期刊文献+

冠状动脉介入治疗术后氯吡格雷抵抗的生化指标分析 被引量:4

Analysis of Biochemical Markers Associated with Clopidogrel Resistance after Percutaneous Coronary Interventions
下载PDF
导出
摘要 目的研究冠心病患者经皮冠状动脉介入治疗术(PCI)后氯吡格雷抵抗(CPGR)的发生率及其相关影响因素。方法 1入选符合研究要求PCI术后患者86例,于服药前、服药24 h后分别采血,采用光透射比浊法测定血浆二磷酸腺苷(ADP)诱导的血小板聚集率(PA),血小板聚集抑制率(△P)≤10%(包含负值)即为CPGR;2根据PA将研究组分为CPGR组和非CPGR组,观察CPGR与患者的相关临床生化指标的关系。结果 86例患者CPGR的发生率为38.4%(33/86)。两组患者空腹血糖值、糖化血红蛋白、血小板平均体积(MPV)、脂蛋白a的差异有统计学意义(P<0.05)。Logistic回归分析结果显示,氯吡格雷的独立危险因素有高空腹血糖、高糖化血红蛋白、高血小板平均体积。结论 1PCI术后服用氯吡格雷药物,确实存在CPGR现象,而测定PA有助于发现此类患者;2高空腹血糖、高糖化血红蛋白与高血小板平均体积可能是冠心病患者发生CPGR现象的危险因素。 Objective To observe the incidence and the influential factors of clopidogrel resistance (CPGR) in patients who received percutancous coronary interventions(PCI). Methods Eighty six patients with PCI were subjected to the study. Light transmittance aggregometry was used to measure platclet aggregation (PA) induced by adenosine diphosphate (ADP) before and 5-7 days after clopidogrel intake. The AP measurements were based on the standard of AP ≤ 10% CPGR (negative values included) . The patients were divided into CPGR group and none CPGR group according to the △P. The relation between CPGR and the patients' relevant clinical biochemical indexes was observed. Results Among the 86 patients, the incidence rate of CPGR was 38.4% (33/86). Significant differences were noted of fasting plasma glucose, glycosylated hemoglobin and MPV between the two groups (P〈0.05). Logistic regression analysis revealed that fasting plasma glucose, glycosylated hemoglobin and PDW were independent risk factors of clopidogrel resistance. Conclusion Patients with percutaneous coronary interventions may have CPGR following clopidogrel treatment, which may be diagnosed by PA detection. Fasting plasma glucose, glycosylated hemoglobin and PDW are risk factors of clopidogrel resistance in patients with coronary heart disease.
机构地区 广东省人民医院
出处 《临床输血与检验》 CAS 2016年第3期251-254,共4页 Journal of Clinical Transfusion and Laboratory Medicine
基金 广东省医学科研基金(No.A2015442)资助
关键词 氯吡格雷 冠状动脉介入治疗术 生化指标 影响因素 Clopidogrel Percutaneous coronary interventions Biochemical parameters Influential factors
  • 相关文献

参考文献9

  • 1李蕾,韩江莉,李海燕,乔蕊,于海奕,张捷,高炜.冠心病患者氯吡格雷抵抗与血小板参数的相关性分析[J].中华医学杂志,2013,93(12):916-920. 被引量:45
  • 2余长永,张勇,邹建军,燕翔,马海涛,倪斌,朱余兵,樊宏伟,贺春晖.氯吡格雷抵抗原因及对策的研究进展[J].中国临床药理学与治疗学,2009,14(10):1168-1173. 被引量:21
  • 3Gurbel PA,Bliden KP,Hiatt Bl,et al. Clopidogrel for coronary stenting: response variability drug resistance end the effect of pretreatment platelet reactivity [J]. Circulation, 2003, 107(23):2908.
  • 4谢媛,马向华.抗血小板药物抵抗的研究进展[J].医学综述,2012,18(20):3364-3367. 被引量:5
  • 5王明亮,朱毅,甘洁民.急性冠脉综合征患者中氯吡格雷抵抗的发生率及影响因素[J].中国临床药学杂志,2010,19(3):142-144. 被引量:6
  • 6Hall HM, Baneoee S, McGuire DK. Variability of elopidogrel response in patients with type 2 diabetes mellitus[J]. Diab Vasc Dis Res, 2011, 8(4): 245- 253.
  • 7E1 Ghannudi S, Ohlmann P, Jesel L, et al. Impaired inhibition of P2Y12 by elopidogrel is a major determinant of cardiac death in diabetes mellitus patients treated by percutaneous coronary intervention[J]. Atherosclerusis,2011,217 (2) : 465-472.
  • 8Vizioli L, Muscari S, Muscafi A. The relationship of mean platelet volume with the risk and prognosis of cardiovascular diseases[J]. Int J Clin Praet, 2009,63 (10) : 1509-1515.
  • 9Lance MD, Slocp M, Henskens YM, et al. Mean platelet volume as a diagnostic marker for cardiovascular disease: drawbacks ofpreanalytical conditions and measuring techniques[J]. Clin ApplThrombHemost, 2012, 18 (6) : 561-568.

二级参考文献72

  • 1李小鹰.阿司匹林在动脉硬化性心血管疾病中的临床应用:中国专家共识(2005)[J].中华心血管病杂志,2006,34(3):281-284. 被引量:194
  • 2谭丽玲,贾三庆,王明生,李虹伟,王雷,赵敏,沈潞华,贾宁,孙志军.急性冠脉综合征患者氯吡格雷抵抗的影响因素[J].中国心血管病研究,2006,4(9):680-682. 被引量:14
  • 3Gurbel PA, Bliden KP, Hiatt BI, et al. Clopidogrel for coronary stenting: response variability drug resistance and the effect of pretreatment platelet reactivity[J]. Circulation, 2003,107(23) :2908.
  • 4CAPRIE Steering Committee. A randomized blinded trial of clopidogrel versus aspirin in patients at risk of ischemic events[J]. Lancet, 1996, 348(9068) : 1329.
  • 5The CURE Investigation. Effects of clopidogrd in addition to aspirin in patients with acute coronary syndromes without ST-segment devation[J]. N Engl J Med, 2001,345(7) :494.
  • 6Mehta SR, Yusuf S, Peter RJ, et al. Effects of pretreatment with elopi- dogrel and aspirin followed by long-tern1 therapy in patients undergoing percutaneous coronary intervention: file PCI-CURE study[J]. Lancet, 2001,358: 527.
  • 7Steinhubl SR, Berber PB, Mann JT, et al. Early and sustained dual oral antiplatelet therapy following percutaneous coronary intervention: a randomized controlled trial[J]. J Am Med Assoc, 2002,288:2411.
  • 8Lau WC, Gurbel PA, Watkins PB, ct al. Contribution of hepatic cytochrome p450 3A4 metabolic activity to the phenomenon of clopidogrel resistance[J]. Circulation, 2004,109(2) : 166.
  • 9Mitsios JV, Papathanasiou AP, Rodis FI, et al. Atorvastatin does not affect the antiplatelet potency of clopidogrel when it is administered concomitantly for 5 weeks in patients with acute coronary syndromes[J]. Circulation, 2004,109 ( 11 ) : 1335.
  • 10Forbes CD, Lowe GD, Maclaren M, et al. Clopidogrel compatibility with concomitant cardiac co-medications: a study of its interactions with a beta-blocker and a calcium uptake antagonist [ J ]. Semin Thromb Hemost, 1999,5 (Supply 2 ) : 55.

共引文献71

同被引文献40

引证文献4

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部