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©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Pathophysiol. May 24, 2024; 15(2): 92791
Published online May 24, 2024. doi: 10.4291/wjgp.v15.i2.92791
Metabolic dysfunction-associated steatotic liver disease heterogeneity: Need of subtyping
Shahid Habib
Shahid Habib, Department of Hepatology, Liver Institute PLLC, Tucson, AZ 85716, United States
Author contributions: Habib S hypothesis genesis, data collection, critical data review and synthesis, manuscript writing and submission.
Conflict-of-interest statement: There is no conflict of interest associated with any of the senior author or other coauthors contributed their efforts in this manuscript.
Corresponding author: Shahid Habib, MD, Doctor, Researcher, Department of Hepatology, Liver Institute PLLC, 3232 E Speedway Bvd, Tucson, AZ 85716, United States. shabib@liverinstitutepllc.org
Received: February 5, 2024
Revised: April 4, 2024
Accepted: April 24, 2024
Published online: May 24, 2024
Processing time: 107 Days and 14.4 Hours
Core Tip

Core Tip: Metabolic dysfunctions-associated steatotic liver disease (MASLD) is a pathogenically heterogeneous disease with dynamic pathological features. The cardiometabolic risk of MASLD varies based on underlying etiopathogenic processes. Four subtypes of MASLD have been identified: Diabetic, non-diabetic (insulin resistance), genetic and mixed. These subtypes have not been clearly defined yet as separate entities. Given such heterogeneity, the behavior and outcome of MASLD in each patient is expected to be different. Therefore, a single drug is not expected to work for all patients with MASLD. The natural history of MASLD subtypes is unknown. There is an unmet need to categorize its subtypes and prospective studies are needed to characterize each subtype.