Modulating kidney transplant interstitial fibrosis and tubular atrophy: is the RAAS an important target?
Author(s) -
Hatem Amer,
Matthew D. Griffin
Publication year - 2014
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1038/ki.2013.400
Subject(s) - medicine , fibrosis , atrophy , kidney , pathology , kidney tubules , kidney glomerulus , kidney transplantation , urology , glomerulonephritis
In follow-up to a recently published randomized controlled clinical trial, Issa et al. provide evidence that systemic activity and physiological responsiveness of the renin aldosterone angiotensin system (RAAS) are well within normal limits in most kidney recipients during the first 5 years post-transplant. Implications of the results include the need to better understand intra-renal RAAS activity in transplanted kidneys and to identify patients in which the graft-protective effects of RAAS blockade are most relevant.
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