Peng Qian, Chen Changhui, Zhang Yu, He Hailan, Wu Qing, Liao Jing, Li Bo, Luo Caidan, Hu Xiaoping, Zheng Zhi, Yang Yuan
Department of Pediatrics, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, 610072, Sichuan, China.
Pediatr Cardiol. 2012 Oct;33(7):1046-53. doi: 10.1007/s00246-012-0223-x. Epub 2012 Feb 24.
Kawasaki disease (KD) is characterized by acute systemic vasculitis and frequently is complicated by coronary artery lesions (CALs). The inositol 1,4,5-trisphosphate 3-kinase C (ITPKC) gene rs28493229 was recently found to be associated with the risk for KD in the Japanese population, suggesting that the ITPKC gene may contribute to KD susceptibility. This study investigated the association of ITPKC polymorphisms with KD in a Han Chinese population. Five ITPKC Single-nucleotide polymorphisms, including rs28493229, were genotyped in 223 unrelated patients who had KD and 318 non-KD control subjects. The allele, genotype, and haplotype frequencies were compared between the patients and the control subjects, between the patients with and those without CALs, and between patients resistant to intravenous immunoglobulin treatment and those responsive to such treatment. Multiple alleles were observed for rs28493229 and rs2290692. No significant differences in the frequencies of the C allele, the CC genotype, or the C carriers of rs28493229 were observed in the comparisons. Interestingly, significantly higher frequencies of the C allele (p < 0.001), the CC genotype (p = 0.001), and the C carriers (p = 0.003) were observed for rs2290692 among the patients than among the control subjects, and similar differences were observed between the patients with and those without CALs. The GC haplotype for rs28493229 and rs2290692 was more common among the patients than among the control subjects. The results indicate that the C allele of the ITPKC gene rs2290692 is linked to a significantly higher risk for KD in the studied population, which provides new evidence to support the importance of the ITPKC gene in the occurrence of KD. More notably, this finding suggests that there may be an unidentified ITPKC polymorphism in strong linkage disequilibrium to rs2290692, significantly affecting susceptibility to KD in the Han population.
川崎病(KD)以急性全身性血管炎为特征,常并发冠状动脉病变(CALs)。最近发现肌醇1,4,5 -三磷酸3 -激酶C(ITPKC)基因rs28493229与日本人群患KD的风险相关,这表明ITPKC基因可能与KD易感性有关。本研究调查了中国汉族人群中ITPKC基因多态性与KD的关联。对223例无亲缘关系的KD患者和318例非KD对照者进行了包括rs28493229在内的5个ITPKC单核苷酸多态性的基因分型。比较了患者与对照者之间、有CALs和无CALs的患者之间以及对静脉注射免疫球蛋白治疗有抗性和有反应的患者之间的等位基因、基因型和单倍型频率。rs28493229和rs2290692观察到多个等位基因。在比较中,未观察到rs28493229的C等位基因、CC基因型或C携带者频率有显著差异。有趣的是,在患者中观察到rs2290692的C等位基因频率(p <0.001)、CC基因型频率(p = 0.001)和C携带者频率(p = 0.003)显著高于对照者,在有和无CALs的患者之间也观察到类似差异。rs28493229和rs2290692的GC单倍型在患者中比在对照者中更常见。结果表明,在研究人群中,ITPKC基因rs2290692的C等位基因与患KD的风险显著更高相关,这为支持ITPKC基因在KD发生中的重要性提供了新证据。更值得注意的是,这一发现表明可能存在一个与rs2290692处于强连锁不平衡状态的未鉴定的ITPKC多态性,显著影响汉族人群对KD的易感性。