Hernandez-Suarez Dagmar F, Scott Stuart A, Tomey Matthew I, Melin Kyle, Lopez-Candales Angel, Buckley Charlotte E, Duconge Jorge
ORCID ID: 0000-0003-1850-9078, University of Puerto Rico School of Medicine, Medical Sciences Building, PO Box 365067, San Juan, 00936-5067, Puerto Rico.
Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ther Adv Cardiovasc Dis. 2017 Sep;11(9):235-241. doi: 10.1177/1753944717718718. Epub 2017 Jul 4.
Clopidogrel is by far the most prescribed platelet adenosine diphosphate (ADP) antagonist in Puerto Rico despite the advent of newer agents (prasugrel and ticagrelor). Given the paucity of data on clopidogrel responsiveness in Hispanics, we sought to determine the association between clinical characteristics and platelet reactivity in Puerto Rican patients on clopidogrel therapy.
A total of 100 Puerto Rican patients on clopidogrel therapy were enrolled and allocated into two groups: Group I, without high on-treatment platelet reactivity (HTPR); and Group II, with HTPR. Platelet function was measured ex vivo using the VerifyNow® P2Y12 assay.
The cohort was comprised of Hispanic patients with coronary artery disease (57%), peripheral artery disease (32%), carotid artery stenosis (7%), cerebral artery aneurysm (2%), and stroke (2%). Mean platelet reactivity was 200 ± 61 P2Y12 reaction units (PRUs) (range: 8-324), and 35% of patients had HTPR (PRUs ⩾ 230). Multivariable logistic regression analysis determined that diabetes mellitus (DM) [odds ratio (OR) = 3.27; 95% confidence interval (CI): 1.20-8.96], use of proton-pump inhibitors (PPIs) (OR = 3.60; 95% CI: 1.09-11.82), and calcium channel blockers (CCBs) (OR = 3.10; 95% CI: 1.09-8.83) were independent predictors of HTPR ( p < 0.05) after adjusting for other clinical variables.
In a sample of 100 Puerto Rican Hispanic patients on clopidogrel, 35% had HTPR. Furthermore, DM, PPIs and CCBs predicted HTPR. Clinical outcome data are needed to identify appropriate PRU thresholds for risk prediction in the Puerto Rican population.
尽管有新型药物(普拉格雷和替格瑞洛)问世,但氯吡格雷仍是波多黎各目前处方最多的血小板二磷酸腺苷(ADP)拮抗剂。鉴于西班牙裔人群中关于氯吡格雷反应性的数据匮乏,我们试图确定接受氯吡格雷治疗的波多黎各患者的临床特征与血小板反应性之间的关联。
共有100名接受氯吡格雷治疗的波多黎各患者入组,并分为两组:第一组,无治疗期间高血小板反应性(HTPR);第二组,有HTPR。使用VerifyNow® P2Y12分析体外测量血小板功能。
该队列由患有冠状动脉疾病(57%)、外周动脉疾病(32%)、颈动脉狭窄(7%)、脑动脉瘤(2%)和中风(2%)的西班牙裔患者组成。平均血小板反应性为200±61 P2Y12反应单位(PRU)(范围:8 - 324),35%的患者有HTPR(PRU⩾230)。多变量逻辑回归分析确定,在调整其他临床变量后,糖尿病(DM)[比值比(OR)= 3.27;95%置信区间(CI):1.20 - 8.96]、使用质子泵抑制剂(PPI)(OR = 3.60;95% CI:1.09 - 11.82)和钙通道阻滞剂(CCB)(OR = 3.10;95% CI:1.09 - 8.83)是HTPR的独立预测因素(p < 0.05)。
在100名接受氯吡格雷治疗的波多黎各西班牙裔患者样本中,35%有HTPR。此外,DM、PPI和CCB可预测HTPR。需要临床结局数据来确定波多黎各人群中用于风险预测的合适PRU阈值。