Mihara K, Suzuki A, Kondo T, Nagashima U, Ono S, Otani K, Kaneko S
Department of Neuropsychiatry, Hirosaki University School of Medicine, Japan.
Am J Med Genet. 2000 Jun 12;96(3):422-4. doi: 10.1002/1096-8628(20000612)96:3<422::aid-ajmg35>3.0.co;2-5.
The relationship between Taq1 A polymorphism of dopamine D(2) receptor (DRD(2)) gene and extrapyramidal adverse effects of bromperidol and nemonapride, which are both antipsychotic drugs with selective and potent DRD(2) antagonistic property, was investigated in Japanese schizophrenic inpatients. Twenty-seven patients were treated with bromperidol at 6 or 12 or 18 mg/day, while 25 patients were treated with nemonapride at 18 mg/day. The duration of treatment was 3 weeks. The A1 and A2 alleles were determined by PCR. The extrapyramidal adverse effects were assessed by the Udvalg for Kliniske Unders¿ogelser side effects rating scale. Six patients were homozygous for the A1 allele, 27 were heterozygous for the A1 and A2 alleles, and 19 were homozygous for the A2 allele. There were no significant differences in the incidences or severity of extrapyramidal adverse effects between the patients with one or two A1 alleles and those with no A1 allele. The present study suggests that Taq1 A polymorphism is not related to the development of extrapyramidal adverse effects during acute phase of bromperidol and nemonapride treatments.
在日本精神分裂症住院患者中,研究了多巴胺D₂受体(DRD₂)基因的Taq1 A多态性与溴哌利多和尼莫必利锥体外系不良反应之间的关系。这两种药物均为具有选择性和强效DRD₂拮抗特性的抗精神病药物。27例患者接受溴哌利多治疗,剂量为6或12或18mg/天,25例患者接受尼莫必利治疗,剂量为18mg/天。治疗持续时间为3周。通过聚合酶链反应(PCR)确定A1和A2等位基因。采用临床研究不良反应评定量表(Udvalg for Kliniske Undersøgelser side effects rating scale)评估锥体外系不良反应。6例患者为A1等位基因纯合子,27例为A1和A2等位基因杂合子,19例为A2等位基因纯合子。有一个或两个A1等位基因的患者与无A1等位基因的患者相比,锥体外系不良反应的发生率和严重程度无显著差异。本研究表明,在溴哌利多和尼莫必利治疗的急性期,Taq1 A多态性与锥体外系不良反应的发生无关。