The multiple-hit pathogenesis of non-alcoholic fatty liver disease (NAFLD)

被引:2340
作者
Buzzetti, Elena
Pinzani, Massimo
Tsochatzis, Emmanuel A. [1 ,2 ]
机构
[1] Royal Free Hosp, UCL Inst Liver & Digest Hlth, London, England
[2] UCL, London, England
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2016年 / 65卷 / 08期
关键词
Insulin resistance; Lipotoxicity; Gut microbiome; Metabolic syndrome; PNPLA3; ENDOPLASMIC-RETICULUM STRESS; NECROSIS-FACTOR-ALPHA; DE-NOVO LIPOGENESIS; IMPROVES HEPATIC STEATOSIS; 3 GENE PNPLA3; NF-KAPPA-B; INSULIN-RESISTANCE; ADIPOSE-TISSUE; MITOCHONDRIAL DYSFUNCTION; INTESTINAL PERMEABILITY;
D O I
10.1016/j.metabol.2015.12.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) is increasingly prevalent and represents a growing challenge in terms of prevention and treatment. Despite its high prevalence, only a small minority of affected patients develops inflammation and subsequently fibrosis and chronic liver disease, while most of them only exhibit simple steatosis. In this context, the full understanding of the mechanisms underlying the development of NAFLD and nonalcoholic steatohepatitis (NASH) is of extreme importance; despite advances in this field, knowledge on the pathogenesis of NAFLD is still incomplete. The 'two-hit' hypothesis is now obsolete, as it is inadequate to explain the several molecular and metabolic changes that take place in NAFLD. The "multiple hit" hypothesis considers multiple insults acting together on genetically predisposed subjects to induce NAFLD and provides a more accurate explanation of NAFLD pathogenesis. Such hits include insulin resistance, hormones secreted from the adipose tissue, nutritional factors, gut microbiota and genetic and epigenetic factors. In this article, we review the factors that form this hypothesis. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:1038 / 1048
页数:11
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