Suzuki A, Kondo T, Mihara K, Yasui-Furukori N, Otani K, Furukori H, Kaneko S, Inoue Y
Department of Neuropsychiatry, Hirosaki University School of Medicine, Japan.
Eur Arch Psychiatry Clin Neurosci. 2001;251(2):57-9. doi: 10.1007/s004060170053.
The relationship between TaqI A dopamine D2 receptor (DRD2) polymorphism and therapeutic response to bromperidol, a selective dopamine antagonist, was investigated in 30 acutely exacerbated schizophrenic inpatients. Patients were treated with bromperidol 6-18 mg/day for 3 weeks. Clinical symptoms were evaluated by the Brief Psychiatric Rating Scale (BPRS) before and 3 weeks after the treatment. The TaqI A genotypes were determined with the PCR method. There was no significant difference in the percentage improvement of total BPRS or 5-subgrouped symptoms (positive, negative, anxiety-depression, excitement and cognitive symptoms) after the 3-week treatment between the patients with A1 alleles (n=18) and those with no A1 allele (n=12). Although the present study is preliminary, it is suggested that the TaqI A DRD2 polymorphism is not associated with therapeutic response to bromperidol in schizophrenic patients.
在30例急性加重期的精神分裂症住院患者中,研究了TaqI A多巴胺D2受体(DRD2)基因多态性与选择性多巴胺拮抗剂溴哌利多治疗反应之间的关系。患者接受溴哌利多6 - 18毫克/天治疗,为期3周。治疗前及治疗3周后,采用简明精神病评定量表(BPRS)评估临床症状。用聚合酶链反应(PCR)方法确定TaqI A基因型。在有A1等位基因的患者(n = 18)和无A1等位基因的患者(n = 12)中,经过3周治疗后,BPRS总分或5个分组症状(阳性、阴性、焦虑抑郁、兴奋和认知症状)的改善百分比没有显著差异。尽管本研究是初步的,但提示TaqI A DRD2基因多态性与精神分裂症患者对溴哌利多的治疗反应无关。