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CHRN 基因与“头晕”对烟草的关联。

Association of CHRN genes with "dizziness" to tobacco.

机构信息

Institute for Behavioral Genetics, University of Colorado, Boulder, Colorado.

Department of Integrative Physiology, University of Colorado, Boulder, Colorado.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):600-609. doi: 10.1002/ajmg.b.31027.

Abstract

The neuronal nicotinic receptor genes (CHRN) have been implicated in a variety of smoking-related behaviors. Here we tested for association between an early subjective response phenotype, "dizziness," and 226 single nucleotide polymorphisms (SNPs) in CHRN genes. The sample included 789 nicotine-dependent cases and 811 controls, where early "dizziness" reports were significantly associated with case/control status (P < 0.0001). Multiple SNPs in the putative promoter region of the CHRNB3 gene were nominally associated with "dizziness" experience from the first few cigarettes (P < 0.01). Cell culture studies were conducted to examine the ability of different haplotypes in the CHRNB3 promoter to drive luciferase expression. Data from these experiments support the hypothesis that different alleles in the CHRNB3 upstream promoter region may lead to different levels of RNA expression. In addition, a novel finding of association between SNPs in the CHRNA10 gene reached experiment-wide empirical significance (P = 0.048), which implicates another CHRN gene as being involved in early subjective response to tobacco.

摘要

神经元烟碱受体基因 (CHRN) 与多种与吸烟相关的行为有关。在这里,我们测试了早期主观反应表型“头晕”与 CHRN 基因中的 226 个单核苷酸多态性 (SNP) 之间的关联。该样本包括 789 名尼古丁依赖病例和 811 名对照,其中早期“头晕”报告与病例/对照状态显著相关 (P < 0.0001)。CHRNB3 基因假定启动子区域的多个 SNP 与首次吸烟时的“头晕”经历呈名义相关 (P < 0.01)。进行了细胞培养研究,以检查 CHRNB3 启动子中不同单倍型驱动荧光素酶表达的能力。这些实验数据支持这样的假设,即 CHRNB3 上游启动子区域中的不同等位基因可能导致 RNA 表达水平的不同。此外,CHRNA10 基因中的 SNP 之间的关联发现达到了实验范围的经验显著性 (P = 0.048),这表明另一个 CHRN 基因参与了对烟草的早期主观反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9372/2878135/3ef30edcae05/nihms199289f1.jpg

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Association of CHRN genes with "dizziness" to tobacco.CHRN 基因与“头晕”对烟草的关联。
Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):600-609. doi: 10.1002/ajmg.b.31027.

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