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非酒精性脂肪性肝炎的治疗前景

The therapeutic landscape of non-alcoholic steatohepatitis.

作者信息

Perazzo Hugo, Dufour Jean-François

机构信息

Evandro Chagas National Institute of Infectious Disease (INI)-Oswaldo Cruz Foundation (FIOCRUZ), Laboratory of clinical research on STD/AIDS, Manguinhos, Rio de Janeiro, Brazil.

University Clinic for Visceral Surgery and Medicine, University of Bern, Inselspital, Bern, Switzerland.

出版信息

Liver Int. 2017 May;37(5):634-647. doi: 10.1111/liv.13270. Epub 2016 Nov 7.

Abstract

Non-alcoholic steatohepatitis (NASH) is characterized by lobular inflammation and hepatocellular ballooning, and may be associated with liver fibrosis leading to cirrhosis and its complications. A pharmacological approach is necessary to treat NASH because of failure to change dietary habits and lifestyle in most patients. Insulin resistance with an increased release of free fatty acids, oxidative stress and activation of inflammatory cytokines seem to be key features for disease progression. Thiazolidinediones, such as pioglitazone and antioxidant agents, such as vitamin E, were the first pharmacological options to be evaluated for NASH. In recent years, several new molecules that target different pathways related to NASH pathogenesis, such as liver metabolic homeostasis, inflammation, oxidative stress and fibrosis, have been developed. Obeticholic acid (INT-747) and elafibranor (GFT-505) have provided promising results in phase IIb, randomized, placebo-controlled clinical trials and they are being evaluated in ongoing phase III studies. Most of the potential treatments for NASH are under investigation in phase II studies, with some at phase I. This diversity in possible treatments calls for a better understanding of NASH in order to enrich trial populations with patients more susceptible to progress and to respond. This manuscript aims to review the pharmacological NASH treatment landscape.

摘要

非酒精性脂肪性肝炎(NASH)的特征是小叶炎症和肝细胞气球样变,并可能与导致肝硬化及其并发症的肝纤维化有关。由于大多数患者未能改变饮食习惯和生活方式,因此需要采用药物治疗方法来治疗NASH。游离脂肪酸释放增加、氧化应激和炎性细胞因子激活所导致的胰岛素抵抗似乎是疾病进展的关键特征。噻唑烷二酮类药物(如吡格列酮)和抗氧化剂(如维生素E)是首批针对NASH进行评估的药物选择。近年来,已经开发出几种针对与NASH发病机制相关的不同途径(如肝脏代谢稳态、炎症、氧化应激和纤维化)的新分子。奥贝胆酸(INT-747)和依拉伐诺(GFT-505)在IIb期随机安慰剂对照临床试验中取得了有前景的结果,目前正在进行的III期研究中对它们进行评估。大多数NASH的潜在治疗方法正在II期研究中进行调查,有些处于I期。这种可能治疗方法的多样性要求更好地了解NASH,以便在试验人群中纳入更易进展和有反应的患者。本手稿旨在综述NASH的药物治疗前景。

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