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DRD4与COMT之间的基因-基因相互作用调节难治性精神分裂症患者对氯氮平的临床反应。

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

作者信息

Rajagopal Veera M, Rajkumar Anto P, Jacob Kuruthukulangara S, Jacob Molly

机构信息

Departments of Biochemistry.

Department of Biomedicine, Aarhus University, Aarhus, Denmark.

出版信息

Pharmacogenet Genomics. 2018 Jan;28(1):31-35. doi: 10.1097/FPC.0000000000000314.

Abstract

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.

摘要

氯氮平是难治性精神分裂症的首选药物。然而,其使用与不同的临床反应和严重不良反应相关。参与突触神经传递的蛋白质编码基因的多态性可能是造成这种变异性的原因。在此,我们研究了难治性精神分裂症患者中DRD4(120碱基对重复)和COMT(Val158Met)基因多态性与氯氮平临床反应的独立和上位基因关联。我们研究了93名服用稳定剂量氯氮平至少12周的参与者。简明精神病评定量表总分小于或等于35被定义为临床反应。使用逻辑回归分析测试基因关联。所研究的多态性均未被发现与氯氮平反应独立相关。然而,在这些多态性之间观察到了具有统计学意义的基因-基因相互作用。具有COMT Val/Met或Met/Met基因型且同时具有一个或两个DRD4 120碱基对等位基因(120/240和120/120)的参与者对氯氮平表现出显著更好的临床反应。我们的结果突出了在研究氯氮平药物遗传学的同时研究基因-基因相互作用的重要性。

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