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该基因的启动子多态性与韩国人群缺血性中风的易感性有关。

The promoter polymorphism of gene contributes to susceptibility of ischemic stroke in Korean population.

作者信息

Kim Su Kang, Jang Hyang Mi, Kim Dae-Young

机构信息

Department of Biomedical Laboratory Science, Catholic Kwandong University, Gangneung, Korea.

Department of Basic Nursing Science, School of Nursing, Kyungdong University, Wonju, Korea.

出版信息

J Exerc Rehabil. 2018 Dec 27;14(6):1096-1100. doi: 10.12965/jer.1836592.296. eCollection 2018 Dec.

Abstract

The progression of ischemic stroke is associated with inflammatory response, in which the nuclear factor kappa B subunit 1 (NFKB1) plays an important role. The aim of present study was to determine whether promoter single nucleotide polymorphism (SNP) in the gene was contributed to susceptibility of ischemic stroke. One hundred twenty-one Korean adult patients with ischemic stroke (65.7±12.1 years in age) and 291 Korean healthy controls (63.0±9.3 years in age) were recruited. We genotyped a promoter SNP (rs11940017, -1727, C/T) of gene using direct sequencing in 121 Korean ischemic stroke patients and 291 control subjects. The T/C genotype of rs11940017 SNP in the codominant model (vs. the T/T genotype) (odds ratio [OR], 0.38; 95% confidence interval [CI], 0.15-0.92; =0.032) and the genotype containing C allele (T/C and C/C) in the dominant model (vs. the T/T genotype) (OR, 0.33; 95% CI, 0.14-0.81; =0.0068) were associated with a decreased risk of ischemic stroke. The frequency of C allele was decreased in ischemic stroke patients, compared with control subjects (OR, 0.31; 95% CI, 0.13-0.74; =0.008). These results suggest that the promoter SNP (rs11940017, -1727, C/T) of gene may affect ischemic stroke susceptibility in Korean population.

摘要

缺血性中风的进展与炎症反应相关,其中核因子κB亚基1(NFKB1)起重要作用。本研究的目的是确定该基因启动子单核苷酸多态性(SNP)是否与缺血性中风的易感性有关。招募了121名韩国成年缺血性中风患者(年龄65.7±12.1岁)和291名韩国健康对照者(年龄63.0±9.3岁)。我们采用直接测序法对121名韩国缺血性中风患者和291名对照者的该基因启动子SNP(rs11940017,-1727,C/T)进行基因分型。共显性模型中rs11940017 SNP的T/C基因型(相对于T/T基因型)(优势比[OR],0.38;95%置信区间[CI],0.15 - 0.92;P = 0.032)以及显性模型中含C等位基因的基因型(T/C和C/C,相对于T/T基因型)(OR,0.33;95% CI,0.14 - 0.81;P = 0.0068)与缺血性中风风险降低相关。与对照者相比,缺血性中风患者中C等位基因的频率降低(OR,0.31;95% CI,0.13 - 0.74;P = 0.008)。这些结果表明该基因启动子SNP(rs11940017,-1727,C/T)可能影响韩国人群缺血性中风的易感性。

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