Nonalcoholic fatty liver disease: An overview of current insights in pathogenesis, diagnosis and treatment

被引:155
作者
Schreuder, Tim C. M. A. [1 ]
Verwer, Bart J. [1 ]
van Nieuwkerk, Carin M. J. [1 ]
Mulder, Chris J. J. [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Gastroenterol & Hepatol, NL-1007 MB Amsterdam, Netherlands
关键词
non-alcoholic fatty liver disease; non-alcoholic steatohepatitis; insulin resistance; liver; obesity; steatosis;
D O I
10.3748/wjg.14.2474
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Estimates of people suffering from overweight (one billion) and obesity (300 million) are increasing. The accumulation of triglycerides in the liver, in the absence of excess alcohol intake, has been described in the early sixties, It was not until 1980, however, that Ludwig et al named this condition nonalcoholic steatohepatitis (NASH). Subsequently, nonalcoholic fatty liver disease (NAFLD) has been used as a general name for conditions ranging from simple steatosis through steatohepatitis to end-stage liver disease (cirrhosis). Many studies have demonstrated the significant correlation with obesity and insulin resistance. Other studies have revealed a significant correlation between hepatic steatosis, cardiovascular disease and increased intima-media thickness. WHO estimated that at least two million patients will develop cirrhosis due to hepatic steatosis in the years to come. Longitudinal cohort studies have demonstrated that those patients with cirrhosis have a similar risk to develop hepatocellular carcinoma as those with other causes of cirrhosis. Taken all together, NAFLD has become the third most important indication for liver transplantation. Therefore, training programmes in internal medicine, gastroenterology and hepatology should stress the importance of diagnosing this entity and treat properly those at risk for developing complications of portal hypertension and concomittant cardiovascular disease. This review will focus on the clinical characteristics, pathophysiology, imaging techniques and the readily available therapeutic options. (C) 2008 WJG. All rights reserved.
引用
收藏
页码:2474 / 2486
页数:13
相关论文
共 164 条
[1]   Adipose-selective targeting of the GLUT4 gene impairs insulin action in muscle and liver [J].
Abel, ED ;
Peroni, O ;
Kim, JK ;
Kim, YB ;
Boss, O ;
Hadro, E ;
Minnemann, T ;
Shulman, GI ;
Kahn, BB .
NATURE, 2001, 409 (6821) :729-733
[2]  
Adams LA, 2006, J CLIN GASTROENTEROL, V40, pS34
[3]   The natural history of nonalcoholic fatty liver disease: A population-based cohort study [J].
Adams, LA ;
Lymp, JF ;
St Sauver, J ;
Sanderson, SO ;
Lindor, KD ;
Feldstein, A ;
Angulo, P .
GASTROENTEROLOGY, 2005, 129 (01) :113-121
[4]   A pilot trial of pentoxifylline in nonalcoholic steatohepatitis [J].
Adams, LA ;
Zein, CO ;
Angulo, P ;
Lindor, KD .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2004, 99 (12) :2365-2368
[5]   Metabolic syndrome - a new world-wide definition. A consensus statement from the international diabetes federation [J].
Alberti, KGMM ;
Zimmet, P ;
Shaw, J .
DIABETIC MEDICINE, 2006, 23 (05) :469-480
[6]  
American Gastroenterological Association medical position statement, 2002, Gastroenterology, V123, P1702
[7]   Drugs improving insulin resistance for non-alcoholic fatty liver disease and/or non-alcoholic steatohepatitis [J].
Angelico, F. ;
Burattin, M. ;
Alessandri, C. ;
Del Ben, M. ;
Lirussi, F. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2007, (01)
[8]   Insulin resistance, the metabolic syndrome, and nonalcoholic fatty liver disease [J].
Angelico, F ;
Del Ben, M ;
Conti, R ;
Francioso, S ;
Feole, K ;
Fiorello, S ;
Cavallo, MG ;
Zalunardo, B ;
Lirussi, F ;
Alessandri, C ;
Violi, F .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (03) :1578-1582
[9]  
[Anonymous], 2000, Cleve Clin J Med
[10]   Spillover of dietary fatty acids and use of serum nonesterified fatty acids for the synthesis of VLDL-triacylglycerol under two different feeding regimens [J].
Barrows, BR ;
Timlin, MT ;
Parks, EJ .
DIABETES, 2005, 54 (09) :2668-2673