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Authors

Alberto Queiroz Farias,
Anna Curto Vilalta,
Patrícia Momoyo Zitelli,
Gustavo Pereira,
Luciana L Goncalves,
Aldo Torre,
Juan Manuel Diaz,
Adrian C Gadano,
Angelo Z Mattos,
Liliana S C Mendes,
Mario R Alvares-da-Silva,
Paulo L Bittencourt,
Carlos Benitez,
Claudia Alves Couto,
Manuel Mendizabal,
Claudio L Toledo,
Daniel F Mazo,
Mauricio Castillo Barradas,
Eva M Uson Raposo,
P Martín Padilla-Machaca,
Adelina Zarela Lozano Miranda,
René Malé-Velázquez,
André Castro Lyra,
Milagros B Dávalos-Moscol,
Jose L Pérez Hernandez,
Rafael O Ximenes ,
Giovanni Faria Silva,
Oscar A Beltrán-Galvis,
María S González Huezo,
Fernando Bessone,
Tarciso D S Rocha,
Eduardo Fassio,
Carlos Terra,
Juan I Marín,
Patricia Sierra Casas,
Carlos de la Peña-Ramirez,
Ferran Aguilar Parera,
Flavia Fernandes,
Maria da Penha Zago-Gomes,
Osvely Méndez-Guerrero,
Sebastián Marciano,
Angelo A Mattos,
Joao C Oliveira ,
Gabriel T S Guerreiro,
Liana Codes,
Marco Arrese,
Mateus J Nardelli ,
Marcelo O Silva ,
Renato Palma-Fernandez,
Camila Alcantara,
Cristina Sánchez Garrido ,
Jonel Trebicka,
Thierry Gustot,
Javier Fernández,
Joan Clària,
Rajiv Jalan,
Paolo Angeli,
Vicente Arroyo,
Flair J Carrilho,
ACLARA Study Collaborators,

Abstract

Background & aims: Genetic ancestry or racial differences in health outcomes exist in diseases associated with systemic inflammation (eg, COVID-19). This study aimed to investigate the association of genetic ancestry and race with acute-on-chronic 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 who were nonelectively admitted to 44 hospitals from 7 Latin American countries.

Results: Three hundred ninety-five patients (31.0%) had ACLF of any grade at enrollment. Patients with ACLF had a 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 ACLF. In terms of race, a higher percentage of patients with ACLF than patients without ACLF were Native American and a lower percentage of patients with ACLF than patients without ACLF were European American or African American. In multivariable analyses that adjusted for differences in sociodemographic and clinical characteristics, the odds ratio for ACLF at enrollment was 1.08 (95% 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 CONCLUSIONS: In a large cohort of Latin American patients with acutely decompensated cirrhosis, increasing percentages of Native American ancestry and Native American race were factors independently associated with ACLF at enrollment.

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