医学
心力衰竭
盐皮质激素受体
心脏病学
疾病
肾脏疾病
射血分数
内科学
射血分数保留的心力衰竭
重症监护医学
封锁
临床试验
高钾血症
螺内酯
人口
醛固酮
受体
环境卫生
作者
Kasra Shokri,Abbas Mohammadi,Azin Karimian,Muhammad Adeel,Mohammad Ali Mozaffari,William H. Frishman,Wilbert S. Aronow
标识
DOI:10.1097/crd.0000000000000958
摘要
The mineralocorticoid receptor (MR) plays a pivotal role in cardiorenal disease progression, but steroidal MR antagonists (MRAs) are limited by hyperkalemia, hormonal side effects, and uncertain efficacy in heart failure with preserved ejection fraction (HFpEF). Finerenone, a first-in-class nonsteroidal MRA, offers selective MR blockade with balanced tissue distribution, mitigating off-target effects while demonstrating cardiorenal benefits. Phase 3 trials (FIDELIO-DKD, FIGARO-DKD, and FINEARTS-HF) show significant reductions in renal (18–21%) and cardiovascular (13–16%) composite endpoints, including HFpEF, where it reduced worsening heart failure events by 16%. Unlike steroidal MRAs, finerenone reduces off-target effects while maintaining efficacy in HFpEF, a population with limited therapeutic options. This review synthesizes finerenone’s pharmacological innovations, clinical evidence, and practical challenges, highlighting its potential as a transformative therapy in cardiorenal disease.
科研通智能强力驱动
Strongly Powered by AbleSci AI