School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
Leeds Institute for Medical Research and Leeds Institute for Data Analytics, University of Leeds, Leeds, United Kingdom.
Hepatology. 2021 Oct;74(4):1884-1901. doi: 10.1002/hep.31897. Epub 2021 Jun 17.
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.
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.
This systematic analysis provides a framework for phenotypic assessment of NAFLD models and highlights the need for increased standardization and replication.
人类疾病的动物模型是转化性肝脏病学研究的一个关键组成部分,但对于哪种模型最适合非酒精性脂肪性肝病(NAFLD)尚无共识。
我们生成了一个包含 3920 种 NAFLD 啮齿动物模型的数据库。研究设计高度多样化,因此,很少有模型被多次引用。对遗传模型的分析支持了目前关于脂肪功能障碍作用的证据,并提示固有免疫在 NAFLD 进展中的作用。我们发现高脂肪、高果糖饮食最能重现人类 NAFLD 的表型。动物模型的命名法存在很大的差异:需要就专门饮食的术语达成共识。更广泛地说,这种分析表明了临床前研究设计的可变性,这对肝脏病学领域及其他领域的体内实验的可重复性具有更广泛的影响。
这项系统分析为 NAFLD 模型的表型评估提供了一个框架,并强调需要增加标准化和复制。