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Population-based serology reveals risk factors for RSV infection in children younger than 5 years
Respiratory syncytial virus (RSV) infection is a leading cause of hospitalization in infants. Underlying risk factors for RSV infection in the general population are not well understood, as previous work has focused on severe outcomes of infection in a clinical setting. Here we use RSV-specific IgG...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076290/ https://www.ncbi.nlm.nih.gov/pubmed/33903695 http://dx.doi.org/10.1038/s41598-021-88524-w |
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author | Andeweg, Stijn P. Schepp, Rutger M. van de Kassteele, Jan Mollema, Liesbeth Berbers, Guy A. M. van Boven, Michiel |
author_facet | Andeweg, Stijn P. Schepp, Rutger M. van de Kassteele, Jan Mollema, Liesbeth Berbers, Guy A. M. van Boven, Michiel |
author_sort | Andeweg, Stijn P. |
collection | PubMed |
description | Respiratory syncytial virus (RSV) infection is a leading cause of hospitalization in infants. Underlying risk factors for RSV infection in the general population are not well understood, as previous work has focused on severe outcomes of infection in a clinical setting. Here we use RSV-specific IgG and IgA antibody measurements from two population-based cross-sectional serosurveys carried out in the Netherlands (n = 682) to classify children up to 5 years as seronegative or seropositive. We employ a generalized additive model to estimate the probability of prior RSV infection as function of age, date of birth within the year, and other risk factors. The analyses show that the majority of children have experienced a RSV infection before the age of 2 years. Age and birthdate are strong predictors of RSV infection in the first years of life, and children born in summer have higher estimated probability of infection than those born in winter [e.g., 0.56 (95% CI 0.45–0.66) vs. 0.32 (0.21–0.45) at age 1 year]. Our analyses reveal that the mean age at infection depends on date of birth, which has implications for the design of vaccination programmes and prioritisation schemes for the prophylactic use of monoclonal antibodies. |
format | Online Article Text |
id | pubmed-8076290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80762902021-04-27 Population-based serology reveals risk factors for RSV infection in children younger than 5 years Andeweg, Stijn P. Schepp, Rutger M. van de Kassteele, Jan Mollema, Liesbeth Berbers, Guy A. M. van Boven, Michiel Sci Rep Article Respiratory syncytial virus (RSV) infection is a leading cause of hospitalization in infants. Underlying risk factors for RSV infection in the general population are not well understood, as previous work has focused on severe outcomes of infection in a clinical setting. Here we use RSV-specific IgG and IgA antibody measurements from two population-based cross-sectional serosurveys carried out in the Netherlands (n = 682) to classify children up to 5 years as seronegative or seropositive. We employ a generalized additive model to estimate the probability of prior RSV infection as function of age, date of birth within the year, and other risk factors. The analyses show that the majority of children have experienced a RSV infection before the age of 2 years. Age and birthdate are strong predictors of RSV infection in the first years of life, and children born in summer have higher estimated probability of infection than those born in winter [e.g., 0.56 (95% CI 0.45–0.66) vs. 0.32 (0.21–0.45) at age 1 year]. Our analyses reveal that the mean age at infection depends on date of birth, which has implications for the design of vaccination programmes and prioritisation schemes for the prophylactic use of monoclonal antibodies. Nature Publishing Group UK 2021-04-26 /pmc/articles/PMC8076290/ /pubmed/33903695 http://dx.doi.org/10.1038/s41598-021-88524-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Andeweg, Stijn P. Schepp, Rutger M. van de Kassteele, Jan Mollema, Liesbeth Berbers, Guy A. M. van Boven, Michiel Population-based serology reveals risk factors for RSV infection in children younger than 5 years |
title | Population-based serology reveals risk factors for RSV infection in children younger than 5 years |
title_full | Population-based serology reveals risk factors for RSV infection in children younger than 5 years |
title_fullStr | Population-based serology reveals risk factors for RSV infection in children younger than 5 years |
title_full_unstemmed | Population-based serology reveals risk factors for RSV infection in children younger than 5 years |
title_short | Population-based serology reveals risk factors for RSV infection in children younger than 5 years |
title_sort | population-based serology reveals risk factors for rsv infection in children younger than 5 years |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076290/ https://www.ncbi.nlm.nih.gov/pubmed/33903695 http://dx.doi.org/10.1038/s41598-021-88524-w |
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