Genetic Ancestry, Race, and Severity of Acutely Decompensated Cirrhosis in Latin America
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https://www.sciencedirect.com/science/article/pii/S0016508523008065Date
2023-05-30Author(s)
Farias, Alberto Queiroz
Vilalta, Anna Curto
Zitelli, Patrícia Momoyo
Pereira, Gustavo
Goncalves, Luciana L.
Torre, Aldo
Diaz, Juan Manuel
Gadano, Adrian C.
Mattos, Angelo Z.
Mendes, Liliana S.C.
Alvares-da-Silva, Mario R.
Bittencourt, Paulo L.
Benitez, Carlos
Couto, Claudia Alves
Mendizabal, Manuel
Toledo, Claudio L.
Mazo, Daniel F.
Barradas, Mauricio Castillo
Uson Raposo, Eva M.
Padilla-Machaca, P. Martín
Lozano Miranda, Adelina Zarela
Malé-Velázquez, René
Lyra, André Castro
Dávalos-Moscol, Milagros B.
Pérez Hernandez, Jose L
Ximenes, Rafael O.
Silva, Giovanni Faria
Beltrán-Galvis, Oscar A.
González Huezo, María S.
Bessone, Fernando
Rocha, Tarciso D.S.
Fassio, Eduardo
Terra, Carlos
Marín, Juan I.
Casas, Patricia Sierra
Peña-Ramirez, Carlos de la
Parera, Ferran Aguilar
Fernandes, Flavia
da Penha Zago-Gomes, Maria
Méndez-Guerrero, Osvely
Marciano, Sebastián
Mattos, Angelo A.
Oliveira, Joao C.
Guerreiro, Gabriel T.S.
Codes, Liana
Arrese, Marco
Nardelli, Mateus J.
Silva, Marcelo O.
Palma-Fernandez, Renato
Alcantara, Camila
Garrido, Cristina Sánchez
Trebicka, Jonel
Gustot, Thierry
Fernández, Javier
Clària, Joan
Jalan, Rajiv
Angeli, Paolo
Arroyo, Vicente
Moreau, Richard
Carrilho, Flair J.
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Ascendencia genética, raza y gravedad de la cirrosis aguda descompensada en América Latina
Abstract
BACKGROUND & 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.
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