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在一个为期 10 年的成年初级保健患者抑郁症队列中,使用基于药物遗传学处方指南的抗抑郁药。

Use of antidepressants with pharmacogenetic prescribing guidelines in a 10-year depression cohort of adult primary care patients.

机构信息

Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

MyDNA Life, Australia Limited, South Yarra.

出版信息

Pharmacogenet Genomics. 2020 Sep;30(7):145-152. doi: 10.1097/FPC.0000000000000406.

Abstract

OBJECTIVE

To describe the usage patterns of antidepressants with published CYP2D6- and CYP2C19-based prescribing guidelines among depressed primary care patients and estimate the proportion of patients taking antidepressants not recommended for them based on their CYP2C19 and CYP2D6 genotype-predicted metabolizer status.

METHODS

Medication use and pharmacogenetic testing results were collected on 128 primary care patients enrolled in a 10-year depression cohort study. At each 12-month interval, we calculated the proportion of patients that: (1) reported use of one or more of the 13 antidepressant medications (i.e. amitriptyline, citalopram, escitalopram, clomipramine, desipramine, doxepin, fluvoxamine, imipramine, nortriptyline, paroxetine, sertraline, trimipramine, venlafaxine) with published CYP2D6- and CYP2C19-based prescribing guidelines, (2) were taking an antidepressant that was not recommended for them based on their CYP2C19 and CYP2D6 genotype-predicted metabolizer phenotype, and (3) switched medications from the previous 12-month interval.

RESULTS

The annual proportion of individuals taking an antidepressant with a CYP2D6- and CYP2C19-based prescribing guidelines ranged from 45 to 84%. The proportion of participants that used an antidepressant that was not recommended for them, based on available CYP2D6 and CYP2C19 metabolizer phenotype, ranged from 18 to 29% and these individuals tended to switch medications more frequently (10%) compared to their counterparts taking medication aligned with their metabolizer phenotype (6%).

CONCLUSION

One-quarter of primary care patients used an antidepressant that was not recommended for them based on CYP2D6- and CYP2C19-based prescribing guidelines and switching medications tended to be more common in this group. Studies to determine the impact of CYP2D6 and CYP2C19 genotyping on reducing gene-antidepressant mismatches are warranted.

摘要

目的

描述遵循 CYP2D6 和 CYP2C19 指导原则的抗抑郁药物在抑郁初级保健患者中的使用模式,并根据 CYP2C19 和 CYP2D6 基因型预测的代谢物状态估计不建议患者使用的抗抑郁药物的比例。

方法

对参加为期 10 年的抑郁队列研究的 128 名初级保健患者进行了药物使用和药物遗传学检测结果的收集。在每 12 个月的间隔内,我们计算了以下患者的比例:(1)报告使用了一种或多种具有 CYP2D6 和 CYP2C19 指导原则的 13 种抗抑郁药(即阿米替林、西酞普兰、艾司西酞普兰、氯米帕明、去甲替林、多塞平、氟伏沙明、丙咪嗪、去甲丙咪嗪、帕罗西汀、舍曲林、曲米帕明、文拉法辛),(2)服用了不建议根据 CYP2C19 和 CYP2D6 基因型预测的代谢物表型使用的抗抑郁药,以及(3)在上一个 12 个月间隔内更换了药物。

结果

每年服用 CYP2D6 和 CYP2C19 指导原则的抗抑郁药的个体比例为 45%至 84%。根据可用的 CYP2D6 和 CYP2C19 代谢物表型,有 18%至 29%的参与者使用了不建议使用的抗抑郁药,这些人比使用与代谢物表型一致的药物(6%)更频繁地更换药物(10%)。

结论

四分之一的初级保健患者使用了不建议根据 CYP2D6 和 CYP2C19 指导原则使用的抗抑郁药,而且在这一组中更换药物的倾向更为常见。有必要进行研究以确定 CYP2D6 和 CYP2C19 基因分型对抗抑郁药物基因匹配的影响。

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