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Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease

BACKGROUND: As an anti-TNF agent that targets inflammatory process directly, Pentoxifylline has been investigated for treatment of NASH in individual studies and pilot trials for years. We summarized the available information and generating hypotheses for future research. DATA SOURCES: Google, Cochr...

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Autores principales: Li, Wenjun, Zheng, Liu, Sheng, Chunjun, Cheng, Xiaoyun, Qing, Liu, Qu, Shen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3088890/
https://www.ncbi.nlm.nih.gov/pubmed/21477300
http://dx.doi.org/10.1186/1476-511X-10-49
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author Li, Wenjun
Zheng, Liu
Sheng, Chunjun
Cheng, Xiaoyun
Qing, Liu
Qu, Shen
author_facet Li, Wenjun
Zheng, Liu
Sheng, Chunjun
Cheng, Xiaoyun
Qing, Liu
Qu, Shen
author_sort Li, Wenjun
collection PubMed
description BACKGROUND: As an anti-TNF agent that targets inflammatory process directly, Pentoxifylline has been investigated for treatment of NASH in individual studies and pilot trials for years. We summarized the available information and generating hypotheses for future research. DATA SOURCES: Google, Cochrane, MEDLINE, and EMBASE and the Chinese Biomedical data bases for studies restricted to pentoxifylline treatment in humans with NAFLD in all languages until June 2010. Six studies (2 randomized, double-blind, placebo-controlled trials; 4 prospective cohort studies) extracted from 11604 references. RESULTS: Pentoxifylline-treated patients showed a significant decrease AST (n = 37, P = 0.01) and ALT (n = 50, P = 0.03), but no significant effect on IL-6 (n = 36, P = 0.33) and TNF-α (n = 68, P = 0.26) compared with Placebo or UDCA-controlled groups. Improvement in one or more histological variables was reported in two trails, only 1 study showed a reduction in of one or two points in fibrosis stage. LIMITATIONS: The trails did not consistently report all of the outcomes of interest. Sample sizes (117 patients totally) were small and only 2 out of 6 studies had a randomized, controlled design. CONCLUSION: Pentoxifylline reduce AST and ALT levels and may improve liver histological scores in patients with NALFD/NASH, but did not appear to affect cytokines. Large, prospective, and well-designed randomized, controlled studies are needed to address this issue. Novel therapeutic targets for activation of inflammatory signaling pathways by fat also merit investigation.
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spelling pubmed-30888902011-05-07 Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease Li, Wenjun Zheng, Liu Sheng, Chunjun Cheng, Xiaoyun Qing, Liu Qu, Shen Lipids Health Dis Review BACKGROUND: As an anti-TNF agent that targets inflammatory process directly, Pentoxifylline has been investigated for treatment of NASH in individual studies and pilot trials for years. We summarized the available information and generating hypotheses for future research. DATA SOURCES: Google, Cochrane, MEDLINE, and EMBASE and the Chinese Biomedical data bases for studies restricted to pentoxifylline treatment in humans with NAFLD in all languages until June 2010. Six studies (2 randomized, double-blind, placebo-controlled trials; 4 prospective cohort studies) extracted from 11604 references. RESULTS: Pentoxifylline-treated patients showed a significant decrease AST (n = 37, P = 0.01) and ALT (n = 50, P = 0.03), but no significant effect on IL-6 (n = 36, P = 0.33) and TNF-α (n = 68, P = 0.26) compared with Placebo or UDCA-controlled groups. Improvement in one or more histological variables was reported in two trails, only 1 study showed a reduction in of one or two points in fibrosis stage. LIMITATIONS: The trails did not consistently report all of the outcomes of interest. Sample sizes (117 patients totally) were small and only 2 out of 6 studies had a randomized, controlled design. CONCLUSION: Pentoxifylline reduce AST and ALT levels and may improve liver histological scores in patients with NALFD/NASH, but did not appear to affect cytokines. Large, prospective, and well-designed randomized, controlled studies are needed to address this issue. Novel therapeutic targets for activation of inflammatory signaling pathways by fat also merit investigation. BioMed Central 2011-04-08 /pmc/articles/PMC3088890/ /pubmed/21477300 http://dx.doi.org/10.1186/1476-511X-10-49 Text en Copyright ©2011 Li et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Li, Wenjun
Zheng, Liu
Sheng, Chunjun
Cheng, Xiaoyun
Qing, Liu
Qu, Shen
Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease
title Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease
title_full Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease
title_fullStr Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease
title_full_unstemmed Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease
title_short Systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease
title_sort systematic review on the treatment of pentoxifylline in patients with non-alcoholic fatty liver disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3088890/
https://www.ncbi.nlm.nih.gov/pubmed/21477300
http://dx.doi.org/10.1186/1476-511X-10-49
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