Hatano Masakazu, Ikeda Masashi, Saito Takeo, Miyata Masami, Iwata Nakao, Yamada Shigeki
Department of Pharmacotherapeutics and Informatics, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Front Psychiatry. 2025 Mar 27;16:1542000. doi: 10.3389/fpsyt.2025.1542000. eCollection 2025.
Although several guidelines provide dosing recommendations for antidepressants based on patients' genetic information, pharmacogenetic testing for antidepressant use is rarely routinely performed in Japan. To clarify the clinical impact of pharmacogenetic testing, this study estimated the potential drug-gene interactions for first-time antidepressant treatment in Japanese patients with major depressive disorder.
This study retrospectively included Japanese patients who were registered for depressive episodes (F32, International Classification of Diseases, Tenth Revision) and initiated on antidepressants between July 2022 and March 2023. Antidepressant prescription rates were calculated using a nationwide hospital-based database (Medical Data Vision Co., Ltd). The incidence of actionable drug-gene interactions was estimated by multiplying the first-time prescription rate of each relevant antidepressant by the frequency of its corresponding actionable phenotype.
A total of 3,197 patients were included in the analysis. Escitalopram was the most frequently prescribed antidepressant (18.7%, n = 597), followed by mirtazapine (17.5%, n = 561), and sertraline (15.4%, n = 493). Of the patients receiving their first treatment of major depressive disorder, 56.5% (n = 1,807) were prescribed a drug with actionable pharmacogenetic implications, and 26.4% (n = 844) were estimated to have required actionable therapeutic recommendations. The highest incidence of actionable drug-gene interactions was observed in escitalopram and CYP2C19 pairs (12.4%, n = 398). For sertraline and CYP2C19 or CYP2B6 pairs, the incidence was 11.0% (n = 352). Among all antidepressants, paroxetine had the highest incidence of actionable drug-gene interactions related to CYP2D6 at 1.8% (n = 56); this interaction was rarely observed with other antidepressants (<1%).
We estimated that one in four Japanese patients with major depressive disorder who were prescribed first-time antidepressants had actionable drug-gene interactions. These results suggest that pre-emptive pharmacogenetic testing in the treatment of major depressive disorder could have important clinical implications.
尽管有多项指南根据患者的基因信息提供了抗抑郁药的给药建议,但在日本,抗抑郁药使用的药物遗传学检测很少常规进行。为了阐明药物遗传学检测的临床影响,本研究评估了日本重度抑郁症患者首次使用抗抑郁药治疗时潜在的药物-基因相互作用。
本研究回顾性纳入了2022年7月至2023年3月期间登记有抑郁发作(国际疾病分类第十版,F32)并开始使用抗抑郁药的日本患者。使用全国性的基于医院的数据库(Medical Data Vision Co., Ltd)计算抗抑郁药的处方率。通过将每种相关抗抑郁药的首次处方率与其相应可操作表型的频率相乘来估计可操作药物-基因相互作用的发生率。
共有3197名患者纳入分析。艾司西酞普兰是最常处方的抗抑郁药(18.7%,n = 597),其次是米氮平(17.5%,n = 561)和舍曲林(15.4%,n = 493)。在接受重度抑郁症首次治疗的患者中,56.5%(n = 1807)被处方了具有可操作药物遗传学意义的药物,估计26.4%(n = 844)需要可操作的治疗建议。在艾司西酞普兰和CYP2C19配对中观察到可操作药物-基因相互作用的发生率最高(12.4%,n = 398)。对于舍曲林与CYP2C19或CYP2B6配对,发生率为11.0%(n = 352)。在所有抗抑郁药中,帕罗西汀与CYP2D6相关的可操作药物-基因相互作用发生率最高,为1.8%(n = 56);其他抗抑郁药很少观察到这种相互作用(<1%)。
我们估计,在首次处方抗抑郁药的日本重度抑郁症患者中,四分之一的患者存在可操作的药物-基因相互作用。这些结果表明,在重度抑郁症治疗中进行前瞻性药物遗传学检测可能具有重要的临床意义。