da Rocha Felipe Filardi, Malloy-Diniz Leandro, Lage Naira Vassalo, Romano-Silva Marco Aurélio, de Marco Luiz Armando, Correa Humberto
Pharmacology and Molecular Biochemistry Program-UFMG, Belo Horizonte, Brazil.
Behav Brain Res. 2008 Dec 16;195(1):159-63. doi: 10.1016/j.bbr.2008.05.015. Epub 2008 May 29.
Decision-making impairment is an important feature of some psychiatric disorders, such as attention-deficit/hyperactivity disorder and substance-use disorders, and is associated with dysfunction of the fronto-subcortical circuit, mainly the orbitofrontal cortex (OFC). Several data reports support significant correlations between decision-making impairment and the serotonin system. Thus, this neurotransmission system may be a major step in some cognitive features, particularly in OCD because serotonin is associated with this disorder. Therefore, the serotonin transporter promoter polymorphism (5-HTTLPR) may be related to the modulation of these cognitive characteristics. In a sample of Caucasian OCD patients, we explored the link between decision-making and the 5-HTTLPR.
We used the Iowa Gambling Task (IGT) to measure decision-making in 49 OCD patients, according to the DSM-IV criteria. All patients were submitted to Y-BOCS, BDI, BAI, the Raven Progressive Matrices, the Continuous Performance Task, and the Trail Making Test. We grouped S- and/or Lg-carriers in view of the fact that these act in a nearly dominant way.
On IGT, S- and/or Lg-carriers had significantly lower scores on the third, fourth, and fifth blocks. These findings were confirmed after adjusting for clinical and cognitive variables.
Inconclusive findings about the link between OCD and 5-HTTLPR may be better elucidated by studying OCD subgroups that could be more related in some genetic characteristics. Based on our study, low performance on IGT is associated with S- and/or Lg-carriers.
Our results corroborate the hypothesis that the pattern of neuropsychological functioning observed in previous studies may constitute a biological marker or heritable endophenotype of OCD.
决策功能受损是一些精神疾病的重要特征,如注意力缺陷多动障碍和物质使用障碍,且与额-皮质下回路功能障碍有关,主要是眶额皮质(OFC)。多项数据报告支持决策功能受损与血清素系统之间存在显著相关性。因此,该神经传递系统可能是某些认知特征的一个重要因素,特别是在强迫症中,因为血清素与该疾病有关。所以,血清素转运体启动子多态性(5-HTTLPR)可能与这些认知特征的调节有关。在一组白种人强迫症患者样本中,我们探究了决策功能与5-HTTLPR之间的联系。
根据《精神疾病诊断与统计手册》第四版标准,我们使用爱荷华赌博任务(IGT)来测量49名强迫症患者的决策功能。所有患者均接受耶鲁布朗强迫症量表(Y-BOCS)、贝克抑郁量表(BDI)、贝克焦虑量表(BAI)、瑞文渐进矩阵测验、持续性操作任务和连线测验。鉴于S型和/或Lg型携带者的行为方式几乎呈显性,我们将他们归为一组。
在IGT测试中,S型和/或Lg型携带者在第三、第四和第五个板块的得分显著较低。在对临床和认知变量进行调整后,这些结果得到了证实。
通过研究在某些遗传特征上可能更具相关性的强迫症亚组,或许能更好地阐明关于强迫症与5-HTTLPR之间联系的不确定结果。基于我们的研究,IGT测试表现不佳与S型和/或Lg型携带者有关。
我们的结果证实了以下假设,即先前研究中观察到的神经心理功能模式可能构成强迫症的一种生物学标志物或可遗传的内表型。