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Reproducible breath metabolite changes in children with SARS-CoV-2 infection

SARS-CoV-2 infection is diagnosed through detection of specific viral nucleic acid or antigens from respiratory samples. These techniques are relatively expensive, slow, and susceptible to false-negative results. A rapid non-invasive method to detect infection would be highly advantageous. Compellin...

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Autores principales: Berna, Amalia Z., Akaho, Elikplim H., Harris, Rebecca M., Congdon, Morgan, Korn, Emilie, Neher, Samuel, M’Farrej, Mirna, Burns, Julianne, John, Audrey R. Odom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743102/
https://www.ncbi.nlm.nih.gov/pubmed/33330891
http://dx.doi.org/10.1101/2020.12.04.20230755
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author Berna, Amalia Z.
Akaho, Elikplim H.
Harris, Rebecca M.
Congdon, Morgan
Korn, Emilie
Neher, Samuel
M’Farrej, Mirna
Burns, Julianne
John, Audrey R. Odom
author_facet Berna, Amalia Z.
Akaho, Elikplim H.
Harris, Rebecca M.
Congdon, Morgan
Korn, Emilie
Neher, Samuel
M’Farrej, Mirna
Burns, Julianne
John, Audrey R. Odom
author_sort Berna, Amalia Z.
collection PubMed
description SARS-CoV-2 infection is diagnosed through detection of specific viral nucleic acid or antigens from respiratory samples. These techniques are relatively expensive, slow, and susceptible to false-negative results. A rapid non-invasive method to detect infection would be highly advantageous. Compelling evidence from canine biosensors and studies of adults with COVID-19 suggests that infection reproducibly alters human volatile organic compounds (VOCs) profiles. To determine whether pediatric infection is associated with VOC changes, we enrolled SARS-CoV-2-infected and -uninfected children admitted to a major pediatric academic medical center. Breath samples were collected from children and analyzed through state-of-the-art GCxGC-ToFMS. Isolated features included 84 targeted VOCs. Candidate biomarkers that were correlated with infection status were subsequently validated in a second, independent cohort of children. We thus find that six volatile organic compounds are significantly and reproducibly increased in the breath of SARS-CoV-2-infected children. Three aldehydes (octanal, nonanal, and heptanal) drew special attention, as aldehydes are also elevated in the breath of adults with COVID-19. Together, these biomarkers demonstrate high accuracy for distinguishing pediatric SARS-CoV-2 infection and support the ongoing development of novel breath-based diagnostics.
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spelling pubmed-77431022020-12-17 Reproducible breath metabolite changes in children with SARS-CoV-2 infection Berna, Amalia Z. Akaho, Elikplim H. Harris, Rebecca M. Congdon, Morgan Korn, Emilie Neher, Samuel M’Farrej, Mirna Burns, Julianne John, Audrey R. Odom medRxiv Article SARS-CoV-2 infection is diagnosed through detection of specific viral nucleic acid or antigens from respiratory samples. These techniques are relatively expensive, slow, and susceptible to false-negative results. A rapid non-invasive method to detect infection would be highly advantageous. Compelling evidence from canine biosensors and studies of adults with COVID-19 suggests that infection reproducibly alters human volatile organic compounds (VOCs) profiles. To determine whether pediatric infection is associated with VOC changes, we enrolled SARS-CoV-2-infected and -uninfected children admitted to a major pediatric academic medical center. Breath samples were collected from children and analyzed through state-of-the-art GCxGC-ToFMS. Isolated features included 84 targeted VOCs. Candidate biomarkers that were correlated with infection status were subsequently validated in a second, independent cohort of children. We thus find that six volatile organic compounds are significantly and reproducibly increased in the breath of SARS-CoV-2-infected children. Three aldehydes (octanal, nonanal, and heptanal) drew special attention, as aldehydes are also elevated in the breath of adults with COVID-19. Together, these biomarkers demonstrate high accuracy for distinguishing pediatric SARS-CoV-2 infection and support the ongoing development of novel breath-based diagnostics. Cold Spring Harbor Laboratory 2021-05-07 /pmc/articles/PMC7743102/ /pubmed/33330891 http://dx.doi.org/10.1101/2020.12.04.20230755 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Berna, Amalia Z.
Akaho, Elikplim H.
Harris, Rebecca M.
Congdon, Morgan
Korn, Emilie
Neher, Samuel
M’Farrej, Mirna
Burns, Julianne
John, Audrey R. Odom
Reproducible breath metabolite changes in children with SARS-CoV-2 infection
title Reproducible breath metabolite changes in children with SARS-CoV-2 infection
title_full Reproducible breath metabolite changes in children with SARS-CoV-2 infection
title_fullStr Reproducible breath metabolite changes in children with SARS-CoV-2 infection
title_full_unstemmed Reproducible breath metabolite changes in children with SARS-CoV-2 infection
title_short Reproducible breath metabolite changes in children with SARS-CoV-2 infection
title_sort reproducible breath metabolite changes in children with sars-cov-2 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743102/
https://www.ncbi.nlm.nih.gov/pubmed/33330891
http://dx.doi.org/10.1101/2020.12.04.20230755
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