A second update on mapping the human genetic architecture of COVID-19
| dc.contributor.author | COVID-19 Host Genetics Initiative | |
| dc.contributor.organization | fi=biolääketieteen laitos|en=Institute of Biomedicine| | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.77952289591 | |
| dc.converis.publication-id | 380585119 | |
| dc.converis.url | https://research.utu.fi/converis/portal/Publication/380585119 | |
| dc.date.accessioned | 2025-08-27T22:50:31Z | |
| dc.date.available | 2025-08-27T22:50:31Z | |
| dc.description.abstract | <p> The transferability and clinical value of genetic risk scores (GRSs) across populations remain limited due to an imbalance in genetic studies across ancestrally diverse populations. Here we conducted a multi-ancestry genome-wide association study of 156,319 prostate cancer cases and 788,443 controls of European, African, Asian and Hispanic men, reflecting a 57% increase in the number of non-European cases over previous prostate cancer genome-wide association studies. We identified 187 novel risk variants for prostate cancer, increasing the total number of risk variants to 451. An externally replicated multi-ancestry GRS was associated with risk that ranged from 1.8 (per standard deviation) in African ancestry men to 2.2 in European ancestry men. The GRS was associated with a greater risk of aggressive versus non-aggressive disease in men of African ancestry (<em>P</em> = 0.03). Our study presents novel prostate cancer susceptibility loci and a GRS with effective risk stratification across ancestry groups. <br></p> | |
| dc.identifier.eissn | 1476-4687 | |
| dc.identifier.jour-issn | 0028-0836 | |
| dc.identifier.olddbid | 202905 | |
| dc.identifier.oldhandle | 10024/185932 | |
| dc.identifier.uri | https://www.utupub.fi/handle/11111/50487 | |
| dc.identifier.url | https://www.nature.com/articles/s41586-023-06355-3 | |
| dc.identifier.urn | URN:NBN:fi-fe2025082789937 | |
| dc.language.iso | en | |
| dc.okm.affiliatedauthor | Sipeky, Csilla | |
| dc.okm.discipline | 3111 Biomedicine | en_GB |
| dc.okm.discipline | 318 Medical biotechnology | en_GB |
| dc.okm.discipline | 3111 Biolääketieteet | fi_FI |
| dc.okm.discipline | 318 Lääketieteen bioteknologia | fi_FI |
| dc.okm.internationalcopublication | international co-publication | |
| dc.okm.internationality | International publication | |
| dc.okm.type | A1 ScientificArticle | |
| dc.publisher | Springer Nature | |
| dc.publisher.country | United Kingdom | en_GB |
| dc.publisher.country | Britannia | fi_FI |
| dc.publisher.country-code | GB | |
| dc.relation.articlenumber | E7–E26 | |
| dc.relation.doi | 10.1038/s41586-023-06355-3 | |
| dc.relation.ispartofjournal | Nature | |
| dc.relation.issue | 7977 | |
| dc.relation.volume | 621 | |
| dc.source.identifier | https://www.utupub.fi/handle/10024/185932 | |
| dc.title | A second update on mapping the human genetic architecture of COVID-19 | |
| dc.year.issued | 2023 |
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