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dc.contributor.authorFarias, Alberto Queiroz
dc.contributor.authorVilalta, Anna Curto
dc.contributor.authorZitelli, Patrícia Momoyo
dc.contributor.authorPereira, Gustavo
dc.contributor.authorGoncalves, Luciana L.
dc.contributor.authorTorre, Aldo
dc.contributor.authorDiaz, Juan Manuel
dc.contributor.authorGadano, Adrian C.
dc.contributor.authorMattos, Angelo Z.
dc.contributor.authorMendes, Liliana S.C.
dc.contributor.authorAlvares-da-Silva, Mario R.
dc.contributor.authorBittencourt, Paulo L.
dc.contributor.authorBenitez, Carlos
dc.contributor.authorCouto, Claudia Alves
dc.contributor.authorMendizabal, Manuel
dc.contributor.authorToledo, Claudio L.
dc.contributor.authorMazo, Daniel F.
dc.contributor.authorBarradas, Mauricio Castillo
dc.contributor.authorUson Raposo, Eva M.
dc.contributor.authorPadilla-Machaca, P. Martín
dc.contributor.authorLozano Miranda, Adelina Zarela
dc.contributor.authorMalé-Velázquez, René
dc.contributor.authorLyra, André Castro
dc.contributor.authorDávalos-Moscol, Milagros B.
dc.contributor.authorPérez Hernandez, Jose L
dc.contributor.authorXimenes, Rafael O.
dc.contributor.authorSilva, Giovanni Faria
dc.contributor.authorBeltrán-Galvis, Oscar A.
dc.contributor.authorGonzález Huezo, María S.
dc.contributor.authorBessone, Fernando
dc.contributor.authorRocha, Tarciso D.S.
dc.contributor.authorFassio, Eduardo
dc.contributor.authorTerra, Carlos
dc.contributor.authorMarín, Juan I.
dc.contributor.authorCasas, Patricia Sierra
dc.contributor.authorPeña-Ramirez, Carlos de la
dc.contributor.authorParera, Ferran Aguilar
dc.contributor.authorFernandes, Flavia
dc.contributor.authorda Penha Zago-Gomes, Maria
dc.contributor.authorMéndez-Guerrero, Osvely
dc.contributor.authorMarciano, Sebastián
dc.contributor.authorMattos, Angelo A.
dc.contributor.authorOliveira, Joao C.
dc.contributor.authorGuerreiro, Gabriel T.S.
dc.contributor.authorCodes, Liana
dc.contributor.authorArrese, Marco
dc.contributor.authorNardelli, Mateus J.
dc.contributor.authorSilva, Marcelo O.
dc.contributor.authorPalma-Fernandez, Renato
dc.contributor.authorAlcantara, Camila
dc.contributor.authorGarrido, Cristina Sánchez
dc.contributor.authorTrebicka, Jonel
dc.contributor.authorGustot, Thierry
dc.contributor.authorFernández, Javier
dc.contributor.authorClària, Joan
dc.contributor.authorJalan, Rajiv
dc.contributor.authorAngeli, Paolo
dc.contributor.authorArroyo, Vicente
dc.contributor.authorMoreau, Richard
dc.contributor.authorCarrilho, Flair J.
dc.date.accessioned2023-05-30T14:22:38Z
dc.date.available2023-05-30T14:22:38Z
dc.date.issued2023-05-30
dc.identifier.citationGastroenterology. 2023.es_PE
dc.identifier.issn0016-5085
dc.identifier.urihttps://hdl.handle.net/20.500.12959/3755
dc.description.abstractBACKGROUND & AIMS: Genetic ancestry or racial differences in health outcomes exist in diseases associated with systemic inflammation (e.g., Covid-19). This study aimed to investigate the association of genetic ancestry and race with acute-onchronic liver failure (ACLF), which is characterized by acute systemic inflammation, multi-organ failure and high risk of short-term death. METHODS: This prospective cohort study analyzed a comprehensive set of data including genetic ancestry and race, among several others, in 1274 patients with acutely decompensated cirrhosis (ADC) who were nonelectively admitted to 44 hospitals from 7 Latin American countries. RESULTS: 395 (31.0%) had ACLF of any grade at enrollment. Patients with ACLF had higher median percentage of Native American genetic ancestry and lower median percentage of European ancestry than patients without ACLF (22.6% vs 12.9% and 53.4% vs 59.6%, respectively). The median percentage of African genetic ancestry was low among patients with ACLF and among those without. In terms of race, a higher percentage of patients with ACLF than patients without ACLF were Native Americans and a lower percentage of patients with ACLF than patients without were European Americans or African Americans. In multivariable analyses that adjusted for differences in sociodemographic and clinical characteristics, the odds ratio for ACLF at enrollment was 1.08 (95% confidence interval [CI], 1.03-1.13) with Native American genetic ancestry and 2.57 (95% CI, 1.84-3.58) for Native American race vs. European American race.es_PE
dc.formatapplication/pdfes_PE
dc.language.isoenges_PE
dc.publisherInstituto American Gastroenterological Associationes_PE
dc.relation.urihttps://www.sciencedirect.com/science/article/pii/S0016508523008065es_PE
dc.rightsinfo:eu-repo/semantics/openAccesses_PE
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/es_PE
dc.subjectSystemic inflammationes_PE
dc.subjectEthnicityes_PE
dc.subjectSociodemographic dataes_PE
dc.subjectLiver transplantationes_PE
dc.subjectOutcomeses_PE
dc.titleGenetic Ancestry, Race, and Severity of Acutely Decompensated Cirrhosis in Latin Americaes_PE
dc.title.alternativeAscendencia genética, raza y gravedad de la cirrosis aguda descompensada en América Latinaes_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.19es_PE
dc.identifier.doihttps://doi.org/10.1053/j.gastro.2023.05.033


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