Department of Psychiatry and Psychology and Mayo Clinic Depression Center, Mayo Clinic, Rochester, MN.
Department of Anesthesiology, Mayo Clinic, Rochester, MN.
Mayo Clin Proc. 2016 Jul;91(7):897-907. doi: 10.1016/j.mayocp.2016.02.023. Epub 2016 Jun 21.
Antidepressants are commonly prescribed medications in the United States, and there is increasing interest in individualizing treatment selection for more than 20 US Food and Drug Administration-approved treatments for major depressive disorder. Providing greater precision to pharmacotherapeutic recommendations for individual patients beyond the large-scale clinical trials evidence base can potentially reduce adverse effect toxicity profiles and increase response rates and overall effectiveness. It is increasingly recognized that genetic variation may contribute to this differential risk to benefit ratio and thus provides a unique opportunity to develop pharmacogenetic guidelines for psychiatry. Key studies and concepts that review the rationale for cytochrome P450 2D6 (CYP2D6) and cytochrome P450 2C19 (CYP2C19) genetic testing can be delineated by serum levels, adverse events, and clinical outcome measures (eg, antidepressant response). In this article, we report the evidence that contributed to the implementation of pharmacokinetic pharmacogenetic guidelines for antidepressants primarily metabolized by CYP2D6 and CYP2C19.
抗抑郁药是美国常用的处方药,人们越来越有兴趣根据美国食品和药物管理局批准的 20 多种治疗重度抑郁症的方法,为每位患者制定个体化的治疗方案。在大规模临床试验证据基础上,为个别患者提供比药物治疗建议更精确的建议,有可能降低不良反应的毒性,提高反应率和整体疗效。人们越来越认识到,遗传变异可能导致这种风险效益比的差异,因此为精神药理学制定药物遗传学指南提供了独特的机会。关键的研究和概念可以通过血清水平、不良事件和临床结果测量(例如,抗抑郁反应)来审查细胞色素 P450 2D6(CYP2D6)和细胞色素 P450 2C19(CYP2C19)遗传检测的基本原理。在本文中,我们报告了促成主要由 CYP2D6 和 CYP2C19 代谢的抗抑郁药药代动力学药物遗传学指南实施的证据。