Literature DB >> 28771453

Nonsteroidal mineralocorticoid antagonists in diabetic kidney disease.

Farheen K Dojki1, George Bakris.   

Abstract

PURPOSE OF REVIEW: Current data highlight the pathological aspects of excess aldosterone in promoting glomerular hypertrophy, glomerulosclerosis, and proteinuria in diabetic kidney disease (DKD). The role of nonsteroidal mineralocorticoid receptor antagonists (MRAs) in DKD is being evaluated in ongoing clinical trials. RECENT
FINDINGS: Recent studies demonstrate beneficial effects of adding MRAs to the treatment regimen of patients with type 2 diabetes with nephropathy. The MRAs spironolactone and eplerenone can protect against organ damage caused by elevated levels of serum aldosterone in patients with heart failure and DKD but are limited by their side effects, for example, hyperkalemia. Finerenone is more selective for the mineralocorticoid receptor than spironolactone and has greater affinity for the mineralocorticoid receptor than eplerenone. It reduces the concentration of aldosterone without causing significant elevation in serum potassium.
SUMMARY: MRAs have a clear role in reducing albuminuria when used with other renin-angiotensin system blockers in DKD; however, hyperkalemia limits their use. This article provides an overview of clinical studies with a novel MRA, finerenone, and several nonsteroidal MRAs being studied for treatment in DKD.

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Year:  2017        PMID: 28771453     DOI: 10.1097/MNH.0000000000000340

Source DB:  PubMed          Journal:  Curr Opin Nephrol Hypertens        ISSN: 1062-4821            Impact factor:   2.894


  9 in total

Review 1.  The expanding class of mineralocorticoid receptor modulators: New ligands for kidney, cardiac, vascular, systemic and behavioral selective actions.

Authors:  E Bădilă
Journal:  Acta Endocrinol (Buchar)       Date:  2020 Oct-Dec       Impact factor: 0.877

Review 2.  Clinical perspective-evolving evidence of mineralocorticoid receptor antagonists in patients with chronic kidney disease and type 2 diabetes.

Authors:  Peter Rossing
Journal:  Kidney Int Suppl (2011)       Date:  2022-03-18

3.  Spironolactone alleviates diabetic nephropathy through promoting autophagy in podocytes.

Authors:  Dan Dong; Ting-Ting Fan; Ying-Shi Ji; Jin-Yu Yu; Shan Wu; Li Zhang
Journal:  Int Urol Nephrol       Date:  2019-02-08       Impact factor: 2.370

Review 4.  Mineralocorticoid receptor: A hidden culprit for hemodialysis vascular access dysfunction.

Authors:  Bohan Chen; Pei Wang; Andrew Brem; Lance Dworkin; Zhangsuo Liu; Rujun Gong
Journal:  EBioMedicine       Date:  2018-12-05       Impact factor: 8.143

Review 5.  Mitigating risk of aldosterone in diabetic kidney disease.

Authors:  Marie Frimodt-Møller; Frederik Persson; Peter Rossing
Journal:  Curr Opin Nephrol Hypertens       Date:  2020-01       Impact factor: 3.416

6.  Topical Treatment of Human Skin and Cultured Keratinocytes with High-Dose Spironolactone Reduces XPB Expression and Induces Toxicity.

Authors:  M Alexandra Carpenter; Michael G Kemp
Journal:  JID Innov       Date:  2021-05-06

7.  Finerenone in patients with chronic kidney disease and type 2 diabetes with and without heart failure: a prespecified subgroup analysis of the FIDELIO-DKD trial.

Authors:  Gerasimos Filippatos; Bertram Pitt; Rajiv Agarwal; Dimitrios Farmakis; Luis M Ruilope; Peter Rossing; Johann Bauersachs; Robert J Mentz; Peter Kolkhof; Charlie Scott; Amer Joseph; George L Bakris; Stefan D Anker
Journal:  Eur J Heart Fail       Date:  2022-05-19       Impact factor: 17.349

Review 8.  Spironolactone and XPB: An Old Drug with a New Molecular Target.

Authors:  Ryan D Gabbard; Robert R Hoopes; Michael G Kemp
Journal:  Biomolecules       Date:  2020-05-13

9.  Steroidal and non-steroidal mineralocorticoid receptor antagonists in cardiorenal medicine.

Authors:  Rajiv Agarwal; Peter Kolkhof; George Bakris; Johann Bauersachs; Hermann Haller; Takashi Wada; Faiez Zannad
Journal:  Eur Heart J       Date:  2021-01-07       Impact factor: 29.983

  9 in total

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