Wang Hu, Wang Li, Cheng Yujia, Xia Zhiqing, Liao Yifeng, Cao Jiang
Department of Clinical Medicine, Xuzhou Medical University, Xuzhou, Jiangsu 221004, P.R. China.
Department of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu 221002, P.R. China.
Biomed Rep. 2018 Jul;9(1):90-96. doi: 10.3892/br.2018.1100. Epub 2018 May 22.
In the present meta-analysis, the efficacy and safety of orlistat in the treatment of non-alcoholic fatty liver (NAFLD) and non-alcoholic steatohepatitis (NASH) were evaluated. PubMed, Embase, the Cochrane Library, Web of Science, and Wan Fang data were searched for controlled trials of orlistat in patients with NAFLD or NASH, published before August 2017. Three randomized controlled trials and four single-arm trials were included. The involved participants with NAFLD or NASH (330 patients) were analyzed for clinical outcomes including alteration in hepatic histological variables and biomarkers of liver function. Improvements were observed in levels of alanine aminotransferase [standard mean difference (SMD)=-1.41; P=0.01], aspartate aminotransferase (SMD=-2.06; P=0.0005), γ-glutamyl transpeptidase (SMD=-1.91; P=0.05), glucose [mean difference (MD)=-0.51; P=0.01], triglycerides (MD=-0.93; P=0.01), homeostasis model assessment of insulin resistance index (MD=-1.05; P=0.04) and body mass index (MD=-1.97; P=0.02), but not in liver fibrosis score (SMD=-0.14; P=0.71). On sub-analyses of the different patient groups, no significant differences were observed in patients with NASH. Taken together, these findings demonstrate that orlistat could serve as a therapeutic drug to improve biochemical indicators of liver damage, but not as first-choice drug for the management of NAFLD or NASH; thus suggesting a novel palliative drug only for the treatment of NAFLD.
在本次荟萃分析中,评估了奥利司他治疗非酒精性脂肪肝(NAFLD)和非酒精性脂肪性肝炎(NASH)的疗效和安全性。检索了PubMed、Embase、Cochrane图书馆、科学网和万方数据,查找2017年8月之前发表的关于奥利司他治疗NAFLD或NASH患者的对照试验。纳入了三项随机对照试验和四项单臂试验。对纳入的NAFLD或NASH患者(330例)的临床结局进行分析,包括肝脏组织学变量和肝功能生物标志物的变化。观察到丙氨酸氨基转移酶水平有所改善[标准均数差(SMD)=-1.41;P=0.01]、天冬氨酸氨基转移酶(SMD=-2.06;P=0.0005)、γ-谷氨酰转肽酶(SMD=-1.91;P=0.05)、血糖[均数差(MD)=-0.51;P=0.01]、甘油三酯(MD=-0.93;P=0.01)、胰岛素抵抗指数的稳态模型评估(MD=-1.05;P=0.04)和体重指数(MD=-1.97;P=0.02),但肝纤维化评分未改善(SMD=-0.14;P=0.71)。在对不同患者组的亚组分析中,NASH患者未观察到显著差异。综上所述,这些研究结果表明,奥利司他可作为一种治疗药物改善肝损伤的生化指标,但不是治疗NAFLD或NASH的首选药物;因此提示其仅为治疗NAFLD的一种新型姑息药物。