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Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis

BACKGROUND: To assess the relationship between adefovir dipivoxil and renal function after anti-hepatitis B virus therapy and elucidate the risk factors involved. METHODS: Based on the requirements of the Cochrane systematic review methodology, 21 observational articles on adefovir dipivoxil-associa...

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Autores principales: Luo, Qing, Deng, Yong, Cheng, Feifei, Kang, Juan, Zhong, Shan, Zhang, Dazhi, Zeng, Weiqiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268037/
https://www.ncbi.nlm.nih.gov/pubmed/27977591
http://dx.doi.org/10.1097/MD.0000000000005578
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author Luo, Qing
Deng, Yong
Cheng, Feifei
Kang, Juan
Zhong, Shan
Zhang, Dazhi
Zeng, Weiqiong
author_facet Luo, Qing
Deng, Yong
Cheng, Feifei
Kang, Juan
Zhong, Shan
Zhang, Dazhi
Zeng, Weiqiong
author_sort Luo, Qing
collection PubMed
description BACKGROUND: To assess the relationship between adefovir dipivoxil and renal function after anti-hepatitis B virus therapy and elucidate the risk factors involved. METHODS: Based on the requirements of the Cochrane systematic review methodology, 21 observational articles on adefovir dipivoxil-associated renal dysfunction were obtained by searching various databases, between January 1, 1995 and July 1, 2016. The Newcastle Ottawa Scale was used to evaluate risk bias. Parameters for 4276 chronic hepatitis B patients were analyzed by Review Manager and R software, and glomerular filtration rate, creatinine clearance, and serum creatinine values were extracted to evaluate renal function. RESULTS: Renal dysfunction was more likely to occur in patients receiving the adefovir dipivoxil therapy (odds ratio [OR] 1.98, 95% confidence interval [CI] 1.40–2.80) than the none-adefovir dipivoxil group. Subgroup analysis showed that renal function predictive value is higher for glomerular filtration rate (OR 2.42, 95% CI 1.34–3.14), compared with serum creatinine levels (OR 1.51, 95% CI 0.75–3.04). The rate of adefovir dipivoxil-associated renal dysfunction was 12% (95% CI 0.08–0.16). Older patients and patients with renal insufficiency, hypertension, and diabetes mellitus were more prone to developing adefovir dipivoxil-associated renal dysfunction; however, integrated raw data were insufficient for further detailed analysis. CONCLUSION: Long-term adefovir dipivoxil therapy is connected to renal dysfunction in chronic hepatitis B, necessitating the monitoring of kidney function.
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spelling pubmed-52680372017-02-07 Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis Luo, Qing Deng, Yong Cheng, Feifei Kang, Juan Zhong, Shan Zhang, Dazhi Zeng, Weiqiong Medicine (Baltimore) 4200 BACKGROUND: To assess the relationship between adefovir dipivoxil and renal function after anti-hepatitis B virus therapy and elucidate the risk factors involved. METHODS: Based on the requirements of the Cochrane systematic review methodology, 21 observational articles on adefovir dipivoxil-associated renal dysfunction were obtained by searching various databases, between January 1, 1995 and July 1, 2016. The Newcastle Ottawa Scale was used to evaluate risk bias. Parameters for 4276 chronic hepatitis B patients were analyzed by Review Manager and R software, and glomerular filtration rate, creatinine clearance, and serum creatinine values were extracted to evaluate renal function. RESULTS: Renal dysfunction was more likely to occur in patients receiving the adefovir dipivoxil therapy (odds ratio [OR] 1.98, 95% confidence interval [CI] 1.40–2.80) than the none-adefovir dipivoxil group. Subgroup analysis showed that renal function predictive value is higher for glomerular filtration rate (OR 2.42, 95% CI 1.34–3.14), compared with serum creatinine levels (OR 1.51, 95% CI 0.75–3.04). The rate of adefovir dipivoxil-associated renal dysfunction was 12% (95% CI 0.08–0.16). Older patients and patients with renal insufficiency, hypertension, and diabetes mellitus were more prone to developing adefovir dipivoxil-associated renal dysfunction; however, integrated raw data were insufficient for further detailed analysis. CONCLUSION: Long-term adefovir dipivoxil therapy is connected to renal dysfunction in chronic hepatitis B, necessitating the monitoring of kidney function. Wolters Kluwer Health 2016-12-16 /pmc/articles/PMC5268037/ /pubmed/27977591 http://dx.doi.org/10.1097/MD.0000000000005578 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 4200
Luo, Qing
Deng, Yong
Cheng, Feifei
Kang, Juan
Zhong, Shan
Zhang, Dazhi
Zeng, Weiqiong
Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis
title Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis
title_full Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis
title_fullStr Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis
title_full_unstemmed Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis
title_short Relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis B: A meta-analysis
title_sort relationship between nephrotoxicity and long-term adefovir dipivoxil therapy for chronic hepatitis b: a meta-analysis
topic 4200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268037/
https://www.ncbi.nlm.nih.gov/pubmed/27977591
http://dx.doi.org/10.1097/MD.0000000000005578
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