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Gene-gene interaction between DRD4 and COMT modulates clinical response to clozapine in treatment-resistant schizophrenia

机译:DRD4和COMT之间的基因 - 基因相互作用调节治疗抗性精神分裂症中氯氮平的临床反应

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摘要

Clozapine is the drug of choice for treatment-resistant schizophrenia. However, its use is associated with variable clinical responses and serious adverse effects. Polymorphisms in genes encoding proteins involved in synaptic neurotransmission may account for such variability. Here, we studied independent and epistatic genetic associations of polymorphisms in DRD4 (120-bp duplication) and COMT (Val158Met) with clinical response to clozapine in people with treatment-resistant schizophrenia. We studied 93 participants who were on stable doses of clozapine for at least 12 weeks. A total score of less than or equal to 35 on the Brief Psychiatric Rating Scale was defined as a clinical response. The genetic associations were tested using logistic regression analyses. Neither polymorphism studied was found to be independently associated with response to clozapine. However, a statistically significant gene-gene interaction was observed between the polymorphisms. Participants with the COMT Val/Met or Met/Met genotype, who also had one or two DRD4 120-bp alleles (120/240 and 120/120), showed significantly better clinical response to clozapine. Our results highlight the importance of investigating gene-gene interactions, while studying the pharmacogenetics of clozapine.
机译:氯氮平是治疗抗性精神分裂症的首选药物。然而,它的使用与可变的临床反应和严重不利影响有关。编码参与突触神经递质的蛋白质的基因中的多态性可能考虑这种可变性。在这里,我们研究了DRD4(120-BP复制)和COMT(VAL158MET)中多态性的独立和遗传遗传关联,其对抗治疗精神分裂症的人的氯氮平进行临床反应。我们研究了93名参与者,他们在稳定的氯氮平剂量上至少12周。在简短的精神评级规模上的总得分小于或等于35的总分被定义为临床反应。使用Logistic回归分析测试遗传关联。没有发现研究的多态性与对氯氮平的反应独立相关。然而,在多态性之间观察到统计学上显着的基因基因相互作用。与COMT VAL / MET或MET / MET基因型的参与者也有一个或两个DRD4 120-BP等位基因(120/240和120/120),对氯氮平显示出明显更好的临床反应。我们的结果突出了研究基因相互作用的重要性,同时研究氯氮平的药物。

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