Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Semin Liver Dis. 2021 May;41(2):213-224. doi: 10.1055/s-0041-1725023. Epub 2021 May 15.
Chronic liver injury results in cirrhosis and end-stage liver disease (ESLD) which represents a leading cause of death worldwide, affecting people in their most productive years of life. Medical therapy can extend life, but the only definitive treatment is liver transplantation (LT). However, LT remains limited by access to quality donor organs and suboptimal long-term outcomes. The degeneration from healthy-functioning livers to cirrhosis and ESLD involves a dynamic process of hepatocyte damage, diminished hepatic function, and adaptation. However, the mechanisms responsible for deterioration of hepatocyte function and ultimately hepatic failure in man are poorly understood. We review the current understanding of cirrhosis and ESLD as a dynamic process and outline the current mechanisms associated with the development of hepatic failure from the clinical manifestations to energy adaptations, regeneration, and regulation of nuclear transcription factors. A new generation of therapeutics could target stabilization of hepatocyte differentiation and function to avoid the need for transplantation in patients with cirrhosis and ESLD.
慢性肝损伤导致肝硬化和终末期肝病(ESLD),这是全球范围内主要的死亡原因之一,影响了人们生产力最高的年龄段的人群。医学治疗可以延长生命,但唯一的确定性治疗方法是肝移植(LT)。然而,LT 仍然受到优质供体器官的获取和不理想的长期结果的限制。从健康功能的肝脏到肝硬化和 ESLD 的退化涉及肝细胞损伤、肝功能下降和适应的动态过程。然而,导致人类肝细胞功能恶化并最终导致肝衰竭的机制尚不清楚。我们回顾了肝硬化和 ESLD 作为一个动态过程的现有认识,并概述了与从临床表现到能量适应、再生和核转录因子调节的肝衰竭发展相关的当前机制。新一代的治疗方法可以针对稳定肝细胞分化和功能,以避免肝硬化和 ESLD 患者需要进行移植。