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dc.contributor.authorPascall, David J.
dc.contributor.authorVink, Elen
dc.contributor.authorBlacow, Rachel
dc.contributor.authorBulteel, Naomi
dc.contributor.authorCampbell, Alasdair
dc.contributor.authorCampbell, Robyn
dc.contributor.authorClifford, Sarah
dc.contributor.authorDavis, Chris
dc.contributor.authorda Silva Filipe, Ana
dc.contributor.authorEl Sakka, Noha
dc.contributor.authorFjodorova, Ludmila
dc.contributor.authorForrest, Ruth
dc.contributor.authorGoldstein, Emily
dc.contributor.authorGunson, Rory
dc.contributor.authorHaughney, John
dc.contributor.authorHolden, Matthew T. G.
dc.contributor.authorHonour, Patrick
dc.contributor.authorHughes, Joseph
dc.contributor.authorJames, Edward
dc.contributor.authorLewis, Tim
dc.contributor.authorLycett, Samantha
dc.contributor.authorMacLean, Oscar
dc.contributor.authorMcHugh, Martin
dc.contributor.authorMollett, Guy
dc.contributor.authorOnishi, Yusuke
dc.contributor.authorParcell, Ben
dc.contributor.authorRay, Surajit
dc.contributor.authorRobertson, David L.
dc.contributor.authorShabaan, Sharif
dc.contributor.authorShepherd, James G.
dc.contributor.authorSmollett, Katherine
dc.contributor.authorTempleton, Kate
dc.contributor.authorWastnedge, Elizabeth
dc.contributor.authorWilkie, Craig
dc.contributor.authorWilliams, Thomas
dc.contributor.authorThomson, Emma C.
dc.contributor.authorConsortium, The COVID-19 Genomics UK (COG-UK)
dc.date.accessioned2023-04-14T15:30:14Z
dc.date.available2023-04-14T15:30:14Z
dc.date.issued2023-04-13
dc.identifier284110423
dc.identifier257b267d-2394-4745-b7a6-1d6d2cfa2195
dc.identifier85152598538
dc.identifier.citationPascall , D J , Vink , E , Blacow , R , Bulteel , N , Campbell , A , Campbell , R , Clifford , S , Davis , C , da Silva Filipe , A , El Sakka , N , Fjodorova , L , Forrest , R , Goldstein , E , Gunson , R , Haughney , J , Holden , M T G , Honour , P , Hughes , J , James , E , Lewis , T , Lycett , S , MacLean , O , McHugh , M , Mollett , G , Onishi , Y , Parcell , B , Ray , S , Robertson , D L , Shabaan , S , Shepherd , J G , Smollett , K , Templeton , K , Wastnedge , E , Wilkie , C , Williams , T , Thomson , E C & Consortium , T COVID G UK 2023 , ' The SARS-CoV-2 Alpha variant was associated with increased clinical severity of COVID-19 in Scotland : a genomics-based retrospective cohort analysis ' , PLoS ONE , vol. 18 , no. 4 , e0284187 . https://doi.org/10.1371/journal.pone.0284187en
dc.identifier.issn1932-6203
dc.identifier.otherRIS: urn:69585D0C3D6DC310C945BF31624B3411
dc.identifier.otherORCID: /0000-0002-0370-3700/work/133187440
dc.identifier.otherORCID: /0000-0002-4958-2166/work/133187475
dc.identifier.urihttps://hdl.handle.net/10023/27403
dc.descriptionFunding: COG-UK is supported by funding from the Medical Research Council (MRC) part of UK Research & Innovation (UKRI), the National Institute of Health Research (NIHR) and Genome Research Limited, operating as the Wellcome Sanger Institute. Funding was also provided by UKRI through the JUNIPER consortium (MR/V038613/1). Sequencing, bioinformatics and statistical support was funded by the Medical Research Council (MRC) core awards for the MRC-University of Glasgow Centre for Virus Research (MC UU 1201412) and MRC Biostatistics Unit (MC UU 00002/11).en
dc.description.abstractObjectives 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.
dc.format.extent19
dc.format.extent1292185
dc.language.isoeng
dc.relation.ispartofPLoS ONEen
dc.subjectCOVID-19en
dc.subjectRA0421 Public health. Hygiene. Preventive Medicineen
dc.subjectE-DASen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subjectMCCen
dc.subject.lccRA0421en
dc.titleThe SARS-CoV-2 Alpha variant was associated with increased clinical severity of COVID-19 in Scotland : a genomics-based retrospective cohort analysisen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. St Andrews Bioinformatics Uniten
dc.contributor.institutionUniversity of St Andrews. Infection and Global Health Divisionen
dc.identifier.doi10.1371/journal.pone.0284187
dc.description.statusPeer revieweden


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