Zhou Song, Zhu Zezhang, Qiu Xusheng, Wu Weifei, Wang Weijun, Liu Zhen, Lv Feng, Qiu Yong
Nanjing University Medical School, Nanjing, China.
Stud Health Technol Inform. 2012;176:47-51.
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, rs11770843 in CNTNAP2 gene. Statistical analysis of genotype frequencies between AIS patients and controls were performed by χ2 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 IL-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.
最近,几项全基因组关联研究表明,IL-17RC、CHL1、DSCAM和CNTNAP2基因多态性与青少年特发性脊柱侧凸(AIS)相关。为了证实这些关联,我们利用648例AIS患者和573例中国汉族健康青少年的数据进行了这项病例对照研究。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析检测多态性位点的基因型:IL-17RC基因中的rs708567、rs279545,CHL1基因中的rs2055314、rs331894、rs2272524、rs2272522,DSCAM基因中的rs2222973,以及CNTNAP2基因中的rs2710102、rs11770843。采用χ2检验对AIS患者和对照组之间的基因型频率进行统计分析。我们的结果显示,AIS患者和对照组之间rs708567位点的基因型频率和等位基因频率均存在显著差异(P值分别为0.023和0.028)。对于多态性位点rs279545、rs2222973、rs279545、rs2055314、rs331894、rs2272524、rs2272522,AIS患者和对照组之间的基因型频率或等位基因频率均未发现显著差异(p>0.05)。总体而言,我们的研究发现IL-17RC基因多态性与中国汉族人群中的AIS存在显著关联,表明IL-17RC基因可能是AIS的易感基因;而CHL1、CNTNAP2和DSCAM基因与AIS无关,提示这些基因可能不参与AIS的发病机制。然而,需要在其他种族中对这些基因与AIS进行关联研究,以阐明这些基因在AIS病因中的作用。