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慢性精神分裂症患者中多巴胺能和血清素能基因与迟发性运动障碍的关联。

Association of dopaminergic and serotonergic genes with tardive dyskinesia in patients with chronic schizophrenia.

作者信息

Segman R H, Goltser T, Heresco-Levy U, Finkel B, Shalem R, Schlafman M, Yakir A, Greenberg D, Strous R, Lerner A, Shelevoy A, Lerer B

机构信息

Biological Psychiatry Laboratory, Department of Psychiatry, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

出版信息

Pharmacogenomics J. 2003;3(5):277-83. doi: 10.1038/sj.tpj.6500194.

Abstract

Tardive dyskinesia (TD) is a long-term adverse effect of antipsychotic drugs that are dopamine D2 receptor blockers. Serotonin receptor antagonism has been proposed as a common mechanism contributing to the low extrapyramidal side effect profile of atypical antipsychotic drugs. We evaluated candidate dopamine and serotonin genes for association with drug-induced TD. We examined three polymorphisms in the dopamine D2 receptor gene (DRD2), two sites in the 3' region of the dopamine transporter (DAT) gene, two sites in the promoter and coding region of the dopamine D4 (DRD4) receptor gene, as well as polymorphic sites in the serotonin 6 receptor gene, the serotonin transporter gene and the tryptophan hydroxylase gene, for association with TD susceptibility. Schizophrenic patients with (n=59) and without TD (n=63), matched for antipsychotic drug exposure and other relevant variables, were studied. No significant associations were found. Within the limitations imposed by the size of the clinical sample, these findings suggest that the above polymorphic loci do not contribute significantly to risk for TD. Further examination of loci that yielded positive results at a trend level and investigation of other candidate genetic loci coding for antipsychotic drug targets is warranted.

摘要

迟发性运动障碍(TD)是抗精神病药物的一种长期不良反应,这些抗精神病药物是多巴胺D2受体阻滞剂。5-羟色胺受体拮抗作用被认为是导致非典型抗精神病药物锥体外系副作用较低的一种常见机制。我们评估了与药物诱导的TD相关的候选多巴胺和5-羟色胺基因。我们检测了多巴胺D2受体基因(DRD2)中的三种多态性、多巴胺转运体(DAT)基因3'区域中的两个位点、多巴胺D4(DRD4)受体基因启动子和编码区域中的两个位点,以及5-羟色胺6受体基因、5-羟色胺转运体基因和色氨酸羟化酶基因中的多态性位点,以确定它们与TD易感性的关联。我们研究了患有TD(n = 59)和未患TD(n = 63)的精神分裂症患者,这些患者在抗精神病药物暴露和其他相关变量方面相匹配。未发现显著关联。在临床样本量所带来的局限性范围内,这些发现表明上述多态性位点对TD风险的影响不显著。有必要进一步检查在趋势水平上得出阳性结果的位点,并研究其他编码抗精神病药物靶点的候选基因位点。

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