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Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection

PURPOSE OF REVIEW: In chronic kidney disease (CKD), plasma uric acid levels are increased because of the decrease in glomerular filtration rate. However, in addition to CKD, hyperuricemia is frequently associated with a number of other conditions such as hypertension, type 2 diabetes, obesity, and h...

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Autores principales: Kielstein, Jan T., Pontremoli, Roberto, Burnier, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599161/
https://www.ncbi.nlm.nih.gov/pubmed/33128170
http://dx.doi.org/10.1007/s11906-020-01116-3
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author Kielstein, Jan T.
Pontremoli, Roberto
Burnier, Michel
author_facet Kielstein, Jan T.
Pontremoli, Roberto
Burnier, Michel
author_sort Kielstein, Jan T.
collection PubMed
description PURPOSE OF REVIEW: In chronic kidney disease (CKD), plasma uric acid levels are increased because of the decrease in glomerular filtration rate. However, in addition to CKD, hyperuricemia is frequently associated with a number of other conditions such as hypertension, type 2 diabetes, obesity, and heart failure, overweight, and cardiovascular disease. RECENT FINDINGS: It is now becoming increasingly clear that, in many clinical conditions, elevated levels of uric acid have a much greater role beyond just causing gout. The present review will summarize current knowledge on the relation between hyperuricemia, CKD, and existing comorbidities, as well as the mechanisms of uric acid–related renal damage. In addition, the role and evidence for urate-lowering therapy in prevention and cardiovascular protection in CKD patients is discussed with a focus on allopurinol and febuxostat. To date, several clinical studies have provided evidence that urate-lowering therapy may help to prevent and delay the decline of renal function in patients with CKD. SUMMARY: Use of a xanthine oxidase inhibitor should be considered in patients who are at high renal risk and/or with declining renal function in the presence of hyperuricemia with and without deposition, although additional studies are warranted to define treatment targets. Notwithstanding, the possibility to delay deterioration of renal function in patients with CKD merits consideration.
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spelling pubmed-75991612020-11-10 Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection Kielstein, Jan T. Pontremoli, Roberto Burnier, Michel Curr Hypertens Rep Hypertension and the Kidney (RM Carey, Section Editor) PURPOSE OF REVIEW: In chronic kidney disease (CKD), plasma uric acid levels are increased because of the decrease in glomerular filtration rate. However, in addition to CKD, hyperuricemia is frequently associated with a number of other conditions such as hypertension, type 2 diabetes, obesity, and heart failure, overweight, and cardiovascular disease. RECENT FINDINGS: It is now becoming increasingly clear that, in many clinical conditions, elevated levels of uric acid have a much greater role beyond just causing gout. The present review will summarize current knowledge on the relation between hyperuricemia, CKD, and existing comorbidities, as well as the mechanisms of uric acid–related renal damage. In addition, the role and evidence for urate-lowering therapy in prevention and cardiovascular protection in CKD patients is discussed with a focus on allopurinol and febuxostat. To date, several clinical studies have provided evidence that urate-lowering therapy may help to prevent and delay the decline of renal function in patients with CKD. SUMMARY: Use of a xanthine oxidase inhibitor should be considered in patients who are at high renal risk and/or with declining renal function in the presence of hyperuricemia with and without deposition, although additional studies are warranted to define treatment targets. Notwithstanding, the possibility to delay deterioration of renal function in patients with CKD merits consideration. Springer US 2020-10-31 2020 /pmc/articles/PMC7599161/ /pubmed/33128170 http://dx.doi.org/10.1007/s11906-020-01116-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Hypertension and the Kidney (RM Carey, Section Editor)
Kielstein, Jan T.
Pontremoli, Roberto
Burnier, Michel
Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection
title Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection
title_full Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection
title_fullStr Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection
title_full_unstemmed Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection
title_short Management of Hyperuricemia in Patients with Chronic Kidney Disease: a Focus on Renal Protection
title_sort management of hyperuricemia in patients with chronic kidney disease: a focus on renal protection
topic Hypertension and the Kidney (RM Carey, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599161/
https://www.ncbi.nlm.nih.gov/pubmed/33128170
http://dx.doi.org/10.1007/s11906-020-01116-3
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