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惊恐障碍中5-羟色胺1A受体1019C/G(rs6295)启动子及儿茶酚-O-甲基转移酶的基因多态性

Genetic Polymorphism of 1019C/G (rs6295) Promoter of Serotonin 1A Receptor and Catechol-O-Methyltransferase in Panic Disorder.

作者信息

Watanabe Takashi, Ishiguro Shin, Aoki Akiko, Ueda Mikito, Hayashi Yuki, Akiyama Kazufumi, Kato Kazuko, Shimoda Kazutaka

机构信息

Department of Psychiatry, Dokkyo Medical University School of Medicine, Shimotsuga, Tochigi, Japan.

Biological Psychiatry and Neuroscience, Dokkyo Medical University School of Medicine, Shimotsuga, Tochigi, Japan.

出版信息

Psychiatry Investig. 2017 Jan;14(1):86-92. doi: 10.4306/pi.2017.14.1.86. Epub 2016 Dec 29.

Abstract

OBJECTIVE

Family and twin studies have suggested genetic liability for panic disorder (PD) and therefore we sought to determine the role of noradrenergic and serotonergic candidate genes for susceptibility for PD in a Japanese population.

METHODS

In this age- and gender-matched case-control study involving 119 PD patients and 119 healthy controls, we examined the genotype distributions and allele frequencies of the serotonin transporter gene linked polymorphic region (5-HTTLPR), -1019C/G (rs6295) promoter polymorphism of the serotonin receptor 1A (5-HT1A), and catechol-O-methyltransferase (COMT) gene polymorphism (rs4680) and their association with PD.

RESULTS

No significant differences were evident in the allele frequencies or genotype distributions of the COMT (rs4680), 5-HTTLPR polymorphisms or the -1019C/G (rs6295) promoter polymorphism of 5-HT1A between PD patients and controls. Although there were no significant associations of these polymorphisms with in subgroups of PD patients differentiated by gender or in subgroup comorbid with agoraphobia (AP), significant difference was observed in genotype distributions of the -1019C/G (rs6295) promoter polymorphism of 5-HT1A between PD patients without AP and controls (p=0.047).

CONCLUSION

In this association study, the 1019C/G (rs6295) promoter polymorphism of the 5-HT1A receptor G/G genotype was associated with PD without AP in a Japanese population.

摘要

目的

家族和双生子研究提示惊恐障碍(PD)存在遗传易感性,因此我们试图确定去甲肾上腺素能和5-羟色胺能候选基因在日本人群PD易感性中的作用。

方法

在这项年龄和性别匹配的病例对照研究中,纳入119例PD患者和119例健康对照,我们检测了5-羟色胺转运体基因连锁多态性区域(5-HTTLPR)、5-羟色胺受体1A(5-HT1A)的-1019C/G(rs6295)启动子多态性、儿茶酚-O-甲基转移酶(COMT)基因多态性(rs4680)的基因型分布和等位基因频率,以及它们与PD的相关性。

结果

PD患者和对照组之间,COMT(rs4680)、5-HTTLPR多态性或5-HT1A的-1019C/G(rs6295)启动子多态性的等位基因频率或基因型分布无明显差异。虽然这些多态性与按性别区分的PD患者亚组或与广场恐怖症(AP)共病的亚组之间无显著相关性,但在无AP的PD患者和对照组之间,观察到5-HT1A的-1019C/G(rs6295)启动子多态性的基因型分布有显著差异(p=0.047)。

结论

在这项关联研究中,5-HT1A受体的1019C/G(rs6295)启动子多态性的G/G基因型与日本人群中无AP的PD相关。

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Serotonin-2A receptor and catechol-O-methyltransferase polymorphisms in panic disorder.5-羟色胺 2A 受体和儿茶酚-O-甲基转移酶多态性与惊恐障碍。
Prog Neuropsychopharmacol Biol Psychiatry. 2012 Jan 10;36(1):5-10. doi: 10.1016/j.pnpbp.2011.10.010. Epub 2011 Oct 19.

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