dc.contributor.author | Martínez-Sanz, Javier | |
dc.contributor.author | Jiménez, Daniel | |
dc.contributor.author | Martínez-Campelo, Laura | |
dc.contributor.author | Cruz, Raquel | |
dc.contributor.author | Vizcarra, Pilar | |
dc.contributor.author | Sánchez-Conde, Matilde | |
dc.contributor.author | Ron, Raquel | |
dc.contributor.author | Rodríguez, Mario | |
dc.contributor.author | Herrera, Sabina | |
dc.contributor.author | Moreno, Santiago | |
dc.contributor.author | Lopez-Huertas, Maria Rosa | |
dc.contributor.author | Serrano-Villar, Sergio | |
dc.date.accessioned | 2022-03-25T12:56:44Z | |
dc.date.available | 2022-03-25T12:56:44Z | |
dc.date.issued | 2021-12 | |
dc.identifier.citation | Emerg Microbes Infect. 2021 Dec;10(1):493-496. | es_ES |
dc.identifier.uri | http://hdl.handle.net/20.500.12105/13823 | |
dc.description.abstract | We aim to evaluate the role of single-nucleotide polymorphisms of the angiotensin-converting enzyme 2 in susceptibility to SARS-CoV-2 infection. We included 28 uninfected but highly exposed healthcare workers and 39 hospitalized patients with COVID-19. Thirty-five SNPs were rationally selected. Two variants were associated with increased risk of being susceptible to SARS-CoV-2: the minor A allele in the rs2106806 variant (OR 3.75 [95% CI 1.23-11.43]) and the minor T allele in the rs6629110 variant (OR 3.39 [95% CI 1.09-10.56]). Evaluating the role of genetic variants in susceptibility to SARS-CoV-2 infection could help identify more vulnerable individuals and suggest potential drug targets for COVID-19 patients. | es_ES |
dc.description.sponsorship | This work was supported by Instituto de Salud Carlos III: [grant number AC17/00019,COV20/00349,PI18/00154,PT17/0019]; Merck, Sharp & Dohme: [Ref IISP 59181]. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Taylor & Francis | es_ES |
dc.type.hasVersion | VoR | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | * |
dc.subject | COVID-19 | es_ES |
dc.subject | SARS-CoV-2 | es_ES |
dc.subject | Genetic variants | es_ES |
dc.subject | Single-nucleotide polymorphism | es_ES |
dc.subject | Susceptibility | es_ES |
dc.subject.mesh | Genetic Predisposition to Disease | es_ES |
dc.subject.mesh | Health Personnel | es_ES |
dc.subject.mesh | Polymorphism, Single Nucleotide | es_ES |
dc.subject.mesh | SARS-CoV-2 | es_ES |
dc.subject.mesh | Adult | es_ES |
dc.subject.mesh | Aged | es_ES |
dc.subject.mesh | Aged, 80 and over | es_ES |
dc.subject.mesh | Angiotensin-Converting Enzyme 2 | es_ES |
dc.subject.mesh | COVID-19 | es_ES |
dc.subject.mesh | Female | es_ES |
dc.subject.mesh | Humans | es_ES |
dc.subject.mesh | Male | es_ES |
dc.subject.mesh | Middle Aged | es_ES |
dc.title | Role of ACE2 genetic polymorphisms in susceptibility to SARS-CoV-2 among highly exposed but non infected healthcare workers | es_ES |
dc.type | journal article | es_ES |
dc.rights.license | Atribución-NoComercial 4.0 Internacional | * |
dc.identifier.pubmedID | 33704002 | es_ES |
dc.format.volume | 10 | es_ES |
dc.format.number | 1 | es_ES |
dc.format.page | 493-496 | es_ES |
dc.identifier.doi | 10.1080/22221751.2021.1902755 | es_ES |
dc.contributor.funder | Instituto de Salud Carlos III | es_ES |
dc.contributor.funder | Merck, Sharp & Dohme | es_ES |
dc.description.peerreviewed | Sí | es_ES |
dc.identifier.e-issn | 2222-1751 | es_ES |
dc.relation.publisherversion | https://doi.org/10.1080/22221751.2021.1902755 | es_ES |
dc.identifier.journal | Emerging Microbes & Infections | es_ES |
dc.repisalud.centro | ISCIII::Centro Nacional de Microbiología | es_ES |
dc.repisalud.institucion | ISCIII | es_ES |
dc.rights.accessRights | open access | es_ES |
dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/PI18/00154 | es_ES |
dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/PT17/0019 | es_ES |
dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/COV20/00349 | es_ES |
dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/AC17/00019 | es_ES |