Current treatment of non-alcoholic fatty liver disease
- PMID: 35796150
- PMCID: PMC9546342
- DOI: 10.1111/joim.13531
Current treatment of non-alcoholic fatty liver disease
Abstract
Non-alcoholic fatty liver disease (NAFLD) comprises a wide spectrum of pathologies ranging from non-alcoholic fatty liver (NAFL), characterized by simple steatosis without inflammation, to non-alcoholic steatohepatitis (NASH), characterized by steatosis of the liver accompanied by inflammation and hepatocyte ballooning, which can lead to advanced fibrosis, cirrhosis and hepatocellular carcinoma. Apart from lifestyle modifications such as weight loss, a Mediterranean diet and physical activity, only a few NAFLD-specific pharmacological treatment options such as Vitamin E and Pioglitazone are considered by current international guidelines. However, recently randomized controlled trials with GLP-1 agonists, FXR and PPAR ligands as well as other agents have been published and may expand the therapeutic armamentarium for NAFLD in the near future. Finally, knowledge about treating complications of end-stage liver disease due to NASH becomes an increasingly important cornerstone in the treatment of the broad disease spectrum of NAFLD. In this review, we summarize currently available and future treatment options for patients with NAFLD that may help internal medicine specialists treat the complete clinical spectrum of this highly prevalent liver disease.
Keywords: cirrhosis; fibrosis; non-alcoholic fatty liver disease; non-alcoholic steatohepatitis.
© 2022 The Authors. Journal of Internal Medicine published by John Wiley & Sons Ltd on behalf of Association for Publication of The Journal of Internal Medicine.
Conflict of interest statement
MT received speaker fees from Bristol‐Myers Squibb (BMS), Falk Foundation, Gilead, Intercept and Merck Sharp & Dohme (MSD); advisory board fees from Albireo, BiomX, Boehringer Ingelheim, Falk Pharma GmbH, GENFIT, Gilead, Intercept, Janssen, MSD, Novartis, Phenex, Regulus and Shire; travel grants from AbbVie, Falk, Gilead, and Intercept; and research grants from Albireo, Alnylam, CymaBay, Falk, Gilead, Intercept, MSD, Takeda and UltraGenyx. He is also a coinventor of patents on the medical use of norUDCA filed by the Medical Universities of Graz and Vienna.
RP drafted the manuscript, which was then critically revised by MT.
Figures
References
-
- Younossi Z, Anstee QM, Marietti M, Hardy T, Henry L, Eslam M, et al. Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention. Nat Rev Gastroenterol Hepatol. 2018;15:11–20. - PubMed
-
- Younossi ZM, Koenig AB, Abdelatif D, Fazel Y, Henry L, Wymer M. Global epidemiology of nonalcoholic fatty liver disease–meta–analytic assessment of prevalence, incidence, and outcomes. Hepatology. 2016;64:73–84. - PubMed
-
- Ekstedt M, Hagström H, Nasr P, Fredrikson M, Stål P, Kechagias S, et al. Fibrosis stage is the strongest predictor for disease–specific mortality in NAFLD after up to 33 years of follow–up. Hepatology. 2015;61:1547–54. - PubMed
-
- Powell EE, Wong VW–S, Rinella M. Non–alcoholic fatty liver disease. Lancet. 2212–24, 2021. - PubMed
-
- EASL–EASD–EASO Clinical Practice Guidelines for the management of non–alcoholic fatty liver disease. J Hepatol. 2016;64:1388–402. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
