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Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis

Background: Gout is a common disease and is usually treated with uric acid-lowering drugs (the most commonly used of which are febuxostat and allopurinol). However, the cardiovascular safety of febuxostat and allopurinol is still controversial. The purpose of our study is to evaluate the cardiovascu...

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Autores principales: Guan, Xudong, Zhang, Shengzhao, Liu, Jiayan, Wu, Fengbo, Zhou, Lingyan, Liu, Ying, Su, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563376/
https://www.ncbi.nlm.nih.gov/pubmed/36249825
http://dx.doi.org/10.3389/fphar.2022.998441
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author Guan, Xudong
Zhang, Shengzhao
Liu, Jiayan
Wu, Fengbo
Zhou, Lingyan
Liu, Ying
Su, Na
author_facet Guan, Xudong
Zhang, Shengzhao
Liu, Jiayan
Wu, Fengbo
Zhou, Lingyan
Liu, Ying
Su, Na
author_sort Guan, Xudong
collection PubMed
description Background: Gout is a common disease and is usually treated with uric acid-lowering drugs (the most commonly used of which are febuxostat and allopurinol). However, the cardiovascular safety of febuxostat and allopurinol is still controversial. The purpose of our study is to evaluate the cardiovascular safety of the two drugs in patients with gout using one-stage and two-stage meta-analysis. Methods: PubMed, Embase, CBM, CNKI, WanFang, Central, and VIP were searched from inception to 30 January 2022. Randomized controlled trials which evaluated the cardiovascular safety of febuxostat or allopurinol for treating patients with gout were included. Based on the Kaplan–Meier curves of the two studies, individual patient data (IPD) were extracted and reconstructed. We used time-varying risk ratios (RRs) to summarize time-to-event outcomes, and the RRs of MACE incidence, cardiovascular mortality, and all-cause mortality were calculated by a multi-level flexible hazard regression model in 1-stage meta-analyses. p values were calculated using a log-rank test. At the same time, using the reconstructed IPD, we performed 2-stage meta-analyses to inform the quantitative estimates of time-specific relative risks at the six time points (1 , 2, 3, 4, 5, and 6 years) based on a random-effects model. Results: Two RCTs with 12,318 participants were included. In the incidence of major adverse cardiovascular events between the two regimens, there was no significant difference [RR = 0.99 (95% CI, 0.89–1.11), p = 0.87]; at the same time, there was no significant difference in cardiovascular mortality [RR = 1.17 (95% CI, 0.98–1.40),p = 0.08] or all-cause mortality [RR = 1.03 (95% CI, 0.91–1.17),p = 0.62]. In terms of 2-stage meta-analyses, there was no significant difference in any outcomes at any time point (moderate-to low-certainty evidence). Conclusion: In patients without atherosclerotic disease, febuxostat likely has a similar cardiovascular profile to allopurinol. However, in patients with a history of cardiovascular disease, allopurinol treatment is associated with less cardiovascular mortality as compared with febuxostat. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/#loginpage, identifier PROSPERO, CRD42022325656.
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spelling pubmed-95633762022-10-15 Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis Guan, Xudong Zhang, Shengzhao Liu, Jiayan Wu, Fengbo Zhou, Lingyan Liu, Ying Su, Na Front Pharmacol Pharmacology Background: Gout is a common disease and is usually treated with uric acid-lowering drugs (the most commonly used of which are febuxostat and allopurinol). However, the cardiovascular safety of febuxostat and allopurinol is still controversial. The purpose of our study is to evaluate the cardiovascular safety of the two drugs in patients with gout using one-stage and two-stage meta-analysis. Methods: PubMed, Embase, CBM, CNKI, WanFang, Central, and VIP were searched from inception to 30 January 2022. Randomized controlled trials which evaluated the cardiovascular safety of febuxostat or allopurinol for treating patients with gout were included. Based on the Kaplan–Meier curves of the two studies, individual patient data (IPD) were extracted and reconstructed. We used time-varying risk ratios (RRs) to summarize time-to-event outcomes, and the RRs of MACE incidence, cardiovascular mortality, and all-cause mortality were calculated by a multi-level flexible hazard regression model in 1-stage meta-analyses. p values were calculated using a log-rank test. At the same time, using the reconstructed IPD, we performed 2-stage meta-analyses to inform the quantitative estimates of time-specific relative risks at the six time points (1 , 2, 3, 4, 5, and 6 years) based on a random-effects model. Results: Two RCTs with 12,318 participants were included. In the incidence of major adverse cardiovascular events between the two regimens, there was no significant difference [RR = 0.99 (95% CI, 0.89–1.11), p = 0.87]; at the same time, there was no significant difference in cardiovascular mortality [RR = 1.17 (95% CI, 0.98–1.40),p = 0.08] or all-cause mortality [RR = 1.03 (95% CI, 0.91–1.17),p = 0.62]. In terms of 2-stage meta-analyses, there was no significant difference in any outcomes at any time point (moderate-to low-certainty evidence). Conclusion: In patients without atherosclerotic disease, febuxostat likely has a similar cardiovascular profile to allopurinol. However, in patients with a history of cardiovascular disease, allopurinol treatment is associated with less cardiovascular mortality as compared with febuxostat. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/#loginpage, identifier PROSPERO, CRD42022325656. Frontiers Media S.A. 2022-09-30 /pmc/articles/PMC9563376/ /pubmed/36249825 http://dx.doi.org/10.3389/fphar.2022.998441 Text en Copyright © 2022 Guan, Zhang, Liu, Wu, Zhou, Liu and Su. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Guan, Xudong
Zhang, Shengzhao
Liu, Jiayan
Wu, Fengbo
Zhou, Lingyan
Liu, Ying
Su, Na
Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis
title Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis
title_full Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis
title_fullStr Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis
title_full_unstemmed Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis
title_short Cardiovascular safety of febuxostat and allopurinol in patients with gout: A meta-analysis
title_sort cardiovascular safety of febuxostat and allopurinol in patients with gout: a meta-analysis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563376/
https://www.ncbi.nlm.nih.gov/pubmed/36249825
http://dx.doi.org/10.3389/fphar.2022.998441
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