Department of Biomedical & NeuroMotor Sciences, University of Bologna, Bologna, Italy.
Pharmacogenomics. 2020 Oct;21(15):1095-1100. doi: 10.2217/pgs-2019-0086. Epub 2020 Oct 5.
Over 20 years after the initial report of gene variants within the central nervous system modulating antidepressant response, we are now facing for the first time routine clinical pharmacogenetic applications. The scientific community is divided between enthusiasm and skepticism. It seems clear that the benefit of existing tools is not huge, at least for the central nervous system gene variants, while it is generally accepted for the metabolic gene variants. Findings from large international consortia suggest for the first time in psychiatric genetic research history that cumulative scores comprising many variants across the whole genome may reliably constitute liability factors for psychiatric disorders, this approach will most likely improve also present pharmacogenetic tools. A composite genetic score complemented with clinical risk factors for each patient is the most promising approach for a more effective method of targeted treatment for patients with depression.
中枢神经系统内调节抗抑郁反应的基因变异的初步报告发表 20 多年后,我们现在首次面临常规的临床药物遗传学应用。科学界对此既热情又怀疑。现有的工具至少对于中枢神经系统的基因变异,其获益似乎并不巨大,而代谢基因变异则被广泛接受,这一点似乎很清楚。来自大型国际联盟的研究结果首次表明,在精神疾病遗传学研究史上,包含全基因组中许多变异的累积评分可能可靠地构成精神疾病的易患因素,这种方法很可能也会改善现有的药物遗传学工具。对于更有效地针对抑郁症患者进行靶向治疗的方法,为每个患者补充包含临床危险因素的复合遗传评分是最有前途的方法。