Reverse regulation of soluble receptor for advanced glycation end products and proinflammatory factor resistin and S100A12 in Kawasaki disease
© Qi et al.; licensee BioMed Central Ltd. 2012
Received: 12 July 2012
Accepted: 20 November 2012
Published: 21 November 2012
Kawasaki disease (KD), an acute febrile disease, characterized by systemic vasculitis, predominantly affects infants and children under 5 years of age. Coronary artery lesions (CALs) are its most critical complication, and the etiology remains unknown yet. In order to explore the value of resistin, S100A12 and soluble receptor for advanced glycation end products (sRAGE) in the pathophysiology of KD, we studied the serum levels of resistin, S100A12 and sRAGE in different stages of KD.
Serum levels of resistin, S100A12 and sRAGE were measured by enzyme-linked immunosorbent assay (ELISA) method in 15 healthy children and 40 KD patients at acute, afebrile and subacute stage.
The resistin and S100A12 levels, including the ratio of resistin to sRAGE and S100A12 to sRAGE increased significantly in the acute stage, and decreased progressively in the afebrile and subacute stage. However, the sRAGE levels decreased significantly in the acute stage, and increased progressively in the afebrile and subacute stage. In the acute, afebrile and subacute stage, the resistin levels were higher in intravenous immunoglobulin (IVIG) non-responders (0.64 ± 0.30, 0.48 ± 0.35, 0.28 ± 0.19, × 102 ng/ml) than in IVIG responders (0.35 ± 0.24, 0.21 ± 0.19, 0.12 ± 0.05, × 102 ng/ml). In the acute and subacute stage, the S100A12 levels were higher in IVIG non-responders (7.92 ± 2.61, 4.98 ± 4.75, × 102 ng/ml) than in IVIG responders (5.05 ± 3.22, 2.35 ± 2.26, × 102 ng/ml). In the afebrile and subacute stage, the sRAGE levels were lower in IVIG non-responders (3.51 ± 2.64, 3.65 ± 3.27, × 102 pg/ml) than in IVIG responders (6.00 ± 2.78, 7.19 ± 2.88, × 102 pg/ml). The resistin levels were positively correlated with S100A12 levels. The sRAGE levels were negatively related with S100A12 and resistin levels.
Resistin, S100A12 and sRAGE are involved in the pathophysiology of KD.
Kawasaki disease (KD), an acute febrile disease characterized by systemic vasculitis, predominantly affects infants and children under 5 years of age . Coronary artery lesions (CALs) are its most critical complication , and as yet the etiology remains unknown.
Human resistin is a 12.5 kDa cysteine-rich peptide of bioactive molecules produced by the adipose tissue, monocytes and macrophages [3, 4]. Although considered an adipokine, importantly, resistin is expressed in macrophages and plays important roles in systemic inflammation; it also appears to be a predominant pro-inflammatory protein associated with both acute and chronic inflammation [5–9]. Resistin may have a potential role in the development of endothelial dysfunction , thrombosis, angiogenesis, inflammation and smooth muscle cell dysfunction in cardiovascular disease (CVD) and atherosclerosis [11–13]. There is increasing evidence from human clinical and experimental studies that resistin has a pathogenic role in the development and progression of atherosclerosis, coronary artery disease (CAD), and even heart failure . Resistin may have a pivotal role in the pathophysiology of cardiovascular events.
S100A12 is a member of the S100 family of calcium-binding proteins. It is a key ligand of the receptor for advanced glycation end products (RAGE), which is currently secreted by neutrophils, with low expression on lymphocytes and monocytes . S100A12 is also called EN-RAGE (extracellular newly identified RAGE-binding protein), proposed to stress its role as a receptor-mediated signaling pathway. S100A12 binding with RAGE can activate the NF-κB pathway to produce endothelial damage and promote KD . S100A12 is over-expressed at local inflammatory sites, and its serum concentrations are associated with individual disease activity .
It has been identified that soluble RAGE (sRAGE) corresponds to the extracellular domain of circulating RAGE in humans . sRAGE has the same ligand-binding specificity as RAGE and may serve as a competitor by binding pro-inflammatory ligands, and consequently, preventing them from reaching membrane RAGE even preventing the development of inflammatory disease.
Nevertheless, the significance of these critical inflammation proteins to the risk of CALs or intravenous immunoglobulin (IVIG)-resistance in KD remains largely unknown. We found that S100A12 and RAGE expression on circulating endothelial cell surfaces increased significantly in KD . In order to explore the value of resistin, S100A12 and protector sRAGE in the pathophysiology of KD, we studied the serum levels of resistin, S100A12 and sRAGE in different stages of KD.
Materials and methods
The study was approved by the ethical committee of the Children's Hospital, Zhejiang University School of Medicine, China and was based on the institution's guidelines for human studies. The investigation conformed to the principles outlined in the Declaration of Helsinki. Informed consent was obtained from the patients' parents.
Forty patients with KD treated at the Children's Hospital, Zhejiang University School of Medicine were included in this study. All patients fulfilled the diagnostic criteria  and were treated with IVIG at 1 g/kg/d for 2 days and oral aspirin at 30 to 50 mg/kg/d. After 3 to 5 days of treatment when the patient's temperature returned to normal, the dose of aspirin was reduced to 3 to 5 mg/kg/d for 12 weeks. There were four IVIG-resistant KD patients, whose temperature was still higher than 38°C after 48 hours of standard treatment, so they were continued on IVIG at 1 g/kg/d for another 2 days. Nine patients, including five girls and four boys, had CALs (defined as coronary artery z-score > 5)  identified by echocardiography during the disease process. Six patients had CALs in both the left and right coronary arteries, two in the left coronary artery, and one in the right coronary artery. The CALs in the majority of KD patients were temporary and disappeared within 3 months, while in two patients they persisted more than 3 months. Dipyridamole and warfarin were given to patients with CALs depending on the severity of the lesions.
The disease process between 4 to 9 days, 10 to 13 days and 14 to 21 days was defined as acute stage (at the time of diagnosis on admission, prior to the initiation of IVIG treatment), afebrile stage (after IVIG application and the patients' temperature had returned to normal for more than 3 days), and subacute stage (patients had been discharged from hospital). Fifteen healthy children attending for a routine health examination were enrolled into the control group.
Blood samples were respectively collected in acute, afebrile and subacute stages of patients and in healthy children. Two milliliters of blood was collected from the ulnar vein. The samples were centrifuged to yield serum immediately, and were then kept at -20°C until analysis. White blood cell (WBC) counts, platelet counts, serum C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) were measured by conventional methods in our hospital laboratory. Serum levels of resistin, S100A12, and sRAGE were measured by ELISA according to the manufacturer's instructions. Briefly, antibody-antigen reactions were used to capture special proteins. Measurements were performed in duplicate and the results were averaged.
We used the following reagents: human resistin immunoassay (catalog number DRSN00, Quantikine, R&D Systems, Minneapolis, MN, USA); S100A12/EN-RAGE ELISA Kit (catalog number CY-8058, CircuLex™, Nagano, Japan); ELISA kit for measuring sRAGE (catalog number DRG00, Quantikine, R&D Systems, Minneapolis, MN, USA).
SPSS 16.0 software package was used for all statistical analyses. Except where indicated otherwise, the results were expressed as mean (SD). Normal data analysis was performed with analysis of variance (ANOVA) followed by least significant difference (LSD) test for multiple comparisons; nonparametric data were analyzed by the Mann-Whitney test. Correlations were analyzed using the partial correlation test with age and gender as control variables. Differences in parameters were considered significant when the P-values were ≤ 0.05.
Characteristics of the KD patients and healthy children
Characteristics of the patients with Kawasaki disease (KD) and healthy children (control group)
Age, months (range)
Days of fever (range)
Resistin, 102 ng/ml
0.24 (0.22) **
0.14 (0.09) **▲
S100A12, 102 ng/ml
4.07 (3.52) *
2.62 (2.64) **▲
sRAGE, 102 pg/ml
3. 00 (1.91)
5.75 (2.83) **
6.83 (3.07) **
Resistin × S100A12, 104
1.20 (1.19) **
0.24 (0.23) **▲
0.39 (0.28) **
0.21 (0.14) **
0.84 (0.69) **
0.30 (0.25) **
1.01 (0.51) **
1.01 (0.51) **
33.2 (17.2) **
33.4 (17.6) **
50.9 (16.6) **
54.3 (16.7) **
5.68 (2.09) **
6.79 (1.87) **▲▲
25.0 (33.8) **
3.25 (4.12) **▲▲
78.8 (30.4) **
59.2 (28.3) ▲▲
Serum levels of resistin, S100A12, sRAGE in IVIG responder and non-responder KD patients
Serum levels of resistin, S100A12 and soluble receptor for advanced glycation end products (sRAGE) in intravenous immunoglobulin (IVIG) responding or non-responding patients with Kawasaki disease
IVIG responders (n= 36)
IVIG non-responders (n= 4)
Patients with CALs, number
Resistin, 102 ng/ml
0.21 (0.19) **
0.12 (0.05) **▲
S100A12, 102 ng/ml
2.35 (2.26)** ▲
sRAGE, 102 pg/ml
Serum levels of resistin, S100A12, sRAGE in KD patients with and without CALs
Serum levels of resistin, S100A12 and soluble receptor for advanced glycation end products (sRAGE) in Kawasaki disease (KD) with or without coronary artery lesions (CALs)
KD with CALs
KD without CALs
Resistin, 102 ng/ml
0.22 (0.22) *
0.15 (0.08)** ▲
0.13 (0.08) **
S100A12, 102 ng/ml
sRAGE, 102 pg/ml
Correlation between different parameters in patients with KD
Partial correlation coefficients of different parameters in patients with Kawasaki disease
Resistin × S100A12
S100A12 × Resistin
As expected, this study found that the KD patients in the acute stage had elevated resistin and S100A12 serum levels compared with healthy children. The same situation included the product of resistin and S100A12, the ratio of resistin to sRAGE and the ratio of S100A12 to sRAGE. The phenomena show that various types of inflammatory proteins are activated in KD [22, 23]. However, sRAGE levels decreased in KD patients compared with healthy children. Serum levels of resistin and S100A12 in KD patients were peaked in the acute phase before IVIG, and returned to approximately normal levels in the afebrile and subacute stages, respectively. Resistin, S100A12, WBCs, neutrophils, and CRP tended towards a similar pattern of change, which was the opposite of the changes in expression of sRAGE, lymphocytes, monocytes and platelets. Resistin and S100A12 have similar significance to established inflammatory factors in KD patients. Although sRAGE could not be fully confirmed as a protective factor, it can still be a sensitive index response to attack by pro-inflammatory agents like S100A12 or resistin, in view of its negative correlation with them.
Resistin is known to be secreted by adipose tissue and by macrophages and monocytes [3, 4], while S100A12 is normally secreted by neutrophils, with low expression on lymphocytes and monocytes . Although serum levels of S100A12 were significantly higher than the levels of resistin in patients with KD, the change trends were coincident for both S100A12 and resistin in the different stages of KD. A markedly positive correlation between serum resistin and S100A12 levels in KD has been highlighted. Serum resistin and S100A12 levels have shown a negative correlation with sRAGE. Moreover, resistin expression is notably correlated with neutrophils, but the relationship between the sources of resistin and neutrophils still remains unclear. However, we believe that both of them are significant in the process of KD and it seems that resistin, S100A12, and sRAGE are three elements of a balance with positive and negative feedbacks, which could regulate the pathophysiology of KD.
IVIG was not effective for all the children with KD. Patients who did not respond had age and gender differences compared with responders. The response to IVIG depends on children's physiological functions and pathologic state. In the acute, afebrile and subacute stages of KD, resistin levels were higher in IVIG non-responders than in responders, as were S100A12 levels in the acute and subacute stages of KD. This suggests that the inflammatory reaction is more severe in IVIG non-responders than in responders. In the acute stage before IVIG treatment, sRAGE levels were not significantly different in non-responders compared with responders. In the afebrile and subacute stages of KD, sRAGE levels were lower in IVIG non-responders than in responders. This demonstrates that the protective factor against inflammation is lower in IVIG non-responders than in responders. It suggests that it is possible to apply ectogenesis sRAGE to alleviate the inflammatory reaction in IVIG non-responders.
The average serum levels of resistin, S100A12 and sRAGE were not significantly different in the KD patients with CALs compared to those without CALs. Serum levels of resistin, S100A12 and sRAGE are unlikely to predict the risk of CALs in KD patients. The results are consistent with a recent study .
To our knowledge, the present study is the first simultaneous evaluation of resistin, S100A12 and sRAGE in the acute, afebrile and subacute stages of KD. Also it is the first report of higher resistin levels in IVIG non-responders compared to IVIG responders in the acute, afebrile and subacute stages of KD; higher S100A12 levels in IVIG non-responders than in IVIG responders in the acute and subacute stages of KD; and lower sRAGE levels in IVIG non-responders than in IVIG responders in the afebrile and subacute stages of KD.
In KD, sRAGE levels appear to reverse regulation with the pro-inflammatory factor resistin and S100A12 levels. The balance between the levels of resistin, S100A12 and sRAGE may represent a dynamic system with the interaction of positive and negative feedbacks. It suggests that the resistin, S100A12 and sRAGE are involved in the pathophysiology of KD.
analysis of variance
coronary artery disease
coronary artery lesion
enzyme-linked immunosorbent assay
extracellular newly identified RAGE-binding protein
erythrocyte sedimentation rate
least significant difference
receptor for advanced glycation end products
soluble receptor for advanced glycation end products
white blood cell.
This work was supported by the National Nature Scientific Research Foundation [30872799, 30973223]; and the Zhejiang Nature Scientific Research Foundation [Y207201] in China.
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