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首页> 外文期刊>Medical science monitor : >Association Between CHRNA3 and CHRNA5 Nicotine Receptor Subunit Gene Variants and Nicotine Dependence in an Isolated Population of Kashubians in Poland
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Association Between CHRNA3 and CHRNA5 Nicotine Receptor Subunit Gene Variants and Nicotine Dependence in an Isolated Population of Kashubians in Poland

机译:CHRNA3和CHRNA5尼古丁受体亚基基因变异与尼古丁依赖性在波兰Kashubians的孤立人口之间的关联。

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摘要

BACKGROUND Genome-wide and allelic association studies have shown the contribution of [i]CHRNA5-A3-B4[/i] nicotinic receptor subunit gene cluster within chromosome 15 to nicotine dependence (ND). While an association between several single-nucleotide polymorphisms (SNPs) at that locus and smoking quantity (cigarettes per day; CPD) has been well recognized, there are some inconsistencies in demonstrating the influence of these SNPs on other ND phenotypes. This uncertainty motivated us to examine the association of 3 selected SNPs ([i]CHRNA3[/i] rs1051730, rs6495308, and [i]CHRNA5[/i] rs55853898) with ND in an isolated population of Kashubians from Poland.? MATERIAL AND METHODS The study sample consisted of 788 current daily smokers. ND was assessed by CPD, the Fagerstrom Test for Nicotine Dependence (FTND), its brief version - Heavy Smoking Index (HSI), and time to first cigarette after waking (TTF). The correlation between studied SNPs and dichotomized values of ND measures was assessed in the regression analysis. Bonferroni corrected p-value of 0.017 was set for a type 1 error.? RESULTS We found a robust association between risk allele A of rs1051730 and CPD >10 (odds ratio (OR)=1.77, 95% confidence interval (CI): 1.20-2.59, p=0.004), and a weak association, which did not survive correction for multiple testing, with FTND 34. No associations between studied SNPs and HSI or TTF were demonstrated.? CONCLUSIONS Our findings confirm that rs1051730 influences ND phenotype, as defined by CPD.
机译:背景技术全基因组和等位基因关联研究表明,第15号染色体上的[i] CHRNA5-A3-B4 [/ i]烟碱样受体亚基基因簇对尼古丁依赖性(ND)的贡献。尽管已经很好地认识到该位点的多个单核苷酸多态性(SNP)与吸烟量(每天抽烟; CPD)之间的关联,但在证明这些SNP对其他ND表型的影响方面存在一些矛盾之处。这种不确定性促使我们研究了波兰分离的卡舒比人中3个选定的SNP([i] CHRNA3 [/ i] rs1051730,rs6495308和[i] CHRNA5 [/ i] rs55853898))与ND的关联。材料与方法本研究样本包括788名目前的日常吸烟者。 ND通过CPD,法格斯特罗姆尼古丁依赖性测试(FTND),其简短版本-重度吸烟指数(HSI)和醒来后第一次吸烟的时间(TTF)进行评估。在回归分析中评估了研究的SNP与ND测量二分值之间的相关性。对于类型1错误,将Bonferroni校正的p值设置为0.017。结果我们发现rs1051730的风险等位基因A与CPD> 10之间有很强的关联性(优势比(OR)= 1.77,95%置信区间(CI):1.20-2.59,p = 0.004),并且弱关联性不强。在使用FTND 34进行多次测试的校正后,仍然可以幸免。研究的SNP与HSI或TTF之间没有关联。结论我们的发现证实rs1051730影响CPD定义的ND表型。

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