“…This polymorphism is functional in that 3.5R or 4R transcribed 2-10 times more efficiently than those with 2, 3, or 5R (Sabol et al, 1998). Although there are several negative association studies between MAOA-uVNTR gene polymorphism and psychiatric phenotype (Furlong et al, 1999;Yoshida et al, 2002b;Kunugi et al, 1999;Syagailo et al, 2001;Garpenstrand et al, 2002) including an alcoholism study in Han Chinese males (Lu et al, 2002), previous reports demonstrated that this polymorphism may be associated with monoamine metabolite concentrations in the CSF of healthy volunteers (Jonsson et al, 2000) as well as psychiatric diseases such as panic disorder (Deckert et al, 1999), obsessive-compulsive disorder (Camarena et al, 1998), bipolar disorder (Preisig et al, 2000), Alzheimer's disease (Takehashi et al, 2002), and schizophrenia (Jonsson et al, 2003). Considering the possible role of MAOA in the pathogenesis and therapeutic mechanisms, in this study, we investigated the possible association of the MAOA-uVNTR polymorphism with MDD and its antidepressant therapeutic response.…”