Non-alcoholic fatty liver disease.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
05 06 2021
Historique:
received: 07 07 2020
revised: 04 11 2020
accepted: 13 11 2020
pubmed: 25 4 2021
medline: 13 1 2022
entrez: 24 4 2021
Statut: ppublish

Résumé

Non-alcoholic fatty liver disease (NAFLD) has a global prevalence of 25% and is a leading cause of cirrhosis and hepatocellular carcinoma. NAFLD encompasses a disease continuum from steatosis with or without mild inflammation (non-alcoholic fatty liver), to non-alcoholic steatohepatitis (NASH), which is characterised by necroinflammation and faster fibrosis progression than non-alcoholic fatty liver. NAFLD has a bidirectional association with components of the metabolic syndrome, and type 2 diabetes increases the risk of cirrhosis and related complications. Although the leading causes of death in people with NAFLD are cardiovascular disease and extrahepatic malignancy, advanced liver fibrosis is a key prognostic marker for liver-related outcomes and overall mortality, and can be assessed with combinations of non-invasive tests. Patients with cirrhosis should be screened for hepatocellular carcinoma and oesophageal varices. There is currently no approved therapy for NAFLD, although several drugs are in advanced stages of development. Because of the complex pathophysiology and substantial heterogeneity of disease phenotypes, combination treatment is likely to be required for many patients with NAFLD. Healthy lifestyle and weight reduction remain crucial to the prevention and treatment of NAFLD.

Identifiants

pubmed: 33894145
pii: S0140-6736(20)32511-3
doi: 10.1016/S0140-6736(20)32511-3
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2212-2224

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests VW-SW served as a consultant or advisory board member for 3V-BIO, AbbVie, Allergan, Boehringer Ingelheim, US Center for Outcomes Research in Liver Diseases, Echosens, Gilead Sciences, Hanmi Pharmaceutical, Intercept, Merck, Novartis, Novo Nordisk, Perspectum Diagnostics, Pfizer, ProSciento, Sagimet Biosciences, TARGET-NASH, and Terns; and served as a speaker for AbbVie, Bristol-Myers Squibb, Echosens, and Gilead Sciences. VW-SW has also received an unrestricted grant from Gilead Sciences for fatty liver research. MR is a scientific consultant or advisory board member for Centara, Madrigal, Gilead Sciences, Genfit, Galecto, Amgen, Alnylam, Thetis, Lipocine, Coherus, NGM Biopharmaceuticals, Enanta, Immuron, Fractyl, ProSciento, Gelesis, Merck, Metacrine, Viking Therapeutics, Allergan, Cymabay, Boehringer Ingelheim, Genentech, Sagimet Bio, Terns, Siemens, Novartis, Bristol-Myers Squibb, and Intercept Pharmaceuticals. MR has received independent research funding from Novartis, and owns no stocks and does not participate on speakers bureaus. EEP served as a consultant or advisory board member for CSL Behring and has received an unrestricted grant from Siemens Healthineers. EEP owns no stocks and does not participate on speakers bureaus.

Auteurs

Elizabeth E Powell (EE)

Centre for Liver Disease Research, Faculty of Medicine, University of Queensland, Translational Research Institute, Brisbane, QLD, Australia; Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, QLD, Australia. Electronic address: e.powell@uq.edu.au.

Vincent Wai-Sun Wong (VW)

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China; State Key Laboratory of Digestive Disease, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.

Mary Rinella (M)

Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.

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Classifications MeSH