No association between disease severity and respiratory syncytial virus subtypes RSV-A and RSV-B in hospitalized young children in Norway
There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical severity. We aimed to explore the associations between disease severity and RSV subtypes RSV-A and RSV-B and to describe the circulation of RSV subt...
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Published in | PloS one Vol. 19; no. 3; p. e0298104 |
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Abstract | There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical severity. We aimed to explore the associations between disease severity and RSV subtypes RSV-A and RSV-B and to describe the circulation of RSV subtypes pattern by season and age.
Active prospective hospital surveillance for RSV-A and RSV-B in children <59 months of age was conducted during 2015-2018. All febrile children 12-59 months of age were enrolled, whereas children <12 months were eligible if presenting with fever or respiratory symptoms. Risk factors and upper and lower respiratory tract infection was identified by linkage to national registry data and analyzed using penalized maximum likelihood logistic regression.
Both RSV-A and B were found to co-circulate throughout all three study seasons, and no clear seasonal pattern was identified. Likewise, we found no association between sex or measures of severity with RSV-A or RSV-B. There was significantly more RSV-A than RSV-B among children with comorbidities.
No association was found between disease severity or sex and RSV subtypes RSV-A and RSV-B in hospitalized young children in Norway. |
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AbstractList | Objective There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical severity. We aimed to explore the associations between disease severity and RSV subtypes RSV-A and RSV-B and to describe the circulation of RSV subtypes pattern by season and age. Methods Active prospective hospital surveillance for RSV-A and RSV-B in children <59 months of age was conducted during 2015-2018. All febrile children 12-59 months of age were enrolled, whereas children <12 months were eligible if presenting with fever or respiratory symptoms. Risk factors and upper and lower respiratory tract infection was identified by linkage to national registry data and analyzed using penalized maximum likelihood logistic regression. Results Both RSV-A and B were found to co-circulate throughout all three study seasons, and no clear seasonal pattern was identified. Likewise, we found no association between sex or measures of severity with RSV-A or RSV-B. There was significantly more RSV-A than RSV-B among children with comorbidities. Conclusions No association was found between disease severity or sex and RSV subtypes RSV-A and RSV-B in hospitalized young children in Norway. Objective There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical severity. We aimed to explore the associations between disease severity and RSV subtypes RSV-A and RSV-B and to describe the circulation of RSV subtypes pattern by season and age. Methods Active prospective hospital surveillance for RSV-A and RSV-B in children <59 months of age was conducted during 2015–2018. All febrile children 12–59 months of age were enrolled, whereas children <12 months were eligible if presenting with fever or respiratory symptoms. Risk factors and upper and lower respiratory tract infection was identified by linkage to national registry data and analyzed using penalized maximum likelihood logistic regression. Results Both RSV-A and B were found to co-circulate throughout all three study seasons, and no clear seasonal pattern was identified. Likewise, we found no association between sex or measures of severity with RSV-A or RSV-B. There was significantly more RSV-A than RSV-B among children with comorbidities. Conclusions No association was found between disease severity or sex and RSV subtypes RSV-A and RSV-B in hospitalized young children in Norway. OBJECTIVEThere is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical severity. We aimed to explore the associations between disease severity and RSV subtypes RSV-A and RSV-B and to describe the circulation of RSV subtypes pattern by season and age.METHODSActive prospective hospital surveillance for RSV-A and RSV-B in children <59 months of age was conducted during 2015-2018. All febrile children 12-59 months of age were enrolled, whereas children <12 months were eligible if presenting with fever or respiratory symptoms. Risk factors and upper and lower respiratory tract infection was identified by linkage to national registry data and analyzed using penalized maximum likelihood logistic regression.RESULTSBoth RSV-A and B were found to co-circulate throughout all three study seasons, and no clear seasonal pattern was identified. Likewise, we found no association between sex or measures of severity with RSV-A or RSV-B. There was significantly more RSV-A than RSV-B among children with comorbidities.CONCLUSIONSNo association was found between disease severity or sex and RSV subtypes RSV-A and RSV-B in hospitalized young children in Norway. There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical severity. We aimed to explore the associations between disease severity and RSV subtypes RSV-A and RSV-B and to describe the circulation of RSV subtypes pattern by season and age. Active prospective hospital surveillance for RSV-A and RSV-B in children <59 months of age was conducted during 2015-2018. All febrile children 12-59 months of age were enrolled, whereas children <12 months were eligible if presenting with fever or respiratory symptoms. Risk factors and upper and lower respiratory tract infection was identified by linkage to national registry data and analyzed using penalized maximum likelihood logistic regression. Both RSV-A and B were found to co-circulate throughout all three study seasons, and no clear seasonal pattern was identified. Likewise, we found no association between sex or measures of severity with RSV-A or RSV-B. There was significantly more RSV-A than RSV-B among children with comorbidities. No association was found between disease severity or sex and RSV subtypes RSV-A and RSV-B in hospitalized young children in Norway. There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical severity. We aimed to explore the associations between disease severity and RSV subtypes RSV-A and RSV-B and to describe the circulation of RSV subtypes pattern by season and age. Active prospective hospital surveillance for RSV-A and RSV-B in children <59 months of age was conducted during 2015-2018. All febrile children 12-59 months of age were enrolled, whereas children <12 months were eligible if presenting with fever or respiratory symptoms. Risk factors and upper and lower respiratory tract infection was identified by linkage to national registry data and analyzed using penalized maximum likelihood logistic regression. Both RSV-A and B were found to co-circulate throughout all three study seasons, and no clear seasonal pattern was identified. Likewise, we found no association between sex or measures of severity with RSV-A or RSV-B. There was significantly more RSV-A than RSV-B among children with comorbidities. No association was found between disease severity or sex and RSV subtypes RSV-A and RSV-B in hospitalized young children in Norway. |
Audience | Academic |
Author | Leegaard, Truls Michael Havdal, Lise Beier Størdal, Ketil Inchley, Christopher Rojahn, Astrid Elisabeth Debes, Sara Døllner, Henrik Nordbø, Svein Arne Haarr, Elisebet Bøås, Håkon Bekkevold, Terese Kran, Anne-Marte Bakken Barstad, Bjørn Flem, Elmira |
AuthorAffiliation | 14 Department of Microbiology, Oslo University Hospital, Oslo, Norway 7 Department of Microbiology and Infection Control, Akershus University Hospital, Lørenskog, Norway 13 Department of Medical Microbiology, Stavanger University Hospital, Stavanger, Norway 4 Division of Paediatric and Adolescent Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway 5 Department of Pediatrics, St. Olavs University Hospital, Trondheim, Norway 3 Department of Pediatrics, Østfold Hospital, Grålum, Norway Carol Davila University of Medicine and Pharmacy, ROMANIA 1 Norwegian Institute of Public Health, Oslo, Norway 8 Division of Medicine and Laboratory Sciences, Institute of Clinical Medicine - Campus Ahus, University of Oslo, Oslo, Norway 10 Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway 11 Department of Medical Microbiology, Østfold Hospital, Grålum, Norway 12 Department of Pediatrics, Stavanger University Hospital, Stavanger, Norway 2 Department of Paediat |
AuthorAffiliation_xml | – name: 9 Department of Medical Microbiology, St. Olavs University Hospital, Trondheim, Norway – name: 11 Department of Medical Microbiology, Østfold Hospital, Grålum, Norway – name: 7 Department of Microbiology and Infection Control, Akershus University Hospital, Lørenskog, Norway – name: 5 Department of Pediatrics, St. Olavs University Hospital, Trondheim, Norway – name: 14 Department of Microbiology, Oslo University Hospital, Oslo, Norway – name: 3 Department of Pediatrics, Østfold Hospital, Grålum, Norway – name: 1 Norwegian Institute of Public Health, Oslo, Norway – name: 6 Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway – name: 10 Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway – name: 12 Department of Pediatrics, Stavanger University Hospital, Stavanger, Norway – name: 13 Department of Medical Microbiology, Stavanger University Hospital, Stavanger, Norway – name: 2 Department of Paediatric and Adolescent Medicine, Akershus University Hospital, Lørenskog, Norway – name: 8 Division of Medicine and Laboratory Sciences, Institute of Clinical Medicine - Campus Ahus, University of Oslo, Oslo, Norway – name: 4 Division of Paediatric and Adolescent Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway – name: Carol Davila University of Medicine and Pharmacy, ROMANIA |
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Copyright | Copyright: © 2024 Bøås et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. COPYRIGHT 2024 Public Library of Science info:eu-repo/semantics/openAccess 2024 Bøås et al 2024 Bøås et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: Elmira Flem is currently employed by Merck & Co., Inc., North Wales, PA, USA. The work for the current study was conducted by Dr. Flem under the previous affiliation at the Norwegian Institute of Public Health. All other authors hereby declare that no other conflicts of interest exist. A list of members of The Norwegian Enhanced Pediatric Immunisation Surveillance (NorEPIS) Network is provided in the Acknowledgments. |
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Snippet | There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with clinical... Objective There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with... OBJECTIVEThere is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with... Objective There is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with... ObjectiveThere is conflicting evidence whether subtypes of Respiratory syncytial virus have different seasonality or are differentially associated with... |
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SubjectTerms | Analysis Biology and Life Sciences Care and treatment Children Comorbidity Diagnosis Health aspects Hospital patients Infection Medicine and Health Sciences People and Places Respiratory syncytial virus Respiratory tract diseases Risk factors |
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Title | No association between disease severity and respiratory syncytial virus subtypes RSV-A and RSV-B in hospitalized young children in Norway |
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