氟伏沙明
依西酞普兰
西酞普兰
CYP2C19型
帕罗西汀
药物遗传学
舍曲林
加药
医学
药理学
CYP2D6型
氟西汀
精神科
焦虑
血清素
内科学
基因型
抗抑郁药
生物
生物化学
受体
细胞色素P450
新陈代谢
基因
作者
J K Hicks,JR Bishop,Katrin Sangkuhl,Müller Dj,Yuan Ji,SG Leckband,JS Leeder,RL Graham,DL Chiulli,Adrián LLerena,TC Skaar,Stuart A. Scott,Julia Stingl,Teri E. Klein,KE Caudle,Andrea Gaedigk
摘要
Selective serotonin reuptake inhibitors (SSRIs) are primary treatment options for major depressive and anxiety disorders. CYP2D6 and CYP2C19 polymorphisms can influence the metabolism of SSRIs, thereby affecting drug efficacy and safety. We summarize evidence from the published literature supporting these associations and provide dosing recommendations for fluvoxamine, paroxetine, citalopram, escitalopram, and sertraline based on CYP2D6 and/or CYP2C19 genotype (updates at www.pharmgkb.org).
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