Department of Public Health and Epidemiology, Faculty of Medicine, University of Debrecen, 4028 Debrecen, Hungary.
Doctoral School of Health Sciences, University of Debrecen, 4032 Debrecen, Hungary.
Genes (Basel). 2023 Mar 7;14(3):666. doi: 10.3390/genes14030666.
Harmful alcohol consumption has been considered a major public health issue globally, with the amounts of alcohol drunk being highest in the WHO European Region including Hungary. Alcohol consumption behaviors are complex human traits influenced by environmental factors and numerous genes. Beyond alcohol metabolization and neurotransmitter gene polymorphisms, taste preference-related genetic variants may also mediate alcohol consumption behaviors. Applying the Alcohol Use Disorders Identification Test (AUDIT) we aimed to elucidate the underlying genetic determinants of alcohol consumption patterns considering taste preference gene polymorphisms ( rs307355, rs713598, rs10772420 and rs2274333) in the Hungarian general (HG) and Roma (HR) populations. Alcohol consumption assessment was available for 410 HG and 387 HR individuals with 405 HG and 364 HR DNA samples being obtained for genotyping. No significant associations were found between rs307355, rs10772420, and rs2274333 polymorphisms and alcohol consumption phenotypes. Significant associations were identified between TAS2R38 rs713598 and the number of standard drinks consumed in the HG sample (genotype GG negatively correlated with the number of standard drinks; coef: -0.136, = 0.028) and the prevalence of having six or more drinks among Roma (a negative correlation was identified in the recessive model; genotype GG, coef: -0.170, = 0.049), although, none of these findings passed the Bonferroni-corrected probability criterion ( > 0.05). Nevertheless, our findings may suggest that alcohol consumption is partially driven by genetically determined taste preferences in our study populations. Further studies are required to strengthen the findings and to understand the drivers of alcohol consumption behavior in more depth.
有害饮酒已被视为全球主要的公共卫生问题,其中包括匈牙利在内的世界卫生组织欧洲区域的饮酒量最高。饮酒行为是受环境因素和众多基因影响的复杂人类特征。除了酒精代谢和神经递质基因多态性外,味觉偏好相关的遗传变异也可能介导饮酒行为。应用酒精使用障碍识别测试(AUDIT),我们旨在阐明考虑到匈牙利普通人群(HG)和罗姆人群(HR)中味觉偏好基因多态性( rs307355、 rs713598、 rs10772420和 rs2274333)的饮酒模式的潜在遗传决定因素。对 410 名 HG 和 387 名 HR 个体进行了饮酒评估,获得了 405 名 HG 和 364 名 HR 的 DNA 样本进行基因分型。在 rs307355、 rs10772420 和 rs2274333 多态性与饮酒表型之间未发现显著关联。在 HG 样本中,TAS2R38 rs713598 与饮用标准饮品数量之间存在显著关联(基因型 GG 与饮用标准饮品数量呈负相关;系数:-0.136, = 0.028),并且在罗姆人群中存在 6 种或更多饮品的比例(在隐性模型中存在负相关;基因型 GG,系数:-0.170, = 0.049),尽管这些发现均未通过 Bonferroni 校正概率标准( > 0.05)。然而,我们的研究结果表明,在我们的研究人群中,部分饮酒行为受遗传决定的味觉偏好驱动。需要进一步的研究来加强这些发现,并更深入地了解饮酒行为的驱动因素。