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Effect of colesevelam on liver fat quantified by magnetic resonance in nonalcoholic steatohepatitis: a randomized controlled trial.考来烯胺对非酒精性脂肪性肝炎肝脏脂肪含量的磁共振定量影响:一项随机对照试验。
Hepatology. 2012 Sep;56(3):922-32. doi: 10.1002/hep.25731. Epub 2012 Jul 2.
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The impact of bariatric surgery on nonalcoholic steatohepatitis.减重手术对非酒精性脂肪性肝炎的影响。
Semin Liver Dis. 2012 Feb;32(1):80-91. doi: 10.1055/s-0032-1306428. Epub 2012 Mar 13.
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Cellular and molecular mechanisms of metformin: an overview.二甲双胍的细胞和分子机制:概述。
Clin Sci (Lond). 2012 Mar;122(6):253-70. doi: 10.1042/CS20110386.
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Meta-analysis: pioglitazone improves liver histology and fibrosis in patients with non-alcoholic steatohepatitis.荟萃分析:吡格列酮可改善非酒精性脂肪性肝炎患者的肝脏组织学和纤维化。
Aliment Pharmacol Ther. 2012 Jan;35(1):66-75. doi: 10.1111/j.1365-2036.2011.04912.x. Epub 2011 Nov 4.
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Vitamin E and the risk of prostate cancer: the Selenium and Vitamin E Cancer Prevention Trial (SELECT).维生素 E 与前列腺癌风险:硒和维生素 E 癌症预防试验(SELECT)。
JAMA. 2011 Oct 12;306(14):1549-56. doi: 10.1001/jama.2011.1437.
6
Rosiglitazone versus rosiglitazone and metformin versus rosiglitazone and losartan in the treatment of nonalcoholic steatohepatitis in humans: a 12-month randomized, prospective, open- label trial.罗格列酮与罗格列酮加二甲双胍和罗格列酮加氯沙坦治疗非酒精性脂肪性肝炎的随机、前瞻性、开放标签 12 个月试验。
Hepatology. 2011 Nov;54(5):1631-9. doi: 10.1002/hep.24558.
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Pentoxifylline improves nonalcoholic steatohepatitis: a randomized placebo-controlled trial.己酮可可碱改善非酒精性脂肪性肝炎:一项随机安慰剂对照试验。
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8
Glucagon-like peptide-1 receptor activation stimulates hepatic lipid oxidation and restores hepatic signalling alteration induced by a high-fat diet in nonalcoholic steatohepatitis.胰高血糖素样肽-1 受体激动剂可刺激肝脏脂质氧化,并恢复高脂肪饮食诱导的非酒精性脂肪性肝炎中的肝信号转导改变。
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Frequency and outcomes of liver transplantation for nonalcoholic steatohepatitis in the United States.美国非酒精性脂肪性肝炎患者进行肝移植的频率和结果。
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10
Pentoxifylline for the treatment of non-alcoholic steatohepatitis: a randomized controlled trial.己酮可可碱治疗非酒精性脂肪性肝炎:一项随机对照试验。
Ann Hepatol. 2011 Jul-Sep;10(3):277-86.

非酒精性脂肪性肝病和脂肪性肝炎的管理

Management of Non-alcoholic Fatty Liver Disease and Steatohepatitis.

作者信息

Le Thuy-Anh, Loomba Rohit

机构信息

Division of Gastroenterology, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.

Division of Epidemiology, Department of Family and Preventive Medicine, University of California, San Diego, La Jolla, CA 92093, USA.

出版信息

J Clin Exp Hepatol. 2012 Jun;2(2):156-73. doi: 10.1016/S0973-6883(12)60104-2. Epub 2012 Jul 21.

DOI:10.1016/S0973-6883(12)60104-2
PMID:25755424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3940181/
Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of abnormal liver enzymes and chronic liver disease in the US with expected rise in incidence paralleling the epidemic of obesity. A subset of patients with NAFLD have the progressive form of NAFLD that is termed non-alcoholic steatohepatitis (NASH), which is characterized by specific features on liver histology including hepatocellular ballooning degeneration, lobular inflammation, and zone-3 steatosis with or without peri-sinusoidal fibrosis. Non-alcoholic steatohepatitis can progress to cirrhosis and result in liver-related death. Insulin resistance is commonly seen in patients with NASH and often co-exists with other features of the metabolic syndrome including hypertension, hyperlipidemia, and obesity. Although weight loss through lifestyle modifications including dietary changes and increased physical exercise remains the backbone of management of NASH, it has proved challenging for patients to achieve and maintain weight loss goals. Thus, it is often necessary to couple lifestyle changes with another pharmacologic treatment for NASH. Insulin sensitizers including the biguanides (metformin), thiazolidinediones (pioglitazone and rosiglitazone), and glucagon-like peptide-1 receptor agonists (exenatide) are large groups of medications that have been studied for the treatment of NASH. Other agents with anti-inflammatory, anti-apoptotic, or anti-fibrotic properties which have been studied in NASH include vitamin E, pentoxifylline, betaine, and ursodeoxycholic acid. This review will provide a detailed summary on the clinical data behind the full spectrum of treatments that exist for NASH and suggest management recommendations.

摘要

非酒精性脂肪性肝病(NAFLD)是美国肝酶异常和慢性肝病的最常见原因,预计其发病率的上升将与肥胖流行趋势同步。一部分NAFLD患者患有进展性NAFLD,即非酒精性脂肪性肝炎(NASH),其特征是肝脏组织学具有特定特征,包括肝细胞气球样变性、小叶炎症以及3区脂肪变性,伴有或不伴有窦周纤维化。非酒精性脂肪性肝炎可进展为肝硬化并导致肝脏相关死亡。胰岛素抵抗在NASH患者中很常见,且常与代谢综合征的其他特征并存,包括高血压、高脂血症和肥胖。尽管通过包括饮食改变和增加体育锻炼在内的生活方式调整来减轻体重仍然是NASH管理的核心,但事实证明,患者要实现并维持体重减轻目标具有挑战性。因此,通常有必要将生活方式改变与另一种NASH药物治疗相结合。胰岛素增敏剂包括双胍类(二甲双胍)、噻唑烷二酮类(吡格列酮和罗格列酮)以及胰高血糖素样肽-1受体激动剂(艾塞那肽),这些都是已被研究用于治疗NASH的大类药物。在NASH中已被研究的其他具有抗炎、抗凋亡或抗纤维化特性的药物包括维生素E、己酮可可碱、甜菜碱和熊去氧胆酸。本综述将详细总结NASH现有各种治疗方法背后的临床数据,并提出管理建议。