pathophysiology, and glucagon-like peptide-1 receptor (GLP-1R) agonists have shown potential benefits in improving endothelial function. This study aims to explore the relationship between endothelial dysfunction in HFpEF and the mechanisms of action of GLP-1R agonists, highlighting their potential therapeutic benefits. A comprehensive review of the literature was conducted to examine the etiology of HFpEF, the role of endothelial dysfunction, and the effects of GLP-1R agonists on endothelial function and heart failure outcomes. The findings indicate that HFpEF is associated with various comorbidities, such as obesity, diabetes mellitus, and hypertension, which contribute to endothelial dysfunction. GLP-1R agonists, including semaglutide and liraglutide, have demonstrated significant cardioprotective effects, such as improving vascular endothelial function, reducing inflammation, and preventing atherosclerosis. Clinical trials, such as the STEP-HFpEF trial, have shown positive results in reducing symptoms and physical restrictions in HFpEF patients. GLP-1R agonists present a promising therapeutic option for HFpEF by targeting endothelial dysfunction and other pathophysiological mechanisms. Further research is needed to elucidate the precise mechanisms through which GLP-1R agonists exert their benefits and to establish their long-term safety and efficacy in diverse HFpEF populations.
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Declarations. Ethical approval and consent to participate: Not applicable. Our study is a review and does not involve patients. Competing interests: The authors declare no competing interests.
