EASL–EASD–EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD): Executive Summary

European Association for the Study of the Liver, European Association for the Study of Diabetes, European Association for the Study of Obesity

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31 Scopus citations

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD), previously termed non-alcoholic fatty liver disease (NAFLD), is defined as steatotic liver disease (SLD) in the presence of one or more cardiometabolic risk factor(s) and the absence of harmful alcohol intake. The spectrum of MASLD includes steatosis, metabolic dysfunction-associated steatohepatitis (MASH, previously NASH), fibrosis, cirrhosis and MASH-related hepatocellular carcinoma (HCC). This joint EASL–EASD–EASO guideline provides an update on definitions, prevention, screening, diagnosis and treatment for MASLD. Case-finding strategies for MASLD with liver fibrosis, using non-invasive tests, should be applied in individuals with cardiometabolic risk factors, abnormal liver enzymes and/or radiological signs of hepatic steatosis, particularly in the presence of type 2 diabetes or obesity with additional metabolic risk factor(s). A stepwise approach using blood-based scores (such as the fibrosis-4 index [FIB-4]) and, sequentially, imaging techniques (such as transient elastography) is suitable to rule-out/in advanced fibrosis, which is predictive of liver-related outcomes. In adults with MASLD, lifestyle modification—including weight loss, dietary changes, physical exercise and discouraging alcohol consumption—as well as optimal management of comorbidities—including use of incretin-based therapies (e.g. semaglutide, tirzepatide) for type 2 diabetes or obesity, if indicated—is advised. Bariatric surgery is also an option in individuals with MASLD and obesity. If locally approved and dependent on the label, adults with non-cirrhotic MASH and significant liver fibrosis (stage ≥2) should be considered for a MASH-targeted treatment with resmetirom, which demonstrated histological effectiveness on steatohepatitis and fibrosis with an acceptable safety and tolerability profile. No MASH-targeted pharmacotherapy can currently be recommended for the cirrhotic stage. Management of MASH-related cirrhosis includes adaptations of metabolic drugs, nutritional counselling, surveillance for portal hypertension and HCC, as well as liver transplantation in decompensated cirrhosis.

Original languageEnglish
Pages (from-to)2375-2392
Number of pages18
JournalDiabetologia
Volume67
Issue number11
DOIs
StatePublished - Nov 2024

Funding

FundersFunder number
Heinrich-Heine University
Chinese University of Hong Kong
Università degli Studi di Torino
Social Welfare and Health Sciences
Heinrich Heine University
University Hospital
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
Clínica Universidad de Navarra
National Research Council
Charité – Universitätsmedizin Berlin
2Department of Medicine and Therapeutics
Università degli Studi di Padova
Università degli Studi di Milano
Centro de Investigación Biomédica en Red-Fisiopatología de la Obesidad y Nutrición
18Department of Endocrinology and Nutrition
D & Obesity Clinic
University of Haifa, Haifa, Israel
Tel-Aviv
Universitair Ziekenhuis Antwerpen
Tel Aviv University
7Department of Gastroenterology Tel-Aviv Medical Center
Hasharon Hospital-Rabin Medical Center

    Keywords

    • Diabetes
    • Glucagon-like peptide
    • Hepatocellular carcinoma
    • Liver fibrosis
    • MASH
    • MASLD
    • NAFLD
    • NASH
    • Non-invasive tests
    • Resmetirom

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