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The genetic impact (C957T-DRD2) on inhibitory control is magnified by aging

机译:衰老放大了抑制控制的遗传影响(C957T-DRD2)

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Healthy aging beyond the age of 65 is characterized by a general decrease in cognitive control over actions: old adults have more difficulty than young adults in stopping overt responses. Responsible for this cognitive decrement is the continuous decline of striatal and extrastriatal dopamine (DA). The resource-modulation hypothesis assumes that genetic variability is more likely to result in performance differences when brain resources move away from close-to-optimal levels, as in aging. To test this hypothesis we investigated, first, whether individual differences in the C957T polymorphism at DRD2 gene (rs6277) contribute to individual differences in the proficiency to inhibit behavioral responses in a stop-signal task. Second, we assessed whether this genetic effect is magnified in older adults, due to the considerable decline in dopamine function. Our findings show that individuals carrying genotype associated with higher density of extrastriatal D2 receptors (C957T CC) were more efficient in inhibiting unwanted action tendencies, but not in term of response execution. This effect was stronger in older than in younger adults. Our findings support the idea that aging-related decline in dopamine availability alters the balance between genotypes and cognitive functions.
机译:65岁以上的健康衰老的特征是对动作的认知控制普遍下降:在阻止明显反应方面,老年人比年轻人要困难得多。造成这种认知下降的原因是纹状体和纹状体多巴胺(DA)持续下降。资源调节假说假设,当大脑资源偏离接近最佳水平时(如衰老),遗传变异更可能导致性能差异。为了验证该假设,我们首先研究了DRD2基因(rs6277)的C957T多态性的个体差异是否会导致个体能力的差异,从而抑制了停止信号任务中的行为反应。其次,由于多巴胺功能的显着下降,我们评估了这种遗传效应在老年人中是否被放大。我们的研究结果表明,携带基因型与更高密度的纹状体外D2受体(C957T CC)相关的个体在抑制不良行为倾向方面更为有效,但在执行反应方面则更为有效。老年人比年轻人更有效。我们的发现支持这样一种观点,即与衰老相关的多巴胺可用性下降会改变基因型和认知功能之间的平衡。

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