Gutiérrez Blanca, Arias Bárbara, Gastó Cristóbal, Catalán Rosa, Papiol Sergi, Pintor Luis, Fañanás Lourdes
Unitat d'Antropologia, Departament de Biologia Animal, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Psychiatr Genet. 2004 Dec;14(4):203-8. doi: 10.1097/00041444-200412000-00007.
Monoamine oxidase A (MAOA) has been suggested to be involved in human behaviour and physiology due to its key role in the metabolism of several different biological amines including the neurotransmitters serotonin, norepinephrin and dopamine.Recently, a 30 bp repeat in the MAOA gene promoter (uMAOA) has been demonstrated to be polymorphic and to affect transcriptional activity. In the context of an association case-control study design, we analysed the uMAOA polymorphism in 389 unrelated patients affected by severe mood disorders (88 bipolar subjects and 301 major depressive individuals) and in 156 controls. No association was found between the uMAOA locus and bipolar disorder or major depression. However, an increase of high-activity uMAOA alleles was found in major depression female patients presenting a seasonal pattern (chi2=3.013, P=0.05) or psychotic symptoms in their episodes (chi2=2.679, P=0.07). In female bipolar disorder patients, long alleles were associated with longest times of admission (F=4.604, P=0.037). A trend for association with seasonal pattern was also defined in this group (data not corrected for multiple testing). Our results suggest that MAOA gene variation may modulate the expression of some clinical aspects of severe mood disorders, especially in females, and support the existence of a genetic and aetiologic heterogeneity underlying the diagnoses of bipolar disorder and major depression.
单胺氧化酶A(MAOA)因其在包括神经递质5-羟色胺、去甲肾上腺素和多巴胺在内的几种不同生物胺代谢中的关键作用,被认为与人类行为和生理机能有关。最近,MAOA基因启动子中的一个30bp重复序列(uMAOA)已被证明具有多态性,并会影响转录活性。在一项关联病例对照研究设计中,我们分析了389名患有严重情绪障碍的无亲缘关系患者(88名双相情感障碍患者和301名重度抑郁个体)以及156名对照者的uMAOA多态性。未发现uMAOA基因座与双相情感障碍或重度抑郁症之间存在关联。然而,在呈现季节性模式的重度抑郁女性患者(χ2=3.013,P=0.05)或发作时有精神病症状的患者(χ2=2.679,P=0.07)中,发现高活性uMAOA等位基因有所增加。在女性双相情感障碍患者中,长等位基因与最长住院时间相关(F=4.604,P=0.037)。在该组中也确定了与季节性模式相关的一种趋势(数据未进行多重检验校正)。我们的结果表明,MAOA基因变异可能会调节严重情绪障碍某些临床特征的表达,尤其是在女性中,并支持双相情感障碍和重度抑郁症诊断背后存在遗传和病因异质性。