TY - JOUR
T1 - Genetic Ancestry, Race, and Severity of Acutely Decompensated Cirrhosis in Latin America
AU - ACLARA Study Collaborators
AU - Farias, Alberto Queiroz
AU - Curto Vilalta, Anna
AU - Momoyo Zitelli, Patricia
AU - Pereira, Gustavo
AU - Goncalves, Luciana L.
AU - Torre, Aldo
AU - Diaz, Juan Manuel
AU - Gadano, Adrian C.
AU - Mattos, Angelo Z.
AU - Mendes, Liliana S.C.
AU - Alvares-da-Silva, Mario R.
AU - Bittencourt, Paulo L.
AU - Benitez, Carlos
AU - Alves Couto, Claudia
AU - Mendizabal, Manuel
AU - Toledo, Claudio L.
AU - Mazo, Daniel F.C.
AU - Castillo Barradas, Mauricio
AU - Uson Raposo, Eva M.
AU - Padilla-Machaca, P. Martín
AU - Zarela Lozano Miranda, Adelina
AU - Malé-Velázquez, René
AU - Castro Lyra, André
AU - Dávalos-Moscol, Milagros B.
AU - Pérez Hernández, José L.
AU - Ximenes, Rafael O.
AU - Faria Silva, Giovanni
AU - Beltrán-Galvis, Oscar A.
AU - González Huezo, María S.
AU - Bessone, Fernando
AU - Rocha, Tarciso D.S.
AU - Fassio, Eduardo
AU - Terra, Carlos
AU - Marín, Juan I.
AU - Sierra Casas, Patricia
AU - de la Peña-Ramirez, Carlos
AU - Aguilar Parera, Ferran
AU - Fernandes, Flavia
AU - da Penha Zago-Gomes, Maria
AU - Méndez-Guerrero, Osvely
AU - Marciano, Sebastián
AU - Mattos, Angelo A.
AU - Oliveira, Joao C.
AU - Guerreiro, Gabriel T.S.
AU - Codes, Liana
AU - Arrese, Marco
AU - Nardelli, Mateus J.
AU - Silva, Marcelo O.
AU - Palma-Fernandez, Renato
AU - Alcantara, Camila
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/9
Y1 - 2023/9
N2 - 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.
AB - 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.
KW - Ethnicity
KW - Liver Transplantation
KW - Outcomes
KW - Sociodemographic Data
KW - Systemic Inflammation
UR - https://www.scopus.com/pages/publications/85164612561
U2 - 10.1053/j.gastro.2023.05.033
DO - 10.1053/j.gastro.2023.05.033
M3 - Article
C2 - 37263305
AN - SCOPUS:85164612561
SN - 0016-5085
VL - 165
SP - 696
EP - 716
JO - Gastroenterology
JF - Gastroenterology
IS - 3
ER -