Directions of change in intrinsic case severity across successive SARS-CoV-2 variant waves have been inconsistent

David J. Pascall(University of Cambridge), Elen Vink(MRC University of Glasgow Centre for Virus Research), Rachel Blacow(NHS Greater Glasgow and Clyde), Naomi Bulteel(NHS Fife), Alasdair Campbell(NHS Lothian), Robyn Campbell(NHS Lothian), Sarah Clifford(NHS Lothian), Christopher Davis(MRC University of Glasgow Centre for Virus Research), Ana da Silva Filipe(MRC University of Glasgow Centre for Virus Research), Noha El Sakka(NHS Grampian), Ludmila Fjodorova(NHS Greater Glasgow and Clyde), Ruth Forrest(NHS Fife), Emily J. Goldstein(NHS Greater Glasgow and Clyde), Rory Gunson(NHS Greater Glasgow and Clyde), John Haughney(NHS Greater Glasgow and Clyde), Matthew T. G. Holden(University of St Andrews), Patrick Honour(Borders General Hospital), Joseph Hughes(MRC University of Glasgow Centre for Virus Research), Edward James(Borders General Hospital), Tim Lewis(NHS Lothian), Oscar A. MacLean(MRC University of Glasgow Centre for Virus Research), M. McHugh(NHS Lothian), Guy Mollett(MRC University of Glasgow Centre for Virus Research), Tommy Nyberg(MRC Biostatistics Unit), Yusuke Onishi(NHS Grampian), Ben Parcell(University of Dundee), Surajit Ray(University of Glasgow), David L. Robertson(MRC University of Glasgow Centre for Virus Research), Shaun R. Seaman(MRC Biostatistics Unit), Sharif Shabaan(Public Health Scotland), James G. Shepherd(MRC University of Glasgow Centre for Virus Research), Katherine Smollett(MRC University of Glasgow Centre for Virus Research), Kate Templeton(NHS Lothian), Elizabeth Wastnedge(NHS Lothian), Craig Wilkie(University of Glasgow), Thomas Williams(University of Edinburgh), Emma C. Thomson(London School of Hygiene & Tropical Medicine)
Journal of Infection
June 1, 2023
Cited by 25Open Access
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Abstract

OBJECTIVES: To determine how the intrinsic severity of successively dominant SARS-CoV-2 variants changed over the course of the pandemic. METHODS: A retrospective cohort analysis in the NHS Greater Glasgow and Clyde (NHS GGC) Health Board. All sequenced non-nosocomial adult COVID-19 cases in NHS GGC with relevant SARS-CoV-2 lineages (B.1.177/Alpha, Alpha/Delta, AY.4.2 Delta/non-AY.4.2 Delta, non-AY.4.2 Delta/Omicron, and BA.1 Omicron/BA.2 Omicron) during analysis periods were included. Outcome measures were hospital admission, ICU admission, or death within 28 days of positive COVID-19 test. We report the cumulative odds ratio; the ratio of the odds that an individual experiences a severity event of a given level vs all lower severity levels for the resident and the replacement variant after adjustment. RESULTS: After adjustment for covariates, the cumulative odds ratio was 1.51 (95% CI: 1.08-2.11) for Alpha versus B.1.177, 2.09 (95% CI: 1.42-3.08) for Delta versus Alpha, 0.99 (95% CI: 0.76-1.27) for AY.4.2 Delta versus non-AY.4.2 Delta, 0.49 (95% CI: 0.22-1.06) for Omicron versus non-AY.4.2 Delta, and 0.86 (95% CI: 0.68-1.09) for BA.2 Omicron versus BA.1 Omicron. CONCLUSIONS: The direction of change in intrinsic severity between successively emerging SARS-CoV-2 variants was inconsistent, reminding us that the intrinsic severity of future SARS-CoV-2 variants remains uncertain.


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