Novel risk loci for COVID-19 hospitalization among admixed American populations
Silvia Diz‐de AlmeidaiD, Raquel CruziD, André Ducati LuchessiiD, Jose Miguel Lorenzo-SalazariD, Miguel López de HerediaiD, Inés QuintelaiD, Rafaela González‐MontelongoiD, Vivian Nogueira SilbigeriD, Marta Sevilla PorrasiD, Jair Antonio TenorioiD, Julián B. NevadoiD, José María AguadoiD, Carlos Aguilar, Sergio AguileraiD, Virginia Almadana PachecoiD, Berta AlmogueraiD, Núria Álvarez, Álvaro Andreu-BernabeuiD, Eunate Arana‐ArriiD, Celso ArangoiD, Maria Jesús ArranziD, María-Jesús ArtigaiD, Raúl Cuauhtemoc Baptista-RosasiD, María Barreda‐SáncheziD, Moncef Belhassen‐GarcíaiD, , Juan Carlos SoutoiD
Abstract
The genetic basis of severe COVID-19 has been thoroughly studied, and many genetic risk factors shared between populations have been identified. However, reduced sample sizes from non-European groups have limited the discovery of population-specific common risk loci. In this second study nested in the SCOURGE consortium, we conducted a GWAS for COVID-19 hospitalization in admixed Americans, comprising a total of 4,702 hospitalized cases recruited by SCOURGE and seven other participating studies in the COVID-19 Host Genetic Initiative. We identified four genome-wide significant associations, two of which constitute novel loci and were first discovered in Latin American populations (BAZ2B and DDIAS). A trans-ethnic meta-analysis revealed another novel cross-population risk locus in CREBBP. Finally, we assessed the performance of a cross-ancestry polygenic risk score in the SCOURGE admixed American cohort. This study constitutes the largest GWAS for COVID-19 hospitalization in admixed Latin Americans conducted to date. This allowed to reveal novel risk loci and emphasize the need of considering the diversity of populations in genomic research.
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