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Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver
The classical drug development pipeline necessitates studies using animal models of human disease to gauge future efficacy in humans, however there is a low conversion rate from success in animals to humans. Non-alcoholic fatty liver disease (NAFLD) is a complex chronic disease without any establish...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647398/ https://www.ncbi.nlm.nih.gov/pubmed/33063664 http://dx.doi.org/10.7554/eLife.56573 |
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author | Hunter, Harriet de Gracia Hahn, Dana Duret, Amedine Im, Yu Ri Cheah, Qinrong Dong, Jiawen Fairey, Madison Hjalmarsson, Clarissa Li, Alice Lim, Hong Kai McKeown, Lorcan Mitrofan, Claudia-Gabriela Rao, Raunak Utukuri, Mrudula Rowe, Ian A Mann, Jake P |
author_facet | Hunter, Harriet de Gracia Hahn, Dana Duret, Amedine Im, Yu Ri Cheah, Qinrong Dong, Jiawen Fairey, Madison Hjalmarsson, Clarissa Li, Alice Lim, Hong Kai McKeown, Lorcan Mitrofan, Claudia-Gabriela Rao, Raunak Utukuri, Mrudula Rowe, Ian A Mann, Jake P |
author_sort | Hunter, Harriet |
collection | PubMed |
description | The classical drug development pipeline necessitates studies using animal models of human disease to gauge future efficacy in humans, however there is a low conversion rate from success in animals to humans. Non-alcoholic fatty liver disease (NAFLD) is a complex chronic disease without any established therapies and a major field of animal research. We performed a meta-analysis with meta-regression of 603 interventional rodent studies (10,364 animals) in NAFLD to assess which variables influenced treatment response. Weight loss and alleviation of insulin resistance were consistently associated with improvement in NAFLD. Multiple drug classes that do not affect weight in humans caused weight loss in animals. Other study design variables, such as age of animals and dietary composition, influenced the magnitude of treatment effect. Publication bias may have increased effect estimates by 37-79%. These findings help to explain the challenge of reproducibility and translation within the field of metabolism. |
format | Online Article Text |
id | pubmed-7647398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-76473982020-11-09 Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver Hunter, Harriet de Gracia Hahn, Dana Duret, Amedine Im, Yu Ri Cheah, Qinrong Dong, Jiawen Fairey, Madison Hjalmarsson, Clarissa Li, Alice Lim, Hong Kai McKeown, Lorcan Mitrofan, Claudia-Gabriela Rao, Raunak Utukuri, Mrudula Rowe, Ian A Mann, Jake P eLife Medicine The classical drug development pipeline necessitates studies using animal models of human disease to gauge future efficacy in humans, however there is a low conversion rate from success in animals to humans. Non-alcoholic fatty liver disease (NAFLD) is a complex chronic disease without any established therapies and a major field of animal research. We performed a meta-analysis with meta-regression of 603 interventional rodent studies (10,364 animals) in NAFLD to assess which variables influenced treatment response. Weight loss and alleviation of insulin resistance were consistently associated with improvement in NAFLD. Multiple drug classes that do not affect weight in humans caused weight loss in animals. Other study design variables, such as age of animals and dietary composition, influenced the magnitude of treatment effect. Publication bias may have increased effect estimates by 37-79%. These findings help to explain the challenge of reproducibility and translation within the field of metabolism. eLife Sciences Publications, Ltd 2020-10-16 /pmc/articles/PMC7647398/ /pubmed/33063664 http://dx.doi.org/10.7554/eLife.56573 Text en © 2020, Hunter et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Medicine Hunter, Harriet de Gracia Hahn, Dana Duret, Amedine Im, Yu Ri Cheah, Qinrong Dong, Jiawen Fairey, Madison Hjalmarsson, Clarissa Li, Alice Lim, Hong Kai McKeown, Lorcan Mitrofan, Claudia-Gabriela Rao, Raunak Utukuri, Mrudula Rowe, Ian A Mann, Jake P Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver |
title | Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver |
title_full | Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver |
title_fullStr | Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver |
title_full_unstemmed | Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver |
title_short | Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver |
title_sort | weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647398/ https://www.ncbi.nlm.nih.gov/pubmed/33063664 http://dx.doi.org/10.7554/eLife.56573 |
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