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A Systematic Review of Animal Models of NAFLD Finds High-Fat, High-Fructose Diets Most Closely Resemble Human NAFLD.
Im, Yu Ri; Hunter, Harriet; de Gracia Hahn, Dana; Duret, Amedine; Cheah, Qinrong; Dong, Jiawen; Fairey, Madison; Hjalmarsson, Clarissa; Li, Alice; Lim, Hong Kai; McKeown, Lorcán; Mitrofan, Claudia-Gabriela; Rao, Raunak; Utukuri, Mrudula; Rowe, Ian A; Mann, Jake P.
Afiliação
  • Im YR; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Hunter H; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • de Gracia Hahn D; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Duret A; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Cheah Q; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Dong J; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Fairey M; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Hjalmarsson C; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Li A; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Lim HK; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • McKeown L; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Mitrofan CG; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Rao R; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Utukuri M; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Rowe IA; Leeds Institute for Medical Research and Leeds Institute for Data Analytics, University of Leeds, Leeds, United Kingdom.
  • Mann JP; Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.
Hepatology ; 74(4): 1884-1901, 2021 10.
Article em En | MEDLINE | ID: mdl-33973269
ABSTRACT
BACKGROUND AND

AIMS:

Animal models of human disease are a key component of translational hepatology research, yet there is no consensus on which model is optimal for NAFLD. APPROACH AND

RESULTS:

We generated a database of 3,920 rodent models of NAFLD. Study designs were highly heterogeneous, and therefore, few models had been cited more than once. Analysis of genetic models supported the current evidence for the role of adipose dysfunction and suggested a role for innate immunity in the progression of NAFLD. We identified that high-fat, high-fructose diets most closely recapitulate the human phenotype of NAFLD. There was substantial variability in the nomenclature of animal models a consensus on terminology of specialist diets is needed. More broadly, this analysis demonstrates the variability in preclinical study design, which has wider implications for the reproducibility of in vivo experiments both in the field of hepatology and beyond.

CONCLUSIONS:

This systematic analysis provides a framework for phenotypic assessment of NAFLD models and highlights the need for increased standardization and replication.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ratos / Síndrome Metabólica / Modelos Animais de Doenças / Dieta Hiperlipídica / Hepatopatia Gordurosa não Alcoólica / Frutose / Camundongos Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ratos / Síndrome Metabólica / Modelos Animais de Doenças / Dieta Hiperlipídica / Hepatopatia Gordurosa não Alcoólica / Frutose / Camundongos Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article