A multisociety Delphi consensus statement on new fatty liver disease nomenclature

Mary E. Rinella(University of Chicago), Jeffrey V. Lazarus(The Graduate Center, CUNY), Vlad Ratziu(Fondation pour l’innovation en Cadiométabolisme et Nutrition), Sven Francque(Antwerp University Hospital), Arun J. Sanyal(Virginia Commonwealth University), Fasiha Kanwal(Michael E. DeBakey VA Medical Center), Diana Romero(The Graduate Center, CUNY), Manal F. Abdelmalek(Mayo Clinic), Quentin M. Anstee(Newcastle University), Juan Pablo Arab(Pontificia Universidad Católica de Chile), Marco Arrese(Pontificia Universidad Católica de Chile), Ramón Bataller(Consorci Institut D'Investigacions Biomediques August Pi I Sunyer), Ulrich Beuers(Amsterdam University Medical Centers), Jérôme Boursier(Université d'Angers), Elisabetta Bugianesi(University of Turin), Christopher D. Byrne(University Hospital Southampton NHS Foundation Trust), Graciela Castro‐Narro(Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán), Abhijit Chowdhury, Helena Cortez‐Pinto(University of Lisbon), Donna R. Cryer(Liver Institute Northwest), Kenneth Cusi(University of Florida), Mohamed El‐Kassas(Helwan University), Samuel Klein(Washington University in St. Louis), Wayne Eskridge, Jian‐Gao Fan(XinHua Hospital), Samer Gawrieh(Indiana University – Purdue University Indianapolis), Cynthia D. Guy(Duke University Health System), Stephen A. Harrison(University of Oxford), Seung Up Kim(Yonsei University), Bart G.P. Koot(University of Amsterdam), Marko Korenjak(European Federation of Allergy and Airways Diseases Patients Associations), Kris V. Kowdley(Washington State University), Florence Lacaille(Hôpital Necker-Enfants Malades), Rohit Loomba(University of California San Diego), Robert Mitchell-Thain(PBC Foundation), Timothy R. Morgan(University of California, Irvine), Elisabeth E. Powell(QIMR Berghofer Medical Research Institute), Michael Roden(German Center for Diabetes Research), Manuel Romero‐Gómez(Instituto de Biomedicina de Sevilla), Marcelo Silva(Austral University), Shivaram Prasad Singh, Silvia Sookoian(Universidad Abierta Interamericana), C Wendy Spearman(University of Cape Town), Dina Tiniakos(National and Kapodistrian University of Athens), Luca Valenti(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Miriam B. Vos(Children's Healthcare of Atlanta), Vincent Wai‐Sun Wong(Chinese University of Hong Kong), Stavra A. Xanthakos(Cincinnati Children's Hospital Medical Center), Yusuf Yılmaz(Recep Tayyip Erdoğan University), Zobair M. Younossi(Inova Health System), Ansley Hobbs(The Graduate Center, CUNY), Marcela Villota‐Rivas(Barcelona Institute for Global Health), Philip N. Newsome(University Hospitals Birmingham NHS Foundation Trust)
Journal of Hepatology
June 24, 2023
Cited by 2,630Open Access
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Abstract

The principal limitations of the terms NAFLD and NASH are the reliance on exclusionary confounder terms and the use of potentially stigmatising language. This study set out to determine if content experts and patient advocates were in favour of a change in nomenclature and/or definition. A modified Delphi process was led by three large pan-national liver associations. The consensus was defined a priori as a supermajority (67%) vote. An independent committee of experts external to the nomenclature process made the final recommendation on the acronym and its diagnostic criteria. A total of 236 panellists from 56 countries participated in 4 online surveys and 2 hybrid meetings. Response rates across the 4 survey rounds were 87%, 83%, 83%, and 78%, respectively. Seventy-four percent of respondents felt that the current nomenclature was sufficiently flawed to consider a name change. The terms "nonalcoholic" and "fatty" were felt to be stigmatising by 61% and 66% of respondents, respectively. Steatotic liver disease was chosen as an overarching term to encompass the various aetiologies of steatosis. The term steatohepatitis was felt to be an important pathophysiological concept that should be retained. The name chosen to replace NAFLD was metabolic dysfunction-associated steatotic liver disease (MASLD). There was consensus to change the definition to include the presence of at least 1 of 5 cardiometabolic risk factors. Those with no metabolic parameters and no known cause were deemed to have cryptogenic steatotic liver disease. A new category, outside pure metabolic dysfunction-associated steatotic liver disease, termed metabolic and alcohol related/associated liver disease (MetALD), was selected to describe those with metabolic dysfunction-associated steatotic liver disease, who consume greater amounts of alcohol per week (140-350 g/wk and 210-420 g/wk for females and males, respectively). The new nomenclature and diagnostic criteria are widely supported and non-stigmatising, and can improve awareness and patient identification.


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