Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality.
dc.contributor.author | Nakanishi, Tomoko | |
dc.contributor.author | Pigazzini, Sara | |
dc.contributor.author | Degenhardt, Frauke | |
dc.contributor.author | Cordioli, Mattia | |
dc.contributor.author | Butler-Laporte, Guillaume | |
dc.contributor.author | Maya-Miles, Douglas | |
dc.contributor.author | Nafría-Jiménez, Beatriz | |
dc.contributor.author | Bouysran, Youssef | |
dc.contributor.author | Niemi, Mari | |
dc.contributor.author | Palom, Adriana | |
dc.contributor.author | Ellinghaus, David | |
dc.contributor.author | Khan, Atlas | |
dc.contributor.author | Martínez-Bueno, Manuel | |
dc.contributor.author | Rolker, Selina | |
dc.contributor.author | Amitano, Sara | |
dc.contributor.author | Tato, Luisa Roade | |
dc.contributor.author | FinnGen, The COVID-19 Host Genetics Initiative | |
dc.contributor.author | Fava, Francesca | |
dc.contributor.author | Spinner, Christoph D | |
dc.contributor.author | Prati, Daniele | |
dc.contributor.author | Bernardo, David | |
dc.contributor.author | Garcia, Federico | |
dc.contributor.author | Darcis, Gilles | |
dc.contributor.author | Fernández-Cadenas, Israel | |
dc.contributor.author | Holter, Jan Cato | |
dc.contributor.author | Banales, Jesus | |
dc.contributor.author | Frithiof, Robert | |
dc.contributor.author | Kiryluk, Krzysztof | |
dc.contributor.author | Duga, Stefano | |
dc.contributor.author | Asselta, Rosanna | |
dc.contributor.author | Pereira, Alexandre C | |
dc.contributor.author | Romero-Gómez, Manuel | |
dc.contributor.author | Bujanda, Luis | |
dc.contributor.author | Hov, Johannes R | |
dc.contributor.author | Migeotte, Isabelle | |
dc.contributor.author | Renieri, Alessandra | |
dc.contributor.author | Planas, Anna M | |
dc.contributor.author | Ludwig, Kerstin U | |
dc.contributor.author | Buti, Maria | |
dc.contributor.author | Rahmouni, Souad | |
dc.contributor.author | Alarcón-Riquelme, Marta E | |
dc.contributor.author | Schulte, Eva C | |
dc.contributor.author | Franke, Andre | |
dc.contributor.author | Karlsen, Tom H | |
dc.contributor.author | Valenti, Luca | |
dc.contributor.author | Zeberg, Hugo | |
dc.contributor.author | Richards, J Brent | |
dc.contributor.author | Ganna, Andrea | |
dc.date.accessioned | 2025-01-07T13:08:12Z | |
dc.date.available | 2025-01-07T13:08:12Z | |
dc.date.issued | 2021-03-12 | |
dc.description.abstract | There is considerable variability in COVID-19 outcomes amongst younger adults-and some of this variation may be due to genetic predisposition. We characterized the clinical implications of the major genetic risk factor for COVID-19 severity, and its age-dependent effect, using individual-level data in a large international multi-centre consortium. The major common COVID-19 genetic risk factor is a chromosome 3 locus, tagged by the marker rs10490770. We combined individual level data for 13,424 COVID-19 positive patients (N=6,689 hospitalized) from 17 cohorts in nine countries to assess the association of this genetic marker with mortality, COVID-19-related complications and laboratory values. We next examined if the magnitude of these associations varied by age and were independent from known clinical COVID-19 risk factors. We found that rs10490770 risk allele carriers experienced an increased risk of all-cause mortality (hazard ratio [HR] 1·4, 95% confidence interval [CI] 1·2-1·6) and COVID-19 related mortality (HR 1·5, 95%CI 1·3-1·8). Risk allele carriers had increased odds of several COVID-19 complications: severe respiratory failure (odds ratio [OR] 2·0, 95%CI 1·6-2·6), venous thromboembolism (OR 1·7, 95%CI 1·2-2·4), and hepatic injury (OR 1·6, 95%CI 1·2-2·0). Risk allele carriers ≤ 60 years had higher odds of death or severe respiratory failure (OR 2·6, 95%CI 1·8-3·9) compared to those > 60 years OR 1·5 (95%CI 1·3-1·9, interaction p-value=0·04). Amongst individuals ≤ 60 years who died or experienced severe respiratory COVID-19 outcome, we found that 31·8% (95%CI 27·6-36·2) were risk variant carriers, compared to 13·9% (95%CI 12·6-15·2%) of those not experiencing these outcomes. Prediction of death or severe respiratory failure among those ≤ 60 years improved when including the risk allele (AUC 0·82 vs 0·84, p=0·016) and the prediction ability of rs10490770 risk allele was similar to, or better than, most established clinical risk factors. The major common COVID-19 risk locus on chromosome 3 is associated with increased risks of morbidity and mortality-and these are more pronounced amongst individuals ≤ 60 years. The effect on COVID-19 severity was similar to, or larger than most established risk factors, suggesting potential implications for clinical risk management. Funding was obtained by each of the participating cohorts individually. | |
dc.identifier.doi | 10.1101/2021.03.07.21252875 | |
dc.identifier.pmc | PMC7987046 | |
dc.identifier.pmid | 33758887 | |
dc.identifier.pubmedURL | https://pmc.ncbi.nlm.nih.gov/articles/PMC7987046/pdf | |
dc.identifier.unpaywallURL | http://www.jci.org/articles/view/152386/files/pdf | |
dc.identifier.uri | https://hdl.handle.net/10668/25276 | |
dc.journal.title | medRxiv : the preprint server for health sciences | |
dc.journal.titleabbreviation | medRxiv | |
dc.language.iso | en | |
dc.organization | SAS - Hospital Universitario Puerta del Mar | |
dc.organization | SAS - Hospital Universitario Reina Sofía | |
dc.organization | Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC) | |
dc.organization | SAS - Hospital Universitario Virgen de las Nieves | |
dc.organization | SAS - Hospital Universitario Regional de Málaga | |
dc.organization | SAS - Hospital Universitario Virgen del Rocío | |
dc.pubmedtype | Preprint | |
dc.rights.accessRights | open access | |
dc.title | Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. | |
dc.type | research article | |
dc.type.hasVersion | VoR |
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SAS - Hospital Universitario Puerta del Mar
Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud (FIMABIS)
Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC)
SAS - Hospital Universitario Reina Sofía
SAS - Hospital Universitario Virgen de las Nieves
SAS - Hospital Universitario Virgen del Rocío
Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud (FIMABIS)
Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC)
SAS - Hospital Universitario Reina Sofía
SAS - Hospital Universitario Virgen de las Nieves
SAS - Hospital Universitario Virgen del Rocío