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Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7
SARS-CoV-2 lineage B.1.1.7, a variant first detected in the United Kingdom in September 2020(1), has spread to multiple countries worldwide. Several studies have established that B.1.1.7 is more transmissible than preexisting variants, but have not identified whether it leads to any change in diseas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872389/ https://www.ncbi.nlm.nih.gov/pubmed/33564794 http://dx.doi.org/10.1101/2021.02.01.21250959 |
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author | Davies, Nicholas G. Jarvis, Christopher I. Edmunds, W. John Jewell, Nicholas P. Diaz-Ordaz, Karla Keogh, Ruth H. |
author_facet | Davies, Nicholas G. Jarvis, Christopher I. Edmunds, W. John Jewell, Nicholas P. Diaz-Ordaz, Karla Keogh, Ruth H. |
author_sort | Davies, Nicholas G. |
collection | PubMed |
description | SARS-CoV-2 lineage B.1.1.7, a variant first detected in the United Kingdom in September 2020(1), has spread to multiple countries worldwide. Several studies have established that B.1.1.7 is more transmissible than preexisting variants, but have not identified whether it leads to any change in disease severity(2). We analyse a dataset linking 2,245,263 positive SARS-CoV-2 community tests and 17,452 COVID-19 deaths in England from 1 September 2020 to 14 February 2021. For 1,146,534 (51%) of these tests, the presence or absence of B.1.1.7 can be identified because of mutations in this lineage preventing PCR amplification of the spike gene target (S gene target failure, SGTF(1)). Based on 4,945 deaths with known SGTF status, we estimate that the hazard of death associated with SGTF is 55% (95% CI 39–72%) higher after adjustment for age, sex, ethnicity, deprivation, care home residence, local authority of residence and test date. This corresponds to the absolute risk of death for a 55–69-year-old male increasing from 0.6% to 0.9% (95% CI 0.8–1.0%) within 28 days after a positive test in the community. Correcting for misclassification of SGTF and missingness in SGTF status, we estimate a 61% (42–82%) higher hazard of death associated with B.1.1.7. Our analysis suggests that B.1.1.7 is not only more transmissible than preexisting SARS-CoV-2 variants, but may also cause more severe illness. |
format | Online Article Text |
id | pubmed-7872389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-78723892021-02-10 Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7 Davies, Nicholas G. Jarvis, Christopher I. Edmunds, W. John Jewell, Nicholas P. Diaz-Ordaz, Karla Keogh, Ruth H. medRxiv Article SARS-CoV-2 lineage B.1.1.7, a variant first detected in the United Kingdom in September 2020(1), has spread to multiple countries worldwide. Several studies have established that B.1.1.7 is more transmissible than preexisting variants, but have not identified whether it leads to any change in disease severity(2). We analyse a dataset linking 2,245,263 positive SARS-CoV-2 community tests and 17,452 COVID-19 deaths in England from 1 September 2020 to 14 February 2021. For 1,146,534 (51%) of these tests, the presence or absence of B.1.1.7 can be identified because of mutations in this lineage preventing PCR amplification of the spike gene target (S gene target failure, SGTF(1)). Based on 4,945 deaths with known SGTF status, we estimate that the hazard of death associated with SGTF is 55% (95% CI 39–72%) higher after adjustment for age, sex, ethnicity, deprivation, care home residence, local authority of residence and test date. This corresponds to the absolute risk of death for a 55–69-year-old male increasing from 0.6% to 0.9% (95% CI 0.8–1.0%) within 28 days after a positive test in the community. Correcting for misclassification of SGTF and missingness in SGTF status, we estimate a 61% (42–82%) higher hazard of death associated with B.1.1.7. Our analysis suggests that B.1.1.7 is not only more transmissible than preexisting SARS-CoV-2 variants, but may also cause more severe illness. Cold Spring Harbor Laboratory 2021-03-05 /pmc/articles/PMC7872389/ /pubmed/33564794 http://dx.doi.org/10.1101/2021.02.01.21250959 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Davies, Nicholas G. Jarvis, Christopher I. Edmunds, W. John Jewell, Nicholas P. Diaz-Ordaz, Karla Keogh, Ruth H. Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7 |
title | Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7 |
title_full | Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7 |
title_fullStr | Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7 |
title_full_unstemmed | Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7 |
title_short | Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7 |
title_sort | increased mortality in community-tested cases of sars-cov-2 lineage b.1.1.7 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872389/ https://www.ncbi.nlm.nih.gov/pubmed/33564794 http://dx.doi.org/10.1101/2021.02.01.21250959 |
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