Symptom prevalence, duration, and risk of hospital admission in individuals infected with SARS-CoV-2 during periods of omicron and delta variant dominance: a prospective observational study from the ZOE COVID Study.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
23 04 2022
Historique:
received: 28 01 2022
revised: 14 02 2022
accepted: 15 02 2022
pubmed: 11 4 2022
medline: 27 4 2022
entrez: 10 4 2022
Statut: ppublish

Résumé

The SARS-CoV-2 variant of concern, omicron, appears to be less severe than delta. We aim to quantify the differences in symptom prevalence, risk of hospital admission, and symptom duration among the vaccinated population. In this prospective longitudinal observational study, we collected data from participants who were self-reporting test results and symptoms in the ZOE COVID app (previously known as the COVID Symptoms Study App). Eligible participants were aged 16-99 years, based in the UK, with a body-mass index between 15 and 55 kg/m Between June 1, 2021, and Jan 17, 2022, we identified 63 002 participants who tested positive for SARS-CoV-2 and reported symptoms in the ZOE app. These patients were matched 1:1 for age, sex, and vaccination dose, across two periods (June 1 to Nov 27, 2021, delta prevalent at >70%; n=4990, and Dec 20, 2021, to Jan 17, 2022, omicron prevalent at >70%; n=4990). Loss of smell was less common in participants infected during omicron prevalence than during delta prevalence (16·7% vs 52·7%, odds ratio [OR] 0·17; 95% CI 0·16-0·19, p<0·001). Sore throat was more common during omicron prevalence than during delta prevalence (70·5% vs 60·8%, 1·55; 1·43-1·69, p<0·001). There was a lower rate of hospital admission during omicron prevalence than during delta prevalence (1·9% vs 2·6%, OR 0·75; 95% CI 0·57-0·98, p=0·03). The prevalence of symptoms that characterise an omicron infection differs from those of the delta SARS-CoV-2 variant, apparently with less involvement of the lower respiratory tract and reduced probability of hospital admission. Our data indicate a shorter period of illness and potentially of infectiousness which should impact work-health policies and public health advice. Wellcome Trust, ZOE, National Institute for Health Research, Chronic Disease Research Foundation, National Institutes of Health, and Medical Research Council.

Sections du résumé

BACKGROUND
The SARS-CoV-2 variant of concern, omicron, appears to be less severe than delta. We aim to quantify the differences in symptom prevalence, risk of hospital admission, and symptom duration among the vaccinated population.
METHODS
In this prospective longitudinal observational study, we collected data from participants who were self-reporting test results and symptoms in the ZOE COVID app (previously known as the COVID Symptoms Study App). Eligible participants were aged 16-99 years, based in the UK, with a body-mass index between 15 and 55 kg/m
FINDINGS
Between June 1, 2021, and Jan 17, 2022, we identified 63 002 participants who tested positive for SARS-CoV-2 and reported symptoms in the ZOE app. These patients were matched 1:1 for age, sex, and vaccination dose, across two periods (June 1 to Nov 27, 2021, delta prevalent at >70%; n=4990, and Dec 20, 2021, to Jan 17, 2022, omicron prevalent at >70%; n=4990). Loss of smell was less common in participants infected during omicron prevalence than during delta prevalence (16·7% vs 52·7%, odds ratio [OR] 0·17; 95% CI 0·16-0·19, p<0·001). Sore throat was more common during omicron prevalence than during delta prevalence (70·5% vs 60·8%, 1·55; 1·43-1·69, p<0·001). There was a lower rate of hospital admission during omicron prevalence than during delta prevalence (1·9% vs 2·6%, OR 0·75; 95% CI 0·57-0·98, p=0·03).
INTERPRETATION
The prevalence of symptoms that characterise an omicron infection differs from those of the delta SARS-CoV-2 variant, apparently with less involvement of the lower respiratory tract and reduced probability of hospital admission. Our data indicate a shorter period of illness and potentially of infectiousness which should impact work-health policies and public health advice.
FUNDING
Wellcome Trust, ZOE, National Institute for Health Research, Chronic Disease Research Foundation, National Institutes of Health, and Medical Research Council.

Identifiants

pubmed: 35397851
pii: S0140-6736(22)00327-0
doi: 10.1016/S0140-6736(22)00327-0
pmc: PMC8989396
pii:
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1618-1624

Subventions

Organisme : Medical Research Council
ID : MR/V027883/1
Pays : United Kingdom

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests TDS, AMV, CJS, and SO are consultants to ZOE. JW, AM, LP, SP, and JC are employees of ZOE. All other authors declare no competing interests.

Références

Trop Med Int Health. 2022 Jun;27(6):564-573
pubmed: 35411997
N Engl J Med. 2020 Apr 30;382(18):1708-1720
pubmed: 32109013
Lancet Public Health. 2021 Jan;6(1):e21-e29
pubmed: 33278917
JAMA. 2022 Feb 8;327(6):583-584
pubmed: 34967859
Lancet. 2022 Jan 29;399(10323):437-446
pubmed: 35065011
Lancet. 2021 May 8;397(10286):1711-1724
pubmed: 33939953
Nature. 2021 Dec;600(7890):577-578
pubmed: 34934198
J Korean Med Sci. 2022 Jan 17;37(3):e31
pubmed: 35040299
Cell Host Microbe. 2021 Jan 13;29(1):44-57.e9
pubmed: 33259788
Cell Mol Immunol. 2022 Feb;19(2):293-295
pubmed: 35017716
BMJ. 2021 Nov 29;375:n2943
pubmed: 34845008
Thorax. 2021 Jul;76(7):723-725
pubmed: 33376145
Lancet Infect Dis. 2022 Jul;22(7):1002-1010
pubmed: 35405090
J Clin Med. 2021 Jan 24;10(3):
pubmed: 33498861
Nat Med. 2020 Jul;26(7):1037-1040
pubmed: 32393804
J Med Virol. 2022 May;94(5):2290-2295
pubmed: 35060146
Lancet. 2021 Dec 11;398(10317):2126-2128
pubmed: 34871545
Nature. 2022 Mar;603(7902):715-720
pubmed: 35104836
J Mol Histol. 2020 Dec;51(6):613-628
pubmed: 33011887

Auteurs

Cristina Menni (C)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK. Electronic address: cristina.menni@kcl.a.uk.

Ana M Valdes (AM)

Nottingham NIHR Biomedical Research Centre at the School of Medicine, University of Nottingham, Nottingham, UK.

Lorenzo Polidori (L)

ZOE, London, UK.

Michela Antonelli (M)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Satya Penamakuri (S)

ZOE, London, UK.

Ana Nogal (A)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.

Panayiotis Louca (P)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.

Anna May (A)

ZOE, London, UK.

Jane C Figueiredo (JC)

Department of Medicine, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles CA, USA.

Christina Hu (C)

ZOE, London, UK.

Erika Molteni (E)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Liane Canas (L)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Marc F Österdahl (MF)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK; Department of Ageing and Health, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Marc Modat (M)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Carole H Sudre (CH)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK; MRC Unit for Lifelong Health and Ageing, University College London, London, UK; Centre for Medical Image Computing, Department of Computer Science, University College London, London, UK.

Ben Fox (B)

ZOE, London, UK.

Alexander Hammers (A)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK; King's College London & Guy's and St Thomas' PET Centre, London, UK.

Jonathan Wolf (J)

ZOE, London, UK.

Joan Capdevila (J)

ZOE, London, UK.

Andrew T Chan (AT)

Clinical and Translational Epidemiology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Sean P David (SP)

NorthShore University Health System & University of Chicago Pritzker School of Medicine, Chicago, IL, USA.

Claire J Steves (CJ)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK; Department of Ageing and Health, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Sebastien Ourselin (S)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Tim D Spector (TD)

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK. Electronic address: tim.spector@kcl.ac.uk.

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Classifications MeSH