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The SARS-CoV-2 Alpha variant was associated with increased clinical severity of COVID-19 in Scotland: A genomics-based retrospective cohort analysis.

Authors :
Pascall, David J.
Vink, Elen
Blacow, Rachel
Bulteel, Naomi
Campbell, Alasdair
Campbell, Robyn
Clifford, Sarah
Davis, Chris
da Silva Filipe, Ana
El Sakka, Noha
Fjodorova, Ludmila
Forrest, Ruth
Goldstein, Emily
Gunson, Rory
Haughney, John
Holden, Matthew T. G.
Honour, Patrick
Hughes, Joseph
James, Edward
Lewis, Tim
Source :
PLoS ONE; 4/13/2023, Vol. 17 Issue 4, p1-19, 19p
Publication Year :
2023

Abstract

Objectives: The SARS-CoV-2 Alpha variant was associated with increased transmission relative to other variants present at the time of its emergence and several studies have shown an association between Alpha variant infection and increased hospitalisation and 28-day mortality. However, none have addressed the impact on maximum severity of illness in the general population classified by the level of respiratory support required, or death. We aimed to do this. Methods: In this retrospective multi-centre clinical cohort sub-study of the COG-UK consortium, 1475 samples from Scottish hospitalised and community cases collected between 1<superscript>st</superscript> November 2020 and 30<superscript>th</superscript> January 2021 were sequenced. We matched sequence data to clinical outcomes as the Alpha variant became dominant in Scotland and modelled the association between Alpha variant infection and severe disease using a 4-point scale of maximum severity by 28 days: 1. no respiratory support, 2. supplemental oxygen, 3. ventilation and 4. death. Results: Our cumulative generalised linear mixed model analyses found evidence (cumulative odds ratio: 1.40, 95% CI: 1.02, 1.93) of a positive association between increased clinical severity and lineage (Alpha variant versus pre-Alpha variants). Conclusions: The Alpha variant was associated with more severe clinical disease in the Scottish population than co-circulating lineages. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19326203
Volume :
17
Issue :
4
Database :
Complementary Index
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
163070379
Full Text :
https://doi.org/10.1371/journal.pone.0284187