Ursodeoxycholic acid and atorvastatin in the treatment of nonalcoholic steatohepatitis

被引:166
作者
Kiyici, M [1 ]
Gulten, M
Gurel, S
Nak, SG
Dolar, E
Savci, G
Adim, SB
Yerci, O
Memik, F
机构
[1] Uludag Univ, Dept Gastroenterol, Fac Med, TR-16059 Bursa, Turkey
[2] Uludag Univ, Dept Radiol, Fac Med, TR-16059 Bursa, Turkey
[3] Uludag Univ, Dept Pathol, Fac Med, TR-16059 Bursa, Turkey
来源
CANADIAN JOURNAL OF GASTROENTEROLOGY | 2003年 / 17卷 / 12期
关键词
atorvastatin; nonalcoholic steatohepatitis; ursodeoxycholic acid;
D O I
10.1155/2003/857869
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND/AIMS: Nonalcoholic steatohepatitis (NASH) is a serious disorder with the potential to gradually progress to cirrhosis. It is generally associated with obesity, diabetes and hyperlipidemia. Currently, there is no established therapy for NASH. The aim of the present study was to evaluate the effectiveness of atorvastatin and ursodeoxycholic acid (UDCA) in the treatment of NASH. METHODS: This prospective study included 44 adult patients (24 men, 20 women) with a mean age of 48.90 +/- 7.69 years and mean body mass index (BMI) of 29.40 +/- 3.82. Ten patients had a history of diabetes. Serological markers for viral hepatitis were negative in all patients and there was no history of alcohol or drug abuse. Patients who had autoimmune hepatitis were excluded from the study. Liver biopsy was performed before therapy to confirm the diagnosis. Among NASH patients, 17 normolipidemic cases received UDCA 13 to 15 mg/kg/day (group 1), while hyperlipidemic cases (n=27) received atorvastatin 10 mg/day (group 2) for six months. The BMI, serum lipids, liver function tests and liver density, assessed by computerized tomography, were evaluated before and after the treatment period. The BMI, serum aminotransferase levels, histological parameters (steatosis, inflammation, fibrosis scores) and liver densities were not statistically different between the groups at the beginning of therapy. RESULTS: The BMI, serum glucose, and triglyceride levels did not change in either group after the treatment period. In group 1, serum alanine aminotransferase (ALT) and gamma-glutamyl-transferase (GOT) levels reduced significantly, and in group 2, serum cholesterol, aspartate aminotransferase, ALT, alkaline phosphatase and GOT levels reduced significantly. Liver densities increased only in group 2, probably as a result of diminishing fat content of liver. The normalization of transaminases was also more prevalent in group 2. Liver steatosis was closely correlated with liver density, but inflammation and fibrosis were not. CONCLUSIONS: The use of atorvastatin in NASH patients with hyperlipidemia was found to be both effective and safe. The benefit of statin and UDCA therapy in normolipidemic patients with NASH requires confirmation with further placebo-controlled trials.
引用
收藏
页码:713 / 718
页数:6
相关论文
共 13 条
[1]   2 CASES FROM THE SPECTRUM OF NONALCOHOLIC STEATOHEPATITIS [J].
ABDELMALEK, M ;
LUDWIG, J ;
LINDOR, KD .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1995, 20 (02) :127-130
[2]   CORRELATIONS OF LIVER ECHO INTENSITY WITH CYTOLOGY AND CHEMICAL MEASUREMENTS OF FAT, WATER AND PROTEIN-CONTENT IN LIVE BURBOTS (LOTA-LOTA) [J].
BONDESTAM, S ;
ALANEN, A ;
TOIKKANEN, S .
ULTRASOUND IN MEDICINE AND BIOLOGY, 1992, 18 (01) :75-80
[3]  
Brunt EM, 1999, AM J GASTROENTEROL, V94, P2467, DOI 10.1111/j.1572-0241.1999.01377.x
[4]   Steatohepatitis: A tale of two "hits"? [J].
Day, CP ;
James, OFW .
GASTROENTEROLOGY, 1998, 114 (04) :842-845
[5]  
Diehl AK, 2002, SLEISENGER FORDTRANS, P1393
[6]   Rapid MRI using a modified Dixon technique: a non-invasive and effective method for detection and monitoring of fatty metamorphosis of the liver [J].
Fishbein, MH ;
Stevens, WR .
PEDIATRIC RADIOLOGY, 2001, 31 (11) :806-809
[7]  
Harrison SA, 2002, GASTROENTEROLOGY, V122, pA669
[8]  
Kumar KS, 2000, MAYO CLIN PROC, V75, P733
[9]  
Laurin J, 1996, HEPATOLOGY, V23, P1464
[10]   Nonalcoholic fatty liver disease - A feature of the metabolic syndrome [J].
Marchesini, G ;
Brizi, M ;
Bianchi, G ;
Tomassetti, S ;
Bugianesi, E ;
Lenzi, M ;
McCullough, AJ ;
Natale, S ;
Forlani, G ;
Melchionda, N .
DIABETES, 2001, 50 (08) :1844-1850