阿司匹林抵抗与环氧化酶-1、环氧化酶-2及血栓烷A2受体基因多态性相关性研究
2016-08-18许晶晶唐晓芳姚懿徐娜张佳慧马元良宋莹袁晋青
许晶晶,唐晓芳,姚懿,徐娜,张佳慧,马元良,宋莹,袁晋青
冠心病研究
阿司匹林抵抗与环氧化酶-1、环氧化酶-2及血栓烷A2受体基因多态性相关性研究
许晶晶,唐晓芳,姚懿,徐娜,张佳慧,马元良,宋莹,袁晋青
目的: 探讨冠心病二级预防中的阿司匹林抵抗现象,及其与环氧化酶-1(COX1)、环氧化酶-2(COX2)、血栓烷A2受体(TBXA2R) 基因多态性之间相关性。
方法:选取连续服用阿司匹林100 mg大于7天的冠心病患者2 881例,选择符合阿司匹林抵抗标准的患者作为阿司匹林抵抗组(AR组),共166例;阿司匹林敏感的患者200例作为对照组。应用花生四烯酸(AA)作诱导剂测定服药后的血小板聚集功能。并采用聚合酶链反应-限制性核酸内切法(PCR-RFLP)检测COX1、COX2、TBXA2R的基因多态性。
结果:阿司匹林抵抗的发生率约为5.76%(166/2 881)。三个基因共8个tagSNPs位点[COX1(rs3842788、rs4273915、rs7866582);、COX2 (rs3218625);TBXA2R(rs2238630、rs2238631、rs2238633、rs3786989)]野 生 型、杂合子及纯合子的基因型频率在两组之间差异无统计学意义。
结论:规律服药的冠心病患者阿司匹林抵抗的发生率并不高。COX1、COX2以及TBXA2R基因单核苷酸多态性与阿司匹林抵抗的发生无明显关系。
阿司匹林抵抗;多态性,单核苷酸;基因
Abstract
Objective: To explore aspirin resistance (AR) phenomenon in patients with coronary artery disease (CAD) for secondary prevention and to study the relationships between AR and COX1, COX2, TBXA2R gene polymorphisms.
Methods: A total of 2881 CAD patients taken aspirin (100 mg/day) in 7 consecutive days were enrolled. Among them, 2 groups were established as AR group, n=166 and Control group, n=200 aspirin sensitive patients. Platelet aggregation function was induced by arachidonic acid (AA), COX1, COX2 and TBXA2R gene polymorphisms were examined by polymerase chain reaction-restricted fragment length polymorphisms (PCR-RFLP) method.
Results: The occurrence rate of AR was 5.76% (166/2881). There were 8 tagSNPs locus in 3 genes as in COX1:(rs3842788), (rs4273915), (rs7866582); in: COX2 (rs3218625); in TBXA2R: (rs2238630), (rs2238631), (rs2238633),(rs3786989). The frequencies of wild type, heterozygous genotype and homozygous genotype were similar between 2 groups.
Conclusion: The incidence rate of AR is not high in CHD patients with regular aspirin medication; single nucleotide gene polymorphisms of COX1, COX2 and TBXA2R have no obvious correlation to AR.
(Chinese Circulation Journal, 2016,31:644.)
冠状动脉粥样硬化性心脏病作为我国居民致残、致死的主要病因,每年大约造成70万人死亡,约占全部死亡的四分之一。抗栓治疗能显著降低因急性心血管事件造成的死亡,在冠心病的治疗中起着至关重要的作用[1]。其中阿司匹林是冠心病二级预防中最重要的抗血小板药物,其主要作用机制是通过不可逆抑制环氧化酶-1(COX1),阻断花生四烯酸生成血栓烷A2(TXA2),从而抑制血小板聚集。……
