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CONTROL: A randomized phase 2 study of obeticholic acid and atorvastatin on lipoproteins in nonalcoholic steatohepatitis patients.对照:奥贝胆酸和阿托伐他汀在非酒精性脂肪性肝炎患者脂蛋白中的随机 2 期研究。
Liver Int. 2019 Nov;39(11):2082-2093. doi: 10.1111/liv.14209. Epub 2019 Sep 10.
2
Obeticholic Acid: An Update of Its Pharmacological Activities in Liver Disorders.奥贝胆酸:其在肝脏疾病中药理活性的最新进展
Handb Exp Pharmacol. 2019;256:283-295. doi: 10.1007/164_2019_227.
3
Prevalence of Alcoholic Fatty Liver Disease Among Adults in the United States, 2001-2016.美国成年人酒精性脂肪肝疾病的患病率,2001-2016 年。
JAMA. 2019 May 7;321(17):1723-1725. doi: 10.1001/jama.2019.2276.
4
The Natural History of Advanced Fibrosis Due to Nonalcoholic Steatohepatitis: Data From the Simtuzumab Trials.非酒精性脂肪性肝炎所致晚期纤维化的自然史:来自 Simtuzumab 试验的数据。
Hepatology. 2019 Dec;70(6):1913-1927. doi: 10.1002/hep.30664. Epub 2019 May 28.
5
Glucocorticosteroids for people with alcoholic hepatitis.用于酒精性肝炎患者的糖皮质激素。
Cochrane Database Syst Rev. 2019 Apr 9;4(4):CD001511. doi: 10.1002/14651858.CD001511.pub4.
6
NGM282 Improves Liver Fibrosis and Histology in 12 Weeks in Patients With Nonalcoholic Steatohepatitis.NGM282 在 12 周内改善非酒精性脂肪性肝炎患者的肝纤维化和组织学。
Hepatology. 2020 Apr;71(4):1198-1212. doi: 10.1002/hep.30590. Epub 2019 Apr 10.
7
Efficacy of Granulocyte Colony-stimulating Factor in the Management of Steroid-Nonresponsive Severe Alcoholic Hepatitis: A Double-Blind Randomized Controlled Trial.粒细胞集落刺激因子治疗类固醇无应答性重症酒精性肝炎的疗效:一项双盲随机对照试验。
Hepatology. 2019 Sep;70(3):802-811. doi: 10.1002/hep.30516. Epub 2019 Mar 25.
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The Nonsteroidal Farnesoid X Receptor Agonist Cilofexor (GS-9674) Improves Markers of Cholestasis and Liver Injury in Patients With Primary Sclerosing Cholangitis.非甾体法尼醇 X 受体激动剂西利福昔(GS-9674)可改善原发性硬化性胆管炎患者的胆汁淤积和肝损伤标志物。
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非酒精性脂肪性肝病和酒精性肝病从基础科学到临床试验:与行业的合作

Basic science to clinical trials in non-alcoholic fatty liver disease and alcohol-related liver disease: collaboration with industry.

作者信息

Asgharpour Amon, Dinani Amreen, Friedman Scott L

机构信息

Division of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Transl Gastroenterol Hepatol. 2021 Jan 5;6:5. doi: 10.21037/tgh.2020.01.04. eCollection 2021.

DOI:10.21037/tgh.2020.01.04
PMID:33409399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7724182/
Abstract

Non-alcoholic fatty liver disease (NAFLD) and alcohol-related liver disease (ALD) are highly prevalent forms of chronic liver diseases globally, associated with rising all-cause morbidity and mortality. While distinct diseases, NAFLD and ALD share several similarities; both can result in fatty liver disease, steatohepatitis, associated hepatic fibrosis and cirrhosis-related complications, including hepatocellular carcinoma (HCC). Our understanding of the pathophysiology and manifestations of these diseases has advanced significantly, which has established a new foundation to identify therapeutic targets and test new treatments. This review underscores emerging pathogenic pathways that establish a template for target identification and clinical trials. Success is critically dependent upon productive interactions between academic investigators and industry to address unmet therapeutic needs in NAFLD and ALD.

摘要

非酒精性脂肪性肝病(NAFLD)和酒精性肝病(ALD)是全球范围内高度流行的慢性肝病形式,与全因发病率和死亡率的上升相关。虽然是不同的疾病,但NAFLD和ALD有几个相似之处;两者都可导致脂肪性肝病、脂肪性肝炎、相关的肝纤维化和肝硬化相关并发症,包括肝细胞癌(HCC)。我们对这些疾病的病理生理学和表现的理解有了显著进展,这为确定治疗靶点和测试新疗法奠定了新基础。本综述强调了新兴的致病途径,这些途径为靶点识别和临床试验建立了模板。成功与否关键取决于学术研究人员和产业界之间富有成效的互动,以满足NAFLD和ALD中未满足的治疗需求。