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非酒精性脂肪性肝病。

Nonalcoholic fatty liver disease.

机构信息

Department of Medicine II, Saarland University Hospital, Homburg, Germany.

出版信息

Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):695-708. doi: 10.1016/j.bpg.2010.08.005.

Abstract

Non-alcoholic fatty liver disease (NAFLD), the most common liver disorder in the Western world, is a clinico-histopathological entity in which excessive triglyceride accumulation in the liver occurs. Non-alcoholic steatohepatitis (NASH) represents the necroinflammatory form, which can lead to advanced liver fibrosis, cirrhosis, and hepatocellular carcinoma. The pathogenesis of NAFLD/NASH is complex but increased visceral adiposity plus insulin resistance with increased free fatty acids release play an initial key role for the onset and perpetuation of liver steatosis. Further events in the liver include oxidative stress and lipid peroxidation, decreased antioxidant defences, early mitochondrial dysfunction, iron accumulation, unbalance of adipose-derived adipokines with a chronic proinflammatory status, and gut-derived microbial adducts. New gene polymorphisms increasing the risk of fatty liver, namely APOC3 and PNPLA3, have been lately identified allowing further insights into the pathogenesis of this condition. In our review pathophysiological, genetic, and essential diagnostic and therapeutic aspects of NAFLD are examined with future trends in this field highlighted.

摘要

非酒精性脂肪性肝病(NAFLD)是西方世界最常见的肝脏疾病,是一种临床病理实体,其特征是肝脏中甘油三酯过度积聚。非酒精性脂肪性肝炎(NASH)代表了坏死性炎症形式,可导致晚期肝纤维化、肝硬化和肝细胞癌。NAFLD/NASH 的发病机制很复杂,但内脏脂肪增加加上胰岛素抵抗导致游离脂肪酸释放增加,在肝脂肪变性的发生和持续中起着最初的关键作用。肝脏中的进一步事件包括氧化应激和脂质过氧化、抗氧化防御能力下降、早期线粒体功能障碍、铁积累、脂肪来源的脂肪细胞因子失衡导致慢性炎症状态以及肠道衍生的微生物加合物。最近发现了一些新的增加脂肪肝风险的基因多态性,即 APOC3 和 PNPLA3,这使得我们对这种疾病的发病机制有了更深入的了解。在我们的综述中,检查了 NAFLD 的病理生理、遗传和基本诊断及治疗方面,并强调了该领域的未来趋势。

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