Rao P A, Pickar D, Gejman P V, Ram A, Gershon E S, Gelernter J
Department of Psychiatry, West Haven, Conn Veterans Affairs Medical Center.
Arch Gen Psychiatry. 1994 Nov;51(11):912-7. doi: 10.1001/archpsyc.1994.03950110072009.
To test the hypothesis that interindividual differences in response to clozapine therapy might be attributable to the D4 dopamine receptor (DRD4) alleles they carry. Different alleles of the D4 dopamine receptor, coded by the DRD4 gene, differ in the affinity with which they bind the atypical antipsychotic drug clozapine in vitro. This may have physiologic implications. Clinical response to clozapine therapy varies among patients. The observation that, in vitro, clozapine binds the protein products of different DRD4 alleles with differing affinity characteristics suggested this hypothesis.
The region of the DRD4 gene that encodes the putative third cytoplasmic loop of the D4 receptor contains a 48-base pair sequence repeated a variable number of times. With use of polymerase chain reaction amplification, we assessed this variable number of tandem repeats polymorphism in a series of schizophrenic and schizoaffective subjects who had been treated with clozapine, and related genotype with treatment response, to test the hypothesis that DRD4 alleles lead to varying response to clozapine.
Allelic variation at the DRD4 locus does not predict clinical response to clozapine relative to either fluphenazine hydrochloride or placebo in subjects with treatment-refractory schizophrenia or schizoaffective disorder.
DRD4 alleles do not predict therapeutic response to clozapine in schizophrenic and schizoaffective patients. There are implications from these data for the pathophysiology of schizophrenia and the mechanism of clozapine's therapeutic effect are discussed.
检验以下假设,即对氯氮平治疗反应的个体差异可能归因于个体所携带的D4多巴胺受体(DRD4)等位基因。由DRD4基因编码的D4多巴胺受体的不同等位基因,在体外与非典型抗精神病药物氯氮平结合的亲和力方面存在差异。这可能具有生理学意义。患者对氯氮平治疗的临床反应各不相同。体外实验观察到氯氮平与不同DRD4等位基因的蛋白质产物结合时具有不同的亲和力特征,由此提出了这一假设。
DRD4基因中编码D4受体假定的第三个胞质环的区域包含一段48个碱基对的序列,其重复次数可变。我们利用聚合酶链反应扩增技术,在一系列接受氯氮平治疗的精神分裂症和分裂情感性障碍患者中评估了这种可变数量的串联重复多态性,并将基因型与治疗反应相关联,以检验DRD4等位基因导致对氯氮平反应不同的假设。
在难治性精神分裂症或分裂情感性障碍患者中,相对于盐酸氟奋乃静或安慰剂,DRD4基因座的等位基因变异并不能预测对氯氮平的临床反应。
DRD4等位基因不能预测精神分裂症和分裂情感性障碍患者对氯氮平的治疗反应。本文讨论了这些数据对精神分裂症病理生理学的意义以及氯氮平治疗作用的机制。