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非酒精性脂肪性肝炎

Nonalcoholic Steatohepatitis.

作者信息

Mulhall Brian P, Younossi Zobair M

机构信息

Center for Liver Diseases, Department of Medicine, Inova Fairfax Hospital, 3300 Gallows Road, Falls Church, VA 22042, USA.

出版信息

Curr Treat Options Gastroenterol. 2004 Dec;7(6):423-430. doi: 10.1007/s11938-004-0001-9.

DOI:10.1007/s11938-004-0001-9
PMID:15527708
Abstract

Nonalcoholic steatohepatitis (NASH) is an important medical condition and there is great public health concern related to its increasing incidence and potential implications for the development of end-stage liver disease. NASH represents a progression beyond simple lipid deposition in the liver parenchyma, requiring histologic evidence for hepatocyte injury such as ballooning degeneration, Mallory bodies, and/or pericellular fibrosis that can potentially lead to progressive liver injury and eventually cirrhosis. It is believed that several insults contribute to the evolution of hepatic injury such as insulin dysregulation, lipid deposition, oxidative free radicals, and lipid perioxidation. Initial treatment protocols for NASH focus on various aspects of injury in an attempt to control insulin imbalances, improve lipid regulation, reduce free radicals, and ameliorate the inflammatory process. No therapy is conclusively beneficial in all individuals, but preliminary data suggest several approaches that hold promise.

摘要

非酒精性脂肪性肝炎(NASH)是一种重要的医学病症,其发病率不断上升以及对终末期肝病发展的潜在影响引发了极大的公共卫生关注。NASH代表了肝脏实质内单纯脂质沉积之外的一种进展,需要有肝细胞损伤的组织学证据,如气球样变性、马洛里小体和/或细胞周围纤维化,这些可能导致进行性肝损伤并最终发展为肝硬化。据信,多种损伤因素促成了肝损伤的演变,如胰岛素调节异常、脂质沉积、氧化自由基和脂质过氧化。NASH的初始治疗方案侧重于损伤的各个方面,试图控制胰岛素失衡、改善脂质调节、减少自由基并减轻炎症过程。没有一种疗法对所有个体都有确凿的益处,但初步数据表明有几种方法具有前景。

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引用本文的文献

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A novel diagnostic biomarker panel for obesity-related nonalcoholic steatohepatitis (NASH).一种用于肥胖相关非酒精性脂肪性肝炎(NASH)的新型诊断生物标志物组合。
Obes Surg. 2008 Nov;18(11):1430-7. doi: 10.1007/s11695-008-9506-y. Epub 2008 May 24.

本文引用的文献

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Nonalcoholic fatty liver disease: Improvement in liver histological analysis with weight loss.非酒精性脂肪性肝病:体重减轻可改善肝脏组织学分析结果
Hepatology. 2004 Jun;39(6):1647-54. doi: 10.1002/hep.20251.
2
Effect of pioglitazone on biochemical indices of non-alcoholic fatty liver disease in upper body obesity.吡格列酮对上半身肥胖的非酒精性脂肪性肝病生化指标的影响。
Clin Gastroenterol Hepatol. 2003 Sep;1(5):384-7. doi: 10.1053/s1542-3565(03)00198-8.
3
Nonalcoholic fatty liver disease in patients with type 2 diabetes.2型糖尿病患者的非酒精性脂肪性肝病
Clin Gastroenterol Hepatol. 2004 Mar;2(3):262-5. doi: 10.1016/s1542-3565(04)00014-x.
4
Ursodeoxycholic acid for treatment of nonalcoholic steatohepatitis: results of a randomized trial.熊去氧胆酸治疗非酒精性脂肪性肝炎:一项随机试验的结果
Hepatology. 2004 Mar;39(3):770-8. doi: 10.1002/hep.20092.
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Pathologic features associated with fibrosis in nonalcoholic fatty liver disease.非酒精性脂肪性肝病中与纤维化相关的病理特征。
Hum Pathol. 2004 Feb;35(2):196-9. doi: 10.1016/j.humpath.2003.09.018.
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A pilot study of pioglitazone treatment for nonalcoholic steatohepatitis.吡格列酮治疗非酒精性脂肪性肝炎的一项初步研究。
Hepatology. 2004 Jan;39(1):188-96. doi: 10.1002/hep.20012.
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Combined treatment with ursodeoxycholic acid and pioglitazone in a patient with NASH associated with type 2 diabetes and psoriasis.
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Effects of surgical treatment of the metabolic syndrome on liver fibrosis and cirrhosis.
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Vitamin E and vitamin C treatment improves fibrosis in patients with nonalcoholic steatohepatitis.维生素E和维生素C治疗可改善非酒精性脂肪性肝炎患者的纤维化。
Am J Gastroenterol. 2003 Nov;98(11):2485-90. doi: 10.1111/j.1572-0241.2003.08699.x.
10
Is weight reduction an effective therapy for nonalcoholic fatty liver? A systematic review.减轻体重是非酒精性脂肪肝的有效治疗方法吗?一项系统评价。
Am J Med. 2003 Nov;115(7):554-9. doi: 10.1016/s0002-9343(03)00449-2.