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首页> 外文期刊>Pediatric cardiology >Promoter polymorphism (rs3755724, -55C/T) of tissue inhibitor of metalloproteinase 4 (TIMP4) as a risk factor for Kawasaki disease with coronary artery lesions in a Korean population.
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Promoter polymorphism (rs3755724, -55C/T) of tissue inhibitor of metalloproteinase 4 (TIMP4) as a risk factor for Kawasaki disease with coronary artery lesions in a Korean population.

机译:金属蛋白酶4(TIMP4)组织抑制剂的启动子多态性(rs3755724,-55C / T)是韩国人群川崎病合并冠状动脉病变的危险因素。

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摘要

Kawasaki disease (KD) is an acute febrile vasculitis that predominantly affects infants and young children. Tissue inhibitors of matrix metalloproteinases (TIMPs) comprise a family of four members, of which TIMP4 is characterized by its restriction to cardiovascular structures. In KD pathophysiology, TIMP4 is considered to be involved in the development of coronary artery lesions (CALs). Therefore, this study investigated single-nucleotide polymorphisms (SNPs) of the TIMP4 gene as risk factors for KD with CALs in Korean children. To observe this association, two SNPs (rs3755724, -55C/T, promoter; rs17035945, 3'-untranslated region) were genotyped in TIMP4 using direct sequencing. There were no SNPs in the coding region of TIMP4, and two SNPs were selected in the exon and promoter regions. This study recruited 250 control and 101 KD subjects. For data analysis, SNPStats, SNPAnalyzer, and Helixtree programs were used. These SNPs were not associated with KD. However, in the recessive model, a significant association was found between rs3755724 and the development of CALs in KD (P = 0.02; odds ratio, 0.31; 95% confidence interval, 0.11-0.85). The minor allele (C) of rs3755724 showed the susceptibility of CALs to risk in KD patients. These results suggest that TIMP4 is related to the development of KD with CALs in Korean children.
机译:川崎病(KD)是一种急性发热性血管炎,主要影响婴幼儿。基质金属蛋白酶(TIMPs)的组织抑制剂包括四个成员的家族,其中TIMP4的特征在于其对心血管结构的限制。在KD病理生理学中,TIMP4被认为与冠状动脉病变(CAL)的发生有关。因此,本研究调查了TIMP4基因的单核苷酸多态性(SNP)作为韩国儿童发生CAL的KD危险因素。为了观察这种关联,使用直接测序在TIMP4中对两个SNP(rs3755724,-55C / T,启动子; rs17035945,3'-非翻译区)进行基因分型。 TIMP4的编码区域中没有SNP,并且在外显子和启动子区域中选择了两个SNP。该研究招募了250名对照和101名KD受试者。对于数据分析,使用了SNPStats,SNPAnalyzer和Helixtree程序。这些SNP与KD不相关。但是,在隐性模型中,发现rs3755724与KD中CAL的发展之间存在显着关联(P = 0.02;优势比为0.31; 95%置信区间为0.11-0.85)。 rs3755724的次要等位基因(C)显示CAL对KD患者的风险易感性。这些结果表明,TIMP4与韩国儿童中伴有CAL的KD的发展有关。

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