Effect of HCV eradication by DAAs on liver steatosis, carotid atherosclerosis, and associated metabolic comorbidities: A systematic review

Liver Int. 2024 May;44(5):1075-1092. doi: 10.1111/liv.15876. Epub 2024 Feb 22.

Abstract

Background and aims: The beneficial effect of Hepatitis C virus (HCV) eradication by direct antiviral agents (DAAs) on liver fibrosis is well defined. Despite this, the impact of viral eradication in both hepatic and extra-hepatic metabolic features is underreached. This systematic review aimed to synthesize the evidence on the impact of HCV eradication by DAAs on liver steatosis, carotid atherosclerosis, glucidic impairment, dyslipidaemia, and weight gain.

Methods: A systematic search of the existing literature (up to December 2022) identified 97 original studies that fulfilled the inclusion criteria.

Results: Whereas total cholesterol and low-density lipoprotein (LDL) seem to increase after viral eradication, the cardiovascular damage expressed as carotid plaques and intima-media thickness seems to improve. Otherwise, the effect on liver steatosis, glucidic homeostasis, and weight seems to be strictly dependent on the presence of baseline metabolic disorders.

Conclusion: Despite high heterogeneity and relatively short follow-up of included studies, we can conclude that the presence of metabolic risk factors should be strictly evaluated due to their impact on liver steatosis, glucidic and lipid homeostasis, and on weight gain to better identify patients at risk of liver disease progression despite the virus eradication.

Keywords: body weight; carotid atherosclerosis; diabetes mellitus; dyslipidaemia; fatty liver; hepatitis C virus.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Antiviral Agents / therapeutic use
  • Carotid Artery Diseases* / chemically induced
  • Carotid Artery Diseases* / drug therapy
  • Carotid Intima-Media Thickness
  • Fatty Liver* / chemically induced
  • Hepacivirus
  • Hepatitis C* / drug therapy
  • Hepatitis C, Chronic* / drug therapy
  • Humans
  • Weight Gain

Substances

  • Antiviral Agents