Meta-analysis: insulin sensitizers for the treatment of non-alcoholic steatohepatitis

被引:156
作者
Rakoski, M. O. [1 ]
Singal, A. G. [1 ]
Rogers, M. A. M. [2 ]
Conjeevaram, H. [1 ]
机构
[1] Univ Michigan, Med Ctr, Div Gastroenterol, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Med Ctr, Div Gen Med, Ann Arbor, MI 48109 USA
关键词
FATTY LIVER-DISEASE; IMPAIRED GLUCOSE-TOLERANCE; PLACEBO-CONTROLLED TRIAL; CARDIOVASCULAR-DISEASE; VITAMIN-E; PIOGLITAZONE; RESISTANCE; THERAPY; RISK; THIAZOLIDINEDIONE;
D O I
10.1111/j.1365-2036.2010.04467.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
P>Background Non-alcoholic fatty liver disease generally has a benign course; however, patients with non-alcoholic steatohepatitis (NASH) may progress to cirrhosis and hepatocellular carcinoma. Currently, there is a lack of consensus about optimal NASH treatment. Aim To assess the efficacy of insulin-sensitizing agents on histological and biochemical outcomes in randomized control trials of biopsy-proven NASH. Methods Multiple online databases and conference abstracts were searched. Random effects meta-analyses were performed, with assessment for heterogeneity and publication bias. Results Nine trials were included; five trials using thiazolidinediones (glitazones), three using metformin and one trial using both drugs. There was no publication bias. Compared with controls, glitazones resulted in improved steatosis (WMD = 0.57, 95% CI 0.36-0.77, P = < 0.001), hepatocyte ballooning (WMD = 0.36, 95% CI 0.24-0.49, P < 0.001) and ALT (WMD = 16.4, 95% CI 7.7-25.0, P < 0.001), but not inflammation (P = 0.09) or fibrosis (P = 0.11). In patients without diabetes, glitazones significantly improved all histological and biochemical outcomes, most importantly including fibrosis (WMD = 0.29, 95% CI 0.078-0.51, P = 0.008). Metformin failed to improve any pooled outcome. Conclusions Treatment of NASH with glitazones, but not metformin, demonstrates a significant histological and biochemical benefit, especially in patients without diabetes. Additional studies are needed to investigate long-term outcomes of glitazone therapy in patients without diabetes.
引用
收藏
页码:1211 / 1221
页数:11
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