Turku PET Centre, University of Turku, Turku 20500, Finland.
Institute of Clinical Physiology, National Research Council, Pisa 56124, Italy.
World J Gastroenterol. 2021 Aug 14;27(30):4999-5018. doi: 10.3748/wjg.v27.i30.4999.
Metabolic associated fatty liver disease (MAFLD), formerly named "nonalcoholic fatty liver disease" occurs in about one-third of the general population of developed countries worldwide and behaves as a major morbidity and mortality risk factor for major causes of death, such as cardiovascular, digestive, metabolic, neoplastic and neuro-degenerative diseases. However, progression of MAFLD and its associated systemic complications occur almost invariably in patients who experience the additional burden of intrahepatic and/or systemic inflammation, which acts as disease accelerator. Our review is focused on the new knowledge about the brain-gut-liver axis in the context of metabolic dysregulations associated with fatty liver, where insulin resistance has been assumed to play an important role. Special emphasis has been given to digital imaging studies and in particular to positron emission tomography, as it represents a unique opportunity for the noninvasive in vivo study of tissue metabolism. An exhaustive revision of targeted animal models is also provided in order to clarify what the available preclinical evidence suggests for the causal interactions between fatty liver, dysregulated endogenous glucose production and insulin resistance.
代谢相关性脂肪性肝病(MAFLD),以前称为“非酒精性脂肪性肝病”,在世界上大多数发达国家的一般人群中约占三分之一,并且是心血管、消化、代谢、肿瘤和神经退行性疾病等主要死亡原因的主要发病和死亡风险因素。然而,MAFLD 的进展及其相关的全身并发症几乎总是发生在那些经历肝内和/或全身炎症额外负担的患者中,这种炎症是疾病的加速因素。我们的综述重点关注与脂肪性肝病相关的代谢紊乱背景下的脑-肠-肝轴的新知识,其中胰岛素抵抗被认为起着重要作用。特别强调了数字成像研究,特别是正电子发射断层扫描,因为它为组织代谢的非侵入性体内研究提供了独特的机会。还提供了针对动物模型的详尽修订,以阐明现有临床前证据对脂肪性肝病、内源性葡萄糖生成失调和胰岛素抵抗之间的因果相互作用的提示。