脂肪肝
非酒精性脂肪肝
医学
疾病
胰岛素抵抗
肠道菌群
微生物群
发病机制
生物信息学
免疫学
内科学
生物
胰岛素
作者
Jie Ji,Liwei Wu,Jue Wei,Jianye Wu,Chuanyong Guo
出处
期刊:Journal of clinical and translational hepatology
[Xia & He Publishing]
日期:2022-07-14
卷期号:000 (000): 000-000
被引量:7
标识
DOI:10.14218/jcth.2022.00136
摘要
Metabolic-associated fatty liver disease (MAFLD) is a new disease definition, and is proposed to replace the previous name, nonalcoholic fatty liver disease (NAFLD). Globally, MAFLD/NAFLD is the most common liver disease, with an incidence rate ranging from 6% to 35% in adult populations. The pathogenesis of MAFLD/NAFLD is closely related to insulin resistance (IR), and the genetic susceptibility to acquired metabolic stress-associated liver injury. Similarly, the gut microbiota in MAFLD/NAFLD is being revaluated by scientists, as the gut and liver influence each other via the gut-liver axis. Ferroptosis is a novel form of programmed cell death caused by iron-dependent lipid peroxidation. Emerging evidence suggests that ferroptosis has a key role in the pathological progression of MAFLD/NAFLD, and inhibition of ferroptosis may become a novel therapeutic strategy for the treatment of NAFLD. This review focuses on the main mechanisms behind the promotion of MAFLD/NAFLD occurrence and development by the intestinal microbiota and ferroptosis. It outlines new strategies to target the intestinal microbiota and ferroptosis to facilitate future MAFLD/NAFLD therapies.
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