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Epidemiology, pathophysiology and clinical aspects of Hepatocellular Carcinoma in MAFLD patients

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dc.contributor.author김미나-
dc.contributor.author안상훈-
dc.date.accessioned2025-04-17T08:21:10Z-
dc.date.available2025-04-17T08:21:10Z-
dc.date.issued2024-10-
dc.identifier.issn1936-0533-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/204576-
dc.description.abstractHepatocellular carcinoma (HCC) is undergoing a transformative shift, with metabolic-associated fatty liver disease (MAFLD) emerging as a dominant etiology. Diagnostic criteria for MAFLD involve hepatic steatosis and metabolic dysregulation. Globally, MAFLD prevalence stands at 38.77%, significantly linked to the escalating rates of obesity. Epidemiological data indicate a dynamic shift in the major etiologies of hepatocellular carcinoma (HCC), transitioning from viral to metabolic liver diseases. Besides the degree of liver fibrosis, several modifiable lifestyle risk factors, such as type 2 diabetes, obesity, alcohol use, smoking, and HBV, HCV infection contribute to the pathogenesis of HCC. Moreover gut microbiota and genetic variants may contribute to HCC development.The pathophysiological link between MAFLD and HCC involves metabolic dysregulation, impairing glucose and lipid metabolism, inflammation and oxidative stress. Silent presentation poses challenges in early MAFLD-HCC diagnosis. Imaging, biopsy, and AI-assisted techniques aid diagnosis, while HCC surveillance in non-cirrhotic MAFLD patients remains debated.ITA.LI.CA. group proposes a survival-based algorithm for treatment based on Barcelona clinic liver cancer (BCLC) algorithm. Liver resection, transplantation, ablation, and locoregional therapies are applied based on the disease stage. Systemic treatments is promising, with initial immunotherapy results indicating a less favorable response in MAFLD-related HCC.Adopting lifestyle interventions and chemopreventive measures with medications, including aspirin, metformin, and statins, constitute promising approaches for the primary prevention of HCC.Prognosis is influenced by multiple factors, with MAFLD-HCC associated with prolonged survival. Emerging diagnostic biomarkers and epigenomic markers, show promising results for early HCC detection in the MAFLD population.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherSpringer-
dc.relation.isPartOfHEPATOLOGY INTERNATIONAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHCarcinoma, Hepatocellular* / diagnosis-
dc.subject.MESHCarcinoma, Hepatocellular* / epidemiology-
dc.subject.MESHCarcinoma, Hepatocellular* / etiology-
dc.subject.MESHCarcinoma, Hepatocellular* / therapy-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms* / diagnosis-
dc.subject.MESHLiver Neoplasms* / epidemiology-
dc.subject.MESHLiver Neoplasms* / etiology-
dc.subject.MESHLiver Neoplasms* / therapy-
dc.subject.MESHNon-alcoholic Fatty Liver Disease / diagnosis-
dc.subject.MESHNon-alcoholic Fatty Liver Disease / epidemiology-
dc.subject.MESHNon-alcoholic Fatty Liver Disease / physiopathology-
dc.subject.MESHNon-alcoholic Fatty Liver Disease / therapy-
dc.subject.MESHRisk Factors-
dc.titleEpidemiology, pathophysiology and clinical aspects of Hepatocellular Carcinoma in MAFLD patients-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorMaria Eva Argenziano-
dc.contributor.googleauthorMi Na Kim-
dc.contributor.googleauthorMichele Montori-
dc.contributor.googleauthorAlessandro Di Bucchianico-
dc.contributor.googleauthorDaniele Balducci-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorGianluca Svegliati Baroni-
dc.identifier.doi10.1007/s12072-024-10692-4-
dc.contributor.localIdA00440-
dc.contributor.localIdA02226-
dc.relation.journalcodeJ00986-
dc.identifier.eissn1936-0541-
dc.identifier.pmid39012579-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s12072-024-10692-4-
dc.subject.keywordHepatocellular carcinoma-
dc.subject.keywordMAFLD-
dc.subject.keywordPrevention-
dc.subject.keywordRisk factor-
dc.contributor.alternativeNameKim, Mi Na-
dc.contributor.affiliatedAuthor김미나-
dc.contributor.affiliatedAuthor안상훈-
dc.citation.volume18-
dc.citation.numberSUPPL 2-
dc.citation.startPage922-
dc.citation.endPage940-
dc.identifier.bibliographicCitationHEPATOLOGY INTERNATIONAL, Vol.18(SUPPL 2) : 922-940, 2024-10-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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