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Dazed and confused: A molecular genetic approach to everyday cognitive failure

机译:茫然而困惑:解决日常认知衰竭的分子遗传学方法

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摘要

An individual's susceptibility to everyday cognitive failure constitutes a risk factor for physical and mental health. Different factors such as inefficiency of executive functioning and high trait impulsivity have been shown to affect this susceptibility. Furthermore, twin studies indicate a high heritability of failure susceptibility revealing genetic variables as an important biological influence. We tested for a molecular genetic association between variants on the dopamine D2 receptor gene (DRD2), which relate to executive control and impulsivity, and susceptibility to everyday cognitive failure as assessed by the cognitive failure questionnaire (CFQ) in a sample of N=500 (n = 140 male, n = 360 female, mean age M=24.62, SD = 7.98) healthy participants of central European descent. Moreover, we assessed whether trait impulsivity as measured by the Barratt impulsiveness scale (BIS-11) qualifies as a mediator between DRD2 variants and CFQ scores. We found a positive association between DRD2 variants and the CFQ. This effect was in part yet not completely mediated by trait impulsivity. The DRD2 C/C variant constitutes a protective factor for the susceptibility to everyday cognitive failure. Results point towards at least two biopsychological pathways that may explain the observed effect.
机译:个人对日常认知衰竭的敏感性构成了身心健康的风险因素。已经显示出不同的因素,例如执行功能效率低下和特质冲动性,会影响这种敏感性。此外,双胞胎研究表明,失败敏感性的遗传力很高,揭示出遗传变量是重要的生物学影响。我们测试了多巴胺D2受体基因(DRD2)上的变体之间的分子遗传关联,该变体与执行控制和冲动有关,并由N = 500的认知衰竭问卷(CFQ)评估了对日常认知衰竭的敏感性。 (n = 140男性,n = 360女性,平均年龄M = 24.62,SD = 7.98)中欧血统的健康参与者。此外,我们评估了通过Barratt冲动量表(BIS-11)测得的性冲动是否符合DRD2变异与CFQ评分之间的介导条件。我们发现DRD2变体与CFQ之间存在正相关。这种影响部分地还没有完全由特质冲动所介导。 DRD2 C / C变体构成了对日常认知衰竭易感性的保护因素。结果指向至少两个可以解释观察到的效果的生物心理学途径。

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