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沙库巴曲缬沙坦用于广泛的心力衰竭患者(从作用机制到特定人群的治疗结果)。

Sacubitril/valsartan in a wide spectrum of heart failure patients (from mechanisms of action to outcomes in specific populations).

作者信息

Rajzer Przemyslaw, Biegus Jan

机构信息

University of Glasgow School of Medicine, Glasgow, Scotland, UK.

Institute of Heart Diseases, Wroclaw Medical University, Wroclaw, Poland.

出版信息

Heart Fail Rev. 2025 Mar;30(2):387-405. doi: 10.1007/s10741-024-10471-1. Epub 2025 Jan 7.

DOI:10.1007/s10741-024-10471-1
PMID:39776087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11802626/
Abstract

Heart failure (HF) represents a significant global health challenge, characterized by high morbidity and mortality rates, decreased quality of life and a significant financial and economic burden. The prevalence of HF continues to rise, driven by an ageing population and an increasing burden of comorbidities such as hypertension, diabetes and obesity. Understanding the complex pathophysiology and developing effective treatments are critical for improving patient outcomes, yet the range of effective, life-prolonging medication classes has remained mostly constant in the last few decades. The introduction of angiotensin receptor neprilysin inhibitors (ARNI) was a major breakthrough in HF management, for the first time targeting the natriuretic peptide system in addition to the renin-angiotensin-aldosterone pathway to potentiate the effects of older drug classes. ARNI shows superiority in clinical outcomes compared to previous guideline-directed therapies, especially in patients with reduced ejection fraction (EF). It has now been implemented into international guidelines, endorsing its use in patients with HF and reduced ejection fraction (HFrEF) and HF with mildly reduced ejection fraction (HFmrEF). This review summarises the mechanism of action of Sac/Val, presents key clinical trials in a range of patient populations and HF aetiologies and outlines gaps in knowledge and potential novel uses of Sac/Val.

摘要

心力衰竭(HF)是一项重大的全球健康挑战,其特征为高发病率和死亡率、生活质量下降以及巨大的财政和经济负担。受人口老龄化以及高血压、糖尿病和肥胖等合并症负担增加的推动,HF的患病率持续上升。了解复杂的病理生理学并开发有效的治疗方法对于改善患者预后至关重要,然而在过去几十年中,有效的延长生命的药物类别范围基本保持不变。血管紧张素受体脑啡肽酶抑制剂(ARNI)的引入是HF管理中的一项重大突破,它除了作用于肾素-血管紧张素-醛固酮途径外,首次靶向利钠肽系统,以增强旧有药物类别的效果。与先前的指南指导疗法相比,ARNI在临床结局方面显示出优越性,尤其是在射血分数(EF)降低的患者中。它现已被纳入国际指南,批准用于射血分数降低的心力衰竭(HFrEF)患者和射血分数轻度降低的心力衰竭(HFmrEF)患者。本综述总结了沙库巴曲缬沙坦的作用机制,介绍了一系列患者群体和HF病因的关键临床试验,并概述了知识空白以及沙库巴曲缬沙坦的潜在新用途。

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Sacubitril/valsartan in a wide spectrum of heart failure patients (from mechanisms of action to outcomes in specific populations).沙库巴曲缬沙坦用于广泛的心力衰竭患者(从作用机制到特定人群的治疗结果)。
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本文引用的文献

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Reply: Patients With Cardiac Amyloidosis Are More Prone to Hypotension.回复:心脏淀粉样变性患者更容易出现低血压。
J Am Coll Cardiol. 2024 Oct 8;84(15):e235. doi: 10.1016/j.jacc.2024.07.040.
2
Incidence and risk factors of hypotension-related adverse events among Japanese patients with heart failure receiving sacubitril/valsartan or enalapril: Results from the PARALLEL-HF study.在接受沙库巴曲缬沙坦或依那普利治疗的日本心力衰竭患者中,低血压相关不良事件的发生率及危险因素:PARALLEL-HF研究结果
J Cardiol. 2025 Mar;85(3):241-247. doi: 10.1016/j.jjcc.2024.09.002. Epub 2024 Sep 14.
3
The role of sacubitril/valsartan in abnormal renal function patients combined with heart failure: a meta-analysis and systematic analysis.
沙库巴曲缬沙坦在肾功能异常合并心力衰竭患者中的作用:一项荟萃分析与系统分析
Ren Fail. 2024 Dec;46(1):2349135. doi: 10.1080/0886022X.2024.2349135. Epub 2024 Jun 13.
4
Sacubitril/Valsartan-Related Hypotension in Patients With Heart Failure and Preserved or Mildly Reduced Ejection Fraction.沙库巴曲缬沙坦相关低血压在射血分数保留或轻度降低的心力衰竭患者中的作用。
J Am Coll Cardiol. 2024 May 7;83(18):1731-1739. doi: 10.1016/j.jacc.2024.02.035. Epub 2024 Mar 25.
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Sacubitril/Valsartan in Patients Hospitalized With Decompensated Heart Failure.沙库巴曲缬沙坦在射血分数降低的心力衰竭患者中的应用。
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Unraveling the complex pathophysiology of heart failure: insights into the role of renin-angiotensin-aldosterone system (RAAS) and sympathetic nervous system (SNS).揭示心力衰竭复杂的病理生理学机制:深入了解肾素-血管紧张素-醛固酮系统 (RAAS) 和交感神经系统 (SNS) 的作用。
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ESC Heart Fail. 2023 Dec;10(6):3677-3689. doi: 10.1002/ehf2.14559. Epub 2023 Oct 7.
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ESC Heart Fail. 2023 Dec;10(6):3656-3666. doi: 10.1002/ehf2.14358. Epub 2023 Oct 6.