Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, P. R. China.
Shaanxi Provincial Research Center for the Project of Prevention and Treatment of Respiratory Diseases, Xi'an 710061, P. R. China.
Sci Rep. 2017 Jan 6;7:40151. doi: 10.1038/srep40151.
The role of telomere in genomic stability is an established fact. Variation in leukocyte telomere length (LTL) has been considered a crucial factor that associated with age-associated diseases. To elucidate the association between LTL variation and ischemic stroke (IS) risk, we selected ten single nucleotide polymorphisms (SNPs) in three genes (TERC, TERT and RTEL1) that previously reported link to LTL, and genotyped SNPs of these genes in a case-control study. The association between polymorphisms and IS risk were tested by Chi squared test and haplotype analysis. In allele association analysis, allele "C" in rs10936599 of TERC gene and allele "G" in rs2853677 of TERT gene were found to have an increased risk of IS when compared with allele "T" and "A", respectively. Model association analysis showed that genotype "G/A" in the overdominant model and genotypes "G/A" and "A/A" in the dominant model of rs2242652 presented a more likelihood to have IS. Another TERT locus (rs2853677) with genotype "G" was also found IS-related risky in the log-additive model. Taken together, our results suggest a potential association between LTL related TERC, TERT gene variants and ischemic stroke risk.
端粒在基因组稳定性中的作用是一个既定事实。白细胞端粒长度(LTL)的变化被认为是与年龄相关疾病相关的关键因素。为了阐明 LTL 变化与缺血性中风(IS)风险之间的关联,我们选择了三个基因(TERC、TERT 和 RTEL1)中先前报道与 LTL 相关的十个单核苷酸多态性(SNP),并在病例对照研究中对这些基因的 SNP 进行了基因分型。通过卡方检验和单倍型分析来检验多态性与 IS 风险之间的关联。在等位基因关联分析中,与等位基因“T”相比,TERC 基因 rs10936599 中的等位基因“C”和 TERT 基因 rs2853677 中的等位基因“G”与 IS 风险增加相关。模型关联分析显示,rs2242652 的超显性模型中的基因型“G/A”和显性模型中的基因型“G/A”和“A/A”更有可能发生 IS。另一个 TERT 基因座(rs2853677)中的基因型“G”在对数相加模型中也与 IS 相关。总之,我们的结果表明 LTL 相关的 TERC、TERT 基因变异与缺血性中风风险之间存在潜在关联。