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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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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. |
format | Online Article Text |
id | pubmed-8021362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
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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