Department of Psychiatry, University of Muenster, Albert-Schweitzer-Strasse 11, 48149 Muenster, Germany.
J Psychiatr Res. 2010 Oct;44(14):930-7. doi: 10.1016/j.jpsychires.2010.02.006. Epub 2010 Mar 23.
Adenosine A(2A) receptors are suggested to play an important role in different brain circuits and pathways involved in anxiety reactions. A variant within the corresponding ADORA2A gene (rs5751876) increased the risk for panic disorder (PD), for elevated anxiety during challenge tests in healthy probands and for anxiety-related arousal in blood-injury phobia. These multiple effects may mirror a more general effect of the SNP on basic personality traits. In the present study we therefore aimed to replicate the original finding in a large PD sample and extend it by investigating an additional proband sample characterized for different anxiety-related personality scores. In addition, as rs5751876 is assumed not to be the disease variant itself but to be in linkage disequilibrium (LD) with the true functional polymorphism other SNPs of potentially functional relevance were identified by re-sequencing the whole gene including several newly identified regions of putative regulatory potential and analysed for their impact on PD and anxious personality. We were indeed able to replicate rs5751876 as risk factor for PD, particularly PD with agoraphobia. Rs5751876 and several other variants in high LD (rs5751862, rs2298383 and rs3761422) as well as the corresponding haplotypes were also associated with different anxiety-related personality scores (Bonferroni corrected P(all) < 0.05). Of these variants, rs2298383 shows functional potential based on in silico analyses and might therefore represent the true underlying causal variant. Our data provide further support for an important role of ADORA2A variants in the pathogenesis of anxiety disorders and anxious personality reflecting their potential as basic susceptibility factors.
腺苷 A(2A) 受体被认为在不同的脑回路和参与焦虑反应的途径中发挥重要作用。相应的 ADORA2A 基因(rs5751876)中的一个变体增加了恐慌障碍 (PD) 的风险,增加了健康个体在挑战测试中焦虑的风险,以及在血液损伤恐惧症中与焦虑相关的唤醒。这些多重效应可能反映了 SNP 对基本人格特质的更普遍影响。在本研究中,我们旨在在一个大型 PD 样本中复制原始发现,并通过研究具有不同与焦虑相关的人格评分的额外个体样本来扩展它。此外,由于 rs5751876 被认为不是疾病变体本身,而是与真正的功能多态性处于连锁不平衡 (LD) 中,因此通过重新测序整个基因,包括几个新鉴定的潜在调节潜力区域,鉴定出具有潜在功能相关性的其他 SNP,并分析它们对 PD 和焦虑人格的影响。我们确实能够复制 rs5751876 作为 PD 的风险因素,特别是伴有广场恐怖症的 PD。rs5751876 和几个处于高度 LD(rs5751862、rs2298383 和 rs3761422)的其他变体以及相应的单倍型也与不同的与焦虑相关的人格评分相关(经 Bonferroni 校正的 P(all) < 0.05)。在这些变体中,rs2298383 基于计算机分析显示出功能潜力,因此可能代表真正的潜在因果变体。我们的数据为 ADORA2A 变体在焦虑障碍和焦虑人格发病机制中的重要作用提供了进一步的支持,反映了它们作为基本易感因素的潜力。