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Molecular Pathogenesis of Nonalcoholic Steatohepatitis- (NASH-) Related Hepatocellular Carcinoma.非酒精性脂肪性肝炎-(NASH-)相关肝细胞癌的分子发病机制。
Can J Gastroenterol Hepatol. 2018 Aug 29;2018:8543763. doi: 10.1155/2018/8543763. eCollection 2018.
2
Pathogenesis of Nonalcoholic Steatohepatitis and Hormone-Based Therapeutic Approaches.非酒精性脂肪性肝炎的发病机制及基于激素的治疗方法。
Front Endocrinol (Lausanne). 2018 Aug 24;9:485. doi: 10.3389/fendo.2018.00485. eCollection 2018.
3
GS-0976 Reduces Hepatic Steatosis and Fibrosis Markers in Patients With Nonalcoholic Fatty Liver Disease.GS-0976 可降低非酒精性脂肪性肝病患者的肝脂肪变性和纤维化标志物。
Gastroenterology. 2018 Nov;155(5):1463-1473.e6. doi: 10.1053/j.gastro.2018.07.027. Epub 2018 Jul 27.
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The Influence of Gut Microbial Metabolism on the Development and Progression of Non-alcoholic Fatty Liver Disease.肠道微生物代谢对非酒精性脂肪性肝病发生发展的影响。
Adv Exp Med Biol. 2018;1061:95-110. doi: 10.1007/978-981-10-8684-7_8.
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Diagnosis, Staging, and Management of Hepatocellular Carcinoma: 2018 Practice Guidance by the American Association for the Study of Liver Diseases.肝细胞癌的诊断、分期及管理:美国肝病研究协会2018年实践指南
Hepatology. 2018 Aug;68(2):723-750. doi: 10.1002/hep.29913.
6
Components of metabolic syndrome increase the risk of mortality in nonalcoholic fatty liver disease (NAFLD).代谢综合征的各个组成部分会增加非酒精性脂肪性肝病(NAFLD)的死亡风险。
Medicine (Baltimore). 2018 Mar;97(13):e0214. doi: 10.1097/MD.0000000000010214.
7
A randomised, double-blind, placebo-controlled phase 1 study of the safety, tolerability and pharmacodynamics of volixibat in overweight and obese but otherwise healthy adults: implications for treatment of non-alcoholic steatohepatitis.一项关于volixibat在超重和肥胖但其他方面健康的成年人中的安全性、耐受性和药效学的随机、双盲、安慰剂对照1期研究:对非酒精性脂肪性肝炎治疗的意义
BMC Pharmacol Toxicol. 2018 Mar 16;19(1):10. doi: 10.1186/s40360-018-0200-y.
8
NGM282 for treatment of non-alcoholic steatohepatitis: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial.NGM282 治疗非酒精性脂肪性肝炎:一项多中心、随机、双盲、安慰剂对照的 2 期临床试验。
Lancet. 2018 Mar 24;391(10126):1174-1185. doi: 10.1016/S0140-6736(18)30474-4. Epub 2018 Mar 5.
9
Non-alcoholic steatohepatitis pathogenesis: sublethal hepatocyte injury as a driver of liver inflammation.非酒精性脂肪性肝炎发病机制:亚致死性肝细胞损伤作为肝脏炎症的驱动因素。
Gut. 2018 May;67(5):963-972. doi: 10.1136/gutjnl-2017-315691. Epub 2018 Jan 24.
10
Current and future therapeutic regimens for nonalcoholic fatty liver disease and nonalcoholic steatohepatitis.非酒精性脂肪性肝病和非酒精性脂肪性肝炎的当前和未来治疗方案。
Hepatology. 2018 Jul;68(1):361-371. doi: 10.1002/hep.29724.

非酒精性脂肪性肝炎晚期纤维化管理的进展与挑战

Advances and challenges in the management of advanced fibrosis in nonalcoholic steatohepatitis.

作者信息

Sayiner Mehmet, Lam Brian, Golabi Pegah, Younossi Zobair M

机构信息

Department of Medicine, Inova Fairfax Hospital, Falls Church, VA.

Betty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA.

出版信息

Therap Adv Gastroenterol. 2018 Nov 15;11:1756284818811508. doi: 10.1177/1756284818811508. eCollection 2018.

DOI:10.1177/1756284818811508
PMID:30479664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6243399/
Abstract

Nonalcoholic fatty liver disease (NAFLD) is rapidly becoming the most common type of chronic liver disease worldwide. From the spectrum of NAFLD, it is nonalcoholic steatohepatitis (NASH) that predominantly predisposes patients to higher risk for development of cirrhosis and hepatocellular carcinoma. There is growing evidence that the risk of progression to cirrhosis and hepatocellular carcinoma is not uniform among all patients with NASH. In fact, NASH patients with increasing numbers of metabolic diseases such as diabetes, hypertension, visceral obesity and dyslipidemia are at a higher risk of mortality. Additionally, patients with higher stage of liver fibrosis are also at increased risk of mortality. In this context, NASH patients with fibrosis are in the most urgent need of treatment. Also, the first line of treatment for NASH is lifestyle modification with diet and exercise. Nevertheless, the efficacy of lifestyle modification is quite limited. Additionally, vitamin E and pioglitazone may be considered for subset of patients with NASH. There are various medications targeting one or more steps in the pathogenesis of NASH being developed. These drug regimens either alone or in combination, may provide potential treatment option for patients with NASH.

摘要

非酒精性脂肪性肝病(NAFLD)正迅速成为全球最常见的慢性肝病类型。在NAFLD的范围内,主要是非酒精性脂肪性肝炎(NASH)使患者更容易发展为肝硬化和肝细胞癌。越来越多的证据表明,并非所有NASH患者进展为肝硬化和肝细胞癌的风险都是一致的。事实上,患有越来越多代谢性疾病(如糖尿病、高血压、内脏肥胖和血脂异常)的NASH患者死亡风险更高。此外,肝纤维化程度较高的患者死亡风险也会增加。在这种情况下,有纤维化的NASH患者最急需治疗。而且,NASH的一线治疗是通过饮食和运动进行生活方式的改变。然而,生活方式改变的疗效相当有限。此外,对于一部分NASH患者,可以考虑使用维生素E和吡格列酮。目前正在研发针对NASH发病机制中一个或多个步骤的各种药物。这些药物方案单独使用或联合使用,可能为NASH患者提供潜在的治疗选择。