Department of Psychiatry, College of Medicine, Korea University, Seoul, Republic of Korea.
Psychiatry Res. 2010 Jan 30;175(1-2):63-6. doi: 10.1016/j.psychres.2008.09.011. Epub 2009 Dec 11.
Catechol-O-methyltransferase (COMT) is a candidate gene for the pathogenesis of some psychiatric disorders. The aim of this study is to examine the role of the COMT gene Val158Met polymorphism on the clinical aspects of bipolar disorder including symptomatology and therapeutic response. This study comprised 144 unrelated manic patients who met strict DSM-IV criteria for bipolar I disorder and 157 healthy unrelated controls. All subjects were of Korean ethnicity. To evaluate the clinical symptoms, we used the Young Mania Rating Scale at baseline and 6 weeks after treatment. No statistically significant difference in genotype distribution was found between manic patients and normal controls. There was also no significant difference in symptomatology among the genotypes in manic patients. In therapeutic response, however, patients with the Met/Met genotype were significantly more frequent in the non-responder than in the responder group. Our results suggest that the COMT gene polymorphism in the therapeutic response to mood stabilizers in manic patients. Further studies with a larger number of subjects and well-controlled design will be required to better understand the role of the COMT gene polymorphism on the therapeutic response to mood stabilizer in manic patients.
儿茶酚-O-甲基转移酶(COMT)是某些精神疾病发病机制的候选基因。本研究旨在探讨 COMT 基因 Val158Met 多态性对双相障碍临床方面的作用,包括症状和治疗反应。本研究包括 144 例无亲缘关系的躁狂患者,均符合 DSM-IV 双相 I 型障碍的严格标准,以及 157 例无亲缘关系的健康对照。所有受试者均为韩国人。为了评估临床症状,我们在基线和治疗 6 周后使用 Young 躁狂评定量表进行评估。躁狂患者和正常对照组之间的基因型分布无统计学差异。在躁狂患者中,不同基因型之间的症状也没有显著差异。然而,在治疗反应方面,Met/Met 基因型的患者在无反应者中比在反应者中更为常见。我们的结果表明,COMT 基因多态性与躁狂患者对心境稳定剂的治疗反应有关。需要进一步进行更多样本和良好对照设计的研究,以更好地了解 COMT 基因多态性对躁狂患者心境稳定剂治疗反应的作用。