[Maternal bonding style, cholinergic receptor gene polymorphisms in association with smoking-related depressive symptoms].

Q3 Pharmacology, Toxicology and Pharmaceutics
Neuropsychopharmacologia Hungarica Pub Date : 2017-12-01
Iren Csala, Peter Dome, Judit Lazary
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引用次数: 0

Abstract

Backgorund: There is accumulating evidence on the association between the cholinergic system and nicotine dependence (ND) in the literature and the bidirectional relationship of ND and depression. However, the molecular background of the development of ND and related affective phenotype is not clear.

Methods: We recruited 255 tretament-seeking smokers into our study. For phenotyping assessments we used the Fagerstrom Nicotine Dependence Test; The Minnessotta Nicotine Withdrawal Scale; the Zung Self-Rating Depression Scale and the Parental Bonding Instrument. DNA was isolated from buccal mucosa sample and CHRNA4 and CHRNB2 gene SNPs were genotyped with MassArray Sequenom techniques. For statistical analyses ANOVA test, Mann-Whitney U test, linear regression, two-step cluster analyses and hapscore tests were performed.

Results: Two-step cluster analysis revealed 3 well-differentiated subgroups among smokers based on phenotypic characteristics. One subgroup was associated with the highest withdrawal and depressive scores. Frequency of the risk haplotype of CHRNA4 was significantly higher in this subgroup (p=0.019). Further, lifetime prevalence of major depression was also significantly higher in this subgroup. Besides, CHRNB2 gén variants showed a significant interacting effect with maternal bonding style on suicide thoughts (p=0.005).

Conclusions: Our results confirmed the genetic effect of CHRNA4 and CHRNB2 on smoking-related depression. These findings suggest that a genetically vulnerable subgroup can be distinguished among smokers and this subphenotype is more prone to withdrawal and depressive symptoms. Our data suggest that suicidal risk depends on both CHRNB2 gene variants and maternal bonding style. Pharmacogenetic concerns of CHRNA4 and CHRNB2 genes might be significant considering suicide as side effect of quitting therapy. Further pharmacogenetic investigations are requierd to clarify this possibility.

[母亲结合方式、胆碱能受体基因多态性与吸烟相关抑郁症状的关系]。
背景:文献中越来越多的证据表明胆碱能系统与尼古丁依赖(ND)之间存在关联,ND与抑郁之间存在双向关系。然而,ND发生的分子背景和相关的情感表型尚不清楚。方法:我们招募了255名寻求治疗的吸烟者加入我们的研究。对于表型评估,我们使用Fagerstrom尼古丁依赖测试;明尼苏达尼古丁戒断量表;Zung抑郁自评量表和亲代依恋量表。从口腔黏膜样品中分离DNA,采用MassArray测序技术对CHRNA4和CHRNB2基因snp进行基因分型。统计分析采用方差分析、Mann-Whitney U检验、线性回归、两步聚类分析和hapscore检验。结果:两步聚类分析显示吸烟者的表型特征有3个分化良好的亚群。其中一个亚组的戒断和抑郁评分最高。在该亚组中,CHRNA4风险单倍型的频率显著高于其他亚组(p=0.019)。此外,在这个亚组中,重度抑郁症的终生患病率也明显更高。此外,CHRNB2基因变异与母亲结合方式对自杀念头的交互作用显著(p=0.005)。结论:我们的研究结果证实了CHRNA4和CHRNB2在吸烟相关性抑郁中的遗传作用。这些发现表明,在吸烟者中可以区分出一个遗传易感的亚群,这个亚表型更容易出现戒断和抑郁症状。我们的数据表明,自杀风险取决于CHRNB2基因变异和母亲结合方式。考虑到自杀是戒烟治疗的副作用,CHRNA4和CHRNB2基因的药理学关注可能是重要的。需要进一步的药理学研究来澄清这种可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuropsychopharmacologia Hungarica
Neuropsychopharmacologia Hungarica Medicine-Medicine (all)
CiteScore
1.60
自引率
0.00%
发文量
8
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