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The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia

Febrile neutropenia is a common complication during chemotherapy in paediatric cancer care. In this setting, clinical features and current diagnostic tests do not reliably distinguish between bacterial and viral infections. Children with cancer (n = 63) presenting with fever and neutropenia were rec...

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Autores principales: Aasa, Johannes, Tiselius, Eva, Sinha, Indranil, Edman, Gunnar, Wahlund, Martina, Hedengren, Shanie Saghafian, Nilsson, Anna, Berggren, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297134/
https://www.ncbi.nlm.nih.gov/pubmed/37371198
http://dx.doi.org/10.3390/children10060966
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author Aasa, Johannes
Tiselius, Eva
Sinha, Indranil
Edman, Gunnar
Wahlund, Martina
Hedengren, Shanie Saghafian
Nilsson, Anna
Berggren, Anna
author_facet Aasa, Johannes
Tiselius, Eva
Sinha, Indranil
Edman, Gunnar
Wahlund, Martina
Hedengren, Shanie Saghafian
Nilsson, Anna
Berggren, Anna
author_sort Aasa, Johannes
collection PubMed
description Febrile neutropenia is a common complication during chemotherapy in paediatric cancer care. In this setting, clinical features and current diagnostic tests do not reliably distinguish between bacterial and viral infections. Children with cancer (n = 63) presenting with fever and neutropenia were recruited for extensive microbiological and blood RNA sampling. RNA sequencing was successful in 43 cases of febrile neutropenia. These were classified as having probable bacterial infection (n = 17), probable viral infection (n = 13) and fever of unknown origin (n = 13) based on microbiological defined infections and CRP cut-off levels. RNA expression data with focus on the 2-transcript signature (FAM89A and IFI44L), earlier shown to identify bacterial infections with high specificity and sensitivity, was implemented as a disease risk score. The median disease risk score was higher in the probable bacterial infection group, −0.695 (max 2.795; min −5.478) compared to the probable viral infection group −3.327 (max 0.218; min −7.861), which in ROC analysis corresponded to a sensitivity of 0.88 and specificity of 0.54 with an AUC of 0.80. To further characterise the immune signature, analysis of significantly expressed genes and pathways was performed and upregulation of genes associated to antibacterial responses was present in the group classified as probable bacterial infection. Our results suggest that the 2-transcript signature may have a potential use as a diagnostic tool to identify bacterial infections in immunosuppressed children with febrile neutropenia.
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spelling pubmed-102971342023-06-28 The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia Aasa, Johannes Tiselius, Eva Sinha, Indranil Edman, Gunnar Wahlund, Martina Hedengren, Shanie Saghafian Nilsson, Anna Berggren, Anna Children (Basel) Article Febrile neutropenia is a common complication during chemotherapy in paediatric cancer care. In this setting, clinical features and current diagnostic tests do not reliably distinguish between bacterial and viral infections. Children with cancer (n = 63) presenting with fever and neutropenia were recruited for extensive microbiological and blood RNA sampling. RNA sequencing was successful in 43 cases of febrile neutropenia. These were classified as having probable bacterial infection (n = 17), probable viral infection (n = 13) and fever of unknown origin (n = 13) based on microbiological defined infections and CRP cut-off levels. RNA expression data with focus on the 2-transcript signature (FAM89A and IFI44L), earlier shown to identify bacterial infections with high specificity and sensitivity, was implemented as a disease risk score. The median disease risk score was higher in the probable bacterial infection group, −0.695 (max 2.795; min −5.478) compared to the probable viral infection group −3.327 (max 0.218; min −7.861), which in ROC analysis corresponded to a sensitivity of 0.88 and specificity of 0.54 with an AUC of 0.80. To further characterise the immune signature, analysis of significantly expressed genes and pathways was performed and upregulation of genes associated to antibacterial responses was present in the group classified as probable bacterial infection. Our results suggest that the 2-transcript signature may have a potential use as a diagnostic tool to identify bacterial infections in immunosuppressed children with febrile neutropenia. MDPI 2023-05-29 /pmc/articles/PMC10297134/ /pubmed/37371198 http://dx.doi.org/10.3390/children10060966 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aasa, Johannes
Tiselius, Eva
Sinha, Indranil
Edman, Gunnar
Wahlund, Martina
Hedengren, Shanie Saghafian
Nilsson, Anna
Berggren, Anna
The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia
title The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia
title_full The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia
title_fullStr The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia
title_full_unstemmed The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia
title_short The Applicability of a 2-Transcript Signature to Identify Bacterial Infections in Children with Febrile Neutropenia
title_sort applicability of a 2-transcript signature to identify bacterial infections in children with febrile neutropenia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297134/
https://www.ncbi.nlm.nih.gov/pubmed/37371198
http://dx.doi.org/10.3390/children10060966
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