Jönsson E G, Dahl M L, Roh H K, Jerling M, Sedvall G C
Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
Psychiatr Genet. 1998 Spring;8(1):25-8. doi: 10.1097/00041444-199800810-00004.
Debrisoquine 4-hydroxylase (CYP2D6) is a cytochrome P450 enzyme involved in the metabolism of most neuroleptics, which are the drugs of choice for the treatment of psychotic symptoms. CYP2D6 in the brain was suggested to be functionally similar to the dopamine transporter, thus possibly influencing a neurotransmitter system involved in schizophrenia. Swedish schizophrenic patients (n = 124) and control individuals (n = 85) were investigated for two CYP2D6 polymorphisms, responsible for approximately 90% of mutations leading to poor debrisoquine metabolism. No significant CYP2D6 allele or genotype difference was found between schizophrenic patients and control individuals. Taken together with previous results, no major effect appears to be caused by the CYP2D6 gene on schizophrenia.
异喹胍4-羟化酶(CYP2D6)是一种细胞色素P450酶,参与大多数抗精神病药物的代谢,而抗精神病药物是治疗精神病症状的首选药物。大脑中的CYP2D6被认为在功能上与多巴胺转运体相似,因此可能影响与精神分裂症有关的神经递质系统。对瑞典的精神分裂症患者(n = 124)和对照个体(n = 85)进行了两种CYP2D6多态性的研究,这两种多态性约占导致异喹胍代谢不良的突变的90%。在精神分裂症患者和对照个体之间未发现显著的CYP2D6等位基因或基因型差异。结合先前的结果,CYP2D6基因似乎对精神分裂症没有重大影响。