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中国儿童群体中白细胞介素-27基因多态性与川崎病的关系。

The relationship between Interleukin-27 gene polymorphisms and Kawasaki disease in a population of Chinese children.

作者信息

Si Feifei, Wu Yao, Wang Xianmin, Gao Fang, Yang Dan, Liu Ruixi, Yi Qijian

机构信息

1Department of Padiatric Cardiology,Chengdu Women's and Children's Central Hospital,Chengdu,People's Republic of China.

2Department of Cardiovascular Medicine,Children's Hospital of Chongqing Medical University,Chongqing,People's Republic of China.

出版信息

Cardiol Young. 2018 Sep;28(9):1123-1128. doi: 10.1017/S1047951118000914. Epub 2018 Jul 5.

DOI:10.1017/S1047951118000914
PMID:29973303
Abstract

BACKGROUND

Kawasaki disease is the leading cause of acquired heart disease in children from developed countries. The Interleukin-6/ Interleukin-12 cytokine family has many members, including the paradoxical anti- and pro-inflammatory Interleukin-27. Recent studies have demonstrated that Interleukin-27 plays a role in immune diseases. Given this, we sought to evaluate the association between Interleukin-27 genetic polymorphisms and Kawasaki disease in Chinese children.Methods and resultsInterleukin-27 was genotyped in 100 Kawasaki disease children and 98 healthy children (controls), resulting in the direct sequencing of eight Single-nucleotide Polymorphisms: rs17855750, rs40837, rs26528, rs428253, rs4740, rs4905, rs153109, and rs181206). There were no significant differences in Interleukin-27 genotypes between Kawasaki disease and control groups. Of the eight Single-nucleotide Polymorphisms, there was a significant increase in the risk of Kawasaki disease with coronary arterial lesions in children with the rs17855750 (T>G), rs40837 (A>G), rs4740 (G>A), rs4905 (A>G), rs153109 (T>C), and rs26528 (A>G) Single-nucleotide Polymorphisms. This was particularly true for rs17855750 (T>G), which had a greater frequency in Kawasaki disease children with coronary arterial aneurysm.

CONCLUSION

These findings may be used as risk factors when assessing a child's likelihood of developing Kawasaki disease, as well as for the development of future therapeutic treatments for Kawasaki disease.

摘要

背景

川崎病是发达国家儿童后天性心脏病的主要病因。白细胞介素-6/白细胞介素-12细胞因子家族有许多成员,包括具有矛盾抗炎和促炎作用的白细胞介素-27。最近的研究表明,白细胞介素-27在免疫疾病中起作用。鉴于此,我们试图评估中国儿童白细胞介素-27基因多态性与川崎病之间的关联。

方法与结果

对100例川崎病患儿和98例健康儿童(对照组)进行白细胞介素-27基因分型,对8个单核苷酸多态性进行直接测序:rs17855750、rs40837、rs26528、rs428253、rs4740、rs4905、rs153109和rs181206。川崎病组和对照组之间白细胞介素-27基因型无显著差异。在这8个单核苷酸多态性中,rs17855750(T>G)、rs40837(A>G)、rs4740(G>A)、rs4905(A>G)、rs153109(T>C)和rs26528(A>G)单核苷酸多态性的儿童患川崎病合并冠状动脉病变的风险显著增加。rs17855750(T>G)尤其如此 在患有冠状动脉瘤的川崎病儿童中频率更高。

结论

这些发现可作为评估儿童患川崎病可能性的风险因素,也可用于未来川崎病治疗方法的开发。

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