Université de Lorraine, INSERM, Centre d'Investigations Cliniques 1433, CHRU de Nancy, Inserm 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Nancy, France.
Department of Cardiology, Tokyo Medical University, Tokyo, Japan.
Nephrol Dial Transplant. 2024 Jun 28;39(7):1063-1072. doi: 10.1093/ndt/gfae004.
Kidney disease frequently coexists with cardiovascular (CV) diseases, and this dual presence significantly amplifies the risk of adverse clinical outcomes. Shared pathophysiological mechanisms and common CV risk factors contribute to the increased expression of mineralocorticoid receptors, which in turn can drive the progression of chronic CV-kidney disorders. The steroidal mineralocorticoid receptor antagonists (MRAs) spironolactone and eplerenone have demonstrated efficacy in improving patient outcomes in cases of heart failure with reduced ejection fraction or after a myocardial infarction, but have limited value in patients with chronic kidney disease. The non-steroidal MRA finerenone has now established itself as a foundational guideline-recommended therapy in patients with diabetic kidney disease. To date, these pharmacological agents have been developed in distinct patient populations. The consequences of their distinct pharmacological profiles necessitate further consideration. They have not undergone testing across the entire spectrum of cardiorenal scenarios, and the evidence base is currently being complemented with ongoing trials. In this review, we aim to synthesize the existing body of evidence and chart the future trajectory for the use of spironolactone, eplerenone and finerenone in improving clinical outcomes across the diverse spectrum of cardiorenal diseases. By consolidating the current state of knowledge, we seek to provide valuable insights for informed decision making in the management of patients with these complex and interconnected conditions.
肾脏疾病常与心血管(CV)疾病共存,这种双重存在显著增加了不良临床结局的风险。共同的病理生理机制和常见的 CV 危险因素导致了醛固酮受体的过度表达,进而推动了慢性 CV-肾脏疾病的进展。甾体类醛固酮受体拮抗剂(MRA)螺内酯和依普利酮已被证明在改善射血分数降低的心力衰竭或心肌梗死后患者的预后方面有效,但在慢性肾脏病患者中的价值有限。非甾体类 MRA 非奈利酮现已成为糖尿病肾病患者的基础指南推荐治疗药物。迄今为止,这些药物已在不同的患者群体中开发。其不同的药理学特征的后果需要进一步考虑。它们尚未在整个心脏肾脏疾病谱中进行测试,目前正在进行的试验正在补充证据基础。在这篇综述中,我们旨在综合现有的证据,并为螺内酯、依普利酮和非奈利酮在改善不同心脏肾脏疾病谱的临床结局方面的应用描绘未来的轨迹。通过整合当前的知识状态,我们旨在为这些复杂且相互关联的疾病的患者管理提供有价值的决策依据。