Efficacy and Safety of Finerenone in Patients With Primary Aldosteronism: A Multicenter Prospective Study

医学 前瞻性队列研究 内科学 急诊医学 多中心研究 重症监护医学 儿科 梅德林 不利影响 临床试验 初级保健 疾病 流行病学 初级卫生保健
作者
P. Li,Fan Yang,Yuxing Lou,Z. Zhang,Yunfeng Du,Jie Zhang,Yan Ren,Anli Tong,Zuoling Xie,Bimin Shi,Jianping Liu,Libin Liu,Dalong Zhu
出处
期刊:Hypertension [Lippincott Williams & Wilkins]
卷期号:83 (5): e26048-e26048 被引量:2
标识
DOI:10.1161/hypertensionaha.125.26048
摘要

BACKGROUND: Finerenone is a novel nonsteroidal mineralocorticoid receptor antagonist. However, robust evidence about its efficacy and safety in primary aldosteronism is scarce. METHODS: In this prospective, multicenter, single-arm, and exploratory trial, we enrolled adults (aged ≤75 years) with primary aldosteronism, an office blood pressure (BP) ranging from 140 to 180/90 to 120 mm Hg, and an estimated glomerular filtration rate ≥60 mL/min per 1.73 m². Eligible patients received finerenone (20–40 mg/d) treatment for 12 weeks. The primary outcome was the change in daytime systolic BP at 12 weeks. RESULTS: Fifty-seven patients were ultimately treated. Per-protocol analysis revealed that finerenone treatment significantly reduced mean daytime systolic BP (−6.69±1.60 mm Hg; P <0.001) and diastolic BP (−4.55±1.06 mm Hg; P <0.001) according to ambulatory monitoring. Mean office BP decreased even more substantially (systolic BP, −15.58±1.69 mm Hg; diastolic BP, −8.61±1.02 mm Hg; both P <0.001). The mean increase in serum potassium concentration was 0.39±0.05 mmol/L, and 94.5% of patients exhibited a normal concentration after 12 weeks of treatment (versus baseline 61.8%; P <0.001). Plasma renin activity increased, and 32.7% of patients exhibited a plasma renin activity concentration ≥1 ng/mL per h. According to the Primary Aldosteronism Medical Treatment Outcome criteria, 29.1% and 20.0% of patients achieved complete biochemical and clinical responses, respectively. Treatment was well tolerated. CONCLUSIONS: This study demonstrated the efficacy and safety of finerenone in the treatment of primary aldosteronism, supporting its use as a potential alternative therapy for the condition. Nevertheless, further prospective and head-to-head randomized controlled trials are essential to establish finerenone as a viable substitute for spironolactone. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT06381323.
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