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Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis

To evaluate the effect of astragaloside IV for hepatic fibrosis. The multiple databases like Pubmed, Embase, Cochrane databases, and China National Knowledge database were used to search for the relevant studies, and full-text articles involved in the evaluation on effect of astragaloside IV for hep...

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Detalles Bibliográficos
Autores principales: Han, Zhongying, Zhu, Junfeng, Han, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021362/
https://www.ncbi.nlm.nih.gov/pubmed/33787592
http://dx.doi.org/10.1097/MD.0000000000025105
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author Han, Zhongying
Zhu, Junfeng
Han, Zheng
author_facet Han, Zhongying
Zhu, Junfeng
Han, Zheng
author_sort Han, Zhongying
collection PubMed
description To evaluate the effect of astragaloside IV for hepatic fibrosis. The multiple databases like Pubmed, Embase, Cochrane databases, and China National Knowledge database were used to search for the relevant studies, and full-text articles involved in the evaluation on effect of astragaloside IV for hepatic fibrosis. Review Manager 5.2 was adopted to estimate the effects of the results among selected articles. Forest plots, sensitivity analysis and bias analysis for the articles included were also conducted. Finally, 7 eligible studies were eventually satisfied the included criteria. Alanine aminotransferase (ALT) in model was higher than astragaloside group (mean difference [MD] = −58.01, 95% confidential interval (CI) [−93.97, −22.05], P = .002; I(2) = 99%). The meta-analysis suggested that aspartate aminotransferase (AST) in model group was more than that in astragaloside group (MD = −39.94, 95% CI [−129.38, 49.50], P = .38; I(2) = 100%). Model group had higher α - smooth muscle actin (α-SMA) than astragaloside group (MD was −1.13, P of heterogeneity <.0001, I(2) = 94%, Z = 5.18, P of over effect <.0001). Transforming growth factor β (TGF-β) in model group was higher than that in astragaloside group (MD was −0.55, P of heterogeneity <.00001, I(2) = 97%, Z = 2.54, P of over effect = .01). Limited publication bias was observed in this study. Astragaloside IV is a potential clinical drug for the treatment of liver fibrosis considering liver function and hepatic fibrosis related protein factor in experimental rats are improved.
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spelling pubmed-80213622021-04-07 Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis Han, Zhongying Zhu, Junfeng Han, Zheng Medicine (Baltimore) 4800 To evaluate the effect of astragaloside IV for hepatic fibrosis. The multiple databases like Pubmed, Embase, Cochrane databases, and China National Knowledge database were used to search for the relevant studies, and full-text articles involved in the evaluation on effect of astragaloside IV for hepatic fibrosis. Review Manager 5.2 was adopted to estimate the effects of the results among selected articles. Forest plots, sensitivity analysis and bias analysis for the articles included were also conducted. Finally, 7 eligible studies were eventually satisfied the included criteria. Alanine aminotransferase (ALT) in model was higher than astragaloside group (mean difference [MD] = −58.01, 95% confidential interval (CI) [−93.97, −22.05], P = .002; I(2) = 99%). The meta-analysis suggested that aspartate aminotransferase (AST) in model group was more than that in astragaloside group (MD = −39.94, 95% CI [−129.38, 49.50], P = .38; I(2) = 100%). Model group had higher α - smooth muscle actin (α-SMA) than astragaloside group (MD was −1.13, P of heterogeneity <.0001, I(2) = 94%, Z = 5.18, P of over effect <.0001). Transforming growth factor β (TGF-β) in model group was higher than that in astragaloside group (MD was −0.55, P of heterogeneity <.00001, I(2) = 97%, Z = 2.54, P of over effect = .01). Limited publication bias was observed in this study. Astragaloside IV is a potential clinical drug for the treatment of liver fibrosis considering liver function and hepatic fibrosis related protein factor in experimental rats are improved. Lippincott Williams & Wilkins 2021-04-02 /pmc/articles/PMC8021362/ /pubmed/33787592 http://dx.doi.org/10.1097/MD.0000000000025105 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 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 4800
Han, Zhongying
Zhu, Junfeng
Han, Zheng
Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis
title Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis
title_full Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis
title_fullStr Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis
title_full_unstemmed Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis
title_short Evaluation of astragaloside IV in hepatic fibrosis: A meta-analysis
title_sort evaluation of astragaloside iv in hepatic fibrosis: a meta-analysis
topic 4800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021362/
https://www.ncbi.nlm.nih.gov/pubmed/33787592
http://dx.doi.org/10.1097/MD.0000000000025105
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