Maron Eduard, Tõru Innar, Must Anne, Tasa Gunnar, Toover Egle, Vasar Veiko, Lang Aavo, Shlik Jakov
Department of Psychiatry, University of Tartu, Raja 31, Tartu 50417, Estonia.
Neurosci Lett. 2007 Jan 16;411(3):180-4. doi: 10.1016/j.neulet.2006.09.060. Epub 2006 Nov 22.
Experimental studies on serotonin (5-HT) availability suggest a role for 5-HT synthesis rate in panicogenesis. Recently, it has been discovered that the tryptophan hydroxylase gene isoform 2 (TPH2), rather than TPH1, is preferentially expressed in the neuronal tissue and, therefore, is primarily responsible for the regulation of brain 5-HT synthesis. In the present case-control genetic association study we investigated whether panic disorder (PD) phenotypes are related to two single nucleotide polymorphisms (SNP) of TPH2, rs1386494 A/G and rs1386483 C/T. The study sample consisted of 213 (163 females and 50 males) PD patients with or without affective comorbidity and 303 (212 females and 91 males) matched healthy control subjects. The allelic and genotypic analyses in the total sample did not demonstrate significant association of PD with the studied SNPs, suggesting that these polymorphisms may not play a robust role in predisposition to PD. However, an association with rs1386494 SNP was observed in the subgroup of female patients with pure PD phenotype, indicating a possible gender-specific effect of TPH2 gene variants in PD.
关于血清素(5-羟色胺,5-HT)可用性的实验研究表明5-HT合成速率在惊恐障碍发病机制中起作用。最近,人们发现色氨酸羟化酶基因同工型2(TPH2)而非TPH1在神经组织中优先表达,因此主要负责调节大脑5-HT的合成。在本病例对照基因关联研究中,我们调查了惊恐障碍(PD)的表型是否与TPH2的两个单核苷酸多态性(SNP),即rs1386494 A/G和rs1386483 C/T相关。研究样本包括213名(163名女性和50名男性)有或无情感共病的PD患者以及303名(212名女性和91名男性)匹配的健康对照者。对总样本的等位基因和基因型分析未显示PD与所研究的SNP之间存在显著关联,这表明这些多态性可能在PD易感性中不发挥重要作用。然而,在具有单纯PD表型的女性患者亚组中观察到与rs1386494 SNP存在关联,表明TPH2基因变异在PD中可能存在性别特异性效应。