Comparative mRNA booster effectiveness against death or hospitalization with COVID-19 pneumonia across at-risk US Veteran populations
dc.contributor.author | Kelly, J. Daniel | |
dc.contributor.author | Leonard, Samuel | |
dc.contributor.author | Boscardin, W. John | |
dc.contributor.author | Hoggatt, Katherine J. | |
dc.contributor.author | Lum, Emily N. | |
dc.contributor.author | Austin, Charles C. | |
dc.contributor.author | Byers, Amy | |
dc.contributor.author | Tien, Phyllis C. | |
dc.contributor.author | Austin, Peter C. | |
dc.contributor.author | Bravata, Dawn M. | |
dc.contributor.author | Keyhani, Salomeh | |
dc.contributor.department | Medicine, School of Medicine | |
dc.date.accessioned | 2024-01-04T13:33:05Z | |
dc.date.available | 2024-01-04T13:33:05Z | |
dc.date.issued | 2023-05-23 | |
dc.description.abstract | Studies of comparative mRNA booster effectiveness among high-risk populations can inform mRNA booster-specific guidelines. The study emulated a target trial of COVID-19 vaccinated U.S. Veterans who received three doses of either mRNA-1273 or BNT162b2 vaccines. Participants were followed for up to 32 weeks between July 1, 2021 to May 30, 2022. Non-overlapping populations were average and high risk; high-risk sub-groups were age ≥65 years, high-risk co-morbid conditions, and immunocompromising conditions. Of 1,703,189 participants, 10.9 per 10,000 persons died or were hospitalized with COVID-19 pneumonia over 32 weeks (95% CI: 10.2, 11.8). Although relative risks of death or hospitalization with COVID-19 pneumonia were similar across at-risk groups, absolute risk varied when comparing three doses of BNT162b2 with mRNA-1273 (BNT162b2 minus mRNA-1273) between average-risk and high-risk populations, confirmed by the presence of additive interaction. The risk difference of death or hospitalization with COVID-19 pneumonia for high-risk populations was 2.2 (0.9, 3.6). Effects were not modified by predominant viral variant. In this work, the risk of death or hospitalization with COVID-19 pneumonia over 32 weeks was lower among high-risk populations who received three doses of mRNA-1273 vaccine instead of BNT162b2 vaccine; no difference was found among the average-risk population and age >65 sub-group. | |
dc.eprint.version | Final published version | |
dc.identifier.citation | Kelly JD, Leonard S, Boscardin WJ, et al. Comparative mRNA booster effectiveness against death or hospitalization with COVID-19 pneumonia across at-risk US Veteran populations. Nat Commun. 2023;14(1):2976. Published 2023 May 23. doi:10.1038/s41467-023-38503-8 | |
dc.identifier.uri | https://hdl.handle.net/1805/37611 | |
dc.language.iso | en_US | |
dc.publisher | Springer Nature | |
dc.relation.isversionof | 10.1038/s41467-023-38503-8 | |
dc.relation.journal | Nature Communications | |
dc.rights | Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | PMC | |
dc.subject | BNT162 Vaccine | |
dc.subject | COVID-19 | |
dc.subject | Hospitalization | |
dc.subject | Veterans | |
dc.title | Comparative mRNA booster effectiveness against death or hospitalization with COVID-19 pneumonia across at-risk US Veteran populations | |
dc.type | Article |