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Treatment of chronic kidney disease
Author(s) -
Jeffrey M. Turner,
Carolyn Bauer,
Matthew K. Abramowitz,
Michal L. Melamed,
Thomas H. Hostetter
Publication year - 2011
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.2011.380
Subject(s) - medicine , kidney disease , hyperphosphatemia , glycemic , glycation , end stage renal disease , diabetes mellitus , disease , metabolic acidosis , advanced glycation end product , intensive care medicine , endocrinology
Treatment of chronic kidney disease (CKD) can slow its progression to end-stage renal disease (ESRD). However, the therapies remain limited. Blood pressure control using angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARBs) has the greatest weight of evidence. Glycemic control in diabetes seems likely to retard progression. Several metabolic disturbances of CKD may prove to be useful therapeutic targets but have been insufficiently tested. These include acidosis, hyperphosphatemia, and vitamin D deficiency. Drugs aimed at other potentially damaging systems and processes, including endothelin, fibrosis, oxidation, and advanced glycation end products, are at various stages of development. In addition to the paucity of proven effective therapies, the incomplete application of existing treatments, the education of patients about their disease, and the transition to ESRD care remain major practical barriers to better outcomes.

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