盐皮质激素受体拮抗剂治疗慢性肾病和2型糖尿病患者高钾血症的研究进展

IF 2.9 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Jessica B Kendrick, Angelina Magreni Dixon
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引用次数: 0

摘要

背景:2型糖尿病(T2D)经常与慢性肾脏疾病(CKD)共存,增加了心血管和肾脏并发症的风险。尽管针对肾素-血管紧张素-醛固酮系统(RAAS)的治疗可以减缓CKD的进展并减少心血管事件,但它们也会增加高钾血症的风险。芬纳酮是一种较新的非甾体类矿物皮质激素受体拮抗剂(MRA),具有相对较低的高钾血症风险,提供有效的心肾保护。方法:我们对截至2024年9月发表的随机对照试验(rct)进行了叙述性回顾,这些试验评估了螺内酯、依普利酮或芬尼酮在T2D、CKD或心力衰竭人群中的作用。研究报告了高钾血症发生率、严重程度和管理的明确数据。考虑到研究人群的异质性和高钾血症的定义,对研究结果进行了综合叙述。结果:来自螺内酯和依普利酮试验的证据强调了甾体MRAs在心力衰竭患者中的生存益处,但也显示了显著的高钾血症风险,特别是在晚期CKD患者中。在FIDELIO-DKD、FIGARO-DKD和随后的FIDELITY研究中,Finerenone显示出降低心血管和肾脏预后的强大功效。它主要与轻度至中度高钾血症相关,通过定期监测稳定。严重事件和因高钾血症而中断治疗的发生率很低。FIDELITY的风险预测模型进一步根据高钾血症风险对患者进行分层,揭示了芬烯酮在所有阶层中一致的相对高钾血症风险。结论:在T2D和CKD患者中,高钾血症仍然是一个关键的挑战,经常导致这些救命药物的利用不足。然而,细芬烯酮的安全性,结合勤奋的钾监测和积极的管理策略(例如,饮食指导,钾结合剂,使用利尿剂),可以实现持续的心肾益处。未来的研究应探索这些试验结果在现实世界中的适用性,并进一步完善基于风险的治疗算法,以优化这一高危人群的治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Review of Hyperkalemia Profile for Mineralocorticoid Receptor Antagonist in Patients with Chronic Kidney Disease and Type 2 Diabetes.

Background: Type 2 diabetes (T2D) frequently coexists with chronic kidney disease (CKD), magnifying the risk of both cardiovascular and renal complications. Although therapies targeting the renin-angiotensin-aldosterone system (RAAS) slow CKD progression and reduce cardiovascular events, they also raise the risk of hyperkalemia. Finerenone, a newer nonsteroidal mineralocorticoid receptor antagonist (MRA), offers potent cardiorenal protection with relatively low hyperkalemia risk.

Methods: We conducted a narrative review of randomized controlled trials (RCTs) published up to September 2024 which evaluated spironolactone, eplerenone, or finerenone in populations with T2D, CKD, or heart failure. Studies that reported explicit data on hyperkalemia incidence, severity, and management were included. The findings were synthesized narratively with the consideration of heterogeneity in study population and hyperkalemia definition.

Results: Evidence from spironolactone and eplerenone trials underscores the survival benefits of steroidal MRAs in heart failure patients but also demonstrates a notable hyperkalemia risk, especially in patients with advanced CKD. Finerenone, studied in FIDELIO-DKD, FIGARO-DKD, and subsequently pooled in FIDELITY, demonstrated robust efficacy in reducing cardiovascular and kidney outcomes. It was associated predominantly with mild-to-moderate hyperkalemia which stabilized with regular monitoring. The incidence of severe events and therapy discontinuations due to hyperkalemia were low. A risk-prediction model from FIDELITY further stratified patients by hyperkalemia risk, revealing consistent relative hyperkalemia risk of finerenone across all strata.

Conclusions: Hyperkalemia remains a pivotal challenge when prescribing MRAs in patients with T2D and CKD, often leading to underutilization of these lifesaving agents. However, finerenone's safety profile, combined with diligent potassium surveillance and proactive management strategies (e.g., dietary guidance, potassium binders, use of diuretics), enables sustained cardiorenal benefits. Future research should explore real-world applicability of these trial findings and further refine risk-based treatment algorithms to optimize outcomes in this high-risk population.

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来源期刊
Cardiorenal Medicine
Cardiorenal Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-UROLOGY & NEPHROLOGY
CiteScore
5.40
自引率
2.60%
发文量
25
审稿时长
>12 weeks
期刊介绍: The journal ''Cardiorenal Medicine'' explores the mechanisms by which obesity and other metabolic abnormalities promote the pathogenesis and progression of heart and kidney disease (cardiorenal metabolic syndrome). It provides an interdisciplinary platform for the advancement of research and clinical practice, focussing on translational issues.
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