Epidemiological and clinical insights from SARS-CoV-2 RT-PCR crossing threshold values, France, January to November 2020
dc.rights.license | open | en_US |
dc.contributor.author | ALIZON, Samuel | |
dc.contributor.author | SELINGER, Christian | |
dc.contributor.author | SOFONEA, Mircea | |
dc.contributor.author | HAIM-BOUKOBZA, Stéphanie | |
dc.contributor.author | GIANNOLI, Jean-Marc | |
dc.contributor.author | NINOVE, Laetitia | |
dc.contributor.author | PILLET, Sylvie | |
dc.contributor.author | THIBAULT, V. | |
dc.contributor.author | DE ROUGEMONT, Alexis | |
hal.structure.identifier | Microbiologie Fondamentale et Pathogénicité [MFP] | |
dc.contributor.author | TUMIOTTO, Camille | |
dc.contributor.author | STEPHAN, Robin | |
dc.contributor.author | BRESSOLLETTE-BODIN, Céline | |
dc.contributor.author | SALMONA, Maud | |
dc.contributor.author | L’HONNEUR, Anne-Sophie | |
dc.contributor.author | BEHILLIL, Sylvie | |
dc.contributor.author | LEFEUVRE, Caroline | |
dc.contributor.author | DINA, Julia | |
dc.contributor.author | HANTZ, Sébastien | |
dc.contributor.author | HARTARD, Cédric | |
dc.contributor.author | VEYER, David | |
dc.contributor.author | DELAGRÈVERIE, Héloïse | |
dc.contributor.author | FOURATI, Slim | |
dc.contributor.author | VISSEAUX, Benoît | |
dc.contributor.author | HENQUELL, Cécile | |
dc.contributor.author | LINA, Bruno | |
dc.contributor.author | FOULONGNE, Vincent | |
dc.contributor.author | BURREL, Sonia | |
dc.date.accessioned | 2023-05-16T15:13:58Z | |
dc.date.available | 2023-05-16T15:13:58Z | |
dc.date.issued | 2022 | |
dc.identifier.issn | 1560-7917 | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/182163 | |
dc.description.abstractEn | BackgroundThe COVID-19 pandemic has led to an unprecedented daily use of RT-PCR tests. These tests are interpreted qualitatively for diagnosis, and the relevance of the test result intensity, i.e. the number of quantification cycles (Cq), is debated because of strong potential biases.AimWe explored the possibility to use Cq values from SARS-CoV-2 screening tests to better understand the spread of an epidemic and to better understand the biology of the infection.MethodsWe used linear regression models to analyse a large database of 793,479 Cq values from tests performed on more than 2 million samples between 21 January and 30 November 2020, i.e. the first two pandemic waves. We performed time series analysis using autoregressive integrated moving average (ARIMA) models to estimate whether Cq data information improves short-term predictions of epidemiological dynamics.ResultsAlthough we found that the Cq values varied depending on the testing laboratory or the assay used, we detected strong significant trends associated with patient age, number of days after symptoms onset or the state of the epidemic (the temporal reproduction number) at the time of the test. Furthermore, knowing the quartiles of the Cq distribution greatly reduced the error in predicting the temporal reproduction number of the COVID-19 epidemic.ConclusionOur results suggest that Cq values of screening tests performed in the general population generate testable hypotheses and help improve short-term predictions for epidemic surveillance. | |
dc.language.iso | EN | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
dc.title.en | Epidemiological and clinical insights from SARS-CoV-2 RT-PCR crossing threshold values, France, January to November 2020 | |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.2807/1560-7917.ES.2022.27.6.2100406 | en_US |
dc.subject.hal | Informatique [cs]/Modélisation et simulation | en_US |
dc.subject.hal | Sciences de l'environnement/Biodiversité et Ecologie | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Santé publique et épidémiologie | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Bio-Informatique, Biologie Systémique [q-bio.QM] | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Biodiversité/Evolution [q-bio.PE] | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Biodiversité/Systématique, phylogénie et taxonomie | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Ecologie, Environnement/Ecosystèmes | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Ecologie, Environnement/Interactions entre organismes | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Ecologie, Environnement/Santé | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Génétique/Génétique des populations [q-bio.PE] | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Microbiologie et Parasitologie/Virologie | en_US |
bordeaux.journal | Eurosurveillance | en_US |
bordeaux.page | 2100406 | en_US |
bordeaux.volume | 27 | en_US |
bordeaux.hal.laboratories | MFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234 | en_US |
bordeaux.issue | 6 | en_US |
bordeaux.institution | CNRS | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
bordeaux.import.source | hal | |
hal.identifier | hal-03175551 | |
hal.version | 1 | |
hal.export | false | |
workflow.import.source | hal | |
dc.rights.cc | Pas de Licence CC | en_US |
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