Department of Gastroenterology, Changzhi People’s Hospital, Changzhi, China
Medical College, Qingdao University, Qingdao, China
Curr Pharm Des. 2021;27(29):3235-3243. doi: 10.2174/1381612827666210315144821.
Nonalcoholic fatty liver disease (NAFLD) is one of the most common reasons for the increase in serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels. Moreover, liver- associated death is approximately 10 times higher in patients with NAFLD than in common individuals. In theory, NAFLD is a kind of metabolic syndrome that manifests in the liver, and insulin resistance plays an important role in it. Therefore, drugs that improve insulin sensitivity may be effective for NAFLD.
The aim of this study was to evaluate the effect of metformin treatment on aminotransferase levels, metabolic parameters and body mass index in NAFLD patients via a meta-analysis of clinical trials.
A comprehensive search on PubMed, EMBASE, the Web of Science and the Cochrane Central Register of Controlled Trials was performed for randomized controlled trials (RCTs) on the effect of metformin treatment on aminotransferase levels, metabolic parameters and body mass index in NAFLD patients. Serum hepatic enzyme, lipid, glucose and insulin levels, homeostasis model assessment-insulin resistance (HOMA-IR) index and body mass index (BMI) at different follow-up points exhibited desirable outcomes. The final search was performed in January, 2021.
In total, 10 RCTs with 459 patients were included. Compared with controls, metformin could effectively reduce serum fasting glucose and insulin levels and the HOMA-IR index in NAFLD patients at the 6-month follow-up. In addition, metformin could clearly reduce the serum ALT and HOMA-IR index at the 12-month follow-up. Although metformin was found to be effective in managing lipid metabolism and controlling BMI in NAFLD patients compared with that at baseline, the effect was similar to that in controls. In addition, the speed of metformin treatment seemed to be slower than that of controls.
Compared to the controls, metformin could effectively reduce the serum fasting glucose and insulin levels and the HOMA-IR index in NAFLD patients at the 6-month follow-up and ALT and the HOMA-IR index at the 12-month follow-up.
非酒精性脂肪性肝病(NAFLD)是导致血清丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)水平升高的最常见原因之一。此外,NAFLD 患者的肝相关死亡率比普通人群高约 10 倍。从理论上讲,NAFLD 是一种以肝脏为表现形式的代谢综合征,胰岛素抵抗在其中起着重要作用。因此,改善胰岛素敏感性的药物可能对 NAFLD 有效。
本研究通过对 NAFLD 患者使用二甲双胍治疗的临床试验进行荟萃分析,评估其对氨基转移酶水平、代谢参数和体重指数的影响。
在 PubMed、EMBASE、Web of Science 和 Cochrane 对照试验中心注册数据库中全面检索关于二甲双胍治疗对 NAFLD 患者氨基转移酶水平、代谢参数和体重指数影响的随机对照试验(RCT)。不同随访点的血清肝酶、血脂、血糖和胰岛素水平、稳态模型评估-胰岛素抵抗指数(HOMA-IR)和体重指数(BMI)均为观察指标。最后一次检索时间为 2021 年 1 月。
共纳入 10 项 RCT,涉及 459 例患者。与对照组相比,二甲双胍能有效降低 NAFLD 患者在 6 个月随访时的血清空腹血糖和胰岛素水平以及 HOMA-IR 指数。此外,二甲双胍能明显降低 12 个月随访时的血清 ALT 和 HOMA-IR 指数。尽管与基线相比,二甲双胍在管理 NAFLD 患者的血脂代谢和控制 BMI 方面有一定效果,但与对照组相似。此外,二甲双胍治疗的速度似乎比对照组慢。
与对照组相比,二甲双胍能有效降低 NAFLD 患者在 6 个月随访时的血清空腹血糖和胰岛素水平以及 HOMA-IR 指数,在 12 个月随访时降低 ALT 和 HOMA-IR 指数。