医学
盐皮质激素受体
心力衰竭
血压
肾脏疾病
原发性醛固酮增多症
盐皮质激素
内科学
醛固酮
内分泌学
血管紧张素II
螺内酯
心脏病学
药理学
作者
Dominic Parfianowicz,Swara Shah,Catherine Nguyen,Theresa N. Maitz,Adrija Hajra,Akshay Goel,Jayakumar Sreenivasan,Wilbert S. Aronow,Apurva Vyas,Rahul Gupta
标识
DOI:10.1016/j.cpcardiol.2022.101386
摘要
The renin-angiotensin-aldosterone system is a neurohormonal system responsible for maintaining homeostasis of fluid regulation, sodium balance, and blood pressure. The complexity of this pathway enables it to be a common target for blood pressure and volume-regulating medications. The mineralocorticoid receptor is one of these targets, and is found not only in the kidney, but also tissues making up the heart, blood vessels, and adipose. Mineralocorticoid receptor antagonists have been shown to slow progression of chronic kidney disease, treat refractory hypertension and primary aldosteronism, and improve morbidity and mortality in management of heart failure with reduced ejection fraction. The more well-studied medications were derived from steroid-based compounds, and thus come with a distinct side-effect profile. To avoid these adverse effects, developing a mineralocorticoid receptor antagonist (MRA) from a non-steroidal base compound has gained much interest. This review will focus on the novel non-steroidal MRA, Finerenone, to describe its unique mechanism of action while summarizing the available clinical trials supporting its use in patients with various etiologies of cardiorenal disease.
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