Hori H, Ohmori O, Shinkai T, Kojima H, Nakamura J
Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Am J Med Genet. 2001 Dec 8;105(8):774-8. doi: 10.1002/ajmg.10045.
The dopamine D2 receptor (DRD2) gene is considered one of the candidate genes contributing to the development of tardive dyskinesia (TD). In the present study, we investigated the genetic association between three functional polymorphisms (Ser311Cys, -141C Ins/Del and TaqI A) in the DRD2 gene and TD (200 patients with schizophrenia: 44 with TD and 156 without TD). No significant difference in the allelic and genotypic distribution between patients with TD and those without TD was observed. However, we found a slightly significant association between the -141C Ins/Del polymorphism and the total Abnormal Involuntary Movement Scale (AIMS) score (P = 0.037). The significant association between the -141C Ins/Del polymorphism and the total AIMS score did not remain after the regression analysis was taken into account (P = 0.14). Our results suggest that that three functional polymorphisms in DRD2 may not play a major role in the occurrence of TD.
多巴胺D2受体(DRD2)基因被认为是导致迟发性运动障碍(TD)发生的候选基因之一。在本研究中,我们调查了DRD2基因中三个功能性多态性(Ser311Cys、-141C Ins/Del和TaqI A)与TD之间的遗传关联(200例精神分裂症患者:44例患有TD,156例未患TD)。未观察到TD患者与未患TD患者之间等位基因和基因型分布的显著差异。然而,我们发现-141C Ins/Del多态性与异常不自主运动量表(AIMS)总分之间存在轻微显著关联(P = 0.037)。在考虑回归分析后,-141C Ins/Del多态性与AIMS总分之间的显著关联不再存在(P = 0.14)。我们的结果表明,DRD2基因中的三个功能性多态性可能在TD的发生中不发挥主要作用。