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Association of Thrombomodulin Gene C1418T Polymorphism with Susceptibility to Kawasaki Disease in Chinese Children

机译:血栓调节蛋白基因C1418T多态性与中国儿童川崎病易感性的关系

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Kawasaki disease (KD) is an acute systemic vasculitis that predominantly affects children and can result in coronary artery lesions (CALs). Thrombomodulin (TM) is a critical cofactor in the protein C anticoagulant system. The TM C1418T (rs1042579) polymorphism is associated with a high risk of cardiac-cerebral vascular diseases. But the association of the TM C1418T polymorphism with susceptibility to KD, CAL formation, and intravenous immunoglobulin (IVIG) resistance is still unclear. In our study, we examined the TM C1418T polymorphism in 122 children with KD and 126 healthy children and revealed the correlation between the TM C1418T polymorphism and KD, CAL formation, and IVIG resistance.
机译:川崎病(KD)是主要影响儿童的急性系统性血管炎,可导致冠状动脉病变(CAL)。血栓调节蛋白(TM)是C蛋白抗凝系统中的关键辅助因子。 TM C1418T(rs1042579)多态性与心脑血管疾病的高风险相关。但是,TM C1418T基因多态性与KD易感性,CAL形成和静脉内免疫球蛋白(IVIG)耐药性之间的关联仍不清楚。在我们的研究中,我们检查了122名KD儿童和126名健康儿童的TM C1418T多态性,并揭示了TM C1418T多态性与KD,CAL形成和IVIG耐药性之间的相关性。

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