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Metabolic dysfunction-associated fatty liver disease and risk of incident chronic kidney disease: A nationwide cohort study

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dc.contributor.author김승업-
dc.contributor.author박근형-
dc.contributor.author박정탁-
dc.contributor.author안상훈-
dc.contributor.author정찬영-
dc.contributor.author김형우-
dc.contributor.author주영수-
dc.contributor.author고희병-
dc.date.accessioned2022-12-22T02:38:31Z-
dc.date.available2022-12-22T02:38:31Z-
dc.date.issued2022-07-
dc.identifier.issn1262-3636-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/191651-
dc.description.abstractAims: The recently proposed metabolic dysfunction-associated fatty liver disease (MAFLD) has been suggested to better reflect the metabolic components of fatty liver disease (FLD), compared to nonalcoholic fatty liver disease (NAFLD). This study investigated whether MAFLD identifies a higher proportion of individuals at risk of developing chronic kidney disease (CKD). Methods: 268,946 participants aged 40-64 years, who underwent National Health Insurance Service health examinations between 2009 and 2015 were included. Participants were categorized by presence of FLD, according to MAFLD or NAFLD. In participants with FLD, participants were categorized into three groups: non-metabolic risk (non-MR) NAFLD, MAFLD but not NAFLD, and overlapping FLD. Incident CKD was defined as the occurrence of eGFR < 60 mL/min/1.73m2 or proteinuria (≥ trace) on two consecutive health examinations. Results: 73,726 (27.4%) and 88,762 (33.0%) participants had NAFLD and MAFLD, respectively. During a median follow-up of 5.1 years, CKD occurred in 8,335 (6.2/1,000 person-years) participants. Compared to non-NAFLD participants, the adjusted hazard ratio (aHR) for incident CKD was 1.33 (95% CI, 1.27-1.39; P < 0.001) for participants with NAFLD. Compared to non-MAFLD participants, the aHR for participants with MAFLD was 1.39 (95% CI, 1.33-1.46; P < 0.001). When the analysis was confined to participants with FLD, compared to non-MR NAFLD participants, the aHRs for participants with MAFLD but not NAFLD, and those with overlapping FLD were 1.18 (95% CI, 1.01-1.39; P = 0.040) and 1.36 (95% CI, 1.19-1.54; P < 0.001), respectively. Conclusion: MAFLD identified a higher proportion of individuals at risk of developing CKD than NAFLD.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish, French-
dc.publisherMasson-
dc.relation.isPartOfDIABETES & METABOLISM-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHCohort Studies-
dc.subject.MESHHumans-
dc.subject.MESHIncidence-
dc.subject.MESHNon-alcoholic Fatty Liver Disease* / complications-
dc.subject.MESHNon-alcoholic Fatty Liver Disease* / epidemiology-
dc.subject.MESHRenal Insufficiency, Chronic* / complications-
dc.subject.MESHRenal Insufficiency, Chronic* / epidemiology-
dc.subject.MESHRetrospective Studies-
dc.titleMetabolic dysfunction-associated fatty liver disease and risk of incident chronic kidney disease: A nationwide cohort study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorChan-Young Jung-
dc.contributor.googleauthorHee Byung Koh-
dc.contributor.googleauthorKeun Hyung Park-
dc.contributor.googleauthorYoung Su Joo-
dc.contributor.googleauthorHyung Woo Kim-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorJung Tak Park-
dc.contributor.googleauthorSeung Up Kim-
dc.identifier.doi10.1016/j.diabet.2022.101344-
dc.contributor.localIdA00654-
dc.contributor.localIdA05973-
dc.contributor.localIdA01654-
dc.contributor.localIdA02226-
dc.contributor.localIdA06058-
dc.contributor.localIdA01151-
dc.contributor.localIdA03956-
dc.relation.journalcodeJ00719-
dc.identifier.eissn1878-1780-
dc.identifier.pmid35346856-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1262363622000271?via%3Dihub-
dc.subject.keywordChronic kidney disease-
dc.subject.keywordMetabolic dysfunction-associated fatty liver disease-
dc.subject.keywordNonalcoholic fatty liver disease-
dc.subject.keywordOutcomes-
dc.subject.keywordRisk factors-
dc.contributor.alternativeNameKim, Seung Up-
dc.contributor.affiliatedAuthor김승업-
dc.contributor.affiliatedAuthor박근형-
dc.contributor.affiliatedAuthor박정탁-
dc.contributor.affiliatedAuthor안상훈-
dc.contributor.affiliatedAuthor정찬영-
dc.contributor.affiliatedAuthor김형우-
dc.contributor.affiliatedAuthor주영수-
dc.citation.volume48-
dc.citation.number4-
dc.citation.startPage101344-
dc.identifier.bibliographicCitationDIABETES & METABOLISM, Vol.48(4) : 101344, 2022-07-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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