The renin-angiotensin system in progression, remission and regression of chronic nephropathies

Claudio Aros, Giuseppe Remuzzi

Research output: Contribution to journalArticle

Abstract

Chronic proteinuric nephropathies may progress to end-stage renal disease (ESRD) through a series of events relatively independent of the initial insult that causes parenchymal damage when the injury involves a critical number of nephrons. The key event is enhanced glomerular capillary pressure, which, among other effects, impairs glomerular permeability to proteins, which reach the lumen of the proximal tubule. In this pathological process angiotensin II has a central role. Reabsorption of filtered proteins contributes to the interstitial injury by activating intracellular events, including upregulation of vasoactive and inflammatory genes. Both interstitial inflammation and progression of disease can be limited by angiotensin-convetting enzyme (ACE) inhibitors that strengthen the glomerular permeability barrier to proteins, thus limiting proteinuria and filtered protein-dependent inflammatory signals. Clinical evidence suggests that remission is now achievable in some patients with chronic nephropathies. The current lag time between starting treatment and remission, however, is such that a substantial proportion of patients still progress to ESRD before their renal function begins to stabilize. A multimodal approach aimed at reducing or abolishing all the risk factors for progression may shorten the time to remission for the majority of patients with proteinuric nephropathies.

Original languageEnglish
JournalJournal of Hypertension
Volume20
Issue numberSUPPL. 3
DOIs
Publication statusPublished - Jun 2002

Keywords

  • Chronic nephropathies
  • Renal disease progression
  • Renin-angiotensin system blockade

ASJC Scopus subject areas

  • Endocrinology
  • Internal Medicine

Fingerprint Dive into the research topics of 'The renin-angiotensin system in progression, remission and regression of chronic nephropathies'. Together they form a unique fingerprint.

  • Cite this