Aldosterone synthase inhibitors in hypertension and chronic kidney disease: double the benefit?

Curr Opin Nephrol Hypertens. 2026 May 1;35(3):337-346. doi: 10.1097/MNH.0000000000001175. Epub 2026 Mar 12.

Abstract

Purpose of review: Aldosterone synthase inhibitors (ASIs) are novel drugs for cardiorenal protection. These compounds block aldosterone production and lower blood levels by targeting its biosynthesis pathway. ASIs induce a complete suppression of both genomic and nongenomic aldosterone effects, while reducing the risks of hyperkalaemia and aldosterone escape. In the present review, we will summarize the clinical potential of current ASIs in hypertension and chronic kidney disease (CKD).

Recent findings: Selective ASIs have been extensively evaluated in patients with both primary and resistant hypertension, and are promising therapeutic agents in CKD. Baxdrostat and lorundrostat effectively lowered blood pressure in patients with resistant or uncontrolled hypertension and showed favourable effects on renal outcomes. In CKD patients, vicadrostat determined a dose-dependent reduction of albuminuria and additive beneficial effects when used on top of empagliflozin.

Summary: In randomized controlled trials, patients assigned to second generation ASIs had beneficial effects on blood pressure and albuminuria, with enhanced safety profiles. Although long-term clinical outcomes are still under investigation, ASIs have the potential to narrow critical gaps in cardiorenal care.

Keywords: aldosterone synthase inhibitors; chronic kidney disease; hypertension.

Publication types

  • Review

MeSH terms

  • Aldosterone
  • Animals
  • Antihypertensive Agents* / adverse effects
  • Antihypertensive Agents* / therapeutic use
  • Blood Pressure* / drug effects
  • Cytochrome P-450 CYP11B2* / antagonists & inhibitors
  • Cytochrome P-450 CYP11B2* / metabolism
  • Enzyme Inhibitors* / adverse effects
  • Enzyme Inhibitors* / therapeutic use
  • Humans
  • Hypertension* / drug therapy
  • Hypertension* / enzymology
  • Hypertension* / physiopathology
  • Mineralocorticoid Receptor Antagonists / therapeutic use
  • Renal Insufficiency, Chronic* / diagnosis
  • Renal Insufficiency, Chronic* / drug therapy
  • Renal Insufficiency, Chronic* / enzymology
  • Renal Insufficiency, Chronic* / physiopathology
  • Treatment Outcome

Substances

  • Cytochrome P-450 CYP11B2
  • Antihypertensive Agents
  • Enzyme Inhibitors
  • Aldosterone
  • Mineralocorticoid Receptor Antagonists