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白细胞介素-6(-636c/g)基因多态性与韩国川崎病患儿的关系。

Interleukin-6 (-636 c/g) gene polymorphism in korean children with kawasaki disease.

机构信息

Department of Pediatrics, School of Medicine, Ewha Womans University, Seoul, Korea.

出版信息

Korean Circ J. 2011 Jun;41(6):321-6. doi: 10.4070/kcj.2011.41.6.321. Epub 2011 Jun 30.

Abstract

BACKGROUND AND OBJECTIVES

Kawasaki disease (KD) is a multi-systemic vasculitis with coronary artery involvement. Serum interleukin (IL)-6 levels during acute phase showed a significant correlation with the duration of fever in patients with KD who were not treated with intravenous immunoglobulin (IVIG), suggesting that the regulation of IL-6 expression in KD patients may differ from that in normal children. However, there are controversies surrounding the association between IL-6 (-636 C/G) gene polymorphism and development of KD.

SUBJECTS AND METHODS

One hundred and nine children with KD and 191 children with congenital heart disease were included in this study. Echocardiography was performed to examine cardiac involvement in patients with KD. Genotyping of the IL-6 (-636 C/G) gene polymorphism was performed using the single-base extension method, and serum IL-6 concentrations were estimated using the sandwich enzyme immunoassay method.

RESULTS

Neutrophil, platelet count, liver function test, total protein and albumin concentrations were significantly different in the KD group and the serum IL-6 concentration was significantly higher in the KD group than the control group. There was no difference between the patients with coronary arterial dilatation (CAD) and those without CAD in the IL-6 (-636 C/G) polymorphism. The serum albumin concentration was significantly lower in patients with KD who had the -636 C/G or GG genotype compared with the control group. The serum IL-6 concentration was significantly higher in patients with KD who had the -636 C/G or GG genotype.

CONCLUSION

There was no association between the IL-6 (-636 C/G) gene polymorphism and development of coronary arterial lesions in KD. Further multicenter studies are required to establish the relationship between the IL-6 (-636 C/G) gene polymorphism and development of KD.

摘要

背景与目的

川崎病(KD)是一种多系统血管炎,可累及冠状动脉。未接受静脉注射免疫球蛋白(IVIG)治疗的 KD 患者急性期血清白细胞介素(IL)-6 水平与发热持续时间呈显著相关性,提示 KD 患者的 IL-6 表达调控可能与正常儿童不同。然而,IL-6(-636 C/G)基因多态性与 KD 发病之间的关系存在争议。

对象与方法

本研究纳入 109 例 KD 患儿和 191 例先天性心脏病患儿。对 KD 患儿行超声心动图检查,以评估其心脏受累情况。采用单碱基延伸法对 IL-6(-636 C/G)基因多态性进行基因分型,采用夹心酶联免疫吸附法测定血清 IL-6 浓度。

结果

KD 组中性粒细胞、血小板计数、肝功能试验、总蛋白和白蛋白浓度均显著高于对照组,血清 IL-6 浓度也显著高于对照组。KD 患儿中,有冠状动脉扩张(CAD)和无 CAD 患儿之间的 IL-6(-636 C/G)多态性无差异。与对照组相比,KD 患儿中-636 C/G 或 GG 基因型的血清白蛋白浓度显著降低,血清 IL-6 浓度显著升高。

结论

IL-6(-636 C/G)基因多态性与 KD 患者冠状动脉病变的发生无关。需要进一步的多中心研究来确定 IL-6(-636 C/G)基因多态性与 KD 发病之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/647c/3132694/beab88edd8b9/kcj-41-321-g001.jpg

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