dc.contributor.author | Diz-de Almeida, Silvia | |
dc.contributor.author | Cruz, Raquel | |
dc.contributor.author | Luchessi, Andre D. | |
dc.contributor.author | Lorenzo Salazar, José M | |
dc.contributor.author | López de Heredia, Miguel | |
dc.contributor.author | Quintela, Inés | |
dc.contributor.author | González Montelongo, Rafaela | |
dc.contributor.author | Nogueira Silbiger, Vivian | |
dc.contributor.author | Sevilla Porras, Marta | |
dc.contributor.author | Tenorio Castaño, Jair Antonio | |
dc.contributor.author | Nevado, Juan | |
dc.contributor.author | Aguado García, José María | |
dc.contributor.author | Aguilar, Carlos | |
dc.contributor.author | Aguilera Albesa, Sergio | |
dc.contributor.author | Almadana, Virginia | |
dc.contributor.author | Almoguera, Berta | |
dc.contributor.author | Alvarez, Nuria | |
dc.contributor.author | Fariñas Álvarez, María del Carmen | |
dc.contributor.author | Riancho Moral, José Antonio | |
dc.contributor.author | Tamayo Revuelta, Esther | |
dc.contributor.other | Universidad de Cantabria | es_ES |
dc.date.accessioned | 2025-02-28T18:17:11Z | |
dc.date.available | 2025-02-28T18:17:11Z | |
dc.date.issued | 2024 | |
dc.identifier.issn | 2050-084X | |
dc.identifier.uri | https://hdl.handle.net/10902/35812 | |
dc.description.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 genome-wide association study (GWAS) for COVID-19 hospitalization in admixed Americans, comprising a total of 4702 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. | es_ES |
dc.description.sponsorship | Acknowledgements: The contribution of the Centro National de Genotipado (CEGEN) and Centro de Supercomputación de Galicia (CESGA) for funding this project by providing supercomputing infrastructures is also acknowledged. The authors are also particularly grateful for the supply of material and the collaboration of patients, health professionals from participating centers and biobanks. Namely, Biobanc-Mur, and biobancs of the Complexo Hospitalario Universitario de A Coruña, Complexo Hospitalario Universitario de Santiago, Hospital Clínico San Carlos, Hospital La Fe, Hospital Universitario Puerta de Hierro Majadahonda—Instituto de Investigación Sanitaria Puerta de Hierro—Segovia de Arana, Hospital Ramón y Cajal, IDIBGI, IdISBa, IIS Biocruces Bizkaia, IIS Galicia Sur. Also biobanks of the Sistema de Salud de Aragón, Sistema Sanitario Público de Andalucía, and Banco Nacional de ADN. Instituto de Salud Carlos III (COV20_00622 to AC, COV20/00792 to MB, COV20_00181 to CA, COV20_1144 to MAJS and AFR, PI20/00876 to CF); European Union (ERDF) ‘A way of making Europe’. Fundación Amancio Ortega, Banco de Santander (to AC), Estrella de Levante SA and Colabora Mujer Association (to EGN) and Obra Social La Caixa (to RB); Agencia Estatal de Investigación (RTC-2017-6471-1 to CF), Cabildo Insular de Tenerife (CGIEU0000219140 ‘Apuestas científicas del ITER para colaborar en la lucha contra la COVID-19’ to CF) and Fundación Canaria Instituto de Investigación Sanitaria de Canarias (PIFIISC20/57 to CF). SD-DA was supported by a Xunta de Galicia predoctoral fellowship | es_ES |
dc.format.extent | 27 p. | es_ES |
dc.language.iso | eng | es_ES |
dc.rights | © Diz-de Almeida, Cruz et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited. | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.source | eLife, 2024, 13, RP93666 | es_ES |
dc.subject.other | COVID-19 | es_ES |
dc.subject.other | GWAS | es_ES |
dc.subject.other | SNP | es_ES |
dc.subject.other | Genetics | es_ES |
dc.subject.other | Genomics | es_ES |
dc.subject.other | None | es_ES |
dc.title | Novel risk loci for COVID-19 hospitalization among admixed American populations | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.relation.publisherVersion | https://doi.org/10.7554/eLife.93666.3 | es_ES |
dc.rights.accessRights | openAccess | es_ES |
dc.identifier.DOI | 10.7554/eLife.93666 | |
dc.type.version | publishedVersion | es_ES |