
Why Aldosterone Has Become a Key Target in CKD Care, With Marc Richards, MD
Key Takeaways
- ACE inhibitors, ARBs, and SGLT2 inhibitors remain foundational by modulating tubuloglomerular feedback and lowering physiologic stress on the kidney to slow CKD progression.
- Aldosterone is increasingly targeted to mitigate residual cardio-renal injury beyond RAAS blockade, using mineralocorticoid receptor antagonists and upstream aldosterone synthase inhibition.
Michael Richards, MD, discusses aldosterone's role in CKD pathophysiology and why targeting this pathway may reshape kidney disease treatment.
Although inhibition of the renin-angiotensin system with angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs), followed by sodium-glucose cotransporter 2 (SGLT2) inhibitors, has transformed
Among these, aldosterone has emerged as an increasingly important therapeutic target through the development of steroidal and nonsteroidal mineralocorticoid receptor antagonists, as well as newer aldosterone synthase inhibitors designed to reduce hormone production upstream.
In this Q&A with HCPLive, Marc Richards, MD, a nephrologist at Florida Kidney Physicians, discusses how advances in CKD pathophysiology have reshaped treatment over the past several decades, why aldosterone has become a key focus for clinicians, and what its physiologic role means for patients with kidney and cardiovascular disease.
Q&A: Why Aldosterone Has Become a Key Target in CKD Care, With Marc Richards, MD
HCPLive: Over the last couple of years and decades, our understanding of CKD pathophysiology has evolved considerably. Which biological pathways do you think have most changed the way clinicians approach treatment?
Richards: I think the big ones are really with ACE inhibitors, ARBs, and SGLT2 inhibitors; it's really all about tubuloglomerular feedback, reducing stress on the kidney.
And then also now we have a focus on targeting aldosterone as a way of trying to help limit stress on the kidney or limit stress on the heart, with older drugs like spironolactone and eplerenone, newer medicines like finerenone, and even looking into novel agents like aldosterone synthase inhibitors, which recently hit the market, to even prevent the aldosterone from being released in the first place.
HCPLive: Could you give a brief overview of aldosterone—what it does physiologically and why clinicians should pay attention to it?
Richards: Aldosterone is a hormone that's released by the adrenal gland, typically in response to either just being released on its own in cases of primary hyperaldosteronism, or in the setting of excess renin release, which can also increase that release because renin can stimulate that.
We know that aldosterone can lead to hypertension. It can lead to hypokalemia. It can lead to stress in patients with secondary release in patients with heart or liver dysfunction, and it probably has issues in the setting of—can possibly lead to—worsening renal dysfunction as well over time.
Editor’s Note: Richards reports no relevant disclosures.
References
National Institute of Diabetes and Digestive and Kidney Diseases. Kidney Disease Statistics for the United States. Updated 2025. Accessed July 17, 2026.
https://www.niddk.nih.gov/health-information/health-statistics/kidney-disease Fioretti F, Testani JM, Tio MC, Pitt B, et al. Aldosterone and aldosterone modulation in cardio-kidney diseases. J Am Coll Cardiol. 2025;86(5):354-373. doi:10.1016/j.jacc.2025.06.012.










































































