Institut für Klinische Chemie und Pathobiochemie, Klinikum rechts der Isar, Technische Universität München, München, Germany.
Ther Drug Monit. 2010 Aug;32(4):381-6. doi: 10.1097/FTD.0b013e3181e1a78d.
Psychiatry is one of the most promising areas for bringing pharmacogenomics to the patient. Psychiatric disorders such as depression and schizophrenia contribute significantly to worldwide morbidity and mortality. Forecasts rank depression second only to ischemic heart disease by 2020. In depression and schizophrenia, 30% to 50% of all patients do not respond sufficiently to the initial treatment regime. Genetic variability has been demonstrated to play an important role in the response to pharmacotherapy. Most data are available with regard to polymorphisms in the genes coding for drug-metabolizing enzymes and recommendations for the choice of personalized dosages based on genotyping results are available. Clinical outcome, in particular adverse effects, has been shown to correlate with the results from genotyping. Incorporating pharmacogenomics into clinical practice has, however, been slow and it is still not clear in which clinical situations genotyping should be performed and what the benefit of such procedures could be beyond therapeutic drug monitoring. Additionally, many studies in psychiatry focus on genetic variation in candidate genes of drug targets. However, despite promising reports, no clear recommendation can be given at present to perform such testing in clinical use.
精神病学是将药物基因组学应用于患者的最有前途的领域之一。精神障碍,如抑郁症和精神分裂症,对全球发病率和死亡率有重大影响。预测显示,到 2020 年,抑郁症的发病率仅次于缺血性心脏病。在抑郁症和精神分裂症中,所有患者中有 30%到 50%对初始治疗方案反应不足。遗传变异性已被证明在药物治疗反应中起着重要作用。大多数数据可用于编码药物代谢酶的基因中的多态性,并且可以根据基因分型结果为个性化剂量选择提供建议。临床结果,特别是不良反应,已经显示与基因分型结果相关。然而,将药物基因组学纳入临床实践的速度一直很慢,目前仍不清楚在哪些临床情况下应该进行基因分型,以及除治疗药物监测之外,这些程序的益处是什么。此外,精神病学中的许多研究都集中在药物靶点的候选基因的遗传变异上。然而,尽管有很有希望的报告,但目前还不能明确建议在临床使用中进行此类检测。