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本文引用的文献

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Influence of interleukin-1 beta gene polymorphisms on the risk of myocardial infarction and ischemic stroke at young age in vivo and in vitro.白细胞介素-1β基因多态性对年轻人心肌梗死和缺血性中风风险的体内及体外影响。
Int J Clin Exp Pathol. 2015 Nov 1;8(11):13806-13. eCollection 2015.
2
Leucocyte Telomere Length and Risk of Cardiovascular Disease in a Cohort of 1,397 Danish Men and Women.1397名丹麦男性和女性队列中的白细胞端粒长度与心血管疾病风险
Cardiology. 2016;133(3):173-7. doi: 10.1159/000441819. Epub 2015 Dec 15.
3
Sequence variation in telomerase reverse transcriptase (TERT) as a determinant of risk of cardiovascular disease: the Atherosclerosis Risk in Communities (ARIC) study.端粒酶逆转录酶(TERT)基因序列变异作为心血管疾病风险的决定因素:社区动脉粥样硬化风险(ARIC)研究
BMC Med Genet. 2015 Jul 23;16:52. doi: 10.1186/s12881-015-0194-x.
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TERT gene harbors multiple variants associated with pancreatic cancer susceptibility.端粒酶逆转录酶(TERT)基因存在多个与胰腺癌易感性相关的变异体。
Int J Cancer. 2015 Nov 1;137(9):2175-83. doi: 10.1002/ijc.29590. Epub 2015 Jun 19.
5
Stroke prevention--medical and lifestyle measures.中风预防——医学及生活方式措施
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6
The Arabidopsis thaliana homolog of the helicase RTEL1 plays multiple roles in preserving genome stability.解旋酶RTEL1的拟南芥同源物在维持基因组稳定性方面发挥多种作用。
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9
Telomere shortening in neurological disorders: an abundance of unanswered questions.神经疾病中的端粒缩短:大量未解答的问题。
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10
A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese.一项全基因组关联研究确定了 TERT 基因上与汉族人群端粒长度有关的一个位点。
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端粒长度相关 TERC 和 TERT 基因多态性与汉族人群缺血性脑卒中的易感性相关。

Polymorphisms in Telomere Length Associated TERC and TERT predispose for Ischemic Stroke in a Chinese Han population.

机构信息

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.

出版信息

Sci Rep. 2017 Jan 6;7:40151. doi: 10.1038/srep40151.

DOI:10.1038/srep40151
PMID:28057933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5216405/
Abstract

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.

摘要

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。