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组胺H2受体拮抗剂在心力衰竭治疗与预防中的应用

Histamine H2 Receptor Antagonists in the Treatment and Prevention of Heart Failure.

作者信息

Wang Dan, Chen Hailan, Luo Yunhao

机构信息

Department of Cardiology, The First People's Hospital of Shuangliu District (West China Airport Hospital, Sichuan University), Chengdu, People's Republic of China.

Department of Critical Care Medicine, Chengdu First People's Hospital, Chengdu, People's Republic of China.

出版信息

Int J Gen Med. 2024 Dec 11;17:6047-6052. doi: 10.2147/IJGM.S499182. eCollection 2024.

DOI:10.2147/IJGM.S499182
PMID:39678682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11646443/
Abstract

Despite advancements in the treatment of heart failure (HF) and modest improvements in survival rates over the past few decades, mortality rate remains significantly high. HF not only imposes a significant economic burden on patients' families but also presents a substantial challenge to society at large. Therefore, effective treatment and prevention strategies are crucial. Numerous studies have demonstrated that histamine H2 receptor antagonists (H2RAs) can benefit patients with HF through various mechanisms. These mechanisms encompass promoting sodium and water excretion, vasodilation, enhancing cardiac output, reducing levels of inflammatory cytokines, improving ventricular remodeling, and reducing mortality rate. Additionally, H2RAs exert beneficial effects on typical risk factors and may prevent the onset of HF. This review aims to elucidate the mechanisms underlying the treatment and prevention of HF using H2RAs. For patients requiring either prevention or management of HF, and who concurrently have acid-related diseases, H2RAs may represent a suitable therapeutic option.

摘要

尽管在过去几十年中心力衰竭(HF)的治疗取得了进展,生存率也有一定程度的提高,但死亡率仍然显著偏高。HF不仅给患者家庭带来了沉重的经济负担,也给整个社会带来了巨大挑战。因此,有效的治疗和预防策略至关重要。大量研究表明,组胺H2受体拮抗剂(H2RAs)可通过多种机制使HF患者受益。这些机制包括促进钠和水排泄、血管舒张、增加心输出量、降低炎症细胞因子水平、改善心室重塑以及降低死亡率。此外,H2RAs对典型危险因素具有有益作用,可能预防HF的发生。本综述旨在阐明使用H2RAs治疗和预防HF的潜在机制。对于需要预防或管理HF且同时患有酸相关疾病的患者,H2RAs可能是一种合适的治疗选择。

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本文引用的文献

1
Neuroimmune cross-talk in heart failure.心力衰竭中的神经免疫相互作用
Cardiovasc Res. 2025 May 6;121(4):550-567. doi: 10.1093/cvr/cvae236.
2
Device therapies for heart failure with reduced ejection fraction: a new era.射血分数降低的心力衰竭的器械治疗:一个新时代。
Front Cardiovasc Med. 2024 Oct 18;11:1388232. doi: 10.3389/fcvm.2024.1388232. eCollection 2024.
3
Beyond Guideline-Directed Medical Therapy: Nonpharmacologic Management for Patients With Heart Failure.超越指南指导的药物治疗:心力衰竭患者的非药物管理
JACC Heart Fail. 2025 Feb;13(2):185-199. doi: 10.1016/j.jchf.2024.08.018. Epub 2024 Oct 23.
4
Clinical profile, treatment patterns and one-year outcome of heart failure patients admitted in tertiary care hospital of North India.印度北部三级医院收治的心力衰竭患者的临床特征、治疗模式及一年期预后
J Family Med Prim Care. 2024 Aug;13(8):3225-3230. doi: 10.4103/jfmpc.jfmpc_1868_23. Epub 2024 Jul 26.
5
Inflammatory Biomarkers in Patients With Type 2 Diabetes Mellitus and Heart Failure With Preserved Ejection Faction.2 型糖尿病伴射血分数保留心力衰竭患者的炎症生物标志物。
Kardiologiia. 2024 Jul 31;64(7):40-47. doi: 10.18087/cardio.2024.7.n2562.
6
The Role of Oxidative Stress and Inflammatory Parameters in Heart Failure.氧化应激和炎症参数在心力衰竭中的作用。
Medicina (Kaunas). 2024 May 2;60(5):760. doi: 10.3390/medicina60050760.
7
Effect of Histamine H2 Receptor Antagonists on All-Cause Mortality in Critically Ill Patients With Essential Hypertension: A Retrospective Cohort Study.组胺 H2 受体拮抗剂对合并原发性高血压危重症患者全因死亡率的影响:一项回顾性队列研究。
J Clin Pharmacol. 2024 Sep;64(9):1112-1122. doi: 10.1002/jcph.2445. Epub 2024 Apr 25.
8
Safety and tolerability of β-blockers: importance of cardioselectivity.β受体阻滞剂的安全性和耐受性:心脏选择性的重要性。
Curr Med Res Opin. 2024;40(sup1):55-62. doi: 10.1080/03007995.2024.2317433. Epub 2024 Apr 10.
9
Histamine H2 receptor antagonist exhibited comparable all-cause mortality-decreasing effect as β-blockers in critically ill patients with heart failure: a cohort study.组胺H2受体拮抗剂在重症心力衰竭患者中显示出与β受体阻滞剂相当的降低全因死亡率的效果:一项队列研究。
Front Pharmacol. 2023 Nov 13;14:1273640. doi: 10.3389/fphar.2023.1273640. eCollection 2023.
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Eur J Heart Fail. 2023 Jun;25(6):776-791. doi: 10.1002/ejhf.2874. Epub 2023 May 19.