Acetyl-CoA carboxylase inhibitors in non-alcoholic steatohepatitis: Is there a benefit?

World J Gastroenterol. 2021 Oct 21;27(39):6522-6526. doi: 10.3748/wjg.v27.i39.6522.

Abstract

De novo lipogenesis (DNL) plays an important role in the pathogenesis of hepatic steatosis and also appears to be implicated in hepatic inflammation and fibrosis. Accordingly, the inhibition of acetyl-CoA carboxylase, which catalyzes the rate-limiting step of DNL, might represent a useful approach in the management of patients with nonalcoholic fatty liver disease (NAFLD). Animal studies and preliminary data in patients with NAFLD consistently showed an improvement in steatosis with the use of these agents. However, effects on fibrosis were variable and an increase in plasma triglyceride levels was observed. Therefore, more long-term studies are needed to clarify the role of these agents in NAFLD and to determine their risk/benefit profile.

Keywords: Acetyl-CoA carboxylase inhibitors; Fibrosis; Firsocostat; Non-alcoholic steatohepatitis; Steatosis.

Publication types

  • Editorial

MeSH terms

  • Acetyl-CoA Carboxylase / metabolism
  • Animals
  • Humans
  • Lipogenesis
  • Liver / metabolism
  • Non-alcoholic Fatty Liver Disease* / drug therapy
  • Non-alcoholic Fatty Liver Disease* / metabolism

Substances

  • Acetyl-CoA Carboxylase