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(Sorbonne Université), Sven Francque(University of Antwerp), 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(The Graduate Center, CUNY), Juan Pablo Arab(Western University), Marco Arrese(University of Antwerp), Ramón Bataller(Virginia Commonwealth University), Ulrich Beuers(University of Chicago), Jérôme Boursier(Michael E. DeBakey VA Medical Center), Elisabetta Bugianesi(The Graduate Center, CUNY), Christopher D. Byrne(University Hospital Southampton NHS Foundation Trust), Graciela Castro‐Narro(Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán), Abhijit Chowdhury(The Graduate Center, CUNY), Helena Cortez‐Pinto(The Graduate Center, CUNY), Donna R. Cryer(The Graduate Center, CUNY), Kenneth Cusi(The Graduate Center, CUNY), Mohamed El‐Kassas(The Graduate Center, CUNY), Samuel Klein(Washington University in St. Louis), Wayne Eskridge(University of Chicago), Jian‐Gao Fan(The Graduate Center, CUNY), Samer Gawrieh(Indiana University School of Medicine), Cynthia D. Guy(Duke University Health System), Stephen A. Harrison(University of Oxford), Seung Up Kim(University of Antwerp), Bart G.P. Koot(Virginia Commonwealth University), Marko Korenjak(Baylor College of Medicine), Kris V. Kowdley(Michael E. DeBakey VA Medical Center), Florence Lacaille(Hôpital Necker-Enfants Malades), Rohit Loomba(University of California San Diego), Robert Mitchell-Thain(The Graduate Center, CUNY), Timothy R. Morgan(University of California, Irvine), Elisabeth E. Powell(Translational Research Institute), Michael Roden(Düsseldorf University Hospital), Manuel Romero‐Gómez(University of Chicago), Marcelo Silva(The Graduate Center, CUNY), Shivaram Prasad Singh(Antwerp University Hospital), Silvia Sookoian(Consejo Nacional de Investigaciones Científicas y Técnicas), C Wendy Spearman(University of Antwerp), Dina Tiniakos(Virginia Commonwealth University), Luca Valenti(Michael E. DeBakey VA Medical Center), Miriam B. Vos(University of Antwerp), Vincent Wai‐Sun Wong(University of Antwerp), Stavra A. Xanthakos(Cincinnati Children's Hospital Medical Center), Yusuf Yılmaz(University of Antwerp), Zobair M. Younossi(Inova Health System), Ansley Hobbs(The Graduate Center, CUNY), Marcela Villota‐Rivas(University of Antwerp), Philip N. Newsome(University Hospitals Birmingham NHS Foundation Trust), on behalf of the NAFLD Nomenclature consensus group
Hepatology
June 22, 2023
Cited by 2,822Open 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 favor 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 panelists 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. 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 nonstigmatising, and can improve awareness and patient identification.


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