Abstract

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.

Highlights

  • Kawasaki disease (KD) is a systemic vasculitis of early childhood occurring mainly in children under the age of 5 years

  • We focused on C-reactive protein (CRP) and two neutrophil-derived proteins, myeloid-related protein 8/14 (MRP8/14) and human neutrophil elastase (HNE)

  • Our discovery cohort consisted of 48 patients with acute KD (27 pre-intravenous immunoglobulin (IVIG) treatment and 21 shortly after IVIG treatment had been administered, within 3 days)

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Summary

Introduction

Kawasaki disease (KD) is a systemic vasculitis of early childhood occurring mainly in children under the age of 5 years. KD’s most important complication is the development of coronary artery aneurysms (CAA), affecting 25% of the untreated patients [1]. This makes KD the most common cause of acquired heart disease in developed countries in children. The risk of CAA development is decreased 5-fold when the patient is treated with high-dose intravenous immunoglobulin (IVIG) and oral aspirin within 10 days of disease onset [1]. 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). 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

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