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Cited 37 time in webofscience Cited 39 time in scopus
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Non-alcoholic fatty liver diseases: update on the challenge of diagnosis and treatment

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dc.contributor.authorOh, Hyunwoo-
dc.contributor.authorJun, Dae Won-
dc.contributor.authorSaeed, Waqar K.-
dc.contributor.authorNguyen, Mindie H.-
dc.date.accessioned2021-08-02T16:28:02Z-
dc.date.available2021-08-02T16:28:02Z-
dc.date.created2021-05-12-
dc.date.issued2016-09-
dc.identifier.issn2287-2728-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/22210-
dc.description.abstractThe prevalence of non-alcoholic fatty liver disease (NAFLD) is estimated to be 25-30% of the population, and is the most common cause of elevated liver enzymes in Korea. NAFLD is a "hot potato" for pharmaceutical companies. Many clinical trials are underway to develop a first-in-class drug to treat NAFLD. However, there are several challenging issues regarding the diagnosis of NAFLD. Currently, liver biopsy is the gold standard method for the diagnosis of NAFLD and steatohepatitis. Ideally, globally recognized standards for histological diagnosis and methods to optimize observer agreement on biopsy interpretation should be developed. Liver biopsy is the best method rather than a perfect one. Recently, multi-parametric magnetic resonance imagery can estimate the amount of intrahepatic fat successfully and is widely used in clinical trials. But no diagnostic method can discriminate between steatohepatitis and simple steatosis. The other unresolved issue in regard to NAFLD is the absence of satisfactory treatment options. Vitamin E and obeticholic acid have shown protective effects in randomized controlled trials, but this drug has not been approved for use in Korea. This study will provide a description of diagnostic methods and treatments that are currently recommended for NAFLD.-
dc.language영어-
dc.language.isoen-
dc.publisherKOREAN ASSOC STUDY LIVER-
dc.titleNon-alcoholic fatty liver diseases: update on the challenge of diagnosis and treatment-
dc.typeArticle-
dc.contributor.affiliatedAuthorJun, Dae Won-
dc.identifier.doi10.3350/cmh.2016.0049-
dc.identifier.scopusid2-s2.0-85014810867-
dc.identifier.bibliographicCitationCLINICAL AND MOLECULAR HEPATOLOGY, v.22, no.3, pp.327 - 335-
dc.relation.isPartOfCLINICAL AND MOLECULAR HEPATOLOGY-
dc.citation.titleCLINICAL AND MOLECULAR HEPATOLOGY-
dc.citation.volume22-
dc.citation.number3-
dc.citation.startPage327-
dc.citation.endPage335-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusCLINICAL SCORING SYSTEM-
dc.subject.keywordPlusLIFE-STYLE INTERVENTION-
dc.subject.keywordPlusMORBIDLY OBESE-PATIENTS-
dc.subject.keywordPlusHEPATIC STEATOSIS-
dc.subject.keywordPlusSTEATOHEPATITIS NASH-
dc.subject.keywordPlusPLASMA CYTOKERATIN-18-
dc.subject.keywordPlusHISTOLOGICAL LESIONS-
dc.subject.keywordPlusRANDOMIZED-TRIAL-
dc.subject.keywordPlusBIOMARKER PANEL-
dc.subject.keywordPlusFIBROSIS-
dc.subject.keywordAuthorNon-alcoholic fatty liver-
dc.subject.keywordAuthorDiagnosis-
dc.subject.keywordAuthorTreatment-
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