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在一个年轻成年人样本中,基因型与回顾性注意缺陷多动障碍症状之间的相互作用可预测终生吸烟风险。

Interactions between genotype and retrospective ADHD symptoms predict lifetime smoking risk in a sample of young adults.

作者信息

McClernon F Joseph, Fuemmeler Bernard F, Kollins Scott H, Kail Melanie E, Ashley-Koch Allison E

机构信息

Department of Psychiatry and Behavioral Sciences, Duke University Medical Cneter, Durham, NC 27708, USA.

出版信息

Nicotine Tob Res. 2008 Jan;10(1):117-27. doi: 10.1080/14622200701704913.

Abstract

Attention-deficit/hyperactivity disorder (ADHD) symptoms are associated with an increased risk of smoking, and genetic studies have identified similar candidate genes associated with both ADHD and smoking phenotypes. This paper addresses the question of whether ADHD symptoms interact with candidate gene variation to predict smoking risk. Participants were a subsample of individuals from the National Longitudinal Study of Adolescent Health (Add Health), a nationally representative sample of adolescents followed from 1995 to 2002. The sample analyzed included a subset from Add Health of 1,900 unrelated individuals with genotype data. Multiple logistic regression was used to examine relationships between self-reported ADHD symptoms, genotype, and lifetime history of regular smoking. Polymorphisms in the DRD2 gene and, among females, the MAOA gene interacted with retrospective reports of ADHD symptoms in contributing to risk for smoking. Trends were observed for interactions between the DRD4 gene and, among males, the MAOA gene and ADHD symptoms to predict smoking risk. No main effect for any of these polymorphisms was observed. We observed neither main effects nor interactions with CYP2A6, DAT, and SLC6A4 genes. These findings suggest that genotypes associated with catecholamine neurotransmission interact with ADHD symptoms to contribute to smoking risk.

摘要

注意缺陷多动障碍(ADHD)症状与吸烟风险增加相关,并且基因研究已经确定了与ADHD和吸烟表型相关的相似候选基因。本文探讨了ADHD症状是否与候选基因变异相互作用以预测吸烟风险这一问题。研究参与者是青少年健康全国纵向研究(Add Health)中的个体子样本,该研究是对1995年至2002年期间具有全国代表性的青少年样本进行跟踪调查。所分析的样本包括Add Health中1900名具有基因型数据的无亲属关系个体的一个子集。采用多元逻辑回归来检验自我报告的ADHD症状、基因型与规律吸烟终生史之间的关系。DRD2基因的多态性以及在女性中MAOA基因的多态性与ADHD症状的回顾性报告相互作用,共同影响吸烟风险。观察到DRD4基因与男性中的MAOA基因和ADHD症状之间存在相互作用以预测吸烟风险的趋势。未观察到这些多态性中的任何一种的主效应。我们既未观察到与CYP2A6、DAT和SLC6A4基因的主效应,也未观察到它们之间的相互作用。这些发现表明,与儿茶酚胺神经传递相关的基因型与ADHD症状相互作用,从而增加吸烟风险。

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