Treatment of nonalcoholic fatty liver disease

被引:20
作者
Suthat Liangpunsakul
Naga Chalasani
机构
[1] Indiana University School of Medicine,Divisions of Gastroenterology/Hepatology and Clinical Pharmacology
关键词
Metformin; NASH; Rosiglitazone; Pioglitazone; Orlistat;
D O I
10.1007/s11938-003-0047-0
中图分类号
学科分类号
摘要
Nonalcoholic fatty liver disease (NAFLD) is very common in the United States, and in some patients it may lead to cirrhosis, liver failure, and liver cancer. NAFLD encompasses a spectrum of liver injury, ranging from steatosis to steatohepatitis, advanced fibrosis, and cirrhosis. Nonalcoholic steatohepatitis (NASH), an advanced form of NAFLD, histologically comprises steatosis, balloon degeneration, inflammation, and fibrosis in varying degrees. It is generally believed that simple steatosis is benign with minimal risk of progression, whereas NASH is progressive and can lead to cirrhosis. The commonly associated risk factors for NAFLD include obesity, hyperlipidemia, and diabetes mellitus. The pathogenesis of NAFLD and NASH is not fully known; however, current evidence suggests that insulin resistance and lipid peroxidation play a role in the pathogenesis of this condition. Currently, there are no proven effective therapies available for the treatment of NASH. Although there are numerous studies that have explored various treatments for NASH, these generally consist of small numbers of patients with suboptimal endpoints. Treatment strategies for NAFLD and NASH can be broadly divided into 1) treatment or control of underlying risk factors such as hyperlipidemia, diabetes mellitus, and obesity; and 2) specific pharmacologic therapy such as insulin sensitizers, antioxidants, or cytoprotective agents. Newer thiazolidinediones, such as rosiglitazone and pioglitazone, have shown promise in the treatment of NASH in pilot studies. However, these agents should not be used in clinical practice until their efficacy and safety are firmly established in larger studies. Despite encouraging initial studies, the recently completed multicenter, randomized, controlled trial failed to show any efficacy for ursodeoxycholic acid in the treatment of NASH. Other agents, such as vitamin E, betaine, probucol, and atorvastatin, have been explored as therapeutic agents for NASH. However, none of these studies have shown convincingly their utility in the treatment of NASH. Attempts to identify optimal therapy for patients with NASH are being vigorously pursued by the research community and important advances are expected within next several years. Until then, subjects should be advised to avoid alcohol, lose weight, and exercise regularly, and meticulous attention should be paid to the control of their risk factors such as diabetes and hyperlipidemia.
引用
收藏
页码:455 / 463
页数:8
相关论文
共 145 条
[1]  
Neuschwander-Tetri BA(2003)Nonalcoholic steatohepatitis: summary of an AASLD single topic conference Hepatology 37 1202-1219
[2]  
Caldwell SH(2002)Nonalcoholic fatty liver disease Gastroenterology 122 1649-1657
[3]  
Clark JM(2000)Prevalence of and risk factors for hepatic steatosis in northern Italy Ann Intern Med 132 112-117
[4]  
Brancati FL(1998)Liver and biliary sonography in diabetic and non-diabetic obese woman Diabetes Metab 24 458-462
[5]  
Diehl AM(1977)Liver histology in a ‘normal’ population-examination of 503 consecutive fatal traffic casualities Scand J Gastroenterol 12 593-597
[6]  
Ballentani S(2002)Update on nonalcoholic fatty liver disease J Clin Gastroenterol 34 255-262
[7]  
Saccoccio G(1987)Comparison between nonalcoholic steatohepatitis and alcoholic steatohepatitis Am J Gastroenterol 82 650-654
[8]  
Masutti F(1990)Fatty liver hepatitis (steatohepatitis) and obesity: an autopsy with analysis of risk factors Hepatology 12 1106-1110
[9]  
Araujo LM(1990)Liver pathology in morbidly obese patients with and without diabetes Am J Gastroenterol 85 1349-1355
[10]  
DeOliveira A(2002)Nonalcoholic fatty liver disease N Engl J Med 346 1221-1231