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Zerehpooshnesfchi et al. Metab Target Organ Damage. 2025;5:15         Metabolism and
               DOI: 10.20517/mtod.2025.04
                                                                             Target Organ Damage




               Review                                                                        Open Access



               Dual etiology vs. MetALD: how MAFLD and MASLD
               address liver diseases coexistence


                                     1
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               Shadi Zerehpooshnesfchi , Amedeo Lonardo , Jian-Gao Fan , Reda Elwakil , Tawesak Tanwandee , Munira
                        6
                                      7
               Y. Altarrah , Necati Örmeci , Mohammed Eslam 1
               1
                Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney, Westmead 2145,
               Australia.
               2
                Department of Internal Medicine, Ospedale Civile di Baggiovara (-2023), Azienda Ospedaliero-Universitaria, Modena 41125,
               Italy.
               3
                Center for Fatty Liver, Department of Gastroenterology, Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of
               Medicine, Shanghai Key Lab of Pediatric Gastroenterology and Nutrition, Shanghai 200082, China.
               4
                Tropical Medicine Department, Faculty of Medicine, Ain Shams Universit, Cairo 11517, Egypt.
               5
                Division of Gastroenterology, Department of Medicine, Faculty of Medicine Siriraj Hospital(-2023), Mahidol University,
               Bangkok 10700, Thailand.
               6
                Gastroenterology and Transplant Hepatology Unit, Thunayan Al Ghanim Gastroenterology Center, Al Amiri Hospital, Kuwait
               City 35001, Kuwait.
               7
                Department of Gastroenterology, İstanbul Health and Technology University, İstanbul 34452, Türkiye.
               Correspondence to: Prof. Mohammed Eslam, Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital
               and University of Sydney, 176 Hawkesbury Road, Westmead 2145, Australia. E-mail: mohammed.eslam@sydney.edu.au
               How to cite this article: Zerehpooshnesfchi S, Lonardo A, Fan JG, Elwakil R, Tanwandee T, Altarrah MY, Örmeci N, Eslam M.
               Dual etiology vs. MetALD: how MAFLD and MASLD address liver diseases coexistence. Metab Target Organ Damage. 2025;5:15.
               https://dx.doi.org/10.20517/mtod.2025.04
               Received: 13 Jan 2025  First Decision: 28 Feb 2025  Revised: 7 Mar 2025  Accepted: 21 Mar 2025  Published: 27 Mar 2025
               Academic Editor: Linda L. Henry  Copy Editor: Ting-Ting Hu  Production Editor: Ting-Ting Hu
               Abstract
               Fatty liver disease associated with metabolic dysfunction has emerged as a significant global health challenge. This
               condition often coexists with other liver diseases, such as alcohol-related liver disease and viral hepatitis,
               complicating both diagnosis and management. To address the limitations of the non-alcoholic fatty liver disease
               (NAFLD) classification, two alternative frameworks have been proposed: metabolic dysfunction-associated fatty
               liver disease (MAFLD) in 2020 and metabolic dysfunction-associated steatotic liver disease (MASLD) in 2023. A
               key difference between these definitions is how they consider fatty liver disease in relation to the coexistence of
               other liver conditions. MAFLD adopts a dual etiology concept, creating a unified classification system that aligns
               with contemporary clinical and epidemiological needs. In contrast, MASLD introduces a new term, MetALD
               (metabolic and alcohol-related/associated liver disease), to describe patients who have both metabolic





                           © The Author(s) 2025. Open Access This article is licensed under a Creative Commons Attribution 4.0
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