Abstract
Aim: Kawasaki disease (KD) is a systemic vasculitis with unknown etiology. In addition to cardiovascular system involvement, it can also have other multiple organs involved. This study is aimed at investigating the correlation between anti-cardiolipin antibody (ACA)/D dimer/C reactive protein (CRP) and coronary artery lesions (CAL)/multiple-organ lesions in children with KD.Methods: Retrospective analysis was performed in 284 KD/IKD patients from May 2015 to April 2016. Among them, 175 were males (61.6%), with average age of 2 years and 5 months old. Patients were divided into ACA+ group and ACA- group, elevated D dimer group (DDE) and normal D dimer group (DDN), and coronary artery injury (CAL) group and non-coronary artery injury (NCAL) group.Results: ACA was most likely tested positive in younger KD children (p < 0.05). ACA+ and hypoproteinemia were correlated with CAL, thrombocytosis, and granulocytopenia (p < 0.05–0.01). Levels of cTnI and CK in the CAL group were significantly higher than those in the NCAL group (p < 0.05). CAL was more frequently detected in younger patients and patients with prolonged fever, later IVIG treatment, and elevated CRP over 100 mg/l, but there was no statistically significant difference (all p > 0.05). In the KD with DDE group, the incidence of granulopenia, thrombocytosis, myocardial damage, cholestasis, hypoproteinemia, and aseptic urethritis was significantly higher than that in the KD with DDN group (p < 0.05–0.01). However, elevated D dimer was not associated with CAL. CRP elevation was highly correlated with D dimer, but not with CAL.Conclusion: Higher incidence of CAL and myocardial damage occurred in KD patients with positive ACA and hypoproteinemia. In the current study, ACA was only tested for positive and negative, which is a limitation to this study. To further elucidate the association, ACA titers would establish its significance in drawing a conclusion for the significance of ACA in CAL and myocardial damages. In addition, higher incidence of CAL occurred in younger patients. The higher D dimer was associated with increased multiple-organ damage (MOD). CRP was closely correlated with D dimer, but not correlated with ACA and CAL.
Highlights
Kawasaki disease (KD) is a systemic vasculitis with unknown etiology
An increase in IgA anticardiolipin antibodies in KD patients suggests that the degree of increase in these antibodies correlates with the degree of systemic inflammation [26]
We found that KD with macrophage activation syndrome (MAS) complication and necrotizing pneumonia was not associated with CAL, patients had fever which lasted for more than 2 weeks
Summary
Kawasaki disease (KD) is a systemic vasculitis with unknown etiology. It is one of the common connective tissue diseases in children. KD has emerged as a major pediatric disorder throughout the developed world [1]. KD is currently being diagnosed and reported in both China and India [2,3,4]. Multiple organs/systems can be involved in KD. Even in patients receiving IVIG treatment within 10 days of disease onset, the incidence of CAL is still about 5% [5]. Prediction of the occurrence of CAL and MOD by utilizing laboratory examination has become a priority for pediatric cardiologists
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