European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) steatotic liver disease special interest group position paper on screening, diagnosis and investigation of paediatric metabolic dysfunction‐associated steatotic liver disease
26 affiliations
- 1Department of Immunology & Immunotherapy, School of Infection, Inflammation and Immunology, College of Medicine and Health University of Birmingham Birmingham UK
- 2Liver Unit (Including Small Bowel Transplantation) Birmingham Women′s and Children′s NHS Foundation Trust Birmingham UK
- 3Hepatology Research Unit, Department of Internal Medicine and Pediatrics Ghent University Ghent Belgium
- 4Genetic of Complex Phenotype Research Unit Bambino Gesù Children′s Hospital, IRCCS Rome Italy
- 5Department of Pediatric Gastroenterology and Organ Transplant Koç University School of Medicine Istanbul Turkey
- 6Department of Gastroenterology, Hepatology and Nutrition, University Children′s Hospital Ljubljana, and Department of Pediatrics, Faculty of Medicine University of Ljubljana Ljubljana Slovenia
- 7Department of Histopathology Birmingham Children′s Hospital Birmingham UK
- 8Department of Health Sciences University of Milan Milan Italy
- 9Pediatric Unit Foundation IRCCS Ca′ Granda Ospedale Maggiore Policlinico Milan Italy
- 10Department of Paediatric Gastroenterology and Hepatology Children′s Health Ireland Dublin Ireland
- 11Department of Gastroenterology and Hepatology Antwerp University Hospital Edegem Belgium
- 12InflaMed Centre of Excellence, Laboratory for Experimental Medicine and Paediatrics, Translational Sciences in Inflammation and Immunology, Faculty of Medicine and Health Sciences University of Antwerp Wilrijk Belgium
- 13Department of Paediatric Gastroenterology, Nephrology and Metabolic Diseases Charité – Universitätsmedizin Berlin Berlin Germany
- 14Department of Gastroenterology, Hepatology, Feeding Disorders and Pediatrics Children′s Memorial Health Institute Warsaw Poland
- 15Department of Pediatric Gastroenterology, Emma Children′s Hospital, Amsterdam UMC University of Amsterdam Amsterdam The Netherlands
- 16Department of Paediatrics Paidon P&A Kyriakou Children′s Hospital Athens Greece
- 17Department of Pediatrics, Dr. von Hauner Children′s Hospital KUM University Hospital LMU Munich Munich Germany
- 18Department of Medicine, Surgery and Dentistry University of Salerno Baronissi Italy
- 19Pediatric Hepatology and Liver Transplant Unit, Department of Pediatrics Vall d′Hebron Hospital Campus, ERN Rare Liver, ERN TransplantChild Barcelona Spain
- 20Department of Pediatric Gastroenterology, Dana‐Dwek Children′s Hospital, Faculty of Medicine Tel Aviv University Tel Aviv Israel
- 21Pediatric Department for the Treatment and Study of Abdominal Diseases and Abdominal Transplantation Mediterranean Institute for Transplantation and Advanced Specialized Therapies (IRCCS ISMETT) Palermo Italy
- 22Division of Gastroenterology & Hepatology, 1st Pediatrics Department, National and Kapodistrian University of Athens “Agia Sofia” Children′s Hospital Athens Greece
- 23Department of Paediatrics Aalborg University Hospital Aalborg Denmark
- 24Department of Paediatrics and Child Health Stellenbosch University Cape Town South Africa
- 25Centre for Overweight Adolescent and Children′s Healthcare (COACH), Department of Pediatrics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University Medical Center+ MosaKids Children′s Hospital Maastricht The Netherlands
- 26Department of Pediatric Gastroenterology SI “Institute of Gastroenterology of the National Academy of Medical Sciences” Dnipro Ukraine
Abstract
Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common reason for elevated liver enzymes in children in Europe, affecting more than 5% of all children. Since the last iteration of this position paper, there have been substantial advances in our understanding of the disease. After a detailed literature review and thorough discussion, we established consensus recommendations for the diagnosis and assessment of MASLD in children. Alanine aminotransferase (ALT) ≥ 30 IU/L is a suitable screening test for MASLD in children over 10 years of age with obesity (body mass index z-score ≥+2), or in children of any age with additional risk factors. All patients with suspected MASLD should be assessed for alternative or concomitant diagnoses, as well as comorbidities. Patients who are not overweight, under 8 years old, or have any other red flags should be promptly referred for specialist assessment. Liver biopsy remains the gold standard for diagnosis and staging of MASLD, but should be reserved for diagnostic uncertainty, to guide treatment decisions, and risk stratification (e.g., prior to transition to adult care). While there is emerging data for non-invasive tests (e.g., transient elastography), it is unclear how to routinely implement these investigations in clinical practice. Combined changes of ≥20% in both ALT and gamma-glutamyl transferase may represent a useful non-invasive tool for monitoring disease severity over time. Most patients are appropriately investigated and managed by non-specialists where the focus is on holistic management of obesity and its complications. Future research should focus on how to use non-invasive tests to risk-stratify children, in particular, how to identify those with advanced fibrosis.
Related
- Hypertransaminasemia in hospitalized children: Insights from a national multicenter study by the Italian Society of Pediatric Gastroenterology, Hepatology, and Nutrition
- Predictors and outcomes of early left ventricular dysfunction in paediatric patients postoperative for ventricular septal defect: a retrospective cohort study based on myocardial strain and work.
- Paediatric mpox during Sierra Leone’s 2024 to 2025 clade IIb outbreak: A national surveillance and outbreak-investigation study of 415 children
- Patient-reported burden and adverse events of urodynamic investigation in adults with neurogenic lower urinary tract dysfunction
- Hepatology: Emerging Paradigms in MASLD, Viral Hepatitis, Cholestatic Liver Disease, Portal Hypertension and Hepatocellular Carcinoma
BibTeX
@article{mann2026european,
title = {{European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) steatotic liver disease special interest group position paper on screening, diagnosis and investigation of paediatric metabolic dysfunction‐associated steatotic liver disease}},
author = {Jake Peter Mann and Sander Lefere and Maarten Buytaert and Anna Alisi and Cigdem Arikan and Jernej Brecelj and Rachel M. Brown and Irene Degrassi and Giulia Fiore and Emer Fitzpatrick and Sven Francque and Christian A. Hudert and Wojciech Jańczyk and Lauren Johansen and Bart G.P. Koot and Anastasia Konidari and Eberhard Lurz and Claudia Mandato and María Mercadal‐Hally and Hadar Moran‐Lev and Antonella Mosca and Giusy Ranucci and Maria E. Rogalidou and Penelope C. Rose and Piotr Socha and Pietro Vajro and Elvira Verduci and Anita C. E. Vreugdenhil and N.Yu. Zavhorodnia and Aglaia Zellos and Ruth De Bruyne},
journal = {Journal of Pediatric Gastroenterology and Nutrition},
year = {2026},
month = jun,
doi = {10.1002/jpn3.70490},
url = {https://doi.org/10.1002/jpn3.70490},
note = {CC BY},
}
RIS
TY - JOUR
TI - European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) steatotic liver disease special interest group position paper on screening, diagnosis and investigation of paediatric metabolic dysfunction‐associated steatotic liver disease
AU - Jake Peter Mann
AU - Sander Lefere
AU - Maarten Buytaert
AU - Anna Alisi
AU - Cigdem Arikan
AU - Jernej Brecelj
AU - Rachel M. Brown
AU - Irene Degrassi
AU - Giulia Fiore
AU - Emer Fitzpatrick
AU - Sven Francque
AU - Christian A. Hudert
AU - Wojciech Jańczyk
AU - Lauren Johansen
AU - Bart G.P. Koot
AU - Anastasia Konidari
AU - Eberhard Lurz
AU - Claudia Mandato
AU - María Mercadal‐Hally
AU - Hadar Moran‐Lev
AU - Antonella Mosca
AU - Giusy Ranucci
AU - Maria E. Rogalidou
AU - Penelope C. Rose
AU - Piotr Socha
AU - Pietro Vajro
AU - Elvira Verduci
AU - Anita C. E. Vreugdenhil
AU - N.Yu. Zavhorodnia
AU - Aglaia Zellos
AU - Ruth De Bruyne
PY - 2026
DA - 2026/06/30
JO - Journal of Pediatric Gastroenterology and Nutrition
DO - 10.1002/jpn3.70490
UR - https://doi.org/10.1002/jpn3.70490
AB - Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common reason for elevated liver enzymes in children in Europe, affecting more than 5% of all children. Since the last iteration of this position paper, there have been substantial advances in our understanding of the disease. After a detailed literature review and thorough discussion, we established consensus recommendations for the diagnosis and assessment of MASLD in children. Alanine aminotransferase (ALT) ≥ 30 IU/L is a suitable screening test for MASLD in children over 10 years of age with obesity (body mass index z-score ≥+2), or in children of any age with additional risk factors. All patients with suspected MASLD should be assessed for alternative or concomitant diagnoses, as well as comorbidities. Patients who are not overweight, under 8 years old, or have any other red flags should be promptly referred for specialist assessment. Liver biopsy remains the gold standard for diagnosis and staging of MASLD, but should be reserved for diagnostic uncertainty, to guide treatment decisions, and risk stratification (e.g., prior to transition to adult care). While there is emerging data for non-invasive tests (e.g., transient elastography), it is unclear how to routinely implement these investigations in clinical practice. Combined changes of ≥20% in both ALT and gamma-glutamyl transferase may represent a useful non-invasive tool for monitoring disease severity over time. Most patients are appropriately investigated and managed by non-specialists where the focus is on holistic management of obesity and its complications. Future research should focus on how to use non-invasive tests to risk-stratify children, in particular, how to identify those with advanced fibrosis.
SN - 0277-2116
SN - 1536-4801
ER -