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Published on: October 26, 2020
Renal protective effects of the renin-angiotensin-aldosterone system blockade: from evidence-based approach to
Leszek Tylicki1, Wojciech Larczynski, Bolesław Rutkowski
1Department of Nephrology, Transplantology and Internal Medicine, Medical University of Gdańsk, Poland. leszek.tylicki@amg.gda.pl
Insights
Renin-angiotensin-aldosterone system (RAAS) blockade, using ACE inhibitors or ARBs, is key for slowing chronic kidney disease progression. Early initiation and maximal doses are crucial for optimal renoprotection in proteinuric nephropathies.
Area of Science:
- Nephrology
- Pharmacology
- Cardiovascular Medicine
Background:
- The renin-angiotensin-aldosterone system (RAAS) plays a critical role in regulating blood pressure and fluid balance.
- Dysregulation of the RAAS is implicated in the progression of various chronic kidney diseases (CKDs).
- RAAS blockade represents a cornerstone therapy for managing proteinuric nephropathies.
Purpose of the Study:
- To review the evidence-based approach for utilizing RAAS-inhibiting agents in kidney diseases.
- To outline treatment strategies for RAAS blockade in diverse clinical scenarios of nephropathy.
- To discuss future perspectives on RAAS blockade for renal protection.
Main Methods:
- Systematic review of existing literature on RAAS blockade in nephropathies.
- Analysis of clinical trial data regarding the efficacy of ACE inhibitors (CEIs) and ARBs.
- Evidence-based guideline formulation for RAAS inhibitor use in proteinuric kidney diseases.
Main Results:
- RAAS blockade with CEIs or ARBs is recommended for all patients with chronic proteinuric nephropathy, regardless of diabetic status or baseline renal function.
- Early initiation of therapy before overt proteinuria or reduced kidney function enhances renoprotection.
- High-dose CEIs and ARBs are necessary to maximize proteinuria reduction and achieve blood pressure targets (<130/80 mmHg, or <125/75 mmHg for those with proteinuria >1 g/24h).
Conclusions:
- RAAS blockade is the most effective strategy for delaying the progression of chronic nephropathies.
- Combination therapy with CEIs and ARBs is indicated for patients with non-diabetic proteinuric nephropathies unresponsive to monotherapy.
- Optimal management involves early, high-dose RAAS inhibition tailored to individual patient characteristics and proteinuria levels.
Abstract:
The renin-angiotensin-aldosterone system (RAAS) blockade is currently the best-documented treatment strategy to delay the progression of chronic nephropathies. Angiotensin-converting enzyme inhibitors (CEIs) or angiotensin II type 1 receptor antagonists (ARBs) should be used in every normotensive and hypertensive patient with chronic proteinuric nephropathy of both diabetic and non-diabetic origin. The therapy should be initiated as early as possible, bearing in mind that the renoprotection is more effective if used before overt proteinuria or a reduction in kidney function is present. The therapy should be offered to all patients, regardless of renal function, as well as to subjects with severely impaired glomerular filtration. CEIs and ARBs should be administered in therapeutic doses as high as possible to achieve maximal possible proteinuria reduction and systemic blood pressure target <130/80 mm Hg, and 125/75 mm Hg in those subjects with renal insufficiency who present with proteinuria above 1 g/24 h. The combined therapy with the concomitant use of CEIs and ARBs should be offered to all patients with proteinuric non-diabetic chronic nephropathies who do not achieve full and persistent remission of proteinuria with CEI or ARB alone. The article reviews an evidence-based approach on the use of RAAS-inhibiting agents in kidney diseases, considers treatment strategies in different clinical situations and discusses some perspectives related to the implementation of the RAAS blockade in renal protection.
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