Division of Cardiology, Department of Internal Medicine, Texas Tech University Health Sciences Center, Paul L. Foster School of Medicine, 4800 Alberta Avenue, El Paso, TX, 79905, USA.
Curr Cardiol Rep. 2024 Jul;26(7):675-680. doi: 10.1007/s11886-024-02071-0. Epub 2024 May 28.
Identification of a reliable discriminatory test to accurately stratify patient responses to antiplatelet therapy following coronary revascularization has become increasingly desirable to optimize therapeutic efficacy and safety.
The expansion of platelet function testing to include genotype assessment has been an evolutionary journey, initially fraught with confounding results. However, more recent and rigorous data analysis suggests that genotype testing- guided, tailored antiplatelet therapy may hold promise in optimizing treatment of patients after coronary intervention. Current evidence increasingly supports the use of genotype guided CYP2C19 testing to better match the post coronary intervention patient with the most efficacious and least risky antiplatelet inhibitor. The risk stratification of poor, intermediate, and good metabolizers of these drugs with such testing promises to yield clinical dividends in terms of morbidity, mortality and cost control, in this growing patient population.
识别一种可靠的鉴别性检测方法,以准确分层经冠状动脉血运重建治疗后的患者对抗血小板治疗的反应,这对于优化治疗效果和安全性变得越来越重要。
血小板功能检测的扩展,包括基因型评估,是一个不断发展的过程,最初充满了相互矛盾的结果。然而,最近更严格的数据分析表明,基因型检测指导下的个体化抗血小板治疗可能有希望优化经冠状动脉介入治疗后的患者的治疗。越来越多的现有证据支持使用基因型指导的 CYP2C19 检测,以更好地将经冠状动脉介入治疗后的患者与最有效和风险最小的抗血小板抑制剂相匹配。对这些药物的代谢不良、中间和良好的个体进行风险分层,通过这种检测有望在发病率、死亡率和成本控制方面为这一不断增长的患者群体带来临床收益。