Tomson Katrin, Vaht Mariliis, Laas Kariina, Veidebaum Toomas, Harro Jaanus
Division of Neuropsychopharmacology, Department of Psychology, University of Tartu, Ravila 14A, Tartu, Estonia; Department of Public Health, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Division of Neuropsychopharmacology, Department of Psychology, University of Tartu, Ravila 14A, Tartu, Estonia.
J Affect Disord. 2016 Dec;206:23-30. doi: 10.1016/j.jad.2016.07.036. Epub 2016 Jul 19.
Impulsivity is multidimensional: Low impulse control may result in behavioural disorders, but acting on the spur of moment may also be advantageous. Previous studies have shown negative associations between different facets of impulsivity and serotonergic function. Other investigations have found negative correlations between serum lipid levels and impulsivity.
We have investigated whether the functional polymorphism -1438A/G in the serotonin 5-HT receptor gene (HTR2A) is associated with impulsivity levels and whether there is any interaction with serum lipid levels. This analysis was based on data of the population-representative Estonian Children Personality Behaviour and Health Study at age 25. Impulsivity was self-reported with the Adaptive and Maladaptive Impulsivity Scale.
Subjects with the A/A genotype of the HTR2A -1438A/G polymorphism had higher scores of Maladaptive impulsivity, but not Adaptive impulsivity. In females, high LDL and total cholesterol levels increased the genotype effect. In males, in the highest quartile of total or LDL cholesterol the genotype effect was altered, with G/G homozygotes having the highest Maladaptive impulsivity levels.
Only one cohort of the European Youth Heart Study (EYHS) was used in the current study and impulsivity measures were self-reported.
Our results do not support the notion that low cholesterol levels universally lead to higher impulsivity, but it was found that high total and LDL cholesterol levels moderate the effect of the HTR2A gene promoter polymorphism. This suggests that future studies on impulsivity need to consider the interaction of serotonergic measures with the whole range of cholesterol levels.
冲动性是多维度的:低冲动控制可能导致行为障碍,但一时冲动行事也可能具有优势。先前的研究表明冲动性的不同方面与血清素能功能之间存在负相关。其他调查发现血清脂质水平与冲动性之间存在负相关。
我们研究了血清素5-HT受体基因(HTR2A)中的功能性多态性-1438A/G是否与冲动性水平相关,以及是否与血清脂质水平存在任何相互作用。该分析基于具有人群代表性的爱沙尼亚25岁儿童个性行为与健康研究的数据。冲动性通过适应性和适应不良冲动性量表进行自我报告。
HTR2A -1438A/G多态性的A/A基因型受试者具有较高的适应不良冲动性得分,但适应性冲动性得分不高。在女性中,高LDL和总胆固醇水平增强了基因型效应。在男性中,在总胆固醇或LDL胆固醇最高四分位数中,基因型效应发生改变,G/G纯合子具有最高的适应不良冲动性水平。
本研究仅使用了欧洲青年心脏研究(EYHS)的一个队列,且冲动性测量是自我报告的。
我们的结果不支持低胆固醇水平普遍导致更高冲动性的观点,但发现高总胆固醇和LDL胆固醇水平会调节HTR2A基因启动子多态性的效应。这表明未来关于冲动性的研究需要考虑血清素能测量与整个胆固醇水平范围之间的相互作用。