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Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia

In vitro and animal models described lower replication capacity and virulence of SARS-CoV-2 Omicron lineage in lower respiratory airways compared to wild type and other variants of concern (oVOCs). Among adult subjects admitted to our hospital (Turin, Italy) due to wild type, oVOCs, and Omicron SARS...

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Autores principales: Trunfio, Mattia, Portesani, Francesca, Vicinanza, Sabrina, Nespoli, Paola, Traverso, Federico, Cortese, Giancarlo, Bonora, Stefano, Calcagno, Andrea, Di Perri, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483268/
https://www.ncbi.nlm.nih.gov/pubmed/36114845
http://dx.doi.org/10.1007/s00408-022-00566-7
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author Trunfio, Mattia
Portesani, Francesca
Vicinanza, Sabrina
Nespoli, Paola
Traverso, Federico
Cortese, Giancarlo
Bonora, Stefano
Calcagno, Andrea
Di Perri, Giovanni
author_facet Trunfio, Mattia
Portesani, Francesca
Vicinanza, Sabrina
Nespoli, Paola
Traverso, Federico
Cortese, Giancarlo
Bonora, Stefano
Calcagno, Andrea
Di Perri, Giovanni
author_sort Trunfio, Mattia
collection PubMed
description In vitro and animal models described lower replication capacity and virulence of SARS-CoV-2 Omicron lineage in lower respiratory airways compared to wild type and other variants of concern (oVOCs). Among adult subjects admitted to our hospital (Turin, Italy) due to wild type, oVOCs, and Omicron SARS-CoV-2-related pneumonia (n = 100 for each lineage), the cases of Omicron pneumonia showed lower degree of lung parenchyma involvement (aβ -1.471, p = 0.037), less tendency to parenchyma consolidation (aOR 0.500, p = 0.011), and better respiratory functions (assessed by ambient air arterial blood gas analysis). After adjusting for demographic, previous immunity, and comorbidities, Omicron pneumonia still associated with lower risk of respiratory failure (for severe respiratory failure, Wild-type versus Omicron aOR 15.6, p = 0.005 and oVOCs versus Omicron aOR 31.7, p < 0.001). These observations are in line with preliminary findings from in vitro and animal models and could explain why Omicron infection has been associated with lower mortality and hospitalization in human.
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spelling pubmed-94832682022-09-19 Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia Trunfio, Mattia Portesani, Francesca Vicinanza, Sabrina Nespoli, Paola Traverso, Federico Cortese, Giancarlo Bonora, Stefano Calcagno, Andrea Di Perri, Giovanni Lung Covid-19 In vitro and animal models described lower replication capacity and virulence of SARS-CoV-2 Omicron lineage in lower respiratory airways compared to wild type and other variants of concern (oVOCs). Among adult subjects admitted to our hospital (Turin, Italy) due to wild type, oVOCs, and Omicron SARS-CoV-2-related pneumonia (n = 100 for each lineage), the cases of Omicron pneumonia showed lower degree of lung parenchyma involvement (aβ -1.471, p = 0.037), less tendency to parenchyma consolidation (aOR 0.500, p = 0.011), and better respiratory functions (assessed by ambient air arterial blood gas analysis). After adjusting for demographic, previous immunity, and comorbidities, Omicron pneumonia still associated with lower risk of respiratory failure (for severe respiratory failure, Wild-type versus Omicron aOR 15.6, p = 0.005 and oVOCs versus Omicron aOR 31.7, p < 0.001). These observations are in line with preliminary findings from in vitro and animal models and could explain why Omicron infection has been associated with lower mortality and hospitalization in human. Springer US 2022-09-17 2022 /pmc/articles/PMC9483268/ /pubmed/36114845 http://dx.doi.org/10.1007/s00408-022-00566-7 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Covid-19
Trunfio, Mattia
Portesani, Francesca
Vicinanza, Sabrina
Nespoli, Paola
Traverso, Federico
Cortese, Giancarlo
Bonora, Stefano
Calcagno, Andrea
Di Perri, Giovanni
Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia
title Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia
title_full Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia
title_fullStr Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia
title_full_unstemmed Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia
title_short Real-life Evidence of Lower Lung Virulence in COVID-19 Inpatients Infected with SARS-CoV-2 Omicron Variant Compared to Wild-Type and Delta SARS-CoV-2 Pneumonia
title_sort real-life evidence of lower lung virulence in covid-19 inpatients infected with sars-cov-2 omicron variant compared to wild-type and delta sars-cov-2 pneumonia
topic Covid-19
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483268/
https://www.ncbi.nlm.nih.gov/pubmed/36114845
http://dx.doi.org/10.1007/s00408-022-00566-7
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