Severity of Severe Acute Respiratory System Coronavirus 2 (SARS-CoV-2) Alpha Variant (B.1.1.7) in England

Author:

Grint Daniel J1ORCID,Wing Kevin1,Houlihan Catherine2,Gibbs Hamish P1,Evans Stephen J W1,Williamson Elizabeth1,McDonald Helen I1,Bhaskaran Krishnan1,Evans David3,Walker Alex J3,Hickman George3,Nightingale Emily4,Schultze Anna1,Rentsch Christopher T1,Bates Chris5,Cockburn Jonathan5,Curtis Helen J3,Morton Caroline E3,Bacon Sebastian3,Davy Simon3,Wong Angel Y S1,Mehrkar Amir3,Tomlinson Laurie1,Douglas Ian J1,Mathur Rohini1,MacKenna Brian3,Ingelsby Peter3,Croker Richard3,Parry John5,Hester Frank5,Harper Sam5,DeVito Nicholas J3,Hulme Will3,Tazare John1,Smeeth Liam1,Goldacre Ben3,Eggo Rosalind M1

Affiliation:

1. Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom

2. Division of Infection and Immunity, University College London, London, United Kingdom

3. The DataLab, Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom

4. Faculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, London, United Kingdom

5. TPP, Horsforth, Leeds, United Kingdom

Abstract

Abstract Background The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) alpha variant (B.1.1.7) is associated with higher transmissibility than wild-type virus, becoming the dominant variant in England by January 2021. We aimed to describe the severity of the alpha variant in terms of the pathway of disease from testing positive to hospital admission and death. Methods With the approval of NHS England, we linked individual-level data from primary care with SARS-CoV-2 community testing, hospital admission, and Office for National Statistics all-cause death data. We used testing data with S-gene target failure as a proxy for distinguishing alpha and wild-type cases, and stratified Cox proportional hazards regression to compare the relative severity of alpha cases with wild-type diagnosed from 16 November 2020 to 11 January 2021. Results Using data from 185 234 people who tested positive for SARS-CoV-2 in the community (alpha = 93 153; wild-type = 92 081), in fully adjusted analysis accounting for individual-level demographics and comorbidities as well as regional variation in infection incidence, we found alpha associated with 73% higher hazards of all-cause death (adjusted hazard ratio [aHR]: 1.73; 95% confidence interval [CI]: 1.41–2.13; P < .0001) and 62% higher hazards of hospital admission (1.62; 1.48–1.78; P < .0001) compared with wild-type virus. Among patients already admitted to the intensive care unit, the association between alpha and increased all-cause mortality was smaller and the CI included the null (aHR: 1.20; 95% CI: .74–1.95; P = .45). Conclusions The SARS-CoV-2 alpha variant is associated with an increased risk of both hospitalization and mortality than wild-type virus.

Funder

UK Research and Innovation

National Institute for Health Research

Asthma UK–British Lung Foundation

Wellcome Trust

Health Data Research UK

Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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