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Published on: August 30, 2011
Significance of Differential Characteristics in Infantile Kawasaki Disease
Ji Hee Kwak1, JungHwa Lee2, Kee Soo Ha3
1Department of Pediatrics, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Insights
Kawasaki disease (KD) laboratory values differ significantly between infants and older children. Age-adjusted hemoglobin and C-reactive protein levels can help distinguish KD in infants from simple febrile illness.
Area of Science:
- Pediatric Immunology
- Hematology
- Clinical Laboratory Science
Background:
- Kawasaki disease (KD) exhibits age-specific immunological variations.
- Previous studies have not specifically compared laboratory values between infant and non-infant KD patients.
- Understanding these differences is crucial for accurate diagnosis and management.
Purpose of the Study:
- To compare age-adjusted laboratory values, specifically white and red blood cell counts, between infants and non-infants diagnosed with Kawasaki disease.
- To identify laboratory markers that can aid in differentiating KD in infants.
Main Methods:
- Retrospective analysis of 192 infants and 667 non-infants with KD from 2003-2015.
- Determination of age-unadjusted raw values (R) and age-adjusted Z-values (Z) for blood cell counts.
- Comparison of laboratory values between infant and non-infant KD cohorts.
Main Results:
- Infants with KD showed distinct patterns including lymphopenia, eosinophilia, low neutrophil ratios, anemia, thrombocytosis, and reduced erythrocyte sedimentation rates compared to non-infants.
- Pre-intravenous immunoglobulin (IVIG) Z-hemoglobin <-0.01 effectively predicted KD in all patients (AUC, 0.914).
- Pre-IVIG C-reactive protein (CRP) >40 mg/L differentiated KD infants from febrile controls (AUC, 0.811).
Conclusions:
- Laboratory findings provide a basis for differentiating between infant and non-infant Kawasaki disease.
- These hematological differences enhance the understanding of KD pathophysiology across age groups.
- Pre-IVIG Z-hemoglobin and CRP are valuable for distinguishing incomplete KD in infants from simple febrile illnesses.
Background And Objectives:
Immunological variability in Kawasaki disease (KD) shows age-specific differences; however, specific differences in laboratory values have not been compared between infants and non-infants with KD. We compared age-adjusted Z-values (Z) of white and red blood cells in infants with KD with those in non-infants with KD.
Methods:
This study retrospectively investigated 192 infants and 667 non-infants recruited between 2003 and 2015 at the Korea University Hospital. Laboratory values for infants with KD and non-infants with KD were analyzed and age-unadjusted raw values (R) and age-adjusted Z for blood cells counts were determined.
Results:
Z in infants with KD during pre-intravenous immunoglobulin (IVIG), post-IVIG, and chronic phases showed increased lymphopenia and eosinophilia, low neutrophil:lymphocyte and neutrophil:eosinophil ratios, worse anemia, increased thrombocytosis, and reduced erythrocyte sedimentation rates compared with those in non-infants with KD. The optimal cut-off value for pre-IVIG Z-hemoglobin for prediction of KD in all patients was <-0.01 (area under the curve [AUC], 0.914; sensitivity/specificity, 0.999/0.886; p=0.04). The optimal cut-off value for pre-IVIG C-reactive protein (CRP) for prediction of KD in infants compared to that in febrile control infants was >40 mg/L (AUC, 0.811; sensitivity/specificity, 0.712/0.700; p=0.04).
Conclusions:
Laboratory characteristics enable differentiation between infants and non-infants with KD and contribute to a better understanding of changes in blood cell counts. Infants with incomplete KD can be more easily differentiated from infants with simple febrile illness using pre-IVIG Z-hemoglobin and pre-IVIG CRP values.
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