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惊恐障碍中新型脑特异性色氨酸羟化酶-2基因

The novel brain-specific tryptophan hydroxylase-2 gene in panic disorder.

作者信息

Mössner Rainald, Freitag Christine M, Gutknecht Lise, Reif Andreas, Tauber Ralf, Franke Petra, Fritze Jürgen, Wagner Gerd, Peikert Gregor, Wenda Berit, Sand Philipp, Rietschel Marcella, Garritsen Henk, Jacob Christian, Lesch K Peter, Deckert Jürgen

机构信息

Department of Psychiatry and Psychotherapy, University of Würzburg, Würzburg, Germany.

出版信息

J Psychopharmacol. 2006 Jul;20(4):547-52. doi: 10.1177/0269881106059704. Epub 2006 Jan 9.

Abstract

Panic disorder is a common psychiatric disorder characterized by recurrent anxiety attacks and anticipatory anxiety. Due to the severity of the symptoms of the panic attacks and the frequent additional occurrence of agoraphobia, panic disorder is an often debilitating disease. Elevation of central serotonin levels by drugs such as clomipramine represents one of the most effective treatment options for panic disorder. This points to an important role of dysregulation of the serotonergic system in the genetic etiology of panic disorder. The novel brain-specific 5-HT synthesizing enzyme, tryptophan hydroxylase-2 (TPH2), which represents the rate-limiting enzyme of 5-HT production in the brain, may therefore be of particular importance in panic disorder. We focused on the putative transcriptional control region of TPH2 and identified two novel common single nucleotide polymorphisms (SNPs) of TPH2 in and close to this region. Moreover, a recently described loss-of-function mutation of TPH2 which results in an 80% reduction of serotonin production, was assessed. In an analysis of the putative transcriptional control region SNPs in a sample of panic disorder patients and controls no association of the disorder with the TPH2 SNPs or haplotypes was found. Moreover, the loss-of-function R441H mutation of TPH2 was not present in the panic disorder patients. The results of this first study of TPH2 in panic disorder argue against an importance of allelic variation of TPH2 in the pathogenesis of panic disorder with or without agoraphobia.

摘要

惊恐障碍是一种常见的精神障碍,其特征为反复出现焦虑发作和预期性焦虑。由于惊恐发作症状的严重性以及广场恐惧症的频繁并发,惊恐障碍常常是一种使人衰弱的疾病。使用氯米帕明等药物提高中枢血清素水平是治疗惊恐障碍最有效的选择之一。这表明血清素能系统失调在惊恐障碍的遗传病因中起重要作用。新型脑特异性5-羟色胺合成酶色氨酸羟化酶-2(TPH2)是大脑中5-羟色胺生成的限速酶,因此在惊恐障碍中可能特别重要。我们聚焦于TPH2的假定转录控制区域,并在该区域及其附近鉴定出TPH2的两个新型常见单核苷酸多态性(SNP)。此外,对最近描述的导致血清素生成减少80%的TPH2功能丧失突变进行了评估。在对惊恐障碍患者和对照组样本中的假定转录控制区域SNP进行分析时,未发现该障碍与TPH2 SNP或单倍型之间存在关联。此外,惊恐障碍患者中不存在TPH2的功能丧失性R441H突变。这项关于TPH2在惊恐障碍中的首次研究结果表明,无论有无广场恐惧症,TPH2的等位基因变异在惊恐障碍发病机制中并不重要。

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