Human Coronavirus in Hospitalized Children With Respiratory Tract Infections: A 9-Year Population-Based Study From Norway.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
08 04 2019
Historique:
received: 10 09 2018
accepted: 06 11 2018
pubmed: 13 11 2018
medline: 9 1 2020
entrez: 13 11 2018
Statut: ppublish

Résumé

The burden of human coronavirus (HCoV)-associated respiratory tract infections (RTIs) in hospitalized children is poorly defined. We studied the occurrence and hospitalization rates of HCoV over 9 years. Children from Sør-Trøndelag County, Norway, hospitalized with RTIs and asymptomatic controls, were prospectively enrolled from 2006 to 2015. Nasopharyngeal aspirates were analyzed with semiquantitative polymerase chain reaction (PCR) tests for HCoV subtypes OC43, 229E, NL63, and HKU1, and 13 other respiratory pathogens. HCoV was present in 9.1% (313/3458) of all RTI episodes: 46.6% OC43, 32.3% NL63, 16.0% HKU1, and 5.8% 229E. Hospitalization rates for HCoV-positive children with lower RTIs were 1.5 and 2.8 per 1000 <5 and <1 years of age, respectively. The detection rate among controls was 10.2% (38/373). Codetections occurred in 68.1% of the patients and 68.4% of the controls. In a logistic regression analysis, high HCoV genomic loads (cycle threshold <28 in PCR analysis) were associated with RTIs (odds ratio = 3.12, P = .016) adjusted for relevant factors. HCoVs occurred in 1 of 10 hospitalized children with RTIs and asymptomatic controls. A high HCoV genomic load was associated with RTI. HCoVs are associated with a substantial burden of RTIs in need of hospitalization.

Sections du résumé

BACKGROUND
The burden of human coronavirus (HCoV)-associated respiratory tract infections (RTIs) in hospitalized children is poorly defined. We studied the occurrence and hospitalization rates of HCoV over 9 years.
METHODS
Children from Sør-Trøndelag County, Norway, hospitalized with RTIs and asymptomatic controls, were prospectively enrolled from 2006 to 2015. Nasopharyngeal aspirates were analyzed with semiquantitative polymerase chain reaction (PCR) tests for HCoV subtypes OC43, 229E, NL63, and HKU1, and 13 other respiratory pathogens.
RESULTS
HCoV was present in 9.1% (313/3458) of all RTI episodes: 46.6% OC43, 32.3% NL63, 16.0% HKU1, and 5.8% 229E. Hospitalization rates for HCoV-positive children with lower RTIs were 1.5 and 2.8 per 1000 <5 and <1 years of age, respectively. The detection rate among controls was 10.2% (38/373). Codetections occurred in 68.1% of the patients and 68.4% of the controls. In a logistic regression analysis, high HCoV genomic loads (cycle threshold <28 in PCR analysis) were associated with RTIs (odds ratio = 3.12, P = .016) adjusted for relevant factors.
CONCLUSIONS
HCoVs occurred in 1 of 10 hospitalized children with RTIs and asymptomatic controls. A high HCoV genomic load was associated with RTI. HCoVs are associated with a substantial burden of RTIs in need of hospitalization.

Identifiants

pubmed: 30418633
pii: 5168836
doi: 10.1093/infdis/jiy646
pmc: PMC7107437
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1198-1206

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Inger Heimdal (I)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim.

Nina Moe (N)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim.
Department of Pediatrics, St Olavs Hospital, Trondheim University Hospital, Norway.

Sidsel Krokstad (S)

Departments of Medical Microbiology, St Olavs Hospital, Trondheim University Hospital, Norway.

Andreas Christensen (A)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim.
Departments of Medical Microbiology, St Olavs Hospital, Trondheim University Hospital, Norway.

Lars Høsøien Skanke (LH)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim.
Department of Pediatrics, St Olavs Hospital, Trondheim University Hospital, Norway.

Svein Arne Nordbø (SA)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim.
Departments of Medical Microbiology, St Olavs Hospital, Trondheim University Hospital, Norway.

Henrik Døllner (H)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim.
Department of Pediatrics, St Olavs Hospital, Trondheim University Hospital, Norway.

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