• 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

非酒精性脂肪性肝炎与代谢综合征

Nonalcoholic steatohepatitis and the metabolic syndrome.

作者信息

Neuschwander-Tetri Brent A

机构信息

Department of Internal Medicine, Division of Gastroenterology and Hepatology, Saint Louis University Liver Center, St. Louis, Missouri 63110, USA.

出版信息

Am J Med Sci. 2005 Dec;330(6):326-35. doi: 10.1097/00000441-200512000-00011.

DOI:10.1097/00000441-200512000-00011
PMID:16355018
Abstract

Relatively recently, the liver has been recognized as a major target of injury in patients with insulin resistance or the metabolic syndrome. Insulin resistance is associated with fat accumulation in the liver, a condition called nonalcoholic fatty liver disease (NAFLD). Excess fat in the liver is not a benign condition. Some patients with NAFLD develop necroinflammatory changes in the liver called nonalcoholic steatohepatitis (NASH) and a fraction of those will develop cirrhosis. About 20% all adults have NAFLD and 2% to 3% of adults have NASH. Approximately 20% of patients with NASH are at risk for developing cirrhosis and subsequently dying from end-stage liver disease. The diagnosis of NASH requires a high index of suspicion, especially in obese patients over the age of 45 years who have diabetes, because these are the patients at greatest risk for developing cirrhosis. Treatment focuses on addressing the underlying insulin resistance with increased exercise and weight reduction.

摘要

直到最近,肝脏才被认为是胰岛素抵抗或代谢综合征患者的主要损伤靶点。胰岛素抵抗与肝脏脂肪堆积有关,这种情况被称为非酒精性脂肪性肝病(NAFLD)。肝脏中的脂肪过多并非良性状况。一些NAFLD患者会出现肝脏坏死性炎症变化,即非酒精性脂肪性肝炎(NASH),其中一部分患者会发展为肝硬化。所有成年人中约20%患有NAFLD,2%至3%的成年人患有NASH。大约20%的NASH患者有发展为肝硬化并随后死于终末期肝病的风险。NASH的诊断需要高度怀疑,尤其是在45岁以上患有糖尿病的肥胖患者中,因为这些患者发生肝硬化的风险最高。治疗重点是通过增加运动和减轻体重来解决潜在的胰岛素抵抗问题。

相似文献

1
Nonalcoholic steatohepatitis and the metabolic syndrome.非酒精性脂肪性肝炎与代谢综合征
Am J Med Sci. 2005 Dec;330(6):326-35. doi: 10.1097/00000441-200512000-00011.
2
Nonalcoholic steatohepatitis and the metabolic syndrome.非酒精性脂肪性肝炎与代谢综合征
Metab Syndr Relat Disord. 2008 Mar;6(1):1-7. doi: 10.1089/met.2007.0026.
3
[Nonalcoholic steatohepatitis: diagnosis, pathogenesis, treatment and prognosis].[非酒精性脂肪性肝炎:诊断、发病机制、治疗与预后]
Ned Tijdschr Geneeskd. 2005 Feb 5;149(6):289-94.
4
From nonalcoholic fatty liver to nonalcoholic steatohepatitis and cirrhosis in HIV-infected patients: diagnosis and management.从非酒精性脂肪肝到 HIV 感染患者的非酒精性脂肪性肝炎和肝硬化:诊断与管理。
Curr Opin Infect Dis. 2012 Feb;25(1):10-6. doi: 10.1097/QCO.0b013e32834ef599.
5
Prevalence of Nonalcoholic Steatohepatitis-Associated Cirrhosis in the United States: An Analysis of National Health and Nutrition Examination Survey Data.美国非酒精性脂肪性肝炎相关肝硬化的患病率:基于国家健康与营养检查调查数据的分析
Am J Gastroenterol. 2017 Apr;112(4):581-587. doi: 10.1038/ajg.2017.5. Epub 2017 Feb 14.
6
Nonalcoholic fatty liver disease: from steatosis to cirrhosis.非酒精性脂肪性肝病:从脂肪变性到肝硬化
Hepatology. 2006 Feb;43(2 Suppl 1):S99-S112. doi: 10.1002/hep.20973.
7
Evolving pathophysiologic concepts in nonalcoholic steatohepatitis.非酒精性脂肪性肝炎不断演变的病理生理概念。
Curr Gastroenterol Rep. 2002 Feb;4(1):31-6. doi: 10.1007/s11894-002-0035-x.
8
Nonalcoholic fatty liver disease.非酒精性脂肪性肝病
Rev Gastroenterol Disord. 2002;2(1):11-9.
9
[Nonalcoholic steatohepatitis: a review].[非酒精性脂肪性肝炎:综述]
Rev Med Liege. 2003 Mar;58(3):147-54.
10
Nutritional modulation of nonalcoholic fatty liver disease and insulin resistance: human data.营养调控非酒精性脂肪性肝病和胰岛素抵抗:人体数据。
Curr Opin Clin Nutr Metab Care. 2010 Nov;13(6):709-14. doi: 10.1097/MCO.0b013e32833f4b34.

引用本文的文献

1
Crosstalk between Epigenetics and Autophagy in Metabolic Dysfunction-Associated Steatotic Liver Disease.代谢功能障碍相关脂肪性肝病中表观遗传学与自噬之间的相互作用
J Obes Metab Syndr. 2025 Jul 30;34(3):253-267. doi: 10.7570/jomes24041. Epub 2025 Jun 16.
2
Impact of Sodium-Glucose Co-Transporter Type-2 Inhibitors on Alanine Aminotransferase Levels in Type-2 Diabetes Patients Having Features of Nonalcoholic Fatty Liver Disease: A Retrospective Cohort Study in Pakistan.2型钠-葡萄糖协同转运蛋白抑制剂对具有非酒精性脂肪性肝病特征的2型糖尿病患者丙氨酸氨基转移酶水平的影响:巴基斯坦的一项回顾性队列研究
Pak J Med Sci. 2024 Dec;40(11):2681-2688. doi: 10.12669/pjms.40.11.8900.
3
"Adjusting internal organs and dredging channelon" electroacupuncture glycolipid metabolism disorders in NAFLD mice by mediating the AMPK/ACC signaling pathway.
“调脏腑、通经络”电针通过介导AMPK/ACC信号通路改善非酒精性脂肪性肝病小鼠糖脂代谢紊乱
Diabetol Metab Syndr. 2024 Jul 25;16(1):173. doi: 10.1186/s13098-024-01416-7.
4
Comparison of the role of alcohol consumption and qualitative abdominal fat on NAFLD and MAFLD in males and females.比较男性和女性中饮酒和定性腹部脂肪对非酒精性脂肪性肝病和代谢相关脂肪性肝病的作用。
Sci Rep. 2022 Sep 26;12(1):16048. doi: 10.1038/s41598-022-20124-8.
5
Just Drink a Glass of Water? Effects of Bicarbonate-Sulfate-Calcium-Magnesium Water on the Gut-Liver Axis.只喝一杯水?碳酸氢盐-硫酸盐-钙-镁水对肠-肝轴的影响。
Front Pharmacol. 2022 Jun 28;13:869446. doi: 10.3389/fphar.2022.869446. eCollection 2022.
6
Early detection of metabolic changes in drug-induced steatosis using metabolomics approaches.利用代谢组学方法早期检测药物性脂肪变性中的代谢变化。
RSC Adv. 2020 Nov 11;10(67):41047-41057. doi: 10.1039/d0ra06577c. eCollection 2020 Nov 9.
7
Alterations in Lysosome Homeostasis in Lipid-Related Disorders: Impact on Metabolic Tissues and Immune Cells.脂质相关疾病中溶酶体稳态的改变:对代谢组织和免疫细胞的影响
Front Cell Dev Biol. 2021 Dec 10;9:790568. doi: 10.3389/fcell.2021.790568. eCollection 2021.
8
Hepatic Response of Magnesium-Restricted Wild Type Mice.镁限制野生型小鼠的肝脏反应。
Metabolites. 2021 Nov 6;11(11):762. doi: 10.3390/metabo11110762.
9
Disturbances in Cholesterol Homeostasis and Non-alcoholic Fatty Liver Diseases.胆固醇稳态紊乱与非酒精性脂肪性肝病
Front Med (Lausanne). 2020 Sep 2;7:467. doi: 10.3389/fmed.2020.00467. eCollection 2020.
10
Novel Insights into the Pathogenesis and Management of the Metabolic Syndrome.对代谢综合征发病机制与管理的新见解
Pediatr Gastroenterol Hepatol Nutr. 2020 May;23(3):189-230. doi: 10.5223/pghn.2020.23.3.189. Epub 2020 May 8.