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Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic

BACKGROUND: Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is clinically diverse, and children have a low risk of developing severe coronavirus disease 2019 (COVID-19). However, children with chronic diseases have a potentially increased risk. METHODS: We performed a pro...

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Autores principales: Hoste, Levi, Prytula, Agnieszka, Dehoorne, Jo, De Bruyne, Ruth, Van Biervliet, Stephanie, De Waele, Kathleen, Maes, Evelyn, Bordon, Victoria, Vanlander, Arnaud, Claes, Karlien, Vande Walle, Johan, Schelstraete, Petra, Van daele, Sabine, Haerynck, Filomeen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440688/
https://www.ncbi.nlm.nih.gov/pubmed/37609364
http://dx.doi.org/10.3389/fped.2023.1210181
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author Hoste, Levi
Prytula, Agnieszka
Dehoorne, Jo
De Bruyne, Ruth
Van Biervliet, Stephanie
De Waele, Kathleen
Maes, Evelyn
Bordon, Victoria
Vanlander, Arnaud
Claes, Karlien
Vande Walle, Johan
Schelstraete, Petra
Van daele, Sabine
Haerynck, Filomeen
author_facet Hoste, Levi
Prytula, Agnieszka
Dehoorne, Jo
De Bruyne, Ruth
Van Biervliet, Stephanie
De Waele, Kathleen
Maes, Evelyn
Bordon, Victoria
Vanlander, Arnaud
Claes, Karlien
Vande Walle, Johan
Schelstraete, Petra
Van daele, Sabine
Haerynck, Filomeen
author_sort Hoste, Levi
collection PubMed
description BACKGROUND: Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is clinically diverse, and children have a low risk of developing severe coronavirus disease 2019 (COVID-19). However, children with chronic diseases have a potentially increased risk. METHODS: We performed a prospective surveillance study with longitudinal serum SARS-CoV-2 anti-nucleocapsid antibody quantification and questionnaires in pediatric tertiary care patients during the first waves of the COVID-19 pandemic (November 2020–September 2021). The results were compared with those of healthy children and adults from the same geographic area. RESULTS: We obtained 525 samples from 362 patients (M/F ratio of 1.3:1; median age of 11.1 years) comprising children with immune-suppressive or immune-modulating drugs (32.9%), inborn errors of immunity (23.5%), type 1 diabetes mellitus (15.2%), and rheumatic diseases (11.9%). A total of 51 (9.7%) samples were seropositive among 37/351 children (10.5%). Seropositivity increased from 5.8% in November–December 2020 to 21.6% in July–September 2021. Compared with adults, a longitudinal analysis revealed reduced seroprevalence but similar kinetics as in children from the same country. Demographic or social variables and disease characteristics did not correlate with seropositivity. Being obese and household contact with COVID-19-infected individuals significantly increased the odds of infection. The majority of seropositive patients had mild symptoms (21/37). One-third were asymptomatic and/or unaware of having COVID-19 (10/37). Four patients (4/37) needed hospitalization, with good clinical outcomes. CONCLUSIONS: Although harboring a chronic disease, we observed a low SARS-CoV-2 incidence in a cohort of pediatric tertiary care patients, comparable with healthy children during the first year of the pandemic. Infection was mostly associated with mild symptoms.
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spelling pubmed-104406882023-08-22 Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic Hoste, Levi Prytula, Agnieszka Dehoorne, Jo De Bruyne, Ruth Van Biervliet, Stephanie De Waele, Kathleen Maes, Evelyn Bordon, Victoria Vanlander, Arnaud Claes, Karlien Vande Walle, Johan Schelstraete, Petra Van daele, Sabine Haerynck, Filomeen Front Pediatr Pediatrics BACKGROUND: Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is clinically diverse, and children have a low risk of developing severe coronavirus disease 2019 (COVID-19). However, children with chronic diseases have a potentially increased risk. METHODS: We performed a prospective surveillance study with longitudinal serum SARS-CoV-2 anti-nucleocapsid antibody quantification and questionnaires in pediatric tertiary care patients during the first waves of the COVID-19 pandemic (November 2020–September 2021). The results were compared with those of healthy children and adults from the same geographic area. RESULTS: We obtained 525 samples from 362 patients (M/F ratio of 1.3:1; median age of 11.1 years) comprising children with immune-suppressive or immune-modulating drugs (32.9%), inborn errors of immunity (23.5%), type 1 diabetes mellitus (15.2%), and rheumatic diseases (11.9%). A total of 51 (9.7%) samples were seropositive among 37/351 children (10.5%). Seropositivity increased from 5.8% in November–December 2020 to 21.6% in July–September 2021. Compared with adults, a longitudinal analysis revealed reduced seroprevalence but similar kinetics as in children from the same country. Demographic or social variables and disease characteristics did not correlate with seropositivity. Being obese and household contact with COVID-19-infected individuals significantly increased the odds of infection. The majority of seropositive patients had mild symptoms (21/37). One-third were asymptomatic and/or unaware of having COVID-19 (10/37). Four patients (4/37) needed hospitalization, with good clinical outcomes. CONCLUSIONS: Although harboring a chronic disease, we observed a low SARS-CoV-2 incidence in a cohort of pediatric tertiary care patients, comparable with healthy children during the first year of the pandemic. Infection was mostly associated with mild symptoms. Frontiers Media S.A. 2023-08-07 /pmc/articles/PMC10440688/ /pubmed/37609364 http://dx.doi.org/10.3389/fped.2023.1210181 Text en © 2023 Hoste, Prytula, Dehoorne, De Bruyne, Van Biervliet, De Waele, Maes, Bordon, Vanlander, Claes, Vande Walle, Schelstraete, Van daele and Haerynck. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Hoste, Levi
Prytula, Agnieszka
Dehoorne, Jo
De Bruyne, Ruth
Van Biervliet, Stephanie
De Waele, Kathleen
Maes, Evelyn
Bordon, Victoria
Vanlander, Arnaud
Claes, Karlien
Vande Walle, Johan
Schelstraete, Petra
Van daele, Sabine
Haerynck, Filomeen
Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic
title Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic
title_full Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic
title_fullStr Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic
title_full_unstemmed Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic
title_short Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic
title_sort comparison of sars-cov-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the covid-19 pandemic
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440688/
https://www.ncbi.nlm.nih.gov/pubmed/37609364
http://dx.doi.org/10.3389/fped.2023.1210181
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