Advancing towards accurate phenotyping based on metabolic and fibrosis risk in metabolic-dysfunction associated steatotic liver disease: one step closer to personalized care
- PMID: 38322230
- PMCID: PMC10839720
- DOI: 10.21037/hbsn-23-563
Advancing towards accurate phenotyping based on metabolic and fibrosis risk in metabolic-dysfunction associated steatotic liver disease: one step closer to personalized care
Keywords: Metabolic-dysfunction associated steatotic liver disease (MASLD); advanced fibrosis; non-invasive tests (NITs); type 2 diabetes (T2D).
Conflict of interest statement
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://hbsn.amegroups.com/article/view/10.21037/hbsn-23-563/coif). S.M.M. reports grant for educational development from Bristol-Myers Squibb, payment honoraria for lectures from Bayer and Asopharma and travel and meeting funding from Bayer, Eisai and MSD. The other authors have no conflicts of interest to declare.
Comment on
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A prospective study on the prevalence of NAFLD, advanced fibrosis, cirrhosis and hepatocellular carcinoma in people with type 2 diabetes.J Hepatol. 2023 Mar;78(3):471-478. doi: 10.1016/j.jhep.2022.11.010. Epub 2022 Nov 19. J Hepatol. 2023. PMID: 36410554 Free PMC article.
References
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- Huang DQ, Noureddin N, Ajmera V, et al. Type 2 diabetes, hepatic decompensation, and hepatocellular carcinoma in patients with non-alcoholic fatty liver disease: an individual participant-level data meta-analysis. Lancet Gastroenterol Hepatol 2023;8:829-36. 10.1016/S2468-1253(23)00157-7 - DOI - PMC - PubMed
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