Bschor T, Baethge C, Hiemke C, Müller-Oerlinghausen B
Abteilung für Psychiatrie, Schlosspark-Klinik, Heubnerweg 2, 14059, Berlin, Deutschland.
Klinik und Poliklinik für Psychiatrie und Psychotherapie, Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden, Dresden, Deutschland.
Nervenarzt. 2017 May;88(5):495-499. doi: 10.1007/s00115-017-0310-6.
In clinical practice, there is a need for a more individualized selection of antidepressants and adequate dosage. The investigation of pharmacokinetically relevant genes is a promising approach to assist this selection. In the past 2 years, two commercially available tests have been subject of advertisement, a test from Stada, which analyses variants of the cytochrome P450 isoenzymes CYP2D6 and CYP2C19 and a test from HMNC Brain Health, which analyses variants of the ABCB1 gene. The costs for both kits are not covered by the statutory health insurance and it is therefore proposed that the patients are invoiced directly in the form of individual healthcare payment. The companies claim that by applying the tests antidepressant treatment failure can be avoided and that patients will respond faster to the antidepressant used. These claims are not based on appropriate clinical trials, which are either lacking or reveal conflicting results. Hence, the routine use of these tests is not recommended. In accordance with the German S3 Guideline for unipolar depression, therapeutic drug monitoring (TDM) of serum levels should be carried out in cases of non-response to an antidepressant with adequate dosage and duration. As a rule the costs for TDM are covered by the statutory health insurance. Cytochrome P450 genotyping is only indicated when the serum level is not within the expected range and other reasons to explain this discrepancy are excluded. Many laboratories provide these analyses and in individual cases the costs are reimbursed by the statutory health insurance. Further research should be carried out to investigate the importance of the ABCB1 gene for the treatment with antidepressants.
在临床实践中,需要更个体化地选择抗抑郁药并确定合适的剂量。对药物代谢动力学相关基因进行研究是辅助这一选择的一种有前景的方法。在过去两年中,有两种商业可用的检测成为广告宣传的对象,一种是施达德公司的检测,它分析细胞色素P450同工酶CYP2D6和CYP2C19的变体;另一种是HMNC脑健康公司的检测,它分析ABCB1基因的变体。这两种试剂盒的费用均不在法定医疗保险范围内,因此建议直接向患者开具个人医疗费用账单。这些公司声称,通过应用这些检测可以避免抗抑郁治疗失败,并且患者对抗抑郁药的反应会更快。这些说法并非基于适当的临床试验,要么缺乏临床试验,要么结果相互矛盾。因此,不建议常规使用这些检测。根据德国关于单相抑郁症的S3指南,对于使用了足够剂量和疗程的抗抑郁药仍无反应的情况,应进行血清水平的治疗药物监测(TDM)。通常,TDM的费用由法定医疗保险支付。仅当血清水平不在预期范围内且排除了其他解释这种差异的原因时,才进行细胞色素P450基因分型。许多实验室提供这些分析,在个别情况下,费用可由法定医疗保险报销。应开展进一步研究,以调查ABCB1基因在抗抑郁药治疗中的重要性。