Anti-obesity Medications for the Management of Nonalcoholic Fatty Liver Disease.
Curr Obes Rep · 2022
Last updated 2026-05-28Research shows that some weight-loss medications, including liraglutide and semaglutide (GLP-1 drugs), as well as orlistat, may improve liver fat buildup and inflammation in people with nonalcoholic fatty liver disease (NAFLD). However, these medications do not appear to improve liver scarring (fibrosis). Other weight-loss drugs, such as lorcaserin, setmelanotide, and phentermine-based treatments, have not been well studied for NAFLD.
AI summary of the abstract below.
| Journal | Curr Obes Rep, 2022 |
|---|---|
| Citations | 31 |
| Relative citation ratio | 2.77 |
| NIH percentile | 82 |
| Molecules | — |
| Conditions studied | Obesity, Mash |
Abstract
PURPOSE OF REVIEW: Obesity is closely associated with nonalcoholic fatty liver disease (NAFLD), a highly prevalent disease without any approved medication. The aim of this review was to summarize the evidence on the effect of anti-obesity medications on NAFLD, especially focusing on hepatic histology.
RECENT FINDINGS: Orlistat and some glucagon-like peptide-1 receptor analogs, including liraglutide and semaglutide, have beneficial effects on hepatic steatosis and inflammation, but not fibrosis. Other anti-obesity medications, including lorcaserin, setmelanotide, phentermine hydrochloric, phentermine/topiramate, and naltrexone/bupropion, have been minimally investigated in NAFLD. Furthermore, medications like sodium-glucose cotransporter-2 inhibitors and farnesoid X receptor have shown beneficial effects in both NAFLD and obesity, but they have not been licensed for either disease. Liraglutide, semaglutide, and orlistat may be currently used in selected patients with obesity and NAFLD. Further research is warranted, since targeting obesity may provide additional benefits on its comorbidities, including NAFLD.
Verbatim abstract via PubMed 35501557 ↗