Department of Public Health, Hjelt Institute, University of Helsinki, Helsinki, Finland.
1] Department of Public Health, Hjelt Institute, University of Helsinki, Helsinki, Finland [2] National Institute for Health and Welfare, Helsinki, Finland.
Mol Psychiatry. 2014 May;19(5):615-24. doi: 10.1038/mp.2013.72. Epub 2013 Jun 11.
Smoking is a major risk factor for several somatic diseases and is also emerging as a causal factor for neuropsychiatric disorders. Genome-wide association (GWA) and candidate gene studies for smoking behavior and nicotine dependence (ND) have disclosed too few predisposing variants to account for the high estimated heritability. Previous large-scale GWA studies have had very limited phenotypic definitions of relevance to smoking-related behavior, which has likely impeded the discovery of genetic effects. We performed GWA analyses on 1114 adult twins ascertained for ever smoking from the population-based Finnish Twin Cohort study. The availability of 17 smoking-related phenotypes allowed us to comprehensively portray the dimensions of smoking behavior, clustered into the domains of smoking initiation, amount smoked and ND. Our results highlight a locus on 16p12.3, with several single-nucleotide polymorphisms (SNPs) in the vicinity of CLEC19A showing association (P<1 × 10(-6)) with smoking quantity. Interestingly, CLEC19A is located close to a previously reported attention-deficit hyperactivity disorder (ADHD) linkage locus and an evident link between ADHD and smoking has been established. Intriguing preliminary association (P<1 × 10(-5)) was detected between DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, 4th edition) ND diagnosis and several SNPs in ERBB4, coding for a Neuregulin receptor, on 2q33. The association between ERBB4 and DSM-IV ND diagnosis was replicated in an independent Australian sample. Recently, a significant increase in ErbB4 and Neuregulin 3 (Nrg3) expression was revealed following chronic nicotine exposure and withdrawal in mice and an association between NRG3 SNPs and smoking cessation success was detected in a clinical trial. ERBB4 has previously been associated with schizophrenia; further, it is located within an established schizophrenia linkage locus and within a linkage locus for a smoker phenotype identified in this sample. In conclusion, we disclose novel tentative evidence for the involvement of ERBB4 in ND, suggesting the involvement of the Neuregulin/ErbB signalling pathway in addictions and providing a plausible link between the high co-morbidity of schizophrenia and ND.
吸烟是多种躯体疾病的主要危险因素,也逐渐成为神经精神障碍的致病因素。全基因组关联 (GWA) 和候选基因研究已经发现了吸烟行为和尼古丁依赖 (ND) 的少数易感变体,但这些变体还不足以解释高遗传率。以前的大规模 GWA 研究对与吸烟相关的行为的表型定义非常有限,这可能阻碍了遗传效应的发现。我们对来自基于人群的芬兰双胞胎队列研究中为吸烟而确定的 1114 名成年双胞胎进行了 GWA 分析。17 种与吸烟相关的表型的可用性使我们能够全面描述吸烟行为的维度,这些维度聚类为吸烟起始、吸烟量和 ND 领域。我们的研究结果突出了 16p12.3 上的一个基因座,该基因座附近的几个单核苷酸多态性 (SNP) 与 CLEC19A 与吸烟量相关 (P<1×10(-6))。有趣的是,CLEC19A 位于先前报道的注意力缺陷多动障碍 (ADHD) 连锁基因座附近,并且已经建立了 ADHD 与吸烟之间的明显联系。在 DSM-IV (精神障碍诊断与统计手册,第 4 版) ND 诊断和 2q33 上编码神经调节蛋白受体的 ERBB4 中的几个 SNP 之间检测到初步的关联 (P<1×10(-5))。在澳大利亚的一个独立样本中,对 ERBB4 与 DSM-IV ND 诊断之间的关联进行了复制。最近,在慢性尼古丁暴露和戒断后,在小鼠中发现 ErbB4 和 Neuregulin 3 (Nrg3) 的表达显著增加,并且在临床试验中检测到 NRG3 SNP 与戒烟成功之间的关联。ERBB4 先前与精神分裂症有关;此外,它位于已建立的精神分裂症连锁基因座内,并且位于该样本中确定的吸烟者表型的连锁基因座内。总之,我们揭示了 ERBB4 参与 ND 的新的暂定证据,表明神经调节蛋白/ErbB 信号通路在成瘾中的参与,并为精神分裂症和 ND 的高共病率提供了一个合理的联系。