Kleinjan Marloes, Engels Rutger C M E, DiFranza Joseph R
Trimbos Institute (Netherlands Institute of Mental Health and Addiction), Da Costakade 45, 3521 VS, Utrecht, The Netherlands.
Behavioural Science Institute, Radboud University Nijmegen, Montessorilaan 3, 6525 HR, Nijmegen, The Netherlands.
BMC Pulm Med. 2015 Oct 8;15:115. doi: 10.1186/s12890-015-0114-z.
Among adolescent novice smokers, craving is often the first, and is the most reported, symptom of nicotine dependence. Until now, little has been known about the development of craving symptoms in novice smokers. The aim of this study was to identify specific genetic (i.e., DRD2 Taq1A, DRD4 48 bp VNTR, and OPRM1 A118G polymorphisms) and environmental mechanisms that underlie the emergence of both cue-induced and cognitive craving among adolescent novice smokers.
A five-wave longitudinal, genetically-informed survey study was conducted with intervals of four months. The sample included 376 early adolescent smokers (12-13 years of age at baseline). Self-report questionnaires were completed regarding smoking behavior, observed parental smoking behavior, and both cue-induced and cognitive craving.
Data were analyzed with a latent growth curve approach. For both cue-induced and cognitive craving, significant interaction effects were found for DRD2 Taq1A with parental smoke exposure. A1-allele carriers did not seem to be influenced by the environment with regard to craving development. Adolescents who are homozygous for the A2-allele and who are more exposed to parental smoking experience the highest levels of both types of craving over time. No significant interaction effects were found between parental smoke exposure and DRD4 48 bp VNTR or OPRM1 A118G.
Previous studies identified DRD2 Taq1A A1-allele carriers as vulnerable to developing nicotine dependence. However, this study showed that parental smoking increased the chances of developing dependence more rapidly for early adolescents who are considered to be less sensitive to the rewarding effects of nicotine according to their DRD2 Taq1A genotype. It is thus especially important that these young people not be exposed to smoking in their social environment.
在青少年初吸者中,渴求通常是尼古丁依赖的首个且被报告最多的症状。到目前为止,对于初吸者渴求症状的发展了解甚少。本研究的目的是确定青少年初吸者中线索诱导性渴求与认知性渴求出现背后的特定遗传机制(即多巴胺D2受体基因Taq1A多态性、多巴胺D4受体基因48碱基对可变数目串联重复序列多态性和阿片μ受体基因A118G多态性)及环境机制。
进行了一项为期五个阶段的纵向、基于遗传信息的调查研究,间隔为四个月。样本包括376名青少年早期吸烟者(基线时年龄为12 - 13岁)。完成了关于吸烟行为、观察到的父母吸烟行为以及线索诱导性渴求与认知性渴求的自我报告问卷。
采用潜在增长曲线方法分析数据。对于线索诱导性渴求与认知性渴求,均发现多巴胺D2受体基因Taq1A与父母吸烟暴露存在显著的交互作用。A1等位基因携带者在渴求发展方面似乎不受环境影响。A2等位基因纯合且父母吸烟暴露较多的青少年,随着时间推移,两种渴求水平最高。未发现父母吸烟暴露与多巴胺D4受体基因48碱基对可变数目串联重复序列或阿片μ受体基因A118G之间存在显著的交互作用。
先前的研究将多巴胺D2受体基因Taq1A A1等位基因携带者确定为易患尼古丁依赖。然而,本研究表明,对于根据其多巴胺D2受体基因Taq1A基因型被认为对尼古丁奖励作用不太敏感的青少年早期吸烟者,父母吸烟会增加其更快发展为尼古丁依赖的几率。因此,尤其重要的是,这些年轻人不应在其社交环境中接触到吸烟行为。