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Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD

Introduction: Chronic inflammation is the core mechanism of the development of chronic obstructive pulmonary disease (COPD). Corticosteroid resistance in COPD limits its anti-inflammatory potency. p38 MAPKIs were suggested as an alternative to corticosteroids despite the fact that there is currently...

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Autores principales: Yu, Haichuan, Su, Xiaojie, Lei, Ting, Zhang, Lu, Feng, Zhouzhou, Zhang, Chuchu, Zhang, Meng, Wang, Yalei, Chen, Xinlong, Liu, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554617/
https://www.ncbi.nlm.nih.gov/pubmed/36249771
http://dx.doi.org/10.3389/fphar.2022.950035
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author Yu, Haichuan
Su, Xiaojie
Lei, Ting
Zhang, Lu
Feng, Zhouzhou
Zhang, Chuchu
Zhang, Meng
Wang, Yalei
Chen, Xinlong
Liu, Jian
author_facet Yu, Haichuan
Su, Xiaojie
Lei, Ting
Zhang, Lu
Feng, Zhouzhou
Zhang, Chuchu
Zhang, Meng
Wang, Yalei
Chen, Xinlong
Liu, Jian
author_sort Yu, Haichuan
collection PubMed
description Introduction: Chronic inflammation is the core mechanism of the development of chronic obstructive pulmonary disease (COPD). Corticosteroid resistance in COPD limits its anti-inflammatory potency. p38 MAPKIs were suggested as an alternative to corticosteroids despite the fact that there is currently no systematic review evaluating existing evidence. Methods: This randomized controlled trials (RCT)-based systematic review with meta-analysis was conducted following the PRISMA statement. RCTs were searched and screened from 8 databases. Three types of data, including basic information of included studies, pre-defined outcome data, and quality assessment information were extracted. Pooling values and associated 95 % confidence intervals were deemed as statistically significant only when two-tailed p values were smaller than 0.05. Results: This study included 10 RCTs with a total population of 1,751 [age, mean (SD) = 64.39 (8.06)]. Safety and several efficacy indicators of lung function, inflammatory biomarkers, and quality of life were meta-analyzed. Despite the improvement of post-bronchodilator-forced vital capacity (FVC), no difference between p38 MAPKIs and placebo was found in both safety and efficacy. Conclusion: Compared with placebo, p38 MAPKIs are safe but did not show any significant effects in the COPD population. Results of this study should be regarded with caution due to the small number of included studies and heterogeneity from combining different p38 MAPKIs as a whole. Systematic Review registration: PROSPERO #CRD42022302890.
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spelling pubmed-95546172022-10-13 Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD Yu, Haichuan Su, Xiaojie Lei, Ting Zhang, Lu Feng, Zhouzhou Zhang, Chuchu Zhang, Meng Wang, Yalei Chen, Xinlong Liu, Jian Front Pharmacol Pharmacology Introduction: Chronic inflammation is the core mechanism of the development of chronic obstructive pulmonary disease (COPD). Corticosteroid resistance in COPD limits its anti-inflammatory potency. p38 MAPKIs were suggested as an alternative to corticosteroids despite the fact that there is currently no systematic review evaluating existing evidence. Methods: This randomized controlled trials (RCT)-based systematic review with meta-analysis was conducted following the PRISMA statement. RCTs were searched and screened from 8 databases. Three types of data, including basic information of included studies, pre-defined outcome data, and quality assessment information were extracted. Pooling values and associated 95 % confidence intervals were deemed as statistically significant only when two-tailed p values were smaller than 0.05. Results: This study included 10 RCTs with a total population of 1,751 [age, mean (SD) = 64.39 (8.06)]. Safety and several efficacy indicators of lung function, inflammatory biomarkers, and quality of life were meta-analyzed. Despite the improvement of post-bronchodilator-forced vital capacity (FVC), no difference between p38 MAPKIs and placebo was found in both safety and efficacy. Conclusion: Compared with placebo, p38 MAPKIs are safe but did not show any significant effects in the COPD population. Results of this study should be regarded with caution due to the small number of included studies and heterogeneity from combining different p38 MAPKIs as a whole. Systematic Review registration: PROSPERO #CRD42022302890. Frontiers Media S.A. 2022-09-28 /pmc/articles/PMC9554617/ /pubmed/36249771 http://dx.doi.org/10.3389/fphar.2022.950035 Text en Copyright © 2022 Yu, Su, Lei, Zhang, Feng, Zhang, Zhang, Wang, Chen and Liu. 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
Yu, Haichuan
Su, Xiaojie
Lei, Ting
Zhang, Lu
Feng, Zhouzhou
Zhang, Chuchu
Zhang, Meng
Wang, Yalei
Chen, Xinlong
Liu, Jian
Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD
title Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD
title_full Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD
title_fullStr Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD
title_full_unstemmed Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD
title_short Safety and efficacy of p38 mitogen-activated protein kinase inhibitors (MAPKIs) in COPD
title_sort safety and efficacy of p38 mitogen-activated protein kinase inhibitors (mapkis) in copd
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554617/
https://www.ncbi.nlm.nih.gov/pubmed/36249771
http://dx.doi.org/10.3389/fphar.2022.950035
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