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Association study of IL-17RC, CHL1,DSCAM and CNTNAP2 genes polymorphisms with adolescent idiopathic scoliosis susceptibility in a Chinese Han population

机译:IL-17RC,CHL1,DSCAM和CNTNAP2基因多态性研究中国汉族人群青少年特发性脊柱缺损性研究

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Recently, several genome wide association studies suggested IL-17RC, CHL1, DSCAM and CNTNAP2 genes polymorphisms were associated with AIS. To confirm these associations, we performed this case-control study using data from 648 AIS patients and 573 healthy adolescent of Chinese Han population. A polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis was performed to detect the genotypes of polymorphic loci: rs708567 rs279545 in IL-17RC gene, and rs2055314, rs331894, rs2272524, rs2272522 in CHL1 gene, and rs2222973 in DSCAM gene, and rs2710102, rsl 1770843 in CNTNAP2 gene. Statistical analysis of genotype frequencies between AIS patients and controls were performed by y2 test. Our results show that both the genotype frequency and allele frequency of loci rs708567 were significantly different between AIS patients and controls (P = 0.023, 0.028, respectively). As for polymorphic loci rs279545, rs2222973, rs279545, rs2055314, rs331894, rs2272524, rs2272522, no significant difference was found between AIS patients and controls either genotype or allele frequencies (p>0.05). Overall, our study found a significant association of IL-17RC gene polymorphisms with AIS in a Chinese Han population, indicating EL-17RC gene may be as a susceptibility gene for AIS; While CHL1, CNTNAP2 and DSCAM genes were not associated with AIS, suggesting that those genes may not be involved in the etiopathogenesis of AIS. However, association study of these genes with AIS in other races is needed to clarify the role of these genes in the etiology of AIS.
机译:最近,几个全基因组关联研究表明IL-17RC,CHL1,DSCAM和CNTNAP2基因多态性与AIS相关。为了确认这些关联,我们使用648名AIS患者和573中国汉族人群的健康青少年数据这种病例对照研究。进行聚合酶链式反应 - 限制性片段长度多态性(PCR-RFLP)分析,以检测多态性位点的基因型:rs708567 rs279545在IL-17RC基因,和rs2055314,rs331894,rs2272524,rs2272522中CHL1基因,和rs2222973中DSCAM基因和rs2710102,RSL 1770843在CNTNAP2基因。 AIS患者和对照之间基因型频率的统计分析通过Y2检验。我们的研究结果表明,无论是基因型频率和基因座rs708567等位基因频率分别为AIS患者和对照(P = 0.023,0.028,分别地)之间显著不同。至于多态位点rs279545,rs2222973,rs279545,rs2055314,rs331894,rs2272524,rs2272522,无显著差异AIS患者和对照任一基因型或等位基因频率(P> 0.05)之间找到。总的来说,我们的研究发现,IL-17RC基因多态性与AIS在中国汉族人群显著的关联,说明EL-17RC基因可能是作为一个易感基因AIS的;而CHL1,CNTNAP2和DSCAM基因没有与AIS相关联,这表明这些基因可能无法在AIS的发病机理有关。然而,需要这些基因与AIS在其他种族的相关性研究,以澄清这些基因在AIS的病因中的作用。

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