Rychel Monika, Suchanecka Aleksandra, Chmielowiec Jolanta, Chmielowiec Krzysztof, Różański Jacek, Masiak Jolanta, Grzywacz Anna, Boroń Agnieszka
Department of Clinical and Molecular Biochemistry, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich 72 St., 70-111 Szczecin, Poland.
Independent Laboratory of Behavioral Genetics and Epigenetics, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich 72 St., 70-111 Szczecin, Poland.
Cells. 2025 May 12;14(10):699. doi: 10.3390/cells14100699.
The dysregulation of the serotonin system has been implicated in the pathophysiology of alcohol use disorders. Meta-analytic evidence suggests a significant correlation between genetic variation in the serotonin transporter gene and the risk of alcohol dependence. Hence, we aimed to analyse the association between polymorphism and alcohol use disorder in a group of women and to perform an interaction analysis of variants, personality traits, and AUD. The study group comprised 213 female volunteers; 101 were diagnosed with alcohol addiction, and 112 were not dependent on any substance or behaviour. The variants were identified by PCR, and the resulting products were separated electrophoretically. When comparing the AUD group with the controls, we observed significant differences in the distribution of genotypes ( = 0.0230) and alleles ( = 0.0046). We also observed a significant impact of the genotype ( = 0.0001) on the Neuroticism and Extraversion ( = 0.0037) scales. Additionally, there was a statistically significant impact of genotype interaction and alcohol dependency or lack of it on the Neuroticism scale ( < 0.0001). The observed interaction suggests that the effect of the on neuroticism may be exacerbated or attenuated in the presence of alcohol addiction. Further investigation is needed to elucidate the precise nature of this interaction. Still, it potentially indicates a gene-environment interaction where the genetic predisposition conferred by the polymorphism interacts with the environmental stressor of alcohol dependence to influence neuroticism.
血清素系统的失调与酒精使用障碍的病理生理学有关。荟萃分析证据表明血清素转运体基因的遗传变异与酒精依赖风险之间存在显著相关性。因此,我们旨在分析一组女性中该多态性与酒精使用障碍之间的关联,并对该变体、人格特质和酒精使用障碍进行交互作用分析。研究组由213名女性志愿者组成;101人被诊断为酒精成瘾,112人不依赖任何物质或行为。通过聚合酶链反应(PCR)鉴定该变体,所得产物通过电泳分离。将酒精使用障碍组与对照组进行比较时,我们观察到该基因型(P = 0.0230)和等位基因(P = 0.0046)的分布存在显著差异。我们还观察到该基因型(P = 0.0001)对神经质和外向性量表(P = 0.0037)有显著影响。此外,该基因型交互作用与酒精依赖或非酒精依赖对神经质量表有统计学显著影响(P < 0.0001)。观察到的交互作用表明,在存在酒精成瘾的情况下,该基因对神经质的影响可能会加剧或减弱。需要进一步研究以阐明这种交互作用的确切性质。不过,这可能表明存在基因-环境交互作用,即该多态性赋予的遗传易感性与酒精依赖的环境应激源相互作用,从而影响神经质。