Maron Eduard, Tõru Innar, Tasa Gunnar, Must Anne, Toover Egle, Lang Aavo, Vasar Veiko, Shlik Jakov
Department of Psychiatry, University of Tartu, Tartu, Estonia.
Neurosci Lett. 2008 Dec 3;446(2-3):88-92. doi: 10.1016/j.neulet.2008.09.052.
Despite continuing efforts to determine genetic vulnerability to panic disorder (PD), the studies of candidate genes in this disorder have produced inconsistent or negative, results. Laboratory panic induction may have a potential in testing genetic substrate of PD. In this study we aimed to explore the effects of several genetic polymorphisms previously implicated in PD on the susceptibility to cholecystokinin-tetrapeptide (CCK-4) challenge in healthy subjects. The study sample consisted of 110 healthy volunteers (47 males and 63 females, mean age 22.2 +/- 5.2) who participated in CCK-4 challenge test. Nine gene-candidates, including 5-HTTLPR, MAO-A VNTR, TPH2 rs1386494, 5-HTR1A -1019C-G, 5-HTR2A 102T-C, CCKR1 246G-A, CCKR2 -215C-A, DRD1 -94G-A and COMT Val158Met, were selected for genotyping based on previous positive findings from genetic association studies in PD. After CCK-4 challenge, 39 (35.5%) subjects experienced a panic attack, while 71 subjects were defined as non-panickers. We detected significant differences for both genotypic and allelic frequencies of 1386494A/G polymorphism in TPH2 gene between panic and non-panic groups with the frequencies of G/G genotype and G allele significantly higher in panickers. None of the other candidate loci were significantly associated with CCK-4-induced panic attacks in healthy subjects. In line with our previous association study in patients with PD, we detected a possible association between TPH2 rs1386494 polymorphism and susceptibility to panic attacks. Other polymorphisms previously associated with PD were unrelated to CCK-4-induced panic attacks, probably due to the differences between complex nature of PD and laboratory panic model.
尽管人们不断努力确定惊恐障碍(PD)的遗传易感性,但该疾病候选基因的研究结果却不一致或呈阴性。实验室诱发惊恐可能在测试PD的遗传基础方面具有潜力。在本研究中,我们旨在探讨先前与PD相关的几种基因多态性对健康受试者胆囊收缩素四肽(CCK-4)激发试验易感性的影响。研究样本包括110名健康志愿者(47名男性和63名女性,平均年龄22.2±5.2岁),他们参与了CCK-4激发试验。基于先前PD遗传关联研究的阳性结果,选择了9个候选基因进行基因分型,包括5-HTTLPR、MAO-A VNTR、TPH2 rs1386494、5-HTR1A -1019C-G、5-HTR2A 102T-C、CCKR1 246G-A、CCKR2 -215C-A、DRD1 -94G-A和COMT Val158Met。CCK-4激发试验后,39名(35.5%)受试者经历了惊恐发作,而71名受试者被定义为非惊恐者。我们检测到惊恐组和非惊恐组之间TPH2基因1386494A/G多态性的基因型和等位基因频率存在显著差异,惊恐者中G/G基因型和G等位基因的频率显著更高。其他候选基因座均与健康受试者中CCK-4诱发的惊恐发作无显著关联。与我们先前对PD患者的关联研究一致,我们检测到TPH2 rs1386494多态性与惊恐发作易感性之间可能存在关联。先前与PD相关的其他多态性与CCK-4诱发的惊恐发作无关,这可能是由于PD的复杂性质与实验室惊恐模型之间存在差异。