van Westrhenen Roos, Aitchison Katherine J, Ingelman-Sundberg Magnus, Jukić Marin M
Department of Psychiatry, Parnassia Group, Amsterdam, Netherlands.
Department of Psychiatry and Neuropsychology, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, Netherlands.
Front Psychiatry. 2020 Mar 12;11:94. doi: 10.3389/fpsyt.2020.00094. eCollection 2020.
In recent decades, very few new psychiatric drugs have entered the market. Thus, improvement in the use of antidepressant and antipsychotic therapy has to focus mainly on enhanced and more personalized treatment with the currently available drugs. One important aspect of such individualization is emphasizing interindividual differences in genes relevant to treatment, an area that can be termed neuropsychopharmacogenomics. Here, we review previous efforts to identify such critical genetic variants and summarize the results obtained to date. We conclude that most clinically relevant genetic variation is connected to phase I drug metabolism, in particular to genetic polymorphism of and . To further improve individualized pharmacotherapy, there is a need to take both common and rare relevant mutations into consideration; we discuss the present and future possibilities of using whole genome sequencing to identify patient-specific genetic variation relevant to treatment in psychiatry. Translation of pharmacogenomic knowledge into clinical practice can be considered for specific drugs, but this requires education of clinicians, instructive guidelines, as well as full attention to polypharmacy and other clinically relevant factors. Recent large patient studies (n > 1,000) have replicated previous findings and produced robust evidence warranting the clinical utility of relevant genetic biomarkers. To further judge the clinical and financial benefits of preemptive genotyping in psychiatry, large prospective randomized trials are needed to quantify the value of genetic-based patient stratification in neuropsychopharmacotherapy and to demonstrate the cost-effectiveness of such interventions.
近几十年来,进入市场的新型精神科药物极少。因此,改善抗抑郁和抗精神病治疗的重点必须主要放在利用现有药物加强治疗并使其更加个性化上。这种个体化的一个重要方面是强调与治疗相关基因的个体间差异,这一领域可称为神经精神药理学基因组学。在此,我们回顾了此前为确定此类关键基因变异所做的努力,并总结了迄今所取得的成果。我们得出的结论是,大多数临床相关的基因变异与I期药物代谢有关,尤其是与[具体基因1]和[具体基因2]的基因多态性有关。为进一步改善个体化药物治疗,有必要同时考虑常见和罕见的相关突变;我们讨论了利用全基因组测序来识别与精神科治疗相关的患者特异性基因变异的现状和未来可能性。对于特定药物,可以考虑将药物基因组学知识转化为临床实践,但这需要对临床医生进行培训、制定指导性准则,并充分关注联合用药及其他临床相关因素。近期大规模患者研究(n > 1000)重复了之前的发现,并提供了有力证据证明相关基因生物标志物的临床实用性。为进一步评判精神科抢先基因分型的临床和经济效益,需要开展大型前瞻性随机试验,以量化基于基因的患者分层在神经精神药物治疗中的价值,并证明此类干预措施的成本效益。