TY - JOUR
T1 - The SARS-CoV-2 Alpha variant was associated with increased clinical severity of COVID-19 in Scotland
T2 - A genomics-based retrospective cohort analysis
AU - The COVID-19 Genomics UK (COG-UK) consortium
AU - Pascall, David J.
AU - Vink, Elen
AU - Blacow, Rachel
AU - Bulteel, Naomi
AU - Campbell, Alasdair
AU - Campbell, Robyn
AU - Clifford, Sarah
AU - Davis, Chris
AU - Filipe, Ana da Silva
AU - Sakka, Noha El
AU - Fjodorova, Ludmila
AU - Forrest, Ruth
AU - Goldstein, Emily
AU - Gunson, Rory
AU - Haughney, John
AU - Holden, Matthew T.G.
AU - Honour, Patrick
AU - Hughes, Joseph
AU - James, Edward
AU - Lewis, Tim
AU - Lycett, Samantha
AU - Loman, Nicholas J.
AU - Jackson, David K.
AU - Aggarwal, Dinesh
AU - Curran, Martin D.
AU - Parmar, Surendra
AU - Underwood, Anthony P.
AU - Peacock, Sharon J.
AU - Osman, Husam
AU - Chand, Meera
AU - de Angelis, Daniela D.
AU - Muir, Peter
AU - Robinson, Esther
AU - Kidd, Stephen P.
AU - Bosworth, Andrew
AU - Iturriza-Gomara, Miren
AU - Asad, Hibo
AU - McKerr, Caoimhe
AU - Ahmad, Shazaad S.Y.
AU - Machin, Nicholas W.
AU - Cole, Kevin
AU - Hopes, Richard
AU - Chalker, Vicki
AU - Harrison, Ian
AU - Bibby, David
AU - Dabrera, Gavin
AU - Ellaby, Nicholas
AU - Gallagher, Eileen
AU - Lackenby, Angie
AU - Twohig, Katherine A.
N1 - Publisher Copyright:
© 2023 Pascall et al.
PY - 2023/4
Y1 - 2023/4
N2 - 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 1st November 2020 and 30th 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.
AB - 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 1st November 2020 and 30th 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.
UR - http://www.scopus.com/inward/record.url?scp=85152598538&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0284187
DO - 10.1371/journal.pone.0284187
M3 - Article
C2 - 37053201
AN - SCOPUS:85152598538
SN - 1932-6203
VL - 18
JO - PLoS ONE
JF - PLoS ONE
IS - 4
M1 - e0284187
ER -