Department of Cardiovascular Medicine.
Department of Molecular Pharmacology and Experimental Therapeutics.
Pharmacogenet Genomics. 2019 Jun;29(4):76-83. doi: 10.1097/FPC.0000000000000368.
To evaluate perceptions toward pharmacogenetic testing of patients undergoing percutaneous coronary intervention (PCI) who are prescribed dual antiplatelet therapy (DAPT) and whether geographical differences in these perceptions exist.
TAILOR-PCI is the largest genotype-based cardiovascular clinical trial randomizing participants to conventional DAPT or prospective genotyping-guided DAPT. Enrolled patients completed surveys before and 6 months after randomization.
A total of 1327 patients completed baseline surveys of whom 28, 29, and 43% were from Korea, Canada and the USA, respectively. Most patients (77%) valued identifying pharmacogenetic variants; however, fewer Koreans (44%) as compared with Canadians (91%) and USA (89%) patients identified pharmacogenetics as being important (P<0.001). After adjusting for age, sex, and country, those who were confident in their ability to understand genetic information were significantly more likely to value identifying pharmacogenetic variants (odds ratio: 30.0; 95% confidence interval: 20.5-43.8). Only 21% of Koreans, as opposed to 86 and 77% of patients in Canada and USA, respectively, were confident in their ability to understand genetic information (P<0.001).
Although genetically mediated clopidogrel resistance is more prevalent amongst Asians, Koreans undergoing PCI identified pharmacogenetic variants as less important to their healthcare, likely related to their lack of confidence in their ability to understand genetic information. To enable successful implementation of pharmacogenetic testing on a global scale, the possibility of international population differences in perceptions should be considered.
评估正在接受经皮冠状动脉介入治疗(PCI)并接受双联抗血小板治疗(DAPT)的患者对药物遗传学检测的看法,以及这些看法是否存在地域差异。
TAILOR-PCI 是一项最大的基于基因型的心血管临床试验,该试验将参与者随机分配至传统 DAPT 或前瞻性基因分型指导的 DAPT。入组患者在随机分组前后完成了调查。
共有 1327 名患者完成了基线调查,其中 28%、29%和 43%分别来自韩国、加拿大和美国。大多数患者(77%)重视确定药物遗传学变异;然而,与加拿大(91%)和美国(89%)患者相比,韩国患者(44%)认为药物遗传学更重要(P<0.001)。在调整年龄、性别和国家后,那些对自己理解遗传信息的能力有信心的患者更有可能重视确定药物遗传学变异(优势比:30.0;95%置信区间:20.5-43.8)。只有 21%的韩国患者,而不是加拿大(86%)和美国(77%)的患者,对自己理解遗传信息的能力有信心(P<0.001)。
尽管亚洲人群中氯吡格雷抵抗的遗传介导更为普遍,但接受 PCI 的韩国患者认为药物遗传学变异对其医疗保健的重要性较低,这可能与他们对理解遗传信息的能力缺乏信心有关。为了在全球范围内成功实施药物遗传学检测,应考虑国际人群在看法上的差异。