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Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis
Objectives: Whether uric acid levels were associated with the progression of chronic kidney disease (CKD) remained controversial. This meta-analysis was aimed to assess the effect of lowering serum uric acid therapy on the progression of CKD to clarify the role of uric acid in the progression of CKD...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014338/ https://www.ncbi.nlm.nih.gov/pubmed/29619870 http://dx.doi.org/10.1080/0886022X.2018.1456463 |
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author | Liu, Xuemei Zhai, Tingting Ma, Ruixia Luo, Congjuan Wang, Huifang Liu, Liqiu |
author_facet | Liu, Xuemei Zhai, Tingting Ma, Ruixia Luo, Congjuan Wang, Huifang Liu, Liqiu |
author_sort | Liu, Xuemei |
collection | PubMed |
description | Objectives: Whether uric acid levels were associated with the progression of chronic kidney disease (CKD) remained controversial. This meta-analysis was aimed to assess the effect of lowering serum uric acid therapy on the progression of CKD to clarify the role of uric acid in the progression of CKD indirectly. Methods: Pubmed, Embase, the Cochrane library, CBM were searched for randomized controlled trials (RCTs) that assessed the efficiency of lowering serum uric acid therapy on the progression of CKD without language restriction. Summary estimates of weighted mean differences (WMDs) and relative risk (RR) were obtained by using random-effect or fixed-effect models. Sensitivity analyses were performed to identify the source of heterogeneity. Results: A total of 12 randomized controlled trials with 832 CKD participants were included in the analysis. Pooled estimate for eGFR was in favor of lowering serum uric acid therapy with a mean difference (MD) of 3.88 ml/min/1.73 m(2), 95% CI 1.26–6.49 ml/min/1.73 m(2), p = .004 and this was consistent with results for serum creatinine. The risk of worsening of kidney function or ESRD or death was significantly decreased in the treatment group compared to the control group (RR 0.39, 95% CI 0.28–0.52, p< .01). Conclusions: Uric acid-lowering therapy may be effective in retarding the progression of CKD. Further randomized controlled trials should be performed to confirm the effect of lowering serum uric acid therapy on the progression of CKD. |
format | Online Article Text |
id | pubmed-6014338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60143382018-06-28 Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis Liu, Xuemei Zhai, Tingting Ma, Ruixia Luo, Congjuan Wang, Huifang Liu, Liqiu Ren Fail Clinical Study Objectives: Whether uric acid levels were associated with the progression of chronic kidney disease (CKD) remained controversial. This meta-analysis was aimed to assess the effect of lowering serum uric acid therapy on the progression of CKD to clarify the role of uric acid in the progression of CKD indirectly. Methods: Pubmed, Embase, the Cochrane library, CBM were searched for randomized controlled trials (RCTs) that assessed the efficiency of lowering serum uric acid therapy on the progression of CKD without language restriction. Summary estimates of weighted mean differences (WMDs) and relative risk (RR) were obtained by using random-effect or fixed-effect models. Sensitivity analyses were performed to identify the source of heterogeneity. Results: A total of 12 randomized controlled trials with 832 CKD participants were included in the analysis. Pooled estimate for eGFR was in favor of lowering serum uric acid therapy with a mean difference (MD) of 3.88 ml/min/1.73 m(2), 95% CI 1.26–6.49 ml/min/1.73 m(2), p = .004 and this was consistent with results for serum creatinine. The risk of worsening of kidney function or ESRD or death was significantly decreased in the treatment group compared to the control group (RR 0.39, 95% CI 0.28–0.52, p< .01). Conclusions: Uric acid-lowering therapy may be effective in retarding the progression of CKD. Further randomized controlled trials should be performed to confirm the effect of lowering serum uric acid therapy on the progression of CKD. Taylor & Francis 2018-04-05 /pmc/articles/PMC6014338/ /pubmed/29619870 http://dx.doi.org/10.1080/0886022X.2018.1456463 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Liu, Xuemei Zhai, Tingting Ma, Ruixia Luo, Congjuan Wang, Huifang Liu, Liqiu Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis |
title | Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis |
title_full | Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis |
title_fullStr | Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis |
title_full_unstemmed | Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis |
title_short | Effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis |
title_sort | effects of uric acid-lowering therapy on the progression of chronic kidney disease: a systematic review and meta-analysis |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014338/ https://www.ncbi.nlm.nih.gov/pubmed/29619870 http://dx.doi.org/10.1080/0886022X.2018.1456463 |
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