Nonalcoholic steatohepatitis: recent advances from experimental models to clinical management

被引:78
作者
Portincasa, P [1 ]
Grattagliano, I [1 ]
Palmieri, VO [1 ]
Palasciano, G [1 ]
机构
[1] Univ Bari, Sch Med, Dept Internal Med & Publ Med, Policlin, I-70124 Bari, Italy
关键词
antioxidants; breath test; choline-deficient diet; insulin resistance; fatty liver; microsomes; mitochondria; nonalcoholic steatohepatitis; oxidative stress; peroxisomes;
D O I
10.1016/j.clinbiochem.2004.10.014
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
A condition defined as nonalcoholic fatty liver disease (NAFLD) is frequently found in humans. Deemed as a benign condition until recently, more emphasis is now put on the potential harmful evolution of the inflammatory form, that is, nonalcoholic steatohepatitis (NASH), toward end-stage liver disease. This review highlights the major morphologic and pathophysiological features of NASH. The link between experimental biochemical findings in animal models and clinical and therapeutic approaches in humans is discussed. Once all the other causes of persistent elevation of serum transaminase levels have been excluded, the diagnosis of NASH can be only confirmed by liver histology. Other noninvasive diagnostic tools, however, are being investigated to assess specific subcellular functions and to allow the follow-up of patients at higher risk for major liver dysfunction. A better understanding of various pathogenic aspects of NASH will help in identifying potential therapeutic approaches in these patients. (C) 2004 The Canadian Society of Clinical Chemists. All rights reserved.
引用
收藏
页码:203 / 217
页数:15
相关论文
共 186 条
[1]  
Abdelmalek MF, 2001, AM J GASTROENTEROL, V96, P2711
[2]   Portal fibrosis and hepatic steatosis in morbidly obese subjects: A spectrum of nonalcoholic fatty liver disease [J].
Abrams, GA ;
Kunde, SS ;
Lazenby, AJ ;
Clements, RH .
HEPATOLOGY, 2004, 40 (02) :475-483
[3]   A modified choline-deficient, ethionine-supplemented diet protocol effectively induces oval cells in mouse liver [J].
Akhurst, B ;
Croager, EJ ;
Farley-Roche, CA ;
Ong, JK ;
Dumble, ML ;
Knight, B ;
Yeoh, GC .
HEPATOLOGY, 2001, 34 (03) :519-522
[4]  
ALPERS DH, 1993, DIS LIVER, P825
[5]   Independent predictors of liver fibrosis in patients with nonalcoholic steatohepatitis [J].
Angulo, P ;
Keach, JC ;
Batts, KP ;
Lindor, KD .
HEPATOLOGY, 1999, 30 (06) :1356-1362
[6]   Insulin resistance and mitochondrial abnormalities in NASH: A cool look into a burning issue [J].
Angulo, P ;
Lindor, KD .
GASTROENTEROLOGY, 2001, 120 (05) :1281-1285
[7]   Review article: breath testing for human liver function assessment [J].
Armuzzi, A ;
Candelli, M ;
Zocco, MA ;
Andreoli, A ;
De Lorenzo, A ;
Nista, EC ;
Miele, L ;
Cremonini, F ;
Cazzato, IA ;
Grieco, A ;
Gasbarrini, G ;
Gasbarrini, A .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 (12) :1977-1996
[8]   NONALCOHOLIC STEATOHEPATITIS - AN EXPANDED CLINICAL ENTITY [J].
BACON, BR ;
FARAHVASH, MJ ;
JANNEY, CG ;
NEUSCHWANDERTETRI, BA .
GASTROENTEROLOGY, 1994, 107 (04) :1103-1109
[9]   Leptin selectively decreases visceral adiposity and enhances insulin action [J].
Barzilai, N ;
Wang, JL ;
Massilon, D ;
Vuguin, P ;
Hawkins, M ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (12) :3105-3110
[10]   A controlled trial of gemfibrozil in the treatment of patients with nonalcoholic steatohepatitis [J].
Basaranoglu, M ;
Acbay, O ;
Sonsuz, A .
JOURNAL OF HEPATOLOGY, 1999, 31 (02) :384-384