Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5766
Title: Diagnosis of childhood febrile illness using a multi-class blood RNA molecular signature
Authors: Habgood-Coote, Dominic
Wilson, Clare
Shimizu, Chisato
Barendregt, Anouk M.
Philipsen, Ria
Galassini, Rachel
Calle, Irene Rivero
Workman, Lesley
Agyeman, Philipp K. A.
Ferwerda, Gerben
Anderson, Suzanne T.
van den Berg, J. Merlijn
Emonts, Marieke
Carrol, Enitan D.
Fink, Colin G.
de Groot, Ronald
Hibberd, Martin L.
Kanegaye, John
Nicol, Mark P.
Paulus, Stéphane
Pollard, Andrew J.
Salas, Antonio
Secka, Fatou
Schlapbach, Luregn J.
Tremoulet, Adriana H.
Walther, Michael
Zenz, Werner
Van der Flier, Michiel
Zar, Heather J.
Kuijpers, Taco
Burns, Jane C.
Martinón-Torres, Federico
Wright, Victoria J.
Coin, Lachlan J. M.
Cunnington, Aubrey J.
Herberg, Jethro A.
Levin, Michael
Kaforou, Myrsini
Issue Date: 2023
Source: Med (New York, N.Y.), 2023 (4) 9 p.635
Pages: 635
Journal Title: Med (New York, N.Y.)
Abstract: Background: Appropriate treatment and management of children presenting with fever depend on accurate and timely diagnosis, but current diagnostic tests lack sensitivity and specificity and are frequently too slow to inform initial treatment. As an alternative to pathogen detection, host gene expression signatures in blood have shown promise in discriminating several infectious and inflammatory diseases in a dichotomous manner. However, differential diagnosis requires simultaneous consideration of multiple diseases. Here, we show that diverse infectious and inflammatory diseases can be discriminated by the expression levels of a single panel of genes in blood.; Methods: A multi-class supervised machine-learning approach, incorporating clinical consequence of misdiagnosis as a "cost" weighting, was applied to a whole-blood transcriptomic microarray dataset, incorporating 12 publicly available datasets, including 1,212 children with 18 infectious or inflammatory diseases. The transcriptional panel identified was further validated in a new RNA sequencing dataset comprising 411 febrile children.; Findings: We identified 161 transcripts that classified patients into 18 disease categories, reflecting individual causative pathogen and specific disease, as well as reliable prediction of broad classes comprising bacterial infection, viral infection, malaria, tuberculosis, or inflammatory disease. The transcriptional panel was validated in an independent cohort and benchmarked against existing dichotomous RNA signatures.; Conclusions: Our data suggest that classification of febrile illness can be achieved with a single blood sample and opens the way for a new approach for clinical diagnosis.; Funding: European Union's Seventh Framework no. 279185; Horizon2020 no. 668303 PERFORM; Wellcome Trust (206508/Z/17/Z); Medical Research Foundation (MRF-160-0008-ELP-KAFO-C0801); NIHR Imperial BRC.; Competing Interests: Declaration of interests The authors declare that a patent application on the method described in this manuscript has been filed (2304229.4/GB/PRV, 23-03-2023). (Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)
DOI: 10.1016/j.medj.2023.06.007
Resources: https://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=37597512&site=ehost-live
Appears in Sites:Children's Health Queensland Publications

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