Wei You-Quan, Wang Dian-Gang, Yang Hao, Cao Heng
Department of Cardiology, The First Affiliated Hospital of Wannan Medical College, Wuhu, China.
Department of Cardiology, The Second People's Hospital of Huangchuan County, Xinyang, China.
PLoS One. 2015 Jul 6;10(7):e0132561. doi: 10.1371/journal.pone.0132561. eCollection 2015.
The cytochrome P450 (CYP450) 2C19 681 genotypes affect the antiplatelet activity of clopidogrel. We investigated the correlation of CYP 2C19 681G > A mutation with clopidogrel resistance (CR). Additionally, we studied the effect of CR on clinical prognosis of patients with acute coronary syndrome (ACS).
One hundred ten ACS patients undergoing percutaneous coronary intervention, who were followed-up for 1 year, were included in the study. The patients were co-administered aspirin 100 mg/d and clopidogrel 75mg/d following a loading dose of 300 mg. CR was assessed on the basis of polymorphism observed in the CYP2C19 subgroup.
Patients in GG genotype group exhibited greater inhibition of platelet aggregation than patients in GA and AA genotype groups (16.2 ± 10.1%; 10.2 ± 9.9%; 8.0 ± 5.9%, respectively, p < 0.01). CYP2C19 681GG genotype group was associated with lower CR than CYP2C19 681A allele (GA + AA) group (9/59 vs. (12+5)/51; p = 0.009). Over a follow-up of 12 months, the incidence of recurrent angina, acute myocardial infarction, and intra-stent thrombosis in CYP2C19 681 GG carriers was significantly lower than that in CYP2C19 681A allele (GA + AA) group (2/59 vs. 8/51, 1/59 vs. 6/51, 0 vs. 4/51, respectively, p < 0.05).
CYP 2C19*2 is associated with reduced clopidogrel antiplatelet activity and might be an important marker for poor prognosis of ACS.
细胞色素P450(CYP450)2C19 681基因型影响氯吡格雷的抗血小板活性。我们研究了CYP 2C19 681G>A突变与氯吡格雷抵抗(CR)的相关性。此外,我们还研究了CR对急性冠状动脉综合征(ACS)患者临床预后的影响。
本研究纳入了110例行经皮冠状动脉介入治疗的ACS患者,并对其进行了1年的随访。患者在给予300mg负荷剂量后,联合服用阿司匹林100mg/d和氯吡格雷75mg/d。根据CYP2C19亚组中观察到的多态性评估CR。
GG基因型组患者的血小板聚集抑制作用大于GA和AA基因型组患者(分别为16.2±10.1%;10.2±9.9%;8.0±5.9%,p<0.01)。CYP2C19 681GG基因型组的CR低于CYP2C19 681A等位基因(GA+AA)组(9/59对(12+5)/51;p=0.009)。在12个月的随访中,CYP2C19 681 GG携带者的复发性心绞痛、急性心肌梗死和支架内血栓形成的发生率显著低于CYP2C19 681A等位基因(GA+AA)组(分别为2/59对8/51、1/59对6/51、0对4/51,p<0.05)。
CYP 2C19*2与氯吡格雷抗血小板活性降低有关,可能是ACS预后不良的重要标志物。