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dc.rights.licenseopenen_US
dc.contributor.authorMALLET, Vincent
dc.contributor.authorPARLATI, Lucia
dc.contributor.authorMARTININO, Alessandro
dc.contributor.authorSCARANO PEREIRA, Juan Pablo
dc.contributor.authorNAVAS JIMENEZ, Carmen
dc.contributor.authorSAKKA, Mehdi
dc.contributor.authorBOUAM, Samir
dc.contributor.authorRETBI, Aurelia
dc.contributor.authorKRASTEVA, Donika
dc.contributor.authorMERITET, Jean Francois
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSCHWARZINGER, Michael
dc.contributor.authorTHABUT, Dominique
dc.contributor.authorRUFAT, Pierre
dc.contributor.authorBONNEFONT-ROUSSELOT, Dominique
dc.contributor.authorSOGNI, Philippe
dc.contributor.authorPOL, Stanislas
dc.contributor.authorTSOCHATZIS, Emmanuel
dc.contributor.authorDEMOSTHENES RESEARCH, Group
dc.date.accessioned2021-12-06T09:25:50Z
dc.date.available2021-12-06T09:25:50Z
dc.date.issued2021-10-01
dc.identifier.issn1600-0641 (Electronic) 0168-8278 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/123985
dc.description.abstractEnBACKGROUND AND AIMS: There are uncertainties on the burden of liver disease in patients with type-2 diabetes (T2D). METHODS: We measured adjusted hazard ratios of liver disease progression to hepatocellular cancer and/or decompensated cirrhosis in a 2010-2020 retrospective, bicentric, longitudinal, cohort of 52,066 hospitalized patients with T2D. RESULTS: Mean age was 64±14 years and 58% were men. Alcohol use disorders accounted for 57% of liver-related complications and were associated with all liver-related risk factors. Non-metabolic liver-related risk factors accounted for 37% of the liver burden. T2D control was not associated with liver disease progression. The incidence (95% confidence interval) of liver-related complications and of competing mortality were 3.9 (3.5-4.3) and 27.8 (26.7-28.9) per 1000 person-years at risk, respectively. The cumulative incidence of liver disease progression exceeded the cumulative incidence of competing mortality only in the presence of a well-identified risk factors of liver disease progression, including alcohol use. The incidence of hepatocellular cancer was 0.3 (95% CI, 0.1-0.5) per 1000 person-year in patients with obesity and it increased with age. The adjusted hazard ratios of liver disease progression were 55.7 (40.5-76.6), 3.5 (2.3-5.2), 8.9 (6.9-11.5), and 1.5 (1.1-2.1), for alcoholic liver disease, alcohol use disorders without alcoholic liver disease, non-metabolic liver-related risk factors, and obesity, respectively. The attributable fractions of alcohol use disorders, non-metabolic liver risk-related risk factors, and obesity to the liver burden were 55%, 14%, and 7%, respectively. CONCLUSIONS: In this analysis of data from two hospital-based cohorts of patients with T2D, alcohol use disorders, rather than obesity, contributed to most of the liver burden. These results suggest that patients with T2D should be advised to drink minimal amounts of alcohol. LAY SUMMARY: • There is uncertainty on the burden of liver-related complications in patients with type-2 diabetes • We studied the risks of liver cancer and complications of liver disease in over 50,000 patients with type-2 diabetes • We found that alcohol was the main factor associated with complications of liver disease • This finding has major implications on the alcohol advice given to patients with type-2 diabetes.
dc.language.isoENen_US
dc.subject.enType-2 diabetes
dc.subject.enHepatocellular carcinoma
dc.subject.enCirrhosis
dc.subject.enAlcohol use disorders
dc.subject.enNon-alcoholic liver disease
dc.subject.enNon-alcoholic steatohepatitis
dc.title.enBurden of liver disease progression in hospitalized patients with type 2 diabetes mellitus
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.jhep.2021.09.030en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed34606913en_US
bordeaux.journalJournal of Hepatologyen_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03466693
hal.version1
hal.date.transferred2021-12-06T09:25:52Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
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