Published online Oct 14, 2020. doi: 10.3748/wjg.v26.i38.5745
Peer-review started: May 21, 2020
First decision: May 29, 2020
Revised: August 25, 2020
Accepted: September 16, 2020
Article in press: September 16, 2020
Published online: October 14, 2020
Processing time: 146 Days and 5.2 Hours
Nonalcoholic steatohepatitis (NASH) is an important indication for liver transplantation in many Western countries due to the epidemic of obesity and insulin resistance. Unfortunately, no medication is approved for NASH and risk factor modification is often advised. Over the last decade, several clinical trials on NASH have been conducted with several ongoing and the future looks promising. Although betaine (trimethyl glycine) was evaluated for NASH, results were mixed in the clinical trials in large part due to the quality of the studies. It seems reasonable to re-evaluate betaine in clinical trials for NASH and alcoholic liver disease due to its low cost, tolerability and mechanism of action.
Core Tip: This article revisits the role of betaine in liver disease with a focus on nonalcoholic steatohepatitis. Although a randomized controlled trial did not report benefit over placebo, there were limitations with the study. Given the excellent safety profile and tolerance of betaine, it appears this would be an appropriate time to re-evaluate betaine for liver diseases such as nonalcoholic and alcoholic liver diseases.