Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort

© 2018 Article author(s). Introduction Viral acute respiratory infections (ARIs) cause substantial child morbidity. Sensitive molecular-based assays aid virus detection, but the clinical significance of positive tests remains uncertain as some viruses may be found in both acutely ill and healthy chi...

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Main Authors: Sarna, Mohinder, Lambert, S., Sloots, T., Whiley, D., Alsaleh, A., Mhango, L., Bialasiewicz, S., Wang, D., Nissen, M., Grimwood, K., Ware, R.
Format: Journal Article
Published: BMJ Group 2018
Online Access:http://hdl.handle.net/20.500.11937/72112
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author Sarna, Mohinder
Lambert, S.
Sloots, T.
Whiley, D.
Alsaleh, A.
Mhango, L.
Bialasiewicz, S.
Wang, D.
Nissen, M.
Grimwood, K.
Ware, R.
author_facet Sarna, Mohinder
Lambert, S.
Sloots, T.
Whiley, D.
Alsaleh, A.
Mhango, L.
Bialasiewicz, S.
Wang, D.
Nissen, M.
Grimwood, K.
Ware, R.
author_sort Sarna, Mohinder
building Curtin Institutional Repository
collection Online Access
description © 2018 Article author(s). Introduction Viral acute respiratory infections (ARIs) cause substantial child morbidity. Sensitive molecular-based assays aid virus detection, but the clinical significance of positive tests remains uncertain as some viruses may be found in both acutely ill and healthy children. We describe disease-pathogen associations of respiratory viruses and quantify virus-specific attributable risk of ARIs in healthy children during the first 2 years of life. Methods One hundred fifty-eight term newborn babies in Brisbane, Australia, were recruited progressively into a longitudinal, community-based, birth cohort study conducted between September 2010 and October 2014. A daily tick-box diary captured predefined respiratory symptoms from birth until their second birthday. Weekly parent-collected nasal swabs were batch-tested for 17 respiratory viruses by PCR assays, allowing calculation of virus-specific attributable fractions in the exposed (AFE) to determine the proportion of virus-positive children whose ARI symptoms could be attributed to that particular virus. Results Of 8100 nasal swabs analysed, 2646 (32.7%) were virus-positive (275 virus codetections, 3.4%), with human rhinoviruses accounting for 2058/2646 (77.8%) positive swabs. Viruses were detected in 1154/1530 (75.4%) ARI episodes and in 984/4308 (22.8%) swabs from asymptomatic periods. Respiratory syncytial virus (AFE: 68% (95% CI 45% to 82%)) and human metapneumovirus (AFE: 69% (95% CI 43% to 83%)) were strongly associated with higher risk of lower respiratory symptoms. Discussion The strong association of respiratory syncytial virus and human metapneumovirus with ARIs and lower respiratory symptoms in young children managed within the community indicates successful development of vaccines against these two viruses should provide substantial health benefits.
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spelling curtin-20.500.11937-721122019-03-18T04:18:41Z Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort Sarna, Mohinder Lambert, S. Sloots, T. Whiley, D. Alsaleh, A. Mhango, L. Bialasiewicz, S. Wang, D. Nissen, M. Grimwood, K. Ware, R. © 2018 Article author(s). Introduction Viral acute respiratory infections (ARIs) cause substantial child morbidity. Sensitive molecular-based assays aid virus detection, but the clinical significance of positive tests remains uncertain as some viruses may be found in both acutely ill and healthy children. We describe disease-pathogen associations of respiratory viruses and quantify virus-specific attributable risk of ARIs in healthy children during the first 2 years of life. Methods One hundred fifty-eight term newborn babies in Brisbane, Australia, were recruited progressively into a longitudinal, community-based, birth cohort study conducted between September 2010 and October 2014. A daily tick-box diary captured predefined respiratory symptoms from birth until their second birthday. Weekly parent-collected nasal swabs were batch-tested for 17 respiratory viruses by PCR assays, allowing calculation of virus-specific attributable fractions in the exposed (AFE) to determine the proportion of virus-positive children whose ARI symptoms could be attributed to that particular virus. Results Of 8100 nasal swabs analysed, 2646 (32.7%) were virus-positive (275 virus codetections, 3.4%), with human rhinoviruses accounting for 2058/2646 (77.8%) positive swabs. Viruses were detected in 1154/1530 (75.4%) ARI episodes and in 984/4308 (22.8%) swabs from asymptomatic periods. Respiratory syncytial virus (AFE: 68% (95% CI 45% to 82%)) and human metapneumovirus (AFE: 69% (95% CI 43% to 83%)) were strongly associated with higher risk of lower respiratory symptoms. Discussion The strong association of respiratory syncytial virus and human metapneumovirus with ARIs and lower respiratory symptoms in young children managed within the community indicates successful development of vaccines against these two viruses should provide substantial health benefits. 2018 Journal Article http://hdl.handle.net/20.500.11937/72112 10.1136/thoraxjnl-2017-210233 http://creativecommons.org/licenses/by-nc/4.0/ BMJ Group fulltext
spellingShingle Sarna, Mohinder
Lambert, S.
Sloots, T.
Whiley, D.
Alsaleh, A.
Mhango, L.
Bialasiewicz, S.
Wang, D.
Nissen, M.
Grimwood, K.
Ware, R.
Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort
title Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort
title_full Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort
title_fullStr Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort
title_full_unstemmed Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort
title_short Viruses causing lower respiratory symptoms in young children: Findings from the ORChID birth cohort
title_sort viruses causing lower respiratory symptoms in young children: findings from the orchid birth cohort
url http://hdl.handle.net/20.500.11937/72112