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在健康志愿者中使用CCK - 4激发试验对惊恐障碍候选基因进行关联测试。

Association testing of panic disorder candidate genes using CCK-4 challenge in healthy volunteers.

作者信息

Maron Eduard, Tõru Innar, Tasa Gunnar, Must Anne, Toover Egle, Lang Aavo, Vasar Veiko, Shlik Jakov

机构信息

Department of Psychiatry, University of Tartu, Tartu, Estonia.

出版信息

Neurosci Lett. 2008 Dec 3;446(2-3):88-92. doi: 10.1016/j.neulet.2008.09.052.

Abstract

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.

摘要

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。

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