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首页> 外文期刊>Biological psychiatry >TTC12-ANKK1-DRD2 and CHRNA5-CHRNA3-CHRNB4 influence different pathways leading to smoking behavior from adolescence to mid-adulthood.
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TTC12-ANKK1-DRD2 and CHRNA5-CHRNA3-CHRNB4 influence different pathways leading to smoking behavior from adolescence to mid-adulthood.

机译:TTC12-ANKK1-DRD2和CHRNA5-CHRNA3-CHRNB4影响从青春期到成年中期吸烟行为的不同途径。

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BACKGROUND: CHRNA5-CHRNA3-CHRNB4 and TTC12-ANKK1-DRD2 gene-clusters influence smoking behavior. Our aim was to test developmental changes in their effects as well as the interplays between them and with nongenetic factors. METHODS: Participants included 4762 subjects from a general population-based, prospective Northern Finland 1966 Birth Cohort (NFBC 1966). Smoking behavior was collected at age 14 and 31 years. Information on maternal smoking, socioeconomic status, and novelty seeking were also collected. Structural equation modeling was used to construct an integrative etiologic model including genetic and nongenetic factors. RESULTS: Several single nucleotide polymorphisms in both gene-clusters were significantly associated with smoking. The most significant were in CHRNA3 (rs1051730, p = 1.1 x 10(-5)) and in TTC12 (rs10502172, p = 9.1 x 10(-6)). CHRNA3-rs1051730[A] was more common among heavy/regular smokers than nonsmokers with similar effect-sizes at age 14 years (odds ratio [95% CI]: 1.27 [1.06-1.52]) and 31 years (1.28 [1.13-1.44]). TTC12-rs10502172[G] was more common among smokers than nonsmokers with stronger association at 14 years (1.33 [1.11-1.60]) than 31 years (1.14 [1.02-1.28]). In adolescence, carriers of three-four risk alleles at either CHRNA3-rs1051730 or TTC12-rs10502172 had almost threefold odds of smoking regularly than subjects with no risk alleles. TTC12-rs10502172 effect on smoking in adulthood was mediated by its effect on smoking in adolescence and via novelty seeking. Effect of CHRNA3-rs1051730 on smoking in adulthood was direct. CONCLUSIONS: TTC12-ANKK1-DRD2s seemed to influence smoking behavior mainly in adolescence, and its effect is partially mediated by personality characteristics promoting drug-seeking behavior. In contrast, CHRNA5-CHRNA3-CHRNB4 is involved in the transition toward heavy smoking in mid-adulthood and in smoking persistence. Factors related to familial and social disadvantages were strong independent predictors of smoking.
机译:背景:CHRNA5-CHRNA3-CHRNB4和TTC12-ANKK1-DRD2基因簇影响吸烟行为。我们的目的是测试其影响的发展变化以及它们之间以及与非遗传因素之间的相互作用。方法:参与者包括来自一般人群的,前瞻性的北部芬兰1966年出生队列(NFBC 1966)的4762名受试者。在14岁和31岁时收集吸烟行为。还收集了有关孕产妇吸烟,社会经济地位和寻求新颖性的信息。结构方程模型用于构建包括遗传因素和非遗传因素的综合病因模型。结果:两个基因簇中的几个单核苷酸多态性与吸烟显着相关。最显着的是CHRNA3(rs1051730,p = 1.1 x 10(-6))和TTC12(rs10502172,p = 9.1 x 10(-6))。 CHRNA3-rs1051730 [A]在重度/定期吸烟者中比在14岁(赔率[95%CI]:1.27 [1.06-1.52])和31岁(1.28 [1.13-1.44] ])。 TTC12-rs10502172 [G]在14岁(1.33 [1.11-1.60])而非31岁(1.14 [1.02-1.28])较不吸烟者中更常见。在青春期,CHRNA3-rs1051730或TTC12-rs10502172处的三至四个风险等位基因携带者的规律吸烟率是无风险等位基因受试者的近三倍。 TTC12-rs10502172对成年吸烟的影响是通过其对青春期吸烟的影响和通过寻求新颖性来介导的。 CHRNA3-rs1051730对成年吸烟的影响是直接的。结论:TTC12-ANKK1-DRD2s似乎主要在青春期影响吸烟行为,其作用部分由促进吸毒行为的人格特征介导。相比之下,CHRNA5-CHRNA3-CHRNB4参与了成年中期向重度吸烟的转变以及吸烟的持续性。与家族和社会不利因素有关的因素是吸烟的独立强烈预测因子。

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