• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

非酒精性脂肪性肝病的发病机制与治疗进展:更新版。

Non-alcoholic fatty liver disease from pathogenesis to management: an update.

机构信息

Gradenigo Hospital, Turin, Italy.

出版信息

Obes Rev. 2010 Jun;11(6):430-45. doi: 10.1111/j.1467-789X.2009.00657.x. Epub 2009 Oct 21.

DOI:10.1111/j.1467-789X.2009.00657.x
PMID:19845871
Abstract

Non-alcoholic fatty liver disease (NAFLD), the most common chronic liver disease in the Western world, is tightly associated with obesity and metabolic syndrome. NAFLD entails an increased cardiometabolic and liver-related risk, the latter regarding almost exclusively non-alcoholic steatohepatitis (NASH), the progressive form of NAFLD. Pathogenetic models encompass altered hepatic lipid partitioning and adipokine action, increased oxidative stress, free fatty acid lipotoxicity. On this basis, lifestyle-, drug- or surgically induced weight loss, insulin sensitizers, antioxidants, lipid-lowering drugs have been evaluated in NAFLD/NASH. Most trials are small, of short duration, nonrandomized, without histological end points, thus limiting assessment of long-term safety and efficacy of proposed treatments. All NAFLD patients should be evaluated for their metabolic, cardiovascular and liver-related risk. Liver biopsy remains the gold standard for staging NAFLD, but non-invasive methods are under intense development. Weight loss through lifestyle intervention is the initial approach, because of established efficacy on NAFLD-associated cardiometabolic abnormalities, and to emerging benefits on necroinflammation and overall disease activity in NASH. Bariatric surgery warrants further evaluation before it can be routinely considered in morbidly obese NASH. Larger- and longer-duration randomized trials assessing safety and benefits of drugs on patient-oriented outcomes are needed before pharmacological treatment can be routinely recommended for NASH.

摘要

非酒精性脂肪性肝病(NAFLD)是西方国家最常见的慢性肝病,与肥胖和代谢综合征密切相关。NAFLD 会增加心血管代谢和肝脏相关的风险,后者几乎仅涉及非酒精性脂肪性肝炎(NASH),即 NAFLD 的进展形式。发病机制模型包括肝脂质分布改变和脂肪因子作用、氧化应激增加、游离脂肪酸脂肪毒性。在此基础上,已经在 NAFLD/NASH 中评估了生活方式、药物或手术引起的体重减轻、胰岛素增敏剂、抗氧化剂、降脂药物。大多数试验规模较小、持续时间短、非随机、没有组织学终点,因此限制了对拟议治疗的长期安全性和疗效的评估。所有 NAFLD 患者都应评估其代谢、心血管和肝脏相关风险。肝活检仍然是 NAFLD 分期的金标准,但非侵入性方法正在深入开发中。通过生活方式干预减轻体重是初始方法,因为它对与 NAFLD 相关的代谢异常具有既定的疗效,并且对 NASH 的坏死性炎症和整体疾病活动也有新的益处。减肥手术需要进一步评估,然后才能在病态肥胖的 NASH 患者中常规考虑。在可以常规推荐药物治疗 NASH 之前,需要进行更大规模和更长时间的随机试验,以评估药物对患者为中心的结局的安全性和益处。

相似文献

1
Non-alcoholic fatty liver disease from pathogenesis to management: an update.非酒精性脂肪性肝病的发病机制与治疗进展:更新版。
Obes Rev. 2010 Jun;11(6):430-45. doi: 10.1111/j.1467-789X.2009.00657.x. Epub 2009 Oct 21.
2
[Non-alcoholic fatty liver disease--new view].[非酒精性脂肪性肝病——新视角]
Pol Merkur Lekarski. 2008 Jun;24(144):568-71.
3
Review article: current management of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis.综述文章:非酒精性脂肪性肝病和非酒精性脂肪性肝炎的当前管理
Aliment Pharmacol Ther. 2008 Jul;28(1):2-12. doi: 10.1111/j.1365-2036.2008.03710.x. Epub 2008 Apr 11.
4
Non-alcoholic steatohepatitis in children.儿童非酒精性脂肪性肝炎
Pediatr Transplant. 2004 Dec;8(6):613-8. doi: 10.1111/j.1399-3046.2004.00241.x.
5
Surgical treatment of non-alcoholic steatohepatitis and non-alcoholic fatty liver disease.非酒精性脂肪性肝炎和非酒精性脂肪性肝病的外科治疗。
Dig Dis. 2010;28(1):274-9. doi: 10.1159/000282102. Epub 2010 May 7.
6
Weight loss: cornerstone in the treatment of non-alcoholic fatty liver disease.体重减轻:非酒精性脂肪性肝病治疗的基石。
Minerva Gastroenterol Dietol. 2010 Jun;56(2):159-67.
7
Update on non-alcoholic fatty liver disease in children.儿童非酒精性脂肪性肝病的最新进展。
Clin Nutr. 2007 Aug;26(4):409-15. doi: 10.1016/j.clnu.2007.02.002. Epub 2007 Apr 20.
8
[Nonalcoholic steatohepatitis--a "new" hepatic disease].非酒精性脂肪性肝炎——一种“新型”肝脏疾病
Ugeskr Laeger. 2003 Mar 10;165(11):1115-8.
9
Effects of weight loss on nonalcoholic fatty liver disease.体重减轻对非酒精性脂肪性肝病的影响。
Semin Liver Dis. 2008 Nov;28(4):427-33. doi: 10.1055/s-0028-1091986. Epub 2008 Oct 27.
10
[Treatment of non-alcoholic fatty liver disease].[非酒精性脂肪性肝病的治疗]
Ned Tijdschr Geneeskd. 2011;155:A3181.

引用本文的文献

1
Targeting cAMP signaling and phosphodiesterase 4 for liver disease treatment.以环磷酸腺苷(cAMP)信号传导和磷酸二酯酶4为靶点治疗肝脏疾病。
Med Chem Res. 2024 Aug;33(8):1339-1353. doi: 10.1007/s00044-024-03267-3. Epub 2024 Jun 26.
2
Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD.靶向代谢组学揭示了非酒精性脂肪性肝病患儿肠道中进入血液循环的生物活性炎症介质。
NPJ Biofilms Microbiomes. 2025 Jul 1;11(1):119. doi: 10.1038/s41522-025-00706-w.
3
Correlation between magnetic resonance imaging proton density fat fraction (MRI-PDFF) and liver biopsy to assess hepatic steatosis in obesity.
磁共振成像质子密度脂肪分数(MRI-PDFF)与肝活检评估肥胖患者肝脂肪变性的相关性。
Sci Rep. 2024 Mar 22;14(1):6895. doi: 10.1038/s41598-024-57324-3.
4
Loss of flavin-containing monooxygenase 3 modulates dioxin-like polychlorinated biphenyl 126-induced oxidative stress and hepatotoxicity.黄素单加氧酶 3 的缺失调节二恶英样多氯联苯 126 诱导的氧化应激和肝毒性。
Environ Res. 2024 Jun 1;250:118492. doi: 10.1016/j.envres.2024.118492. Epub 2024 Feb 17.
5
Identification of Myocardial Insulin Resistance by Using Liver Tests: A Simple Approach for Clinical Practice.利用肝脏检查来识别心肌胰岛素抵抗:一种简单的临床实践方法。
Int J Mol Sci. 2022 Aug 7;23(15):8783. doi: 10.3390/ijms23158783.
6
Gut Microbiota-A Future Therapeutic Target for People with Non-Alcoholic Fatty Liver Disease: A Systematic Review.肠道微生物群——非酒精性脂肪性肝病患者的未来治疗靶点:系统评价。
Int J Mol Sci. 2022 Jul 27;23(15):8307. doi: 10.3390/ijms23158307.
7
Platelet-Activating Factor Promotes the Development of Non-Alcoholic Fatty Liver Disease.血小板活化因子促进非酒精性脂肪性肝病的发展。
Diabetes Metab Syndr Obes. 2022 Jul 8;15:2003-2030. doi: 10.2147/DMSO.S367483. eCollection 2022.
8
The caffeic acid moiety plays an essential role in attenuating lipid accumulation by chlorogenic acid and its analogues.咖啡酸部分在绿原酸及其类似物减轻脂质积累过程中起着至关重要的作用。
RSC Adv. 2019 Apr 17;9(22):12247-12254. doi: 10.1039/c8ra09395d.
9
High alcohol-producing causes fatty liver disease through 2,3-butanediol fermentation pathway .高醇产生菌通过 2,3-丁二醇发酵途径引起脂肪肝疾病。
Gut Microbes. 2021 Jan-Dec;13(1):1979883. doi: 10.1080/19490976.2021.1979883.
10
Hepatoprotective Effects of a Novel Trihoney against Nonalcoholic Fatty Liver Disease: A Comparative Study with Atorvastatin.新型三花蜜对非酒精性脂肪肝的保肝作用:与阿托伐他汀的对比研究。
ScientificWorldJournal. 2020 Oct 9;2020:4503253. doi: 10.1155/2020/4503253. eCollection 2020.