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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
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.
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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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