Dikeos D G, Papadimitriou G N, Avramopoulos D, Karadima G, Daskalopoulou E G, Souery D, Mendlewicz J, Vassilopoulos D, Stefanis C N
Department of Psychiatry, Eginition Hospital, Athens University Medical School, Greece.
Psychiatr Genet. 1999 Dec;9(4):189-95. doi: 10.1097/00041444-199912000-00005.
Dopamine neurotransmission has been implicated in the pathophysiology of schizophrenia and, more recently, affective disorders. Among the dopamine receptors, D3 can be considered as particularly related to affective disorders due to its neuroanatomical localization in the limbic region of the brain and its relation to the serotoninergic activity of the CNS. The possible involvement of dopamine receptor D3 in unipolar (UP) major depression was investigated by a genetic association study of the D3 receptor gene locus (DRD3) on 36 UP patients and 38 ethnically matched controls. An allelic association of DRD3 (Bal I polymorphism) and UP illness was observed, with the Gly-9 allele (allele '2', 206/98 base-pairs long) being more frequent in patients than in controls (49% vs 29%, P < 0.02). The genotypes containing this allele (1-2 and 2-2) were found in 75% of patients vs 50% of controls (P < 0.03, odds ratio = 3.00, 95% CI = 1.12-8.05). The effect of the genotype remained significant (P < 0.02) after sex and family history were controlled by a multiple linear regression analysis. These results further support the hypothesis that dopaminergic mechanisms may be implicated in the pathogenesis of affective disorder. More specifically, the '2' allele of the dopamine receptor D3 gene seems to be associated with unipolar depression and can be considered as a 'phenotypic modifier' for major psychiatric disorders.
多巴胺神经传递已被认为与精神分裂症的病理生理学有关,最近还与情感障碍有关。在多巴胺受体中,D3受体因其在大脑边缘区域的神经解剖定位以及与中枢神经系统5-羟色胺能活性的关系,可被认为与情感障碍特别相关。通过对36名单相(UP)重度抑郁症患者和38名种族匹配的对照进行D3受体基因位点(DRD3)的基因关联研究,调查了多巴胺受体D3在单相(UP)重度抑郁症中的可能作用。观察到DRD3(Bal I多态性)与UP疾病之间存在等位基因关联,患者中Gly-9等位基因(等位基因“2”,长206/98个碱基对)的频率高于对照组(49%对29%,P<0.02)。在75%的患者中发现含有该等位基因的基因型(1-2和2-2),而对照组中为50%(P<0.03,优势比=3.00,95%CI=1.12-8.05)。在通过多元线性回归分析控制性别和家族史后,基因型的影响仍然显著(P<0.02)。这些结果进一步支持了多巴胺能机制可能参与情感障碍发病机制的假说。更具体地说,多巴胺受体D3基因的“2”等位基因似乎与单相抑郁症有关,可被视为主要精神疾病的“表型修饰因子”。