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The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials
BACKGROUND: Silymarin (SIL) is an active extraction of the silybum marianum, milk thistle, which is an ancient medicinal plant for treatment of various liver diseases for centuries. This study is to assess the therapeutic effect of SIL in the treatment of nonalcoholic fatty liver disease through met...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728929/ https://www.ncbi.nlm.nih.gov/pubmed/29245314 http://dx.doi.org/10.1097/MD.0000000000009061 |
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author | Zhong, Sheng Fan, Yuxiang Yan, Qi Fan, Xingyu Wu, Bo Han, Yujuan Zhang, Ying Chen, Yong Zhang, Huimao Niu, Junqi |
author_facet | Zhong, Sheng Fan, Yuxiang Yan, Qi Fan, Xingyu Wu, Bo Han, Yujuan Zhang, Ying Chen, Yong Zhang, Huimao Niu, Junqi |
author_sort | Zhong, Sheng |
collection | PubMed |
description | BACKGROUND: Silymarin (SIL) is an active extraction of the silybum marianum, milk thistle, which is an ancient medicinal plant for treatment of various liver diseases for centuries. This study is to assess the therapeutic effect of SIL in the treatment of nonalcoholic fatty liver disease through meta-analysis. METHODS: Published randomized controlled trials (RCTs) were included from electronic databases (PubMed, Embase, Cochrane library, Web of Science, and so forth). Cochrane handbook was applied to evaluate the methodological quality. All statistical analyses were directed by Revman 5.3 software, and statistical significance was defined as P < .05. RESULTS: Eight RCTs involved 587 patients were included in this study. The results showed that SIL reduced the AST and ALT levels more significantly than the control group (AST UI/L: MD = −6.57; 95% CI, −10.03 to −3.12; P = .0002; ALT UI/L: MD = −9.16; 95% CI, −16.24 to −2.08; P = .01). Compared with other interventions, there were significant differences decreasing AST and ALT levels when SIL was used alone (AST UI/L: MD = −5.44; 95% CI, −8.80 to −2.08; P = .002; ALT UI/L: MD = −5.08; 95% CI, −7.85 to −2.32; P = .0003). CONCLUSION: SIL has positive efficacy to reduce transaminases levels in NAFLD patients. SIL can be an encouraging and considerable phytotherapy for NAFLD patients. |
format | Online Article Text |
id | pubmed-5728929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-57289292017-12-20 The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials Zhong, Sheng Fan, Yuxiang Yan, Qi Fan, Xingyu Wu, Bo Han, Yujuan Zhang, Ying Chen, Yong Zhang, Huimao Niu, Junqi Medicine (Baltimore) 4500 BACKGROUND: Silymarin (SIL) is an active extraction of the silybum marianum, milk thistle, which is an ancient medicinal plant for treatment of various liver diseases for centuries. This study is to assess the therapeutic effect of SIL in the treatment of nonalcoholic fatty liver disease through meta-analysis. METHODS: Published randomized controlled trials (RCTs) were included from electronic databases (PubMed, Embase, Cochrane library, Web of Science, and so forth). Cochrane handbook was applied to evaluate the methodological quality. All statistical analyses were directed by Revman 5.3 software, and statistical significance was defined as P < .05. RESULTS: Eight RCTs involved 587 patients were included in this study. The results showed that SIL reduced the AST and ALT levels more significantly than the control group (AST UI/L: MD = −6.57; 95% CI, −10.03 to −3.12; P = .0002; ALT UI/L: MD = −9.16; 95% CI, −16.24 to −2.08; P = .01). Compared with other interventions, there were significant differences decreasing AST and ALT levels when SIL was used alone (AST UI/L: MD = −5.44; 95% CI, −8.80 to −2.08; P = .002; ALT UI/L: MD = −5.08; 95% CI, −7.85 to −2.32; P = .0003). CONCLUSION: SIL has positive efficacy to reduce transaminases levels in NAFLD patients. SIL can be an encouraging and considerable phytotherapy for NAFLD patients. Wolters Kluwer Health 2017-12-08 /pmc/articles/PMC5728929/ /pubmed/29245314 http://dx.doi.org/10.1097/MD.0000000000009061 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 4500 Zhong, Sheng Fan, Yuxiang Yan, Qi Fan, Xingyu Wu, Bo Han, Yujuan Zhang, Ying Chen, Yong Zhang, Huimao Niu, Junqi The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials |
title | The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials |
title_full | The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials |
title_fullStr | The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials |
title_full_unstemmed | The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials |
title_short | The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials |
title_sort | therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: a meta-analysis (prisma) of randomized control trials |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728929/ https://www.ncbi.nlm.nih.gov/pubmed/29245314 http://dx.doi.org/10.1097/MD.0000000000009061 |
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