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Role of Pharmacogenetics in Improving the Safety of Psychiatric Care by Predicting the Potential Risks of Mania in CYP2D6 Poor Metabolizers Diagnosed With Bipolar Disorder

机译:药物遗传学在通过预测被诊断为双相障碍的CYP2D6弱代谢者中躁狂症的潜在风险中改善精神病治疗安全性的作用

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摘要

One of the main concerns in psychiatric care is safety related to drug management. Pharmacogenetics provides an important tool to assess causes that may have contributed the adverse events during psychiatric therapy. This study illustrates the potential of pharmacogenetics to identify those patients for which pharmacogenetic-guided therapy could be appropriate. It aimed to investigate CYP2D6 genotype in our psychiatric population to assess the value of introducing pharmacogenetics as a primary improvement for predicting side effects.A broad series of 224 psychiatric patients comprising psychotic disorders, depressive disturbances, bipolar disorders, and anxiety disorders was included. The patients were genotyped with the AmpliChip CYP450 Test to analyzing 33 allelic variants of the CYP2D6 gene.All bipolar patients with poor metabolizer status showed maniac switching when CYP2D6 substrates such as selective serotonin reuptake inhibitors were prescribed. No specific patterns were identified for adverse events for other disorders.We propose to utilize pharmacogenetic testing as an intervention to aid in the identification of patients who are at risk of developing affective switching in bipolar disorder treated with selective serotonin reuptake inhibitors, CYP2D6 substrates, and inhibitors.
机译:精神科护理中主要关注的问题之一是与药物管理有关的安全性。药物遗传学提供了一种重要的工具,可以评估可能导致精神病治疗期间不良事件发生的原因。这项研究说明了药物遗传学的潜力,以鉴定那些可能需要进行药物遗传学指导治疗的患者。该研究旨在调查CYP2D6基因型在我们的精神病人群中的价值,以评估引入药物遗传学作为预测副作用的主要改善方法的价值。纳入了224例精神病患者,包括精神病,抑郁症,双相情感障碍和焦虑症。采用AmpliChip CYP450检验对患者进行基因分型,以分析CYP2D6基因的33个等位基因变体。当服用CYP2D6底物(如选择性5-羟色胺再摄取抑制剂)时,所有代谢状况不佳的双相患者均表现出躁狂。未发现其他疾病不良事件的具体模式。我们建议采用药物遗传学检测作为干预措施,以帮助识别在患有选择性5-羟色胺再摄取抑制剂,CYP2D6底物和抑制剂。

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