Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2100
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dc.contributor.authorCarrol, E. D.en
dc.contributor.authorPokorn, M.en
dc.contributor.authorUsuf, E.en
dc.contributor.authorMoll, H. A.en
dc.contributor.authorSchlapbach, L. J.en
dc.contributor.authorPaulus, S.en
dc.contributor.authorKuijpers, T. W.en
dc.contributor.authorLevin, M.en
dc.contributor.authorBurns, J.en
dc.contributor.authorHerberg, J.en
dc.contributor.authorMartinón-Torres, F.en
dc.contributor.authorWright, V. J.en
dc.contributor.authorGalassini, R.en
dc.contributor.authorTremoulet, A.en
dc.contributor.authorShimizu, C.en
dc.contributor.authorYeung, S.en
dc.contributor.authorFink, C.en
dc.contributor.authorTsolia, M.en
dc.contributor.authorZandstra, J.en
dc.contributor.authorvan de Geer, A.en
dc.contributor.authorTanck, M. W. T.en
dc.contributor.authorvan Stijn-Bringas Dimitriades, D.en
dc.contributor.authorAarts, C. E. M.en
dc.contributor.authorDietz, S. M.en
dc.contributor.authorvan Bruggen, R.en
dc.contributor.authorSchweintzger, N. A.en
dc.contributor.authorZenz, W.en
dc.contributor.authorEmonts, M.en
dc.contributor.authorZavadska, D.en
dc.date.accessioned2022-11-07T23:27:56Z-
dc.date.available2022-11-07T23:27:56Z-
dc.date.issued2020en
dc.identifier.citation8 , 2020en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/2100-
dc.description.abstractBackground: Kawasaki disease (KD) is a vasculitis of early childhood mimicking several infectious diseases. Differentiation between KD and infectious diseases is essential as KD's most important complication—the development of coronary artery aneurysms (CAA)—can be largely avoided by timely treatment with intravenous immunoglobulins (IVIG). Currently, KD diagnosis is only based on clinical criteria. The aim of this study was to evaluate whether routine C-reactive protein (CRP) and additional inflammatory parameters myeloid-related protein 8/14 (MRP8/14 or S100A8/9) and human neutrophil-derived elastase (HNE) could distinguish KD from infectious diseases. Methods and Results: The cross-sectional study included KD patients and children with proven infections as well as febrile controls. Patients were recruited between July 2006 and December 2018 in Europe and USA. MRP8/14, CRP, and HNE were assessed for their discriminatory ability by multiple logistic regression analysis with backward selection and receiver operator characteristic (ROC) curves. In the discovery cohort, the combination of MRP8/14+CRP discriminated KD patients (n = 48) from patients with infection (n = 105), with area under the ROC curve (AUC) of 0.88. The HNE values did not improve discrimination. The first validation cohort confirmed the predictive value of MRP8/14+CRP to discriminate acute KD patients (n = 26) from those with infections (n = 150), with an AUC of 0.78. The second validation cohort of acute KD patients (n = 25) and febrile controls (n = 50) showed an AUC of 0.72, which improved to 0.84 when HNE was included. Conclusion: When used in combination, the plasma markers MRP8/14, CRP, and HNE may assist in the discrimination of KD from both proven and suspected infection.L6325000622020-08-11 <br />2020-08-19 <br />en
dc.language.isoenen
dc.relation.ispartofFrontiers in Pediatricsen
dc.titleBiomarkers for the Discrimination of Acute Kawasaki Disease From Infections in Childhooden
dc.typeArticleen
dc.identifier.doi10.3389/fped.2020.00355en
dc.subject.keywordsretrospective studyen
dc.subject.keywordspredictive valueen
dc.subject.keywordsbiological markerC reactive proteinen
dc.subject.keywordscalgranulin Aen
dc.subject.keywordscalgranulin Ben
dc.subject.keywordselastaseen
dc.subject.keywordsimmunoglobulinen
dc.subject.keywordsmyeloid related protein 14en
dc.subject.keywordsmyeloid related protein 8en
dc.subject.keywordsneutrophil derived elastaseen
dc.subject.keywordspeptides and proteinsen
dc.subject.keywordsunclassified drugen
dc.subject.keywordsarticleen
dc.subject.keywordsbacterial infectionen
dc.subject.keywordscase control studyen
dc.subject.keywordschilden
dc.subject.keywordsclinical evaluationen
dc.subject.keywordscohort analysisen
dc.subject.keywordscomparative studyen
dc.subject.keywordscontrolled studyen
dc.subject.keywordsconvalescenceen
dc.subject.keywordscoronary artery aneurysmen
dc.subject.keywordscross-sectional studyen
dc.subject.keywordsdiagnostic erroren
dc.subject.keywordsdiagnostic test accuracy studyen
dc.subject.keywordsdifferential diagnosisen
dc.subject.keywordsEuropeen
dc.subject.keywordsfalse positive resulten
dc.subject.keywordsfemaleen
dc.subject.keywordsfeveren
dc.subject.keywordshumanen
dc.subject.keywordsinfectionen
dc.subject.keywordsinflammationen
dc.subject.keywordsmajor clinical studyen
dc.subject.keywordsmaleen
dc.subject.keywordsmucocutaneous lymph node syndromeen
dc.subject.keywordsnormal valueen
dc.subject.keywordsplasmaen
dc.subject.keywordspediatric patienten
dc.subject.keywordsvirus infectionen
dc.subject.keywordsvalidation studyen
dc.subject.keywordsUnited Statesen
dc.subject.keywordstrue positive resulten
dc.subject.keywordstreatment responseen
dc.subject.keywordssensitivity and specificityen
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L632500062&from=exporthttp://dx.doi.org/10.3389/fped.2020.00355 |en
dc.identifier.risid2670en
item.grantfulltextnone-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
Appears in Sites:Children's Health Queensland Publications
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