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肥胖与射血分数保留的心力衰竭:聚焦于新药及药物治疗的未来方向

Obesity and heart failure with preserved ejection fraction: focus on new drugs and future direction in medical treatment.

作者信息

Kim Se-Eun, Yoo Byung-Su

机构信息

Division of Cardiology, Department of Internal Medicine, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, Korea.

出版信息

Korean J Intern Med. 2025 May;40(3):357-370. doi: 10.3904/kjim.2024.387. Epub 2025 Apr 30.

Abstract

Obesity is a major risk factor for heart failure with preserved ejection fraction (HFpEF) and contributes through multiple pathophysiological pathways, including systemic inflammation, neurohormonal activation, and mechanical inhibition. The treatment of obesity has shown significant potential for improving HFpEF outcomes. Sodium-glucose cotransporter 2 inhibitors have emerged as effective treatments for improving symptoms and quality of life in patients with HFpEF while aiding in weight control. Furthermore, a recent demonstration of the clinical benefits of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in HFpEF showed promising results in reducing weight loss, and improving symptoms and clinical outcomes. In this review article, we discuss the association between HFpEF and obesity, the emerging role of GLP-1 RAs, and future directions for medical therapies targeting obesity-associated HFpEF.

摘要

肥胖是射血分数保留的心力衰竭(HFpEF)的主要危险因素,并通过多种病理生理途径起作用,包括全身炎症、神经激素激活和机械抑制。肥胖的治疗已显示出改善HFpEF预后的巨大潜力。钠-葡萄糖协同转运蛋白2抑制剂已成为改善HFpEF患者症状和生活质量并有助于控制体重的有效治疗方法。此外,最近一项关于胰高血糖素样肽-1受体激动剂(GLP-1 RAs)在HFpEF中的临床益处的研究表明,在减轻体重、改善症状和临床结局方面取得了有前景的结果。在这篇综述文章中,我们讨论了HFpEF与肥胖之间的关联、GLP-1 RAs的新作用以及针对肥胖相关HFpEF的药物治疗的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9724/12081111/f2183d6535c5/kjim-2024-387f1.jpg

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