Hosák Ladislav, Libiger Jan, Cizek Jiri, Beránek Martin, Cermáková Eva
Department of Psychiatry, Charles University in Prague, Faculty of Medicine in Hradec Králové and University Hospital Hradec Králové, Czech Republic.
Neuro Endocrinol Lett. 2006 Dec;27(6):799-802.
Measurable traits of human personality may mark the predisposition to psychopathology. Increased novelty seeking plays an important role in the pathogenesis of substance abuse. Novelty seeking, one of the fundamental traits of the human temperament, is related to dopamine. Catechol-O-methyltransferase (COMT) is essential for dopamine inactivation. The aim of our study was to assess whether the COMT gene Val158Met functional polymorphism in patients dependent on methamphetamine is related to their novelty seeking score.
Patients dependent on methamphetamine who had been treated at the Addiction Treatment Unit in Nechanice in 2004 and 2005 agreed to participate in the investigation. We administered the Temperament and Character Inventory (TCI) questionnaire, assessed their novelty seeking score and analysed their DNA samples for COMT Val158Met genotype.
The subjects were thirty-seven Czech Caucasians (women N=10) dependent on methamphetamine with an average age of 23.6+/-3.8 years. We found a significantly higher mean novelty seeking score among the patients with the Met allele (Met/Met homozygotes+Val/Met heterozygotes; N=28) than in nine Val/Val homozygotes (27.4 vs 24.1; p=0.042, Two-Sample T-Test).
The Met allele of the COMT gene Val158Met polymorphism is associated with low COMT enzyme activity and high endogenous dopamine synaptic levels in the prefrontal cortex. This leads to a decrease in dopaminergic neurotransmission in nucleus accumbens and a need for an increased activity to stimulate it. Novelty seeking behavior corresponds with this need.
人类个性的可测量特征可能标志着心理病理学的易感性。寻求新奇在物质滥用的发病机制中起重要作用。寻求新奇是人类气质的基本特征之一,与多巴胺有关。儿茶酚-O-甲基转移酶(COMT)对多巴胺失活至关重要。我们研究的目的是评估甲基苯丙胺依赖患者中COMT基因Val158Met功能多态性是否与其寻求新奇得分相关。
2004年和2005年在内恰尼采戒毒治疗科接受治疗的甲基苯丙胺依赖患者同意参与调查。我们发放了气质和性格量表(TCI)问卷,评估他们的寻求新奇得分,并分析他们的DNA样本以确定COMT Val158Met基因型。
受试者为37名捷克白种人(女性10名),依赖甲基苯丙胺,平均年龄23.6±3.8岁。我们发现,携带Met等位基因的患者(Met/Met纯合子+Val/Met杂合子;N = 28)的平均寻求新奇得分显著高于9名Val/Val纯合子(27.4对24.1;p = 0.042,双样本T检验)。
COMT基因Val158Met多态性的Met等位基因与低COMT酶活性和前额叶皮质内源性多巴胺突触水平升高有关。这导致伏隔核中多巴胺能神经传递减少,需要增加活动来刺激它。寻求新奇行为与这种需求相对应。