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衰老过程中的非酒精性脂肪性肝病与肝纤维化

Non-alcoholic Fatty Liver Disease and Liver Fibrosis during Aging.

作者信息

Li Yuan, Adeniji Nia T, Fan Weiguo, Kunimoto Koshi, Török Natalie J

机构信息

Gastroenterology and Hepatology, Stanford University, Palo Alto, CA 94305, USA.

出版信息

Aging Dis. 2022 Jul 11;13(4):1239-1251. doi: 10.14336/AD.2022.0318.

Abstract

Non-alcoholic fatty liver disease (NAFLD) and its progressive form non-alcoholic steatohepatitis (NASH) have emerged as the leading causes of chronic liver disease-related mortality. The prevalence of NAFLD/NASH is expected to increase given the epidemics of obesity and type 2 diabetes mellitus. Older patients are disproportionally affected by NASH and related complications such as progressive fibrosis, cirrhosis and hepatocellular carcinoma; however, they are often ineligible for liver transplantation due to their frailty and comorbidities, and effective medical treatments are still lacking. In this review we focused on pathways that are key to the aging process in the liver and perpetuate NAFLD/NASH, leading to fibrosis. In addition, we highlighted recent findings and cross-talks of normal and/or senescent liver cells, dysregulated nutrient sensing, proteostasis and mitochondrial dysfunction in the framework of changing metabolic milieu. Better understanding these pathways during preclinical and clinical studies will be essential to design novel and specific therapeutic strategies to treat NASH in the elderly.

摘要

非酒精性脂肪性肝病(NAFLD)及其进展型非酒精性脂肪性肝炎(NASH)已成为慢性肝病相关死亡的主要原因。鉴于肥胖症和2型糖尿病的流行,预计NAFLD/NASH的患病率将会上升。老年患者受NASH及其相关并发症(如进行性纤维化、肝硬化和肝细胞癌)的影响尤为严重;然而,由于身体虚弱和合并症,他们往往不符合肝移植的条件,而且目前仍缺乏有效的药物治疗方法。在这篇综述中,我们重点关注了肝脏衰老过程中的关键途径,这些途径使NAFLD/NASH持续存在并导致纤维化。此外,我们强调了在代谢环境变化的框架下,正常和/或衰老肝细胞、营养感应失调、蛋白质稳态和线粒体功能障碍的最新研究发现及相互作用。在临床前和临床研究中更好地了解这些途径对于设计治疗老年人NASH的新型特异性治疗策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c2/9286912/795e5e8fe4fe/AD-13-4-1239-g1.jpg

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