Department of Psychiatry, Korea University School of Medicine, Seoul, Korea.
Psychiatry Investig. 2012 Jun;9(2):191-4. doi: 10.4306/pi.2012.9.2.191. Epub 2012 May 22.
Tardive dyskinesia (TD) is a hyperkinetic movement disorder associated with the prolonged use of antipsychotic drugs. Since prostate apoptosis response 4 (Par-4) is a key ligand of the dopamine D2 receptor, the Par-4 gene (PAWR) is a good candidate gene to study in the context of TD susceptibility. We examined the association between PAWR gene polymorphisms and TD. Three single nucleotide polymorphisms of PAWR were selected for the analysis: rs7979987, rs4842318, and rs17005769. Two hundred and eighty unrelated Korean schizophrenic patients participated in this study (105 TD and 175 non-TD patients). Genotype/allele-wise and haplotype-wise analyses were performed. There were no significant differences in genotype and allele frequencies between the two groups. Haplotype analysis also did not reveal a difference between the two groups. Within the limitations imposed by the size of the clinical sample, these findings suggest that PAWR gene variants do not significantly contribute to an increased risk of TD.
迟发性运动障碍(TD)是一种与抗精神病药物长期使用相关的多动障碍。由于前列腺凋亡反应蛋白 4(Par-4)是多巴胺 D2 受体的关键配体,因此 Par-4 基因(PAWR)是研究 TD 易感性的一个很好的候选基因。我们研究了 PAWR 基因多态性与 TD 之间的关系。选择了 PAWR 的三个单核苷酸多态性进行分析:rs7979987、rs4842318 和 rs17005769。280 名无关的韩国精神分裂症患者参与了这项研究(105 名 TD 患者和 175 名非 TD 患者)。进行了基因型/等位基因分析和单倍型分析。两组间的基因型和等位基因频率无显著差异。单倍型分析也未显示两组间存在差异。在临床样本大小所限的范围内,这些发现表明 PAWR 基因变异并不显著增加 TD 的风险。