Department of Infectious Diseases, Xiangya Hospital, Central South University, and Key Laboratory of Viral Hepatitis, Changsha, Hunan, China; Department of Medicine, University of California San Diego, La Jolla, California.
Department of Infectious Diseases, Xiangya Hospital, Central South University, and Key Laboratory of Viral Hepatitis, Changsha, Hunan, China.
Transl Res. 2019 Jul;209:22-38. doi: 10.1016/j.trsl.2019.02.005. Epub 2019 Feb 16.
Liver cirrhosis is a major cause of morbidity and mortality worldwide. The most common chronic liver diseases in western countries are alcohol-associated liver disease (ALD) and non-alcoholic fatty liver disease (NAFLD). Although these diseases have different causes, liver fibrosis develops via shared mechanisms. The liver and intestinal microbiome are linked by the portal vein and have bidirectional interactions. Changes in the intestinal microbiome contribute to the pathogenesis and progression of liver diseases including ALD, NAFLD, viral hepatitis and cholestatic disorders, based on studies in patients and animal models. Intestinal microbial dysbiosis has been associated with liver cirrhosis and its complications. We review the mechanisms by which alterations in the microbiome contribute to liver fibrosis and discuss microbiome-based treatment approaches.
肝硬化是全球范围内发病率和死亡率的主要原因。在西方国家,最常见的慢性肝病是酒精相关性肝病(ALD)和非酒精性脂肪性肝病(NAFLD)。尽管这些疾病的病因不同,但肝纤维化的发生机制是相似的。肝脏和肠道微生物组通过门静脉相连,并存在双向相互作用。基于对患者和动物模型的研究,肠道微生物组的变化会导致包括 ALD、NAFLD、病毒性肝炎和胆汁淤积性疾病在内的肝病的发病机制和进展。肠道微生物失调与肝硬化及其并发症有关。我们综述了微生物组的改变如何导致肝纤维化的机制,并讨论了基于微生物组的治疗方法。