Vericiguat:心力衰竭患者的新希望。

IF 3.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Raquel Chiles, Rami A. Al-Horani
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引用次数: 0

摘要

心力衰竭伴射血分数降低(HFrEF)是指心脏不能充分收缩或射血。这颗心脏不能产生足够的心输出量来灌注重要组织。在基础水平上,已知一氧化氮-可溶性鸟苷环化酶-环鸟苷单磷酸的心脏保护途径在心力衰竭患者中受损。Vericiguat是一种新型的口服小分子,直接刺激可溶性鸟苷环化酶,因此,它可以促进环鸟苷单磷酸的产生。Vericiguat于2021年1月获得FDA批准,用于降低有症状的慢性心力衰竭且射血分数低于45%的成年人因心力衰竭住院或需要门诊静脉利尿剂后心血管死亡和心力衰竭住院的风险。在这篇综述中,我们描述了化学和机械方面,药代动力学,不良反应和禁忌症,以促进其最佳的治疗使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vericiguat: A New Hope for Heart Failure Patients

Vericiguat: A New Hope for Heart Failure Patients

Heart failure with reduced ejection fraction (HFrEF) is the inability of the heart to adequately contract or eject blood. This heart is unable to produce adequate cardiac output to perfuse vital tissues. At a fundamental level, it is known that the cardioprotective pathway of nitric oxide-soluble guanylate cyclase-cyclic guanosine monophosphate is impaired in heart failure patients. Vericiguat is a novel, orally used, small molecule, and direct stimulator of the soluble guanylate cyclase, and thus, it enhances the production of cyclic guanosine monophosphate. Vericiguat was approved by the FDA in January of 2021 to reduce the risk of cardiovascular death and heart failure hospitalization following a hospitalization for heart failure or need for outpatient IV diuretics, in adults with symptomatic chronic heart failure and ejection fraction less than 45%. In this review, we describe the chemical and mechanistic aspects, pharmacokinetics, adverse effects, and contraindications of vericiguat so as to facilitate its optimal therapeutic use.

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来源期刊
Cardiovascular Therapeutics
Cardiovascular Therapeutics 医学-心血管系统
CiteScore
5.60
自引率
0.00%
发文量
55
审稿时长
6 months
期刊介绍: Cardiovascular Therapeutics (formerly Cardiovascular Drug Reviews) is a peer-reviewed, Open Access journal that publishes original research and review articles focusing on cardiovascular and clinical pharmacology, as well as clinical trials of new cardiovascular therapies. Articles on translational research, pharmacogenomics and personalized medicine, device, gene and cell therapies, and pharmacoepidemiology are also encouraged. Subject areas include (but are by no means limited to): Acute coronary syndrome Arrhythmias Atherosclerosis Basic cardiac electrophysiology Cardiac catheterization Cardiac remodeling Coagulation and thrombosis Diabetic cardiovascular disease Heart failure (systolic HF, HFrEF, diastolic HF, HFpEF) Hyperlipidemia Hypertension Ischemic heart disease Vascular biology Ventricular assist devices Molecular cardio-biology Myocardial regeneration Lipoprotein metabolism Radial artery access Percutaneous coronary intervention Transcatheter aortic and mitral valve replacement.
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