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慢性肾脏病中的盐皮质激素受体。

The mineralocorticoid receptor in chronic kidney disease.

机构信息

Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico City, Mexico.

Laboratorio de Fisiología Cardiovascular y Trasplante Renal, Unidad de Investigación UNAM-INC, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.

出版信息

Br J Pharmacol. 2022 Jul;179(13):3152-3164. doi: 10.1111/bph.15734. Epub 2021 Dec 28.

Abstract

Chronic kidney disease (CKD) is a major public health concern, affecting approximately 10% of the population worldwide. CKD of glomerular or tubular origin leads to the activation of stress mechanisms, including the renin-angiotensin-aldosterone system and mineralocorticoid receptor (MR) activation. Over the last two decades, blockade of the MR has arisen as a potential therapeutic approach against various forms of kidney disease. In this review, we summarize the experimental studies that have shown a protective effect of MR antagonists (MRAs) in nondiabetic and diabetic CKD animal models. Moreover, we review the main clinical trials that have shown the clinical application of MRAs to reduce albuminuria and, importantly, to slow CKD progression. Recent evidence from the FIDELIO trial showed that the MRA finerenone can reduce hard kidney outcomes when added to the standard of care in CKD associated with type 2 diabetes. Finally, we discuss the effects of MRAs relative to those of SGLT2 inhibitors, as well as the potential benefit of combination therapy to maximize organ protection. LINKED ARTICLES: This article is part of a themed issue on Emerging Fields for Therapeutic Targeting of the Aldosterone-Mineralocorticoid Receptor Signaling Pathway. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.13/issuetoc.

摘要

慢性肾脏病(CKD)是一个主要的公共卫生关注点,影响着全球约 10%的人口。肾小球或肾小管来源的 CKD 会导致应激机制的激活,包括肾素-血管紧张素-醛固酮系统和盐皮质激素受体(MR)的激活。在过去的二十年中,MR 的阻断已成为针对各种形式肾脏疾病的潜在治疗方法。在这篇综述中,我们总结了表明 MR 拮抗剂(MRAs)在非糖尿病和糖尿病 CKD 动物模型中具有保护作用的实验研究。此外,我们还回顾了主要的临床试验,这些试验表明了 MRAs 在减少蛋白尿方面的临床应用,重要的是,减缓 CKD 的进展。最近来自 FIDELIO 试验的证据表明,MRA 非奈利酮可在与 2 型糖尿病相关的 CKD 患者的标准治疗基础上,减少硬终点事件。最后,我们讨论了 MRAs 相对于 SGLT2 抑制剂的作用,以及联合治疗以最大化器官保护的潜在益处。 相关文章:本文是关于醛固酮-盐皮质激素受体信号通路治疗靶点新兴领域的专题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.13/issuetoc.

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