DR.

GETÚLIO AMARAL

Originally published on Plenya Blog. Read at the source ↗

Clinical ManagementJanuary 2026 · 2 min

Why the nephrologist sees it first — the cardio-renal-metabolic axis

The biggest revolution in preventive medicine in recent years was understanding that heart, kidney, and metabolism are a single system. And that the kidney usually speaks first.

Why the nephrologist sees it first — the cardio-renal-metabolic axis

The biggest revolution in preventive medicine over the past five years was not a surgery, was not an isolated drug. It was a reorganization: understanding that heart, kidney, and metabolism are not three separate systems — they are a single system, with a single inflammatory root and a single therapeutic axis.

The technical name is the cardio-renal-metabolic axis, formalized by the American Heart Association in 2023 in a statement by Ndumele and colleagues. What it organizes, in practice, is the perception that chronic kidney disease rarely begins in the kidney. It begins in long-standing metabolic inflammation, in poorly controlled hypertension, in silent hyperinsulinemia, in subclinical endothelial dysfunction.

And the kidney, by a simple physiologic feature — extremely high-precision filtration over a delicate vascular bed — usually signals first. Microalbuminuria, slow decline of estimated glomerular filtration rate, loss of functional reserve. Signs that appear ten or fifteen years before the severe picture.

Diagram of the cardio-renal-metabolic axis — heart, kidney, and metabolism drawn as three overlapping circles forming a single syndrome. Around them, the four pharmacological pillars of the last decade that protect all three systems in parallel: SGLT2 inhibitors (DAPA-CKD), finerenone (FIDELIO-DKD), semaglutide (FLOW), and renin-angiotensin-aldosterone blockade.
Diagram of the cardio-renal-metabolic axis — heart, kidney, and metabolism drawn as three overlapping circles forming a single syndrome. Around them, the four pharmacological pillars of the last decade that protect all three systems in parallel: SGLT2 inhibitors (DAPA-CKD), finerenone (FIDELIO-DKD), semaglutide (FLOW), and renin-angiotensin-aldosterone blockade.

That is why the nephrologist, when trained to look at the silent window, sees it first. The test most frequently ordered — kidney function — is, paradoxically, one of the best early markers of systemic disease.

The pharmacological landmarks of the last decade confirm the axis in clinical practice. SGLT2 inhibitors came first: DAPA-CKD (Heerspink, NEJM 2020) showed reduction in chronic kidney disease progression and cardiovascular death with dapagliflozin even in non-diabetic patients. EMPA-KIDNEY (NEJM 2023) confirmed the effect in a broader cohort. Finerenone, in FIDELIO-DKD (Bakris, NEJM 2020), demonstrated a reduction in renal and cardiovascular events in type-2 diabetes with nephropathy. More recently, FLOW (Perkovic, NEJM 2024) brought semaglutide into the game: a 24% reduction in the composite renal-cardiovascular endpoint in patients with T2D and CKD.

Three different drug classes, three different targets — all protecting the three systems in parallel. It is not coincidence. It is the clinical confirmation that the axis is real.

Preventive nephrology is not a new specialty. It is a way of reading nephrology that is finally being accepted.

Excerpt from Chapter 9 of the book ANTES — The Silent Window Between Normal and Optimal.

Clinical review. Medical content authored by Dr. Getúlio Amaral Filho · CRM-PR 21,876 · RQE 16,038 (Nephrology). Originally published at plenyasaude.com.br/en/blog.

Educational notice

This content is educational and does not constitute medical prescription. Each case is unique — for individual evaluation and care, consult a physician.