TY - JOUR
T1 - Non-alcoholic fatty liver disease
AU - Powell, Elizabeth E.
AU - Wong, Vincent Wai Sun
AU - Rinella, Mary
N1 - Funding Information:
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.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/6/5
Y1 - 2021/6/5
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85106872103&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85106872103&partnerID=8YFLogxK
U2 - 10.1016/S0140-6736(20)32511-3
DO - 10.1016/S0140-6736(20)32511-3
M3 - Review article
C2 - 33894145
AN - SCOPUS:85106872103
SN - 0140-6736
VL - 397
SP - 2212
EP - 2224
JO - The Lancet
JF - The Lancet
IS - 10290
ER -