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惊恐障碍与儿茶酚-O-甲基转移酶的L/L基因型之间的关联。

The association between panic disorder and the L/L genotype of catechol-O-methyltransferase.

作者信息

Woo Jong-Min, Yoon Kyung-Sik, Choi Young-Hee, Oh Kang-Sub, Lee Young-Sik, Yu Bum-Hee

机构信息

Department of Neuropsychiatry, Inje University Seoul Paik Hospital, Seoul, Republic of Korea.

出版信息

J Psychiatr Res. 2004 Jul-Aug;38(4):365-70. doi: 10.1016/j.jpsychires.2004.01.001.

Abstract

To clarify the role of catechol-O-methyltransferase (COMT) polymorphism in panic disorder (PD), we investigated a large group of Korean PD patients (N = 178) and controls (N = 182) using a case-control study. We also assessed the response to paroxetine treatment and other clinical variables in the PD patients. The increase in the COMT(L) allele was not statistically significant in PD (p = 0.104). However, compared with the sum of the other genotypes, the frequency of the L/L genotype was significantly higher in PD (p = 0.042). The odd ratios (ORs) also indicated a significant effect of the homozygosity for the COMT(L) allele on an increased risk for PD (OR=2.38; 95% CI 1.03-5.51). In addition, patients with L/L genotype had higher trait-anxiety levels (p = 0.030) and poorer treatment response to paroxetine than those with other genotypes (p = 0.002). Our results suggest that the COMT L/L genotype is associated with PD and the genetic variant of the COMT enzyme may be related to the clinical severity and treatment response to paroxetine in PD.

摘要

为阐明儿茶酚-O-甲基转移酶(COMT)基因多态性在惊恐障碍(PD)中的作用,我们采用病例对照研究,对一大组韩国PD患者(N = 178)和对照组(N = 182)进行了调查。我们还评估了PD患者对帕罗西汀治疗的反应及其他临床变量。COMT(L)等位基因在PD患者中的增加无统计学意义(p = 0.104)。然而,与其他基因型总和相比,L/L基因型在PD患者中的频率显著更高(p = 0.042)。比值比(OR)也表明,COMT(L)等位基因纯合性对PD风险增加有显著影响(OR = 2.38;95%可信区间1.03 - 5.51)。此外,L/L基因型患者的特质焦虑水平更高(p = 0.030),且对帕罗西汀的治疗反应比其他基因型患者更差(p = 0.002)。我们的结果表明,COMT L/L基因型与PD相关,且COMT酶的基因变异可能与PD的临床严重程度及对帕罗西汀的治疗反应有关。

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