drugsafety.ch, Seestrasse 221, 8700, Küsnacht, Switzerland.
Institute of Internal Medicine and Nephrology, Clinic Hirslanden, Zurich, Switzerland.
Eur J Clin Pharmacol. 2021 May;77(5):709-716. doi: 10.1007/s00228-020-03050-4. Epub 2020 Nov 26.
The antiplatelet prodrug clopidogrel is bioactivated by the polymorphic enzyme CYP2C19. Prospective clinical studies demonstrated an association between CYP2C19 loss of function (LoF) variants and an increased risk of thrombotic events under clopidogrel, but pharmacogenetic (PGx) testing is not frequently implemented in clinical practice. We report our experience with PGx-guided clopidogrel therapy with particular regard to clinically relevant patient management changes.
We conducted an observational study analyzing patients that underwent PGx testing for clopidogrel therapy at two Swiss hospitals. Primary outcome was the proportion of patients with clinically relevant PGx-based management recommendations and their implementation. The association of recurrent ischemic events under clopidogrel with CYP2C19 LoF variants and other factors was explored in a multivariate case-control analysis.
Among 56 patients undergoing PGx testing, 18 (32.1%) were classified as CYP2C19 intermediate or poor metabolizers. This resulted in 17 recommendations for a change of antiplatelet therapy, which were implemented in 12 patients (70.1%). In the remaining five patients, specific reasons for non-implementation could be identified. Recurrent ischemic events under clopidogrel were associated with LoF variants (OR 2.2, 95% CI 0.3-14.4) and several cardiovascular risk factors. Associations were not statistically significant in our small study, but plausible and in line with estimates from large prospective studies.
PGx-guided clopidogrel therapy can identify patients with an elevated risk of ischemic events and offer evidence-based alternative treatments. Successful implementation in clinical practice requires a personalized interdisciplinary service that evaluates indications and additional risk factors, provides specific recommendations, and proactively follows their implementation.
抗血小板前体药物氯吡格雷通过多态性酶 CYP2C19 被生物激活。前瞻性临床研究表明,CYP2C19 功能丧失(LoF)变异与氯吡格雷下血栓事件风险增加之间存在关联,但药物遗传学(PGx)检测在临床实践中并未广泛实施。我们报告了我们在氯吡格雷治疗中使用 PGx 指导的经验,特别是在与临床相关的患者管理变化方面。
我们进行了一项观察性研究,分析了在瑞士的两家医院接受氯吡格雷治疗的 PGx 检测的患者。主要结果是具有临床相关 PGx 管理建议的患者比例及其实施情况。在多变量病例对照分析中,探讨了氯吡格雷下复发性缺血事件与 CYP2C19 LoF 变异和其他因素的关系。
在接受 PGx 检测的 56 名患者中,有 18 名(32.1%)被归类为 CYP2C19 中间代谢者或弱代谢者。这导致了 17 项改变抗血小板治疗的建议,其中 12 项(70.1%)得到实施。在其余的 5 名患者中,可以确定未实施的具体原因。氯吡格雷下复发性缺血事件与 LoF 变异(OR 2.2,95%CI 0.3-14.4)和多种心血管危险因素相关。在我们的小型研究中,这些关联没有统计学意义,但具有合理性,并且与大型前瞻性研究的估计相符。
PGx 指导的氯吡格雷治疗可以识别出缺血事件风险增加的患者,并提供基于证据的替代治疗方法。在临床实践中的成功实施需要个性化的跨学科服务,该服务评估适应症和其他风险因素,提供具体建议,并积极跟进其实施情况。