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Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis
Astragalus membranaceus (AM) is a traditional Chinese medicine, which possesses a variety of biological activities in the cardiovascular systems. We conducted a clinical and preclinical systematic review of 28 randomized clinical control studies with 2522 participants and 16 animal studies with 634...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652609/ https://www.ncbi.nlm.nih.gov/pubmed/33204391 http://dx.doi.org/10.1155/2020/1560353 |
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author | Zheng, Qun Zhuang, Zhuang Wang, Zi-Hao Deng, Li-Hui Jin, Wang-Jun Huang, Zi-Jun Zheng, Guo-Qing Wang, Yan |
author_facet | Zheng, Qun Zhuang, Zhuang Wang, Zi-Hao Deng, Li-Hui Jin, Wang-Jun Huang, Zi-Jun Zheng, Guo-Qing Wang, Yan |
author_sort | Zheng, Qun |
collection | PubMed |
description | Astragalus membranaceus (AM) is a traditional Chinese medicine, which possesses a variety of biological activities in the cardiovascular systems. We conducted a clinical and preclinical systematic review of 28 randomized clinical control studies with 2522 participants and 16 animal studies with 634 animals to evaluate the efficacy, safety, and possible mechanisms of AM for viral myocarditis (VM). The search strategies were performed in 7 databases from inception to January 2020. Application of the Cochrane Collaboration's tool 7-item checklist, SYRCLE's tool 10-item checklist, and Rev-Man 5.3 software to analyze the risk of bias of studies and data. The results show the score of clinical study quality ranged from 3 to 7 points with an average of 3.32, and the score of animal study quality ranged from 2 to 5 points with an average of 3. In clinical study, AM significantly reduced serum myocardial enzymes and cardiac troponin I levels and improved the clinical treatment efficiency in VM patients compared with the control group (P < 0.05). There was no significant difference in the incidence of adverse reactions (P > 0.05). Significant increase of the survival rate and decrease of the cardiac cardiology score, cardiac enzymes, and cardiac troponin I were compared with the placebo group in animal studies (P < 0.05). The possible mechanisms of AM are largely through antivirus and antivirus receptors, anti-inflammatory, antioxidation, antiapoptotic, antifibrosis, and reducing cardiac calcium load. In conclusion, the findings suggested that AM is a cardioprotection candidate drug for VM. |
format | Online Article Text |
id | pubmed-7652609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-76526092020-11-16 Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis Zheng, Qun Zhuang, Zhuang Wang, Zi-Hao Deng, Li-Hui Jin, Wang-Jun Huang, Zi-Jun Zheng, Guo-Qing Wang, Yan Oxid Med Cell Longev Review Article Astragalus membranaceus (AM) is a traditional Chinese medicine, which possesses a variety of biological activities in the cardiovascular systems. We conducted a clinical and preclinical systematic review of 28 randomized clinical control studies with 2522 participants and 16 animal studies with 634 animals to evaluate the efficacy, safety, and possible mechanisms of AM for viral myocarditis (VM). The search strategies were performed in 7 databases from inception to January 2020. Application of the Cochrane Collaboration's tool 7-item checklist, SYRCLE's tool 10-item checklist, and Rev-Man 5.3 software to analyze the risk of bias of studies and data. The results show the score of clinical study quality ranged from 3 to 7 points with an average of 3.32, and the score of animal study quality ranged from 2 to 5 points with an average of 3. In clinical study, AM significantly reduced serum myocardial enzymes and cardiac troponin I levels and improved the clinical treatment efficiency in VM patients compared with the control group (P < 0.05). There was no significant difference in the incidence of adverse reactions (P > 0.05). Significant increase of the survival rate and decrease of the cardiac cardiology score, cardiac enzymes, and cardiac troponin I were compared with the placebo group in animal studies (P < 0.05). The possible mechanisms of AM are largely through antivirus and antivirus receptors, anti-inflammatory, antioxidation, antiapoptotic, antifibrosis, and reducing cardiac calcium load. In conclusion, the findings suggested that AM is a cardioprotection candidate drug for VM. Hindawi 2020-11-02 /pmc/articles/PMC7652609/ /pubmed/33204391 http://dx.doi.org/10.1155/2020/1560353 Text en Copyright © 2020 Qun Zheng et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Zheng, Qun Zhuang, Zhuang Wang, Zi-Hao Deng, Li-Hui Jin, Wang-Jun Huang, Zi-Jun Zheng, Guo-Qing Wang, Yan Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis |
title | Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis |
title_full | Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis |
title_fullStr | Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis |
title_full_unstemmed | Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis |
title_short | Clinical and Preclinical Systematic Review of Astragalus Membranaceus for Viral Myocarditis |
title_sort | clinical and preclinical systematic review of astragalus membranaceus for viral myocarditis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652609/ https://www.ncbi.nlm.nih.gov/pubmed/33204391 http://dx.doi.org/10.1155/2020/1560353 |
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