Key result
Dihydropyridine CCB use alongside RASi and SGLT2i is linked to ~33% more major adverse kidney events.
Why the study?
Optimal antihypertensive therapy with renoprotective effects is essential to slow diabetic kidney disease progression, but the impact of dihydropyridine calcium channel blockers in patients receiving guideline-directed renin-angiotensin and SGLT2 inhibitors needed evaluation.
Does dihydropyridine calcium channel blocker therapy increase the risk of major adverse kidney events in adults with type 2 diabetes treated with renin-angiotensin system inhibitors and sodium-glucose cotransporter-2 inhibitors?
Cohort (n=31,031)
Does dihydropyridine calcium channel blocker therapy increase the risk of major adverse kidney events in adults with type 2 diabetes treated with renin-angiotensin system inhibitors and sodium-glucose cotransporter-2 inhibitors?
In patients with type 2 diabetes treated with RAS inhibitors and SGLT2 inhibitors, the addition of dihydropyridine calcium channel blockers is associated with a higher risk of adverse kidney outcomes compared to other antihypertensive regimens.
Dihydropyridine CCB use associated with higher MAKE risk; leaves open harm versus residual confounding and should not yet change practice.
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Agur et al. (2026) conducted a cohort in Type 2 diabetes (n=31,031). Dihydropyridine calcium-channel-blockers vs. Dihydropyridine calcium-channel-blockers-free therapy was evaluated on Major adverse kidney event (MAKE; 40% eGFR decline or progression to kidney failure) (HR 1.33, 95% CI 1.03-1.73, p=0.03). Dihydropyridine calcium-channel-blocker use in type 2 diabetes on RAS and SGLT2 inhibitors was associated with higher risk of major adverse kidney events (HR 1.33; 95% CI 1.03-1.73; P=0.03).
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