Published online Sep 15, 2021. doi: 10.4239/wjd.v12.i9.1576
Peer-review started: May 6, 2021
First decision: July 3, 2021
Revised: July 9, 2021
Accepted: August 12, 2021
Article in press: August 12, 2021
Published online: September 15, 2021
Processing time: 123 Days and 16.8 Hours
Nonalcoholic fatty liver disease (NAFLD) is becoming a major chronic liver disorder worldwide. Patients with NAFLD usually experience metabolic disorder complications, including type 2 diabetes mellitus, hyperlipidemia and metabolic syndrome. However, there are no established pharmacotherapies for NAFLD.
The use of antidiabetic drugs, including thiazolidinediones (TZDs), metformin, glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium glucose cotransporter-2 inhibitors (SGLT2), has emerged as a major therapeutic strategy to treat patients with NAFLD. However, it is difficult for clinicians to decide which intervention is best for treating patients with NAFLD due to an absence of comprehensive comparisons among treatments.
In this study, we compared the effectiveness of different treatments for NAFLD. The results provide new evidence that can guide the development of clinical guidelines and thus help clinicians make individualized decisions in clinical practice.
The Cochrane Risk of Bias tool was used to assess the risk of bias of the included studies. Data analysis was performed by Stata 14.0 (Corporation LLC, College Station, United States) and R (X64 3.6.3 version) and included inconsistency modeling, the “node-splitting” technique, Begg’s test and the construction of plots of the surface under the cumulative ranking curve.
GLP-1RAs had a great advantage over other treatments in the improvement of liver enzymes and hepatic fat content (HFC), and promising effectiveness was observed with TZDs with regard to the NAFLD activity score (NAS) set. However, no ranking of SGLT2 was possible for the NAS set due to insufficient research. In addition, the side effects of these drugs were not analyzed in this study.
GLP-1RAs are the optimum therapeutic approach to improve HFC, abnormally elevated liver enzymes and overweight, while TZDs are the most promising intervention to ameliorate liver inflammation.
Large multicenter prospective randomized trials with liver biopsy data regarding new classes of glucose-lowering drugs are needed to obtain robust data and confirm our results.