• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

心力衰竭中的盐皮质激素拮抗作用:既定及新出现的治疗作用

Mineralocorticoid Antagonism in Heart Failure: Established and Emerging Therapeutic Role.

作者信息

Chang Joycie, Ambrosy Andrew P, Vardeny Orly, Van Spall Harriette G C, Mentz Robert J, Sauer Andrew J

机构信息

Saint Luke's Mid America Heart Institute, Kansas City, Missouri, USA; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.

Department of Cardiology, Kaiser Permanente San Francisco Medical Center, San Francisco, California, USA; Division of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.

出版信息

JACC Heart Fail. 2024 Dec;12(12):1979-1993. doi: 10.1016/j.jchf.2024.08.007. Epub 2024 Sep 1.

DOI:10.1016/j.jchf.2024.08.007
PMID:39243242
Abstract

The pathophysiology of heart failure (HF) is related to the overactivation of the mineralocorticoid receptor, leading to fluid retention and adverse myocardial remodeling. Although mineralocorticoid receptor antagonists (MRAs) are recommended for the treatment of heart failure with reduced ejection fraction (HFrEF), they remain underused due to adverse effects such as hyperkalemia; and their efficacy is controversial in heart failure with mildly reduced ejection fraction (HFmrEF) and heart failure with preserved ejection fraction (HFpEF). Recent trials in people with diabetes and kidney disease have supported the use of nonsteroidal MRAs in reducing HF-related morbidity and mortality and have fewer side effects than their steroidal counterparts. The efficacy and safety of nonsteroidal MRAs have not been tested in HF and are currently being evaluated in additional clinical trials. This review comprehensively examines the current data regarding MRAs for HF and the future direction of nonsteroidal MRA research while exploring the causes of MRA underutilization.

摘要

心力衰竭(HF)的病理生理学与盐皮质激素受体过度激活有关,导致液体潴留和不良的心肌重塑。尽管盐皮质激素受体拮抗剂(MRAs)被推荐用于治疗射血分数降低的心力衰竭(HFrEF),但由于高钾血症等不良反应,它们的使用仍然不足;并且它们在射血分数轻度降低的心力衰竭(HFmrEF)和射血分数保留的心力衰竭(HFpEF)中的疗效存在争议。最近在糖尿病和肾病患者中进行的试验支持使用非甾体类MRAs来降低与HF相关的发病率和死亡率,并且其副作用比甾体类MRAs少。非甾体类MRAs的疗效和安全性尚未在HF中进行测试,目前正在其他临床试验中进行评估。本综述全面审视了关于MRAs治疗HF的当前数据以及非甾体类MRA研究的未来方向,同时探讨了MRA未得到充分利用的原因。

相似文献

1
Mineralocorticoid Antagonism in Heart Failure: Established and Emerging Therapeutic Role.心力衰竭中的盐皮质激素拮抗作用:既定及新出现的治疗作用
JACC Heart Fail. 2024 Dec;12(12):1979-1993. doi: 10.1016/j.jchf.2024.08.007. Epub 2024 Sep 1.
2
Mineralocorticoid Receptor Antagonists in Heart Failure: An Update.心力衰竭中盐皮质激素受体拮抗剂的最新进展
Circ Heart Fail. 2024 Dec;17(12):e011629. doi: 10.1161/CIRCHEARTFAILURE.124.011629. Epub 2024 Nov 25.
3
Mineralocorticoid receptor antagonists in heart failure: an individual patient level meta-analysis.心力衰竭中醛固酮受体拮抗剂的个体患者水平荟萃分析。
Lancet. 2024 Sep 21;404(10458):1119-1131. doi: 10.1016/S0140-6736(24)01733-1. Epub 2024 Sep 1.
4
A review regarding the article 'Mineralocorticoid receptor antagonists in heart failure with reduced ejection fraction: a network meta-analysis of 32 randomized trials'.关于文章《射血分数降低的心力衰竭中使用盐皮质激素受体拮抗剂:32 项随机试验的网络荟萃分析》的综述。
Curr Probl Cardiol. 2024 Aug;49(8):102644. doi: 10.1016/j.cpcardiol.2024.102644. Epub 2024 May 13.
5
Reduced Risk of Hyperkalemia During Treatment of Heart Failure With Mineralocorticoid Receptor Antagonists by Use of Sacubitril/Valsartan Compared With Enalapril: A Secondary Analysis of the PARADIGM-HF Trial.与依那普利相比,沙库巴曲缬沙坦治疗心力衰竭时降低了高钾血症风险:PARADIGM-HF 试验的二次分析。
JAMA Cardiol. 2017 Jan 1;2(1):79-85. doi: 10.1001/jamacardio.2016.4733.
6
Mineralocorticoid receptor antagonists for heart failure: systematic review and meta-analysis.用于心力衰竭的盐皮质激素受体拮抗剂:系统评价与荟萃分析。
BMC Cardiovasc Disord. 2016 Dec 1;16(1):246. doi: 10.1186/s12872-016-0425-x.
7
Cardiovascular and Renal Outcomes of Mineralocorticoid Receptor Antagonist Use in PARAGON-HF.PARAGON-HF 研究中醛固酮受体拮抗剂的心血管和肾脏结局。
JACC Heart Fail. 2021 Jan;9(1):13-24. doi: 10.1016/j.jchf.2020.08.014. Epub 2020 Nov 11.
8
Patient selection for mineralocorticoid receptor antagonists in heart failure with mildly reduced or preserved ejection fraction.心力衰竭伴轻度降低或射血分数保留患者选择盐皮质激素受体拮抗剂。
Pharmacotherapy. 2023 Jun;43(6):563-569. doi: 10.1002/phar.2801. Epub 2023 Apr 18.
9
[Mineralocorticoid receptor antagonists in heart failure with preserved/mildly reduced ejection fraction: from TOPCAT to FINEARTS-HF].[射血分数保留/轻度降低的心力衰竭中的盐皮质激素受体拮抗剂:从TOPCAT研究到FINEARTS-HF研究]
G Ital Cardiol (Rome). 2025 Jan;26(1):38-49. doi: 10.1714/4394.43958.
10
Effect of Mineralocorticoid Receptor Antagonists in Heart Failure with Preserved Ejection Fraction and with Reduced Ejection Fraction - A Narrative Review.醛固酮受体拮抗剂在射血分数保留型心力衰竭和射血分数降低型心力衰竭中的作用 - 一篇叙述性综述。
Curr Vasc Pharmacol. 2022;20(1):46-51. doi: 10.2174/1570161119666210720120439.

引用本文的文献

1
The Role of Myocardial Revascularization in Ischemic Heart Failure in the Era of Modern Optimal Medical Therapy.现代最佳药物治疗时代心肌血运重建在缺血性心力衰竭中的作用
Medicina (Kaunas). 2025 Aug 12;61(8):1451. doi: 10.3390/medicina61081451.
2
Heart failure with preserved ejection fraction therapeutics: in search of the pillars.射血分数保留的心力衰竭治疗方法:探寻关键要素。
Heart Fail Rev. 2025 May 22. doi: 10.1007/s10741-025-10524-z.
3
Prognostic Impact of Long-Term Sodium Zirconium Cyclosilicate-Integrated Medical Therapy in Patients with Systolic Heart Failure.
长期使用环硅酸钠锆钠联合药物治疗对收缩性心力衰竭患者的预后影响
J Clin Med. 2025 Apr 20;14(8):2836. doi: 10.3390/jcm14082836.
4
Treatment options for heart failure in individuals with overweight or obesity: a review.超重或肥胖个体心力衰竭的治疗选择:一项综述
Future Cardiol. 2025 Apr;21(5):315-329. doi: 10.1080/14796678.2025.2479378. Epub 2025 Mar 18.
5
Finerenone: a breakthrough mineralocorticoid receptor antagonist for heart failure, diabetes and chronic kidney disease.非奈利酮:一种用于治疗心力衰竭、糖尿病和慢性肾脏病的突破性盐皮质激素受体拮抗剂。
Egypt Heart J. 2024 Dec 16;76(1):159. doi: 10.1186/s43044-024-00586-z.