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ANKRD1 与激酶结构域包含蛋白 1-多巴胺受体 D2 和儿茶酚-O-甲基转移酶单核苷酸多态性的上位效应与立陶宛人群酒精使用障碍易感性的关系。

Epistatic effect of Ankyrin repeat and kinase domain containing 1 - Dopamine receptor D2 and catechol-o-methyltransferase single nucleotide polymorphisms on the risk for hazardous use of alcohol in Lithuanian population.

机构信息

Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.

Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.

出版信息

Gene. 2021 Jan 10;765:145107. doi: 10.1016/j.gene.2020.145107. Epub 2020 Sep 2.

Abstract

AIM

The Lithuanian population has outstanding rates of alcohol consumption and alcohol related mortality. Alteration of brain dopaminergic system play a role in the risk for addiction disorders. We evaluated the association of one single nucleotide polymorphism rs1800497 in the Ankyrin Repeat and Kinase Domain Containing 1 - Dopamine Receptor D2 complex (ANKK1-DRD2) and a catechol-o-methyltransferase (COMT) rs4680 single nucleotide polymorphism with the risk for alcohol use disorder and impulsiveness in Lithuanian population. Both genetic polymorphisms are known to alter brain dopaminergic activity, thus we also investigated the possible interaction effect of these polymorphisms.

METHODS

The study included 329 participants recruited from the local community. Hazardous alcohol use was evaluated using the Alcohol Use Disorder Identification Test (AUDIT). Impulsiveness was measured using the Barratt Impulsiveness Scale - 11 (BIS-11). Between group differences of AUDIT and BIS-11 scores were examined stratified by genetic polymorphisms and their combinations. The independent effect of each polymorphism and their interaction for hazardous alcohol use were evaluated using adjusted logistic regression analyses.

RESULTS

The ANKK1-DRD2 rs1800497 polymorphism was associated with total AUDIT score, but not with the hazardous use of alcohol, as indicated by the AUDIT test cut-off of 8. The COMT rs4680 GG genotype was associated with the hazardous use of alcohol (adjusted OR = 2.094, p = 0.029), but this association was not statistically significant after adjustment for multiple comparisons. Presence of both COMT rs4680 and ANKK1-DRD2 rs1800497 GGxCT/TT polymorphisms was associated with significantly increased risk for hazardous use of alcohol (adjusted OR = 5.016, p = 0.005). The COMT rs4680 and ANKK1-DRD2 rs1800497 genetic polymorphisms, and their combination were not associated with impulsiveness.

CONCLUSIONS

Our study demonstrated that the interaction of COMT rs4680 and ANKK1-DRD2 rs1800497 genetic polymorphisms is associated with a hazardous use of alcohol.

摘要

目的

立陶宛人群的酒精消费水平和与酒精相关的死亡率都很高。改变大脑多巴胺能系统在成瘾障碍的风险中起作用。我们评估了ANKK1-DRD2 复合多巴胺受体 D2(ANKK1-DRD2)中的一个单核苷酸多态性 rs1800497 和儿茶酚-O-甲基转移酶(COMT)rs4680 单核苷酸多态性与酒精使用障碍和立陶宛人群冲动之间的关系。这两种遗传多态性已知会改变大脑多巴胺能活性,因此我们还研究了这些多态性的可能相互作用。

方法

该研究纳入了 329 名从当地社区招募的参与者。使用酒精使用障碍识别测试 (AUDIT) 评估危险的酒精使用。使用巴雷特冲动量表-11(BIS-11)测量冲动性。根据遗传多态性及其组合,检查 AUDIT 和 BIS-11 评分的组间差异。使用调整后的逻辑回归分析评估每种多态性及其相互作用对危险饮酒的独立影响。

结果

ANKK1-DRD2 rs1800497 多态性与总 AUDIT 评分相关,但与 AUDIT 测试截断值为 8 时的危险饮酒无关。COMT rs4680 GG 基因型与危险饮酒相关(调整后的 OR=2.094,p=0.029),但在进行多次比较调整后,这种关联无统计学意义。COMT rs4680 和 ANKK1-DRD2 rs1800497 GGxCT/TT 多态性同时存在与危险饮酒的风险显著增加相关(调整后的 OR=5.016,p=0.005)。COMT rs4680 和 ANKK1-DRD2 rs1800497 遗传多态性及其组合与冲动性无关。

结论

我们的研究表明,COMT rs4680 和 ANKK1-DRD2 rs1800497 遗传多态性的相互作用与危险饮酒有关。

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