Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.

<h4>Background</h4>Rapid detection, isolation, and contact tracing of community COVID-19 cases are essential measures to limit the community spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We aimed to identify a parsimonious set of symptoms that jointly predict CO...

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Autores principales: Joshua Elliott, Matthew Whitaker, Barbara Bodinier, Oliver Eales, Steven Riley, Helen Ward, Graham Cooke, Ara Darzi, Marc Chadeau-Hyam, Paul Elliott
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:df15cc8947f14ab29bd1ca8b23f07a5c2021-12-02T19:56:01ZPredictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.1549-12771549-167610.1371/journal.pmed.1003777https://doaj.org/article/df15cc8947f14ab29bd1ca8b23f07a5c2021-09-01T00:00:00Zhttps://doi.org/10.1371/journal.pmed.1003777https://doaj.org/toc/1549-1277https://doaj.org/toc/1549-1676<h4>Background</h4>Rapid detection, isolation, and contact tracing of community COVID-19 cases are essential measures to limit the community spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We aimed to identify a parsimonious set of symptoms that jointly predict COVID-19 and investigated whether predictive symptoms differ between the B.1.1.7 (Alpha) lineage (predominating as of April 2021 in the US, UK, and elsewhere) and wild type.<h4>Methods and findings</h4>We obtained throat and nose swabs with valid SARS-CoV-2 PCR test results from 1,147,370 volunteers aged 5 years and above (6,450 positive cases) in the REal-time Assessment of Community Transmission-1 (REACT-1) study. This study involved repeated community-based random surveys of prevalence in England (study rounds 2 to 8, June 2020 to January 2021, response rates 22%-27%). Participants were asked about symptoms occurring in the week prior to testing. Viral genome sequencing was carried out for PCR-positive samples with N-gene cycle threshold value < 34 (N = 1,079) in round 8 (January 2021). In univariate analysis, all 26 surveyed symptoms were associated with PCR positivity compared with non-symptomatic people. Stability selection (1,000 penalized logistic regression models with 50% subsampling) among people reporting at least 1 symptom identified 7 symptoms as jointly and positively predictive of PCR positivity in rounds 2-7 (June to December 2020): loss or change of sense of smell, loss or change of sense of taste, fever, new persistent cough, chills, appetite loss, and muscle aches. The resulting model (rounds 2-7) predicted PCR positivity in round 8 with area under the curve (AUC) of 0.77. The same 7 symptoms were selected as jointly predictive of B.1.1.7 infection in round 8, although when comparing B.1.1.7 with wild type, new persistent cough and sore throat were more predictive of B.1.1.7 infection while loss or change of sense of smell was more predictive of the wild type. The main limitations of our study are (i) potential participation bias despite random sampling of named individuals from the National Health Service register and weighting designed to achieve a representative sample of the population of England and (ii) the necessary reliance on self-reported symptoms, which may be prone to recall bias and may therefore lead to biased estimates of symptom prevalence in England.<h4>Conclusions</h4>Where testing capacity is limited, it is important to use tests in the most efficient way possible. We identified a set of 7 symptoms that, when considered together, maximize detection of COVID-19 in the community, including infection with the B.1.1.7 lineage.Joshua ElliottMatthew WhitakerBarbara BodinierOliver EalesSteven RileyHelen WardGraham CookeAra DarziMarc Chadeau-HyamPaul ElliottPublic Library of Science (PLoS)articleMedicineRENPLoS Medicine, Vol 18, Iss 9, p e1003777 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
spellingShingle Medicine
R
Joshua Elliott
Matthew Whitaker
Barbara Bodinier
Oliver Eales
Steven Riley
Helen Ward
Graham Cooke
Ara Darzi
Marc Chadeau-Hyam
Paul Elliott
Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.
description <h4>Background</h4>Rapid detection, isolation, and contact tracing of community COVID-19 cases are essential measures to limit the community spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We aimed to identify a parsimonious set of symptoms that jointly predict COVID-19 and investigated whether predictive symptoms differ between the B.1.1.7 (Alpha) lineage (predominating as of April 2021 in the US, UK, and elsewhere) and wild type.<h4>Methods and findings</h4>We obtained throat and nose swabs with valid SARS-CoV-2 PCR test results from 1,147,370 volunteers aged 5 years and above (6,450 positive cases) in the REal-time Assessment of Community Transmission-1 (REACT-1) study. This study involved repeated community-based random surveys of prevalence in England (study rounds 2 to 8, June 2020 to January 2021, response rates 22%-27%). Participants were asked about symptoms occurring in the week prior to testing. Viral genome sequencing was carried out for PCR-positive samples with N-gene cycle threshold value < 34 (N = 1,079) in round 8 (January 2021). In univariate analysis, all 26 surveyed symptoms were associated with PCR positivity compared with non-symptomatic people. Stability selection (1,000 penalized logistic regression models with 50% subsampling) among people reporting at least 1 symptom identified 7 symptoms as jointly and positively predictive of PCR positivity in rounds 2-7 (June to December 2020): loss or change of sense of smell, loss or change of sense of taste, fever, new persistent cough, chills, appetite loss, and muscle aches. The resulting model (rounds 2-7) predicted PCR positivity in round 8 with area under the curve (AUC) of 0.77. The same 7 symptoms were selected as jointly predictive of B.1.1.7 infection in round 8, although when comparing B.1.1.7 with wild type, new persistent cough and sore throat were more predictive of B.1.1.7 infection while loss or change of sense of smell was more predictive of the wild type. The main limitations of our study are (i) potential participation bias despite random sampling of named individuals from the National Health Service register and weighting designed to achieve a representative sample of the population of England and (ii) the necessary reliance on self-reported symptoms, which may be prone to recall bias and may therefore lead to biased estimates of symptom prevalence in England.<h4>Conclusions</h4>Where testing capacity is limited, it is important to use tests in the most efficient way possible. We identified a set of 7 symptoms that, when considered together, maximize detection of COVID-19 in the community, including infection with the B.1.1.7 lineage.
format article
author Joshua Elliott
Matthew Whitaker
Barbara Bodinier
Oliver Eales
Steven Riley
Helen Ward
Graham Cooke
Ara Darzi
Marc Chadeau-Hyam
Paul Elliott
author_facet Joshua Elliott
Matthew Whitaker
Barbara Bodinier
Oliver Eales
Steven Riley
Helen Ward
Graham Cooke
Ara Darzi
Marc Chadeau-Hyam
Paul Elliott
author_sort Joshua Elliott
title Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.
title_short Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.
title_full Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.
title_fullStr Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.
title_full_unstemmed Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people.
title_sort predictive symptoms for covid-19 in the community: react-1 study of over 1 million people.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/df15cc8947f14ab29bd1ca8b23f07a5c
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