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Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7

Authors :
Davies, Nicholas G.
Jarvis, Christopher I.
van Zandvoort, Kevin
Clifford, Samuel
Sun, Fiona Yueqian
Funk, Sebastian
Medley, Graham
Source :
Nature. May 13, 2021, Vol. 593 Issue 7858, p270, 5 p.
Publication Year :
2021

Abstract

SARS-CoV-2 lineage B.1.1.7, a variant that was first detected in the UK in September 2020.sup.1, has spread to multiple countries worldwide. Several studies have established that B.1.1.7 is more transmissible than pre-existing variants, but have not identified whether it leads to any change in disease severity.sup.2. Here we analyse a dataset that links 2,245,263 positive SARS-CoV-2 community tests and 17,452 deaths associated with COVID-19 in England from 1 November 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 mutations in this lineage prevent PCR amplification of the spike (S) gene target (known as S gene target failure (SGTF).sup.1). On the basis of 4,945 deaths with known SGTF status, we estimate that the hazard of death associated with SGTF is 55% (95% confidence interval, 39-72%) higher than in cases without SGTF after adjustment for age, sex, ethnicity, deprivation, residence in a care home, the local authority of residence and test date. This corresponds to the absolute risk of death for a 55-69-year-old man increasing from 0.6% to 0.9% (95% confidence interval, 0.8-1.0%) within 28 days of a positive test in the community. Correcting for misclassification of SGTF and missingness in SGTF status, we estimate that the hazard of death associated with B.1.1.7 is 61% (42-82%) higher than with pre-existing variants. Our analysis suggests that B.1.1.7 is not only more transmissible than pre-existing SARS-CoV-2 variants, but may also cause more severe illness. Analysis of community-tested cases of SARS-CoV-2 indicates that the B.1.1.7 variant is not only more transmissible than pre-existing variants, but may also cause more severe illness, and is associated with a higher risk of death.<br />Author(s): Nicholas G. Davies [sup.1] , Christopher I. Jarvis [sup.1] , Kevin van Zandvoort [sup.1] , Samuel Clifford [sup.1] , Fiona Yueqian Sun [sup.1] , Sebastian Funk [sup.1] , Graham [...]

Details

Language :
English
ISSN :
00280836
Volume :
593
Issue :
7858
Database :
Gale General OneFile
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
edsgcl.661594096
Full Text :
https://doi.org/10.1038/s41586-021-03426-1