Biomarkers for the Discrimination of Acute Kawasaki Disease From Infections in Childhood.

Judith Zandstra ; Annemarie van de Geer ; Michael WT Tanck ; Diana van Stijn-Bringas Dimitriades ; Cathelijn EM Aarts ; Sanne M Dietz ; Robin van Bruggen ; Nina A Schweintzger ; Werner Zenz ; Marieke Emonts ; +20 more... Dace Zavadska ; Marko Pokorn ; Effua Usuf ORCID logo ; Henriette A Moll ; Luregn J Schlapbach ; Enitan D Carrol ; Stephane Paulus ; Maria Tsolia ; Colin Fink ; Shunmay Yeung ORCID logo ; Chisato Shimizu ; Adriana Tremoulet ; Rachel Galassini ; Victoria J Wright ; Federico Martinón-Torres ; Jethro Herberg ; Jane Burns ; Michael Levin ; Taco W Kuijpers ; EUCLIDS Consortium, PERFORM Consortium and UK Kawasaki Disease G ; (2020) Biomarkers for the Discrimination of Acute Kawasaki Disease From Infections in Childhood. FRONTIERS IN PEDIATRICS, 8. 355-. ISSN 2296-2360 DOI: 10.3389/fped.2020.00355
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Background: 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.


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