Li He, Zhang Yan-Jiao, Li Mu-Peng, Hu Xiao-Lei, Song Pei-Yuan, Peng Li-Ming, Ma Qi-Lin, Tang Jie, Zhang Wei, Chen Xiao-Ping
Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha, China.
Front Pharmacol. 2018 Sep 19;9:1039. doi: 10.3389/fphar.2018.01039. eCollection 2018.
Dual antiplatelet treatment with aspirin and clopidogrel is the standard therapy for patients undergoing percutaneous coronary intervention (PCI). However, a portion of patients suffer from clopidogrel resistance (CR) and consequently with recurrence of cardiovascular events. Genetic factors such as loss-of-function variants of contribute a lot to CR. Recently, the N-6-adenine-specific DNA methyltransferase 1 () rs2254638 polymorphism is reported to be associated with clopidogrel response. To validate the association between rs2254638 polymorphism and clopidogrel response, 435 Chinese CAD patients receiving aspirin and clopidogrel were recruited. rs2254638 and polymorphisms were genotyped. Platelet reaction index (PRI) was measured by VASP-phosphorylation assay after treated with a 300 mg loading dose (LD) clopidogrel or 75 mg daily maintenance dose (MD) clopidogrel for at least 5 days. There was a significant difference in PRI between LD cohort and MD cohort. Carriers of allele showed significantly increased PRI in the entire cohort and in respective of the MD and LD cohorts < 0.001, = 0.003, < 0.001, respectively). However, carriers of allele exhibited significantly higher PRI only in the entire cohort and LD cohort ( = 0.023, = 0.023 respectively). PRI value was significantly higher in PM genotyped patients as compared with those carrying the IM genotypes and EM genotype ( < 0.001). Besides, carriers of the rs2254638 C allele showed significantly higher PRI in entire cohort and in the LD cohort = 0.023 = 0.008, respectively). When the patients were grouped into clopidogrel resistance (CR) and non-clopidogrel resistance (non-CR) groups, was associated with increased risk of CR in the entire cohort, the LD cohort and the MD cohort < 0.001 < 0.001, and = 0.019, respectively). Carriers of the rs2254638 C allele also showed increased risk of CR in the entire cohort and the LD cohort = 0.024, and = 0.028, respectively. N6AMT1 rs2254638 remained as a strong predictor for CR (TC vs. TT: OR = 1.880, 95% CI = 1.099-3.216, = 0.021 CC vs. TT: OR = 1.930, 95% CI = 1.056-3.527, = 0.032; TC + CC vs. TT: OR = 1.846, 95%CI = 1.126-3.026, = 0.015) after adjustment for confounding factors. Our study confirmed the influence of 2 and rs2254638 polymorphisms on clopidogrel resistance in Chinese CAD patients. Both and rs2254638 polymorphism may serve as independent biomarkers to predict CR.
阿司匹林和氯吡格雷双重抗血小板治疗是接受经皮冠状动脉介入治疗(PCI)患者的标准疗法。然而,一部分患者存在氯吡格雷抵抗(CR),进而导致心血管事件复发。功能缺失变异等遗传因素在很大程度上导致了CR。最近,有报道称N-6-腺嘌呤特异性DNA甲基转移酶1()rs2254638多态性与氯吡格雷反应相关。为验证rs2254638多态性与氯吡格雷反应之间的关联,招募了435例接受阿司匹林和氯吡格雷治疗的中国CAD患者。对rs2254638和多态性进行基因分型。在用300mg负荷剂量(LD)氯吡格雷或75mg每日维持剂量(MD)氯吡格雷治疗至少5天后,通过VASP磷酸化试验测量血小板反应指数(PRI)。LD队列和MD队列之间的PRI存在显著差异。等位基因携带者在整个队列以及MD和LD队列中PRI均显著升高(分别为<0.001、=0.003、<0.001)。然而,等位基因携带者仅在整个队列和LD队列中表现出显著更高的PRI(分别为=0.023、=0.023)。与携带IM基因型和EM基因型的患者相比,PM基因型患者的PRI值显著更高(<0.001)。此外,rs2254638 C等位基因携带者在整个队列和LD队列中PRI显著更高(分别为=0.023、=0.008)。当将患者分为氯吡格雷抵抗(CR)组和非氯吡格雷抵抗(非CR)组时,在整个队列、LD队列和MD队列中均与CR风险增加相关(分别为<0.001、<0.001、=0.019)。rs2254638 C等位基因携带者在整个队列和LD队列中也表现出CR风险增加(分别为=0.024、=0.028)。在调整混杂因素后,N6AMT1 rs2254638仍然是CR的有力预测指标(TC与TT:OR = 1.880,95%CI = 1.099 - 3.216,= 0.021;CC与TT:OR = 1.930,95%CI = 1.056 - 3.527,= 0.032;TC + CC与TT:OR = 1.846,95%CI = 1.126 - 3.026,= 0.015)。我们的研究证实了2和rs2254638多态性对中国CAD患者氯吡格雷抵抗的影响。和rs2254638多态性均可作为预测CR的独立生物标志物。