Weight loss, insulin resistance, and study design confound results in a meta-analysis of animal models of fatty liver

Author:

Hunter Harriet1,de Gracia Hahn Dana1,Duret Amedine1,Im Yu Ri1,Cheah Qinrong1,Dong Jiawen1,Fairey Madison1,Hjalmarsson Clarissa1,Li Alice1,Lim Hong Kai1ORCID,McKeown Lorcan1,Mitrofan Claudia-Gabriela1,Rao Raunak1ORCID,Utukuri Mrudula1ORCID,Rowe Ian A2,Mann Jake P3ORCID

Affiliation:

1. School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom

2. Leeds Institute for Medical Research & Leeds Institute for Data Analytics, University of Leeds, Leeds, United Kingdom

3. Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom

Abstract

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.

Funder

Wellcome Trust

European Society for Paediatric Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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