Relationship between Clopidogrel Response,Early Neurological Deterioration and
CYP2C19 Gene Polymorphism in Symptomatic Intracranial Atherosclerotic Stenosis
(sICAS)Patients[J]. Journal of Sun Yat-sen University (Medical Sciences), 2017, 38(6).
Relationship between Clopidogrel Response,Early Neurological Deterioration and
CYP2C19 Gene Polymorphism in Symptomatic Intracranial Atherosclerotic Stenosis
(sICAS)Patients[J]. Journal of Sun Yat-sen University (Medical Sciences), 2017, 38(6).DOI:
【目的】探讨CYP2C19基因多态性与症状性颅内动脉狭窄患者氯吡格雷反应性及早期神经功能恶化的相关 性。【方法】连续性收集症状性颅内动脉狭窄患者116例,根据是否出现早期神经功能恶化分为恶化组22例与非恶化组94 例,记录基线资料,检测CYP2C19基因型,口服氯吡格雷后第8天测定血小板最大聚集率,比较两组CYP2C19基因多态性与 氯吡格雷反应性。【结果】恶化组患者合并糖尿病、既往短暂性脑缺血发作(TIA)史明 显高于非恶化组(P<0.05);恶化组 CYP2C19*2 位点 AA 基因型、A 等位基因频率明显高于非恶化组,GG 基因型频率明显低于非恶化组(27.27% vs 2.13%, 50.00% vs 14.84%,27.27% vs 72.34%)(P<0.01);弱代谢型患者血小板最大聚集率明显高于快代谢型、中间代谢型(P<0.01, P<0.05),中间代谢型血小板最大聚集率明显高于快代谢型(P<0.01);恶化组CYP2C19基因分型快代谢型明显低于非恶化 组,弱代谢型明显高于非恶化组(22.73% vs 65.96%,36.36% vs 5.32%)(P<0.01);发生氯吡格雷抵抗59.09%明显高于非恶化 组28.72%(P<0.05)。【结论】CYP2C19基因多态性与症状性颅内动脉狭窄患者氯吡格雷反应性及早期神经功能恶化有关。
Abstract
【Objective】To investigate the relationship between clopidogrel response,early neurological deterioration and CYP2C19 gene polymorphism in sICAS patients.【Methods】116 sICAS patients were divided into deterioration group and non-deterio? ration group by whether appear early nervous function deterioration. Record included the baseline data,the genotypes of CYP2C19, platelet maximum aggregation rate after 7 days of given clopidogrel,CYP2C19 genotype and clopidogrel reaction were compared be? tween two groups.【Results】The deterioration group combination with diabetes,stroke/TIA were significantly higher than the non-de? terioration group(P<0.05);The frequency of CYP2C19*2 AA genotype and A allele were significantly higher than those in non-dete? rioration group. The frequency of GG genotype were significantly lower than non-deterioration group(27.27% vs 2.13%,50.00% vs 14.84%,27.27% vs 72.34%)(P<0.01);The poor metabolic genotype platelet maximum aggregation rate were significantly higher than that of the fast-metabolic genotype and middle metabolic genotype(P<0.01,P<0.05),Middle metabolic genotype platelet maxi? mum aggregation rate were significantly higher than fast-metabolic genotype(P<0.01);The deterioration group fast-metabolic geno? type were significantly lower than non-deterioration group,poor metabolic genotype were significantly higher than non-deteriorationgroup(22.73% vs 65.96%,36.36% vs 5.32%)(P<0.01);Clopidogrel resistance rate 59.09% were significantly higher non-deteriora? tion group 28.72%(P<0.05). 【Conclusion】Clopidogrel response and early neurological deterioration in sICAS patients is associated with CYP2C19 gene polymorphism.