Maron Eduard, Lang Aavo, Tasa Gunnar, Liivlaid Liivi, Tõru Innar, Must Anne, Vasar Veiko, Shlik Jakov
Department of Psychiatry, University of Tartu, Raja, Estonia.
Int J Neuropsychopharmacol. 2005 Jun;8(2):261-6. doi: 10.1017/S1461145704004985. Epub 2005 Jan 26.
Studies suggest that vulnerability to panic attacks and panic disorder (PD) may be related to a deficient serotonin (5-HT) neurotransmission. In the present case-control study we investigated possible associations between PD phenotype and five candidate polymorphisms including 5-HT transporter (5-HTTLPR and VNTR), monoamine oxidase A (MAOA promoter region), tryptophan hydroxylase 1 (TPH1 218A/C) and 5-HT1B receptor (5-HT1BR 861G/C) genes. The study sample consisted of 158 patients with PD and 215 healthy control subjects. The analysis showed higher frequencies of LL genotype (p = 0.016) and L allele variant (p = 0.007) of 5-HTTLPR in the patients. No significant associations were observed between PD and other candidate gene polymorphisms. However, a higher frequency of longer allele genotypes of the MAOA promoter region was observed in female PD patients with agoraphobia than in female controls (p = 0.016). These findings indicate that genetic variants conceivably related to lower 5-HT neurotransmission may be involved in the development of PD.
研究表明,惊恐发作和惊恐障碍(PD)的易感性可能与血清素(5-羟色胺,5-HT)神经传递不足有关。在本病例对照研究中,我们调查了PD表型与五个候选多态性之间的可能关联,这五个候选多态性包括5-羟色胺转运体(5-HTTLPR和VNTR)、单胺氧化酶A(MAOA启动子区域)、色氨酸羟化酶1(TPH1 218A/C)和5-羟色胺1B受体(5-HT1BR 861G/C)基因。研究样本包括158例PD患者和215名健康对照者。分析显示,患者中5-HTTLPR的LL基因型频率较高(p = 0.016)以及L等位基因变异频率较高(p = 0.007)。未观察到PD与其他候选基因多态性之间存在显著关联。然而,与女性对照相比,患有广场恐怖症的女性PD患者中MAOA启动子区域较长等位基因基因型的频率更高(p = 0.016)。这些发现表明,可能与较低5-HT神经传递相关的基因变异可能参与了PD的发病过程。