Huang San-Yuan, Lin Ming-Teng, Shy Mee-Jen, Lin Wei-Wen, Lin Fang-Yi, Lu Ru-Band
Department of Psychiatry, National Defense Medical Center, Tri-Service General Hospital, No. 325, Cheng-Kung Road, Sec. 2, Nei-Hu District, Taipei, 114, Taiwan.
Eur Arch Psychiatry Clin Neurosci. 2008 Sep;258(6):350-6. doi: 10.1007/s00406-008-0803-1. Epub 2008 Apr 24.
Monoamine oxidase A (MAOA) abnormality has been suggested as a crucial factor in the pathogenesis of mood disorder, because MAOA is associated with the metabolism of monoamines such as serotonin and norepinephrine. Various MAOA gene polymorphisms have been investigated for possible associations with bipolar disorder (BD), but the results are controversial. Our goal was to investigate whether MAOA gene polymorphisms, especially the promoter uVNTR polymorphism and the EcoRV polymorphism, are associated either with BD or with different clinical subtypes of BD. A total of 714 Han Chinese subjects in Taiwan (305 controls and 409 BD patients) were recruited for study. All subjects were interviewed with the Chinese Version of the Modified Schedule of Affective Disorders and Schizophrenia-Lifetime; BD was diagnosed according to DSM-IV criteria. Genotyping for MAOA polymorphisms was performed using PCR and restriction fragment length polymorphism. The MAOA promoter polymorphisms uVNTR and EcoRV were not associated with BD or any of its subtypes, in either the frequencies of alleles or genotypes. In multiple logistic regression and haplotype frequency analysis, we confirmed these negative results in both females and males. Our results suggest that MAOA polymorphisms do not play a major role in pathogenesis of BD or its clinical subtypes in Han Chinese.
单胺氧化酶A(MAOA)异常被认为是情绪障碍发病机制中的一个关键因素,因为MAOA与血清素和去甲肾上腺素等单胺类物质的代谢有关。人们已经对各种MAOA基因多态性与双相情感障碍(BD)的可能关联进行了研究,但结果存在争议。我们的目标是研究MAOA基因多态性,尤其是启动子uVNTR多态性和EcoRV多态性,是否与BD或BD的不同临床亚型有关。我们招募了台湾地区总共714名汉族受试者(305名对照者和409名BD患者)进行研究。所有受试者均接受了中文版修订版情感障碍和精神分裂症终身访谈表的访谈;BD根据《精神疾病诊断与统计手册》第四版标准进行诊断。使用聚合酶链反应(PCR)和限制性片段长度多态性进行MAOA多态性的基因分型。MAOA启动子多态性uVNTR和EcoRV在等位基因或基因型频率上均与BD或其任何亚型无关。在多因素逻辑回归和单倍型频率分析中,我们在女性和男性中均证实了这些阴性结果。我们的结果表明,MAOA多态性在汉族人群BD或其临床亚型的发病机制中不发挥主要作用。