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血清素相关基因多态性与惊恐障碍之间的关联。

Associations between serotonin-related gene polymorphisms and panic disorder.

作者信息

Maron Eduard, Lang Aavo, Tasa Gunnar, Liivlaid Liivi, Tõru Innar, Must Anne, Vasar Veiko, Shlik Jakov

机构信息

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

出版信息

Int J Neuropsychopharmacol. 2005 Jun;8(2):261-6. doi: 10.1017/S1461145704004985. Epub 2005 Jan 26.

Abstract

Studies suggest that vulnerability to panic attacks and panic disorder (PD) may be related to a deficient serotonin (5-HT) neurotransmission. In the present case-control study we investigated possible associations between PD phenotype and five candidate polymorphisms including 5-HT transporter (5-HTTLPR and VNTR), monoamine oxidase A (MAOA promoter region), tryptophan hydroxylase 1 (TPH1 218A/C) and 5-HT1B receptor (5-HT1BR 861G/C) genes. The study sample consisted of 158 patients with PD and 215 healthy control subjects. The analysis showed higher frequencies of LL genotype (p = 0.016) and L allele variant (p = 0.007) of 5-HTTLPR in the patients. No significant associations were observed between PD and other candidate gene polymorphisms. However, a higher frequency of longer allele genotypes of the MAOA promoter region was observed in female PD patients with agoraphobia than in female controls (p = 0.016). These findings indicate that genetic variants conceivably related to lower 5-HT neurotransmission may be involved in the development of PD.

摘要

研究表明,惊恐发作和惊恐障碍(PD)的易感性可能与血清素(5-羟色胺,5-HT)神经传递不足有关。在本病例对照研究中,我们调查了PD表型与五个候选多态性之间的可能关联,这五个候选多态性包括5-羟色胺转运体(5-HTTLPR和VNTR)、单胺氧化酶A(MAOA启动子区域)、色氨酸羟化酶1(TPH1 218A/C)和5-羟色胺1B受体(5-HT1BR 861G/C)基因。研究样本包括158例PD患者和215名健康对照者。分析显示,患者中5-HTTLPR的LL基因型频率较高(p = 0.016)以及L等位基因变异频率较高(p = 0.007)。未观察到PD与其他候选基因多态性之间存在显著关联。然而,与女性对照相比,患有广场恐怖症的女性PD患者中MAOA启动子区域较长等位基因基因型的频率更高(p = 0.016)。这些发现表明,可能与较低5-HT神经传递相关的基因变异可能参与了PD的发病过程。

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