The effects of rosiglitazone, metformin, and diet with exercise in nonalcoholic fatty liver disease

被引:28
作者
Akyuez, Filiz
Demir, Kadir
Oezdil, Sadakat
Aksoy, Nevzat
Poturoglu, Sule
Ibrisim, Duygu
Kaymakoglu, Sabahattin
Besisik, Fatih
Boztas, Guengoer
Cakaloglu, Yilmaz
Mungan, Zeynel
Cevikbas, Ugur
Oekten, Atilla
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Gastroenterohepatol, Istanbul, Turkey
[2] Istanbul Univ, Istanbul Fac Med, Dept Pathol, Istanbul, Turkey
关键词
nonalcoholic fatty liver disease; treatment;
D O I
10.1007/s10620-006-9145-x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Our aim was to evaluate effects of metformin, rosiglitazone, and diet with exercise in nonalcoholic fatty liver disease. Forty-seven patients (mean age, 44 +/- 10 years; 17 female) whose ALT levels had been high for at least 6 months and with hepatosteatosis detected by liver biopsy and/or USG were enrolled in this study. Of these, 12 were treated with 850 mg/day metformin (group 1), 11 with 4 mg/day rosiglitazone (group 2), and 24 with diet and exercise (group 3) for 1 year. ALT normalization at months 6 and 12 was accepted as treatment response. Liver biopsy was performed in all patients in groups 1 and 2 before treatment and 12 patients (4 in group 1, 8 in group 2) after treatment; but in group 3 it was performed only in patients who approved this procedure (12 patients). Body mass index did not change in groups 1 and 2, but it decreased significantly in group 3 (30 +/- 3 to 28 +/- 2 kg/m(2)) at month 12. Treatment response rate was 33.3, 54.5, and 54.2% in groups 1, 2, and 3, respectively, at month 6. This rate was 22.2, 37.5, and 41.2 in groups 1, 2, and 3, respectively, at month 12. Rate of steatosis and stage of fibrosis did not change after treatment. Diet with exercise seems to be superior to metformin and rosiglitazone. Decreasing treatment response at month 12 compared to month 6 may be due to fluctuations of ALT levels. Treatment response should be evalulated histologically.
引用
收藏
页码:2359 / 2367
页数:9
相关论文
共 26 条
  • [1] HEPATIC-EFFECTS OF DIETARY WEIGHT-LOSS IN MORBIDLY OBESE SUBJECTS
    ANDERSEN, T
    GLUUD, C
    FRANZMANN, MB
    CHRISTOFFERSEN, P
    [J]. JOURNAL OF HEPATOLOGY, 1991, 12 (02) : 224 - 229
  • [2] Independent predictors of liver fibrosis in patients with nonalcoholic steatohepatitis
    Angulo, P
    Keach, JC
    Batts, KP
    Lindor, KD
    [J]. HEPATOLOGY, 1999, 30 (06) : 1356 - 1362
  • [3] NONALCOHOLIC STEATOHEPATITIS - AN EXPANDED CLINICAL ENTITY
    BACON, BR
    FARAHVASH, MJ
    JANNEY, CG
    NEUSCHWANDERTETRI, BA
    [J]. GASTROENTEROLOGY, 1994, 107 (04) : 1103 - 1109
  • [4] Nonalcoholic steatohepatitis: A proposal for grading and staging the histological lesions
    Brunt, EM
    Janney, CG
    Di Bisceglie, AM
    Neuschwander-Tetri, BA
    Bacon, BR
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 1999, 94 (09) : 2467 - 2474
  • [5] Expanding the natural history from cryptogenic cirrhosis to of nonalcoholic steatohepatitis: Hepatocellular carcinoma
    Bugianesi, E
    Leone, N
    Vanni, E
    Marchesini, G
    Brunello, F
    Carucci, P
    Musso, A
    De Paolis, P
    Capussotti, L
    Salizzoni, M
    Rizzetto, M
    [J]. GASTROENTEROLOGY, 2002, 123 (01) : 134 - 140
  • [6] Cryptogenic cirrhosis: Clinical characterization and risk factors for underlying disease
    Caldwell, SH
    Oelsner, DH
    Iezzoni, JC
    Hespenheide, EE
    Battle, EH
    Driscoll, CJ
    [J]. HEPATOLOGY, 1999, 29 (03) : 664 - 669
  • [7] Caldwell SH, 2001, AM J GASTROENTEROL, V96, P519
  • [8] NASH and insulin resistance: Insulin hypersecretion and specific association with the insulin resistance syndrome
    Chitturi, S
    Abeygunasekera, S
    Farrell, GC
    Holmes-Walker, J
    Hui, JM
    Fung, C
    Karim, R
    Lin, R
    Samarasinghe, D
    Liddle, C
    Weltman, M
    George, J
    [J]. HEPATOLOGY, 2002, 35 (02) : 373 - 379
  • [9] Hepatic steatosis: Innocent bystander or guilty party?
    Day, CP
    James, OFW
    [J]. HEPATOLOGY, 1998, 27 (06) : 1463 - 1466
  • [10] DAY CP, 2003, NON ALCOHOLIC FATTY, P58