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Brain-gut-liver interactions across the spectrum of insulin resistance in metabolic fatty liver disease

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WORLD JOURNAL OF GASTROENTEROLOGY
卷 27, 期 30, 页码 4999-5018

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BAISHIDENG PUBLISHING GROUP INC
DOI: 10.3748/wjg.v27.i30.4999

关键词

Metabolic associated fatty liver disease; Nonalcoholic fatty liver disease; Endogenous glucose production; Insulin resistance; Steatohepatitis; Inflammation

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MAFLD, formerly known as nonalcoholic fatty liver disease, affects about one-third of the general population in developed countries and is associated with various major diseases. Inflammation is a key factor in the progression of MAFLD, where insulin resistance plays an important role. The study focuses on the brain-gut-liver axis, imaging studies, and animal models to understand the causal interactions between fatty liver, dysregulated glucose production, and insulin resistance.
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.

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