首页> 外文期刊>Pediatric cardiology >Association of miR-146a Gene Polymorphism at loci rs2910164 G/C, rs57095329 A/G, and rs6864584 T/C with Susceptibility to Kawasaki Disease in Chinese Children
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Association of miR-146a Gene Polymorphism at loci rs2910164 G/C, rs57095329 A/G, and rs6864584 T/C with Susceptibility to Kawasaki Disease in Chinese Children

机译:miR-146a基因多态性在基因座2910164 g / c,rs57095329 a / g,和中国儿童川崎病患者的敏感性rs6864584。

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摘要

ObjectiveTo investigate the genetic association of miR-146a gene polymorphisms at loci rs2910164 G/C, rs57095329 A/G, and rs6864584 T/C in patients with Kawasaki disease (KD) and coronary artery lesions (CAL).MethodsThere were 120 patients with KD and 126 healthy subjects in this study. The genotype of loci rs2910164 G/C, rs57095329 A/G, and rs6864584 T/C of miR-146a gene were detected by polymerase chain reaction-sequence-based typing.ResultsFor miR-146a gene polymorphisms at loci rs2910164 G/C, rs57095329 A/G, and rs6864584 T/C, there were no significant difference of genotype frequencies and allele frequencies between KD group and healthy control group, or between the IVIG-resistant group and IVIG-sensitive group (P>0.05). In KD with coronary artery lesions (KD-CAL) group, the genotype frequencies of GG were higher than that in KD without coronary artery lesion (KD-WO) group at locus rs2910164 G/C polymorphisms of miR-146a gene ((2)=6.660, P=0.036), patients with KD carried genotype of GG were at 3.636 times higher risk of getting coronary artery lesions than those of non-carriers ((2)=6.455, P=0.018, OR=3.636, 95%CI=1.280-10.262). While there was no significant difference of allele frequency of G and C between KD-CAL group and KD-WO group (P>0.05). In KD-CAL group, the allele frequency of A was higher than that in KD-WO group at locus rs57095329 A/G polymorphisms of miR-146a gene ((2)=4.745, P=0.035), carriers with allele A were at 2.422 times higher risk of getting coronary artery lesions than those of non-carriers ((2)=4.745, P=0.035, OR=2.422, 95%CI=1.073-5.465), while there was no significant difference of genotype frequency of AA, AG, and GG types between KD-CAL group and KD-WO group (P>0.05). There was no significant difference of genotype frequencies of TT, TC, and CC types and allele frequencies of T and C types between KD-CAL group and KD-WO group at locus rs6864584 T/C polymorphisms of miR-146a gene (P>0.05).ConclusionsThe significant association has been found between the genotype and allele frequency of the miR-146a gene loci rs2910164 G/C and rs57095329 A/G, the genotype GG of rs2910164 G/C, and allele A of rs57095329 A/G were risk factors for getting coronary artery lesions.
机译:ObjectiveTo探讨了Kawasaki疾病(KD)和冠状动脉病变(CAL)患者的LOCI-146A基因多态性,RS57095329 A / G和RS6864584 T / C的遗传关联。致冠状动脉病变(CAL)。方法是120名KD患者这项研究中有126名健康科目。通过基于聚合酶链反应序列的分型检测Loci RS2910164 G / C,RS57095329 A / G和RS6864584 T / C的基因型。鉴定基因酶链反应序列的分型检测MIR-146A基因的RS6864584 T / C.Resultsforsmir-146a基因多态性,在Loci rs2910164 g / c,Rs57095329 A / G和RS6864584 T / C,KD组和健康对照组的基因型频率和等位基因频率没有显着差异,或在IVIG抗性组和IVIG敏感组之间(P> 0.05)之间。在KD冠状动脉病变(KD-CAL)组中,GG的基因型频率高于MIR-146A基因的冠状动脉病变(KD-WO)组的KD中的基因型频率(KD-WO)组((2) = 6.660,P = 0.036),GG的KD携带基因型的患者患有冠状动脉病变的风险较高3.636倍,而不是非载体((2)= 6.455,P = 0.018,或= 3.636,95%CI = 1.280-10.262)。虽然KD-CAL组和KD-WO组等等位基因频率没有显着差异(P> 0.05)。在KD-CAL组中,A的等位基因频率高于KD-WO组,在洛克斯57095329A / g多态性MiR-146a基因的多态性((2)= 4.745,p = 0.035),具有等位基因A的载体获得冠状动脉病变的风险高2.422倍而不是非载体((2)= 4.745,P = 0.035,或= 2.422,95%CI = 1.073-5.465),而AA的基因型频率没有显着差异,AG和KD-WO组之间的GG类型(P> 0.05)。在MIR-146A基因的基因座RS6864584 T / C多态性的KD-CAL组和KD-WO组之间的TT,TC和CC型和C型等等位基因频率没有显着差异(P> 0.05 )。Conclusionsthe在miR-146a基因基因座的基因型和等位基因之间发现了显着的关联和rs57095329 a / g的基因型Gg,以及rs57095329 a / g的等位基因a是风险获得冠状动脉病变的因素。

著录项

  • 来源
    《Pediatric cardiology》 |2019年第3期|共9页
  • 作者单位

    Cent S Univ Xiangya Hosp 3 Dept Pediat 138 Tongzipo Rd Changsha 410013 Hunan Peoples R China;

    Cent S Univ Xiangya Hosp 3 Dept Pediat 138 Tongzipo Rd Changsha 410013 Hunan Peoples R China;

    Cent S Univ Xiangya Hosp 3 Dept Pediat 138 Tongzipo Rd Changsha 410013 Hunan Peoples R China;

    Cent S Univ Xiangya Hosp 3 Dept Pediat 138 Tongzipo Rd Changsha 410013 Hunan Peoples R China;

    Cent S Univ Xiangya Hosp 3 Dept Pediat 138 Tongzipo Rd Changsha 410013 Hunan Peoples R China;

    Cent S Univ Xiangya Hosp 3 Cent Lab Changsha 410013 Hunan Peoples R China;

    Cent S Univ Xiangya Hosp 3 Dept Pediat 138 Tongzipo Rd Changsha 410013 Hunan Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 儿科学;
  • 关键词

    Kawasaki disease; MiR-146a gene; Gene polymorphism;

    机译:川崎病;miR-146a基因;基因多态性;

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