The mineralocorticoid receptor in chronic kidney disease

被引:16
|
作者
Barrera-Chimal, Jonatan [1 ,2 ]
Jaisser, Frederic [3 ,4 ]
Anders, Hans-Joachim [5 ]
机构
[1] Univ Nacl Autifinoma Mexico, Inst Invest Biomed, Ciudad Univ, Mexico City, DF, Mexico
[2] Inst Nacl Cardiol Ignacio Chavez, Unidad Invest UNAM INC, Lab Fisiol Cardiovasc & Trasplante Renal, Mexico City, DF, Mexico
[3] Univ Paris, Sorbonne Univ, Ctr Rech Cordeliers, INSERM,UMRS 1138, 15 Rue Ecole Med, F-75270 Paris 06, France
[4] Univ Lorraine, INSERM Ctr Invest Clin Plurithemat 1433, CHRU Nancy,UMR 1116, French Clin Res Infrastruct Network FCRIN INI CRC, Nancy, France
[5] LMU Klinikum, Med Klin & Poliklin 4, Ziemssenstr 1, D-80336 Munich, Germany
关键词
aldosterone; cardiorenal; fibrosis; kidney disease; RENAL INTERSTITIAL FIBROSIS; DIABETIC-NEPHROPATHY; SGLT2; INHIBITORS; CONCISE GUIDE; AMELIORATES PROTEINURIA; HYPERTENSIVE-RATS; OXIDATIVE STRESS; PODOCYTE INJURY; HEART-FAILURE; SPIRONOLACTONE;
D O I
10.1111/bph.15734
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:3152 / 3164
页数:13
相关论文
共 50 条
  • [1] Mineralocorticoid Receptor Blockade in Chronic Kidney Disease
    Matthew J. Volk
    Andrew S. Bomback
    Philip J. Klemmer
    [J]. Current Hypertension Reports, 2011, 13 : 282 - 288
  • [2] Mineralocorticoid Receptor Antagonism in Chronic Kidney Disease
    Georgianos, Panagiotis I.
    Agarwal, Rajiv
    [J]. KIDNEY INTERNATIONAL REPORTS, 2021, 6 (09): : 2281 - 2291
  • [3] Mineralocorticoid Receptor Blockers and Chronic Kidney Disease
    Jain, Gaurav
    Campbell, Ruth C.
    Warnock, David G.
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 4 (10): : 1685 - 1691
  • [4] MINERALOCORTICOID RECEPTOR ANTAGONISM IN CHRONIC KIDNEY DISEASE
    Gillis, Keith
    Lees, Jennifer
    Jardine, Alan
    Traynor, Jamie
    Mark, Patrick
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2017, 32 : 468 - 469
  • [5] Mineralocorticoid Receptor Blockade in Chronic Kidney Disease
    Bomback, Andrew S.
    Klemmer, Philip J.
    [J]. BLOOD PURIFICATION, 2012, 33 (1-3) : 119 - 124
  • [6] Mineralocorticoid Receptor Blockade in Chronic Kidney Disease
    Volk, Matthew J.
    Bomback, Andrew S.
    Klemmer, Philip J.
    [J]. CURRENT HYPERTENSION REPORTS, 2011, 13 (04) : 282 - 288
  • [7] Mineralocorticoid receptor antagonists in patients with chronic kidney disease
    Cosimato, Cosimo
    Agoritsas, Thomas
    Mavrakanas, Thomas A.
    [J]. PHARMACOLOGY & THERAPEUTICS, 2021, 219
  • [8] Mineralocorticoid receptor antagonist for chronic kidney disease, risk or benefit?
    Huang, Bi
    Mcdowell, Garry
    Rao, Anirudh
    Lip, Gregory Y. H.
    [J]. JOURNAL OF HYPERTENSION, 2024, 42 (03) : 396 - 398
  • [9] Mineralocorticoid Receptor Antagonism in Heart Failure and Chronic Kidney Disease
    Ferro, Charles J.
    Townend, Jonathan N.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2024, 83 (24) : 2437 - 2439
  • [10] Mineralocorticoid Receptor Antagonists-Use in Chronic Kidney Disease
    Baran, Wiktoria
    Krzeminska, Julia
    Szlagor, Magdalena
    Wronka, Magdalena
    Mlynarska, Ewelina
    Franczyk, Beata
    Rysz, Jacek
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (18)