# New Therapies for the Management of Chronic Kidney Disease

**Authors:** Andrew M Treihaft, Manish A Parikh, Kaedrea A Jackson, William H Frishman, Stephen J Peterson

PMC · DOI: 10.7759/cureus.81824 · 2025-04-07

## TL;DR

This paper explores new therapies for managing chronic kidney disease, particularly in patients with type 2 diabetes, focusing on potential advancements in pharmacological treatments.

## Contribution

The paper introduces aldosterone synthase inhibitors as a potential new pillar in CKD management.

## Key findings

- Aldosterone synthase inhibitors like vicadrostat show promise in reducing albuminuria and offering renal protection.
- Incomplete aldosterone block remains a challenge in current CKD treatments.
- Early-phase trials indicate potential benefits of ASIs in slowing kidney damage progression.

## Abstract

A major public health concern gripping the nation is chronic kidney disease (CKD), and for individuals concomitantly diagnosed with type 2 diabetes mellitus (T2DM), the coexistence significantly increases the cardiovascular morbidity and mortality by two to three times higher than patients diagnosed without CKD. CKD management encompasses both non-pharmacological approaches, such as dietary sodium restriction and lifestyle modification for blood pressure control, and pharmacological approaches. Current pharmacological management focuses on four key pillars: renin-angiotensin system inhibitors (RASi), sodium-glucose cotransporter-2 inhibitors (SGLT2i), glucagon-like peptide-1 receptor agonists (GLP-1RA), and mineralocorticoid receptor antagonists (MRAs), all of which have shown renoprotective and cardiovascular benefits. An incomplete block of aldosterone activity remains a challenge and is one of the factors contributing to the progression of kidney damage. Aldosterone synthase inhibitors (ASIs), such as vicadrostat, may represent a new horizon in selectively inhibiting aldosterone synthesis while preserving cortisol production. Early-phase trials have shown reductions in albuminuria and a potential for renal protection. The question is, could ASIs emerge as a fifth pillar in CKD management and help curb the progression?

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, CYP11B2 (cytochrome P450 family 11 subfamily B member 2) [NCBI Gene 1585] {aka ALDOS, CPN2, CYP11B, CYP11BL, CYPXIB2, P-450C18}
- **Diseases:** CKD (MESH:D051436), kidney damage (MESH:D007674), T2DM (MESH:D003924), albuminuria (MESH:D000419)
- **Chemicals:** sodium (MESH:D012964), SGLT2i (-), cortisol (MESH:D006854), aldosterone (MESH:D000450)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12057290/full.md

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Source: https://tomesphere.com/paper/PMC12057290