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Review
. 2024 Nov 2;404(10464):1761-1778.
doi: 10.1016/S0140-6736(24)01811-7.

Steatotic liver disease

Affiliations
Review

Steatotic liver disease

Mads Israelsen et al. Lancet. .

Abstract

Steatotic liver disease is the overarching term for conditions characterised by abnormal lipid accumulation in the liver (liver or hepatic steatosis). Steatotic liver disease encompasses what was previously termed non-alcoholic fatty liver disease (NAFLD), which is now called metabolic dysfunction-associated steatotic liver disease (MASLD). Additionally, steatotic liver disease includes alcohol-related liver disease (ALD) and MetALD, the new classification for the overlap between MASLD and ALD, and rare causes of liver steatosis. Cirrhosis is globally the 11th leading cause of death, and steatotic liver disease has become the leading cause of cirrhosis in the EU and USA. Steatotic liver disease affects around 30% of the global population and is mainly driven by obesity, type 2 diabetes, and alcohol intake, but only a minor proportion with steatotic liver disease progress to cirrhosis. The presence and progression of liver fibrosis led by hepatic inflammation is the main predictor of liver-related death across the entire spectrum of steatotic liver diseases. A combination of recent advancements of widely available biomarkers for early detection of liver fibrosis together with considerable advancements in therapeutic interventions offer the possibility to reduce morbidity and mortality in patients with steatotic liver disease. This Seminar covers the recent reclassification of steatotic liver disease and how it reflects clinical practice and prognosis. For early detection of liver fibrosis, we propose a collaborative diagnostic framework between primary care and liver specialists. Lastly, we discuss current best practices for managing steatotic liver disease, we explore therapeutic targets across the spectrum of steatotic liver diseases, and we review the pipeline of drugs in development for MASLD.

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Conflict of interest statement

Declaration of interests MI received travel support from Novo Nordisk for the 7730 ALD investigator meeting. SF holds a senior clinical investigator fellowship from the Research Foundation Flanders (1802154N); received institutional grants from Astellas, Falk Pharma, Genfit, Gilead Sciences, GlympsBio, Janssens Pharmaceutica, Inventiva, Merck Sharp & Dohme, Pfizer, and Roche; was a consultant for AbbVie, Actelion, Aelin Therapeutics, AgomAb, Aligos Therapeutics, Allergan, Alnylam, Astellas, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol Myers Squibb, CSL Behring, Coherus, Echosens, Dr Falk Pharma, Eisai, Enyo, Galapagos, Galmed, Genentech, Genfit, Genflow Biosciences, Gilead Sciences, Intercept, Inventiva, Janssens Pharmaceutica, PRO.MED.CS Praha, Julius Clinical, Madrigal, Medimmune, Merck Sharp & Dohme, Mursla Bio, NGM Bio, Novartis, Novo Nordisk, Promethera, Roche, and Siemens Healthineers; and has lectured for AbbVie, Allergan, Bayer, Eisai, Genfit, Gilead Sciences, Janssens Cilag, Intercept, Inventiva, Merck Sharp & Dohme, Novo Nordisk, Promethera, and Siemens. EAT served as a speaker for AbbVie, Dr Falk Pharma, Echosens, Novo Nordisk, and Orphalan, and participated in advisory boards for Alexion, Boehringer Ingelheim, Siemens, Merck Sharp & Dohme, Novo Nordisk, Pfizer, Orphalan, and Univar. AK served as a speaker for Novo Nordisk, Norgine, Siemens, and Nordic Bioscience; participated in advisory boards for Siemens, Boehringer Ingelheim, and Novo Nordisk, all outside the submitted work; received research support from Norgine, Siemens, Nordic Bioscience, Astra, Echosense; and is a board member and the co-founder of Evido.

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