醛固酮
医学
血压
安慰剂
利尿剂
醛固酮合酶
内科学
内分泌学
原发性高血压
临床终点
随机对照试验
泌尿科
药理学
胃肠病学
心脏病学
肾素-血管紧张素系统
病理
替代医学
作者
Mason W. Freeman,Yuan‐Di C. Halvorsen,William Marshall,Mackenzie L. Pater,Jon Isaacsohn,Catherine Pearce,Brian Murphy,Nicholas Alp,Ajay Kumar Srivastava,Deepak L. Bhatt,Morris J. Brown
标识
DOI:10.1056/nejmoa2213169
摘要
Aldosterone synthase controls the synthesis of aldosterone and has been a pharmacologic target for the treatment of hypertension for several decades. Selective inhibition of aldosterone synthase is essential but difficult to achieve because cortisol synthesis is catalyzed by another enzyme that shares 93% sequence similarity with aldosterone synthase. In preclinical and phase 1 studies, baxdrostat had 100:1 selectivity for enzyme inhibition, and baxdrostat at several dose levels reduced plasma aldosterone levels but not cortisol levels.
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