Optimization of potassium management in patients with chronic kidney disease and type 2 diabetes on finerenone

医学 高钾血症 肾脏疾病 盐皮质激素受体 重症监护医学 内科学 2型糖尿病 中止 糖尿病 吡格列酮 不利影响 醛固酮 内分泌学
作者
Alberto Órtiz,Roberto Alcázar Arroyo,Pedro Pablo Casado Escribano,Beatriz Fernández‐Fernández,Francisco Martínez Debén,Juan Diego Mediavilla,Alfredo Michán‐Doña,María José Soler,José Luis Górriz
出处
期刊:Expert Review of Clinical Pharmacology [Taylor & Francis]
卷期号:16 (6): 519-531 被引量:3
标识
DOI:10.1080/17512433.2023.2213888
摘要

Patients with type 2 diabetes (T2DM) and chronic kidney disease (CKD) are at high risk of CKD progression and cardiovascular events. Despite treatment with renin-angiotensin system inhibitors and SGLT-2 inhibitors, the residual risk is substantial. There is preclinical and clinical evidence supporting a key role of mineralocorticoid receptor in cardiorenal injury in T2DM.Finerenone is a selective and nonsteroidal mineralocorticoid receptor antagonist that reduces -on preclinical studies- heart and kidney inflammation and fibrosis. Clinical trials have demonstrated that among patients with T2DM and CKD, finerenone reduces CKD progression and the risk of cardiovascular events. The incidence of adverse events is similar than for placebo. Permanent discontinuation of study drug due to hyperkalemia was low (1.7% of finerenone and 0.6% of placebo participants) as was the risk of hyperkalemia-related severe-adverse events (1.1%). We provide an overview of risk factors for hyperkalemia and management of serum potassium in people with CKD and T2DM on finerenone.As finerenone increases potassium levels in a predictable way, patients at risk of hyperkalemia can be identified early in clinical practice and monitored for an easy management. This will allow people with T2DM and CKD to safely benefit from improved cardiorenal outcomes.
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