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Piccolo genotype modulates neural correlates of emotion processing but not executive functioning

机译:短笛基因型调节情绪处理的神经相关性,但不调节执行功能

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Major depressive disorder (MDD) is characterized by affective symptoms and cognitive impairments, which have been associated with changes in limbic and prefrontal activity as well as with monoaminergic neurotransmission. A genome-wide association study implicated the polymorphism rs2522833 in the piccolo (PCLO) gene—involved in monoaminergic neurotransmission—as a risk factor for MDD. However, the role of the PCLO risk allele in emotion processing and executive function or its effect on their neural substrate has never been studied. We used functional magnetic resonance imaging (fMRI) to investigate PCLO risk allele carriers vs noncarriers during an emotional face processing task and a visuospatial planning task in 159 current MDD patients and healthy controls. In PCLO risk allele carriers, we found increased activity in the left amygdala during processing of angry and sad faces compared with noncarriers, independent of psychopathological status. During processing of fearful faces, the PCLO risk allele was associated with increased amygdala activation in MDD patients only. During the visuospatial planning task, we found no genotype effect on performance or on BOLD signal in our predefined areas as a function of increasing task load. The PCLO risk allele was found to be specifically associated with altered emotion processing, but not with executive dysfunction. Moreover, the PCLO risk allele appears to modulate amygdala function during fearful facial processing in MDD and may constitute a possible link between genotype and susceptibility for depression via altered processing of fearful stimuli. The current results may therefore aid in better understanding underlying neurobiological mechanisms in MDD.. ? 2012 Macmillan Publishers Limited
机译:严重抑郁症(MDD)的特征是情感症状和认知障碍,与边缘和额叶活动的改变以及单胺能神经传递有关。全基因组关联研究表明,短笛(PCLO)基因多态性rs2522833(涉及单胺能神经传递)是MDD的危险因素。但是,从未研究过PCLO风险等位基因在情绪加工和执行功能中的作用或其对神经底质的影响。我们使用功能磁共振成像(fMRI)在159名当前的MDD患者和健康对照中进行情绪面部处理任务和视觉空间规划任务期间调查PCLO风险等位基因携带者与非携带者。在PCLO风险等位基因携带者中,我们发现与非携带者相比,处理愤怒和悲伤面孔时左杏仁核的活动增加,而与心理病理状态无关。在处理可怕的面孔期间,仅在MDD患者中,PCLO风险等位基因与杏仁核激活增加有关。在视觉空间规划任务中,我们发现在预定义区域中,没有表现出基因型对性能或BOLD信号的影响,这与任务负荷的增加有关。发现PCLO风险等位基因与情绪处理改变有关,但与执行功能障碍无关。此外,PCLO风险等位基因似乎在MDD中令人恐惧的面部加工过程中调节杏仁核功能,并可能通过改变对恐惧刺激的处理而在基因型和抑郁症易感性之间构成可能的联系。因此,当前的结果可能有助于更好地了解MDD中潜在的神经生物学机制。 2012 Macmillan Publishers Limited

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