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.

译文

单胺氧化酶A (MAOA) 异常已被认为是情绪障碍发病机理中的关键因素,因为MAOA与单胺 (例如5-羟色胺和去甲肾上腺素) 的代谢有关。已经研究了各种MAOA基因多态性与双相情感障碍 (BD) 的可能关联,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的不同临床亚型相关。总共招募了714名台湾汉族受试者 (305名对照和409名BD患者) 进行研究。对所有受试者进行了中文版的《情感障碍和精神分裂症-终生时间表》的访谈; 根据dsm-iv标准诊断BD。使用PCR和限制性片段长度多态性对MAOA多态性进行基因分型。MAOA启动子多态性uVNTR和EcoRV在等位基因或基因型的频率上均与BD或其任何亚型无关。在多元逻辑回归和单倍型频率分析中,我们证实了女性和男性的这些阴性结果。我们的结果表明,MAOA多态性在汉族BD或其临床亚型的发病机理中不起作用。

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