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The SLC6A3 gene possibly affects susceptibility to late-onset alcohol dependence but not specific personality traits in a Han Chinese population

机译:SLC6A3基因可能影响汉族人群晚发性酒精依赖的易感性但不影响特定的人格特质

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摘要

Dopaminergic dysfunction has an important role in the pathoetiology of alcohol dependence (AD). The purpose of this study was to determine whether the solute carrier family 6 member 3 (SLC6A3) gene (also known as the dopamine transporter DAT gene) was associated with AD, and whether variants in the SLC6A3 locus were associated with specific personality traits in patients with AD. Sixteen polymorphisms in SLC6A3 were analyzed using 637 patients with AD and 523 healthy controls. To reduce clinical heterogeneity, patients were classified into two subgroups: early-onset AD (EOAD) and late-onset AD (LOAD). The Tridimensional Personality Questionnaire was used to assess the personality traits novelty seeking (NS) and harm avoidance (HA) in the patients with AD. Using allele frequency and genotype distribution comparisons and logistic regression analysis, we found evidence of association between rs6350 and AD (P < 0.05). Following subgroup analysis, we confirmed evidence of an association in patients with LOAD (P = 0.003), but not in patients with EOAD. Heterozygous carriers of the A allele have a nearly 3 times greater risk to develop LOAD compared to individuals who do not have an A allele. Although we found that patients with AD had higher NS and HA scores compared to controls (P < 0.001), we did not find evidence of association between SLC6A3 polymorphisms and either NS or HA in patients with AD using linear regression analysis. The findings from our study indicate that the SLC6A3 gene may have a role in susceptibility to late-onset AD in the Han Chinese population.
机译:多巴胺能功能障碍在酒精依赖症(AD)的病理学中具有重要作用。这项研究的目的是确定溶质载体家族6成员3(SLC6A3)基因(也称为多巴胺转运蛋白DAT基因)是否与AD相关,以及SLC6A3基因座中的变体是否与患者的特定人格特征相关与广告。使用637例AD患者和523例健康对照者分析了SLC6A3中的16个多态性。为了减少临床异质性,将患者分为两个亚组:早发性AD(EOAD)和晚发性AD(LOAD)。三维人格问卷用于评估AD患者的人格特质(NS)和避免伤害(HA)。使用等位基因频率和基因型分布比较和逻辑回归分析,我们发现rs6350与AD之间存在关联的证据(P <0.05)。在亚组分析之后,我们确认了与LOAD患者相关的证据(P = 0.003),而与EOAD患者无关。与没有A等位基因的个体相比,A等位基因的杂合子携带者患LOAD的风险高将近3倍。尽管我们发现,与对照组相比,AD患者的NS和HA评分更高(P <0.001),但我们没有通过线性回归分析发现SLC6A3基因多态性与AD患者的NS或HA相关。我们的研究结果表明,SLC6A3基因可能在汉族人群中对迟发性AD易感性中起作用。

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