The role of calcium antagonists in chronic kidney disease

Casey N Gashti1, George L Bakris

  • 1Rush University Hypertension/Clinical Research Centre, Department of Preventive Medicine, Rush Presbyterian/St Luke's Medical Centre, Chicago, Illinois 60612, USA.

Insights

Calcium antagonists are safe for managing high blood pressure in chronic kidney disease (CKD). However, non-dihydropyridine types may better preserve kidney function than dihydropyridines when used with renin-angiotensin system blockers.

Area of Science:

  • Nephrology
  • Cardiology
  • Pharmacology

Background:

  • Chronic kidney disease (CKD) management requires strict blood pressure control.
  • Antihypertensive therapies aim to reduce cardiovascular risk and slow CKD progression.

Purpose of the Study:

  • To review current goals for antihypertensive treatment in CKD.
  • To evaluate the role of calcium antagonists in slowing kidney disease progression.

Main Methods:

  • Review of recently published guidelines and clinical studies.
  • Analysis of evidence for different classes of antihypertensive agents, including calcium antagonists.

Main Results:

  • Guidelines recommend blood pressure below 130/80 mmHg for CKD patients.
  • Dihydropyridine calcium antagonists aid blood pressure control and reduce stroke risk but offer divergent evidence for slowing CKD progression.
  • Non-dihydropyridine calcium antagonists show potential in decreasing proteinuria and preserving kidney function over 5-6 years, similar to ACE inhibitors.
  • Calcium antagonists are safe and necessary for achieving blood pressure goals in CKD.

Conclusions:

  • Both dihydropyridine and non-dihydropyridine calcium antagonists are safe and essential for achieving blood pressure targets in CKD.
  • Dihydropyridines may not significantly slow kidney disease progression in patients with nephropathy and macroalbuminuria compared to renin-angiotensin system blockers.
  • Non-dihydropyridines may offer renal protective benefits comparable to renin-angiotensin system blockers.
Abstract

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