Dynamic changes and associated factors of clopidogrel resistance in patients after cerebral infarction

被引:0
作者
Bo Rong Zhou
Hong Ting Shi
Rong Wang
Min Zhang
Hai Tao Guan
Zi Fan Liu
Yan Hua Deng
机构
[1] The Third Affiliated Hospital of Guangzhou Medical University,Department of Neurology
[2] The Third Affiliated Hospital of Guangzhou Medical University,Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes
[3] The Fourth Affiliated Hospital of Guangzhou Medical University,Department of Cerebrovascular
[4] The Third Affiliated Hospital of Guangzhou Medical University,Department of Clinical Laboratory
[5] Guangdong Pharmacy College,Department of Epidemics and Health Statistics
来源
Journal of Neurology | 2013年 / 260卷
关键词
Dynamic changes; Clopidogrel resistance; Cerebral infarction; Secondary prevention; Risk factors;
D O I
暂无
中图分类号
学科分类号
摘要
Stroke victims often exhibit clopidogrel resistance (CR). This prospective study was undertaken to observe changes that influence CR in the secondary prevention of cerebral infarction (CI). The study included 56 cases at high risk of stroke (HRS), 147 cases of CI and 68 control subjects. The CI and HRS groups were divided into CR and NCR (none clopidogrel resistance) subgroups using standard criteria. The NCR group was subdivided into DCR (dynamic CR) and CNCR (continuous NCR) groups. Platelet aggregation rate (PAR) was assessed at baseline and after 2 weeks treatment with clopidogrel 75 mg/day in the CI and HRS groups. In the NCR group, PAR was evaluated after 3 and 6 months of clopidogrel (75 mg/day) treatment. Baseline PAR was higher in the CI group than in the HRS or control groups (P < 0.01). The incidence of CR was 28.6 % in the CI and 13.6 % in the HRS group (P = 0.018). Diabetes mellitus, (OR 16.627; 95 % CI 4.691–58.934) and history of TIA (OR 13.711; 95 % CI 1.667–112.784) (both P < 0.05) were both associated with CR. Other independent risk factors included high total cholesterol, calcium antagonist or ACEI/ARB use. A total of 36 CR and 85 NCR cases completed 6 months follow-up. High total cholesterol was an independent risk factor for DCR (OR 0.415; 95 % CI 0.213–0.808; P = 0.01) which developed in 15 subjects at 6 months. PAR decreased by >10 % after 2 weeks in 71.4 % of patients with CR who subsequently changed drugs or received combination therapy. Dynamic CR may occur after CI. Many factors including DM\TIA\HCT\P2Y12 εC coexistence CYP2Y19 εA\combination drug, associate CR or DCR. Our results highlight the need for PAR monitoring.
引用
收藏
页码:2928 / 2937
页数:9
相关论文
共 239 条
[1]  
Chen ZM(2005)Addition of clopidogrel to aspirin in 45,852 patients with acute myocardial infarction: randomised placebo-controlled trial Lancet 366 1607-1621
[2]  
Jiang LX(1999)Pharmacokinetics of clopidogrel Semin Thromb Hemost 25 25-28
[3]  
Chen YP(2001)Effects of pretreatment with clopidogrel and aspirin followed by long-term therapy in patients undergoing percutaneous coronary intervention: the PCI-CURE study Lancet 358 527-533
[4]  
Xie JX(2007)Variability in individual responsiveness to clopidogrel: clinical implications, management, and future perspectives J Am Coll Cardiol 49 1505-1516
[5]  
Pan HC(2006)Aspirin and clopidogrel resistance: an emerging clinical entity Eur Heart J 27 647-654
[6]  
Peto R(2010)Clopidogrel non-responsiveness and risk of cardiovascular morbidity. An updated meta-analysis Thromb Haemost 103 841-848
[7]  
Collins R(2006)Role of the P2Y12 gene polymorphism in platelet responsiveness to clopidogrel in healthy subjects J Thromb Haemost 4 2096-2097
[8]  
Liu LS(2013)Clopidogrel resistance in North Indian patients of coronary artery disease and lack of its association with platelet ADP receptors P2Y1 and P2Y12 gene polymorphisms Platelets 24 297-302
[9]  
Caplain H(2006)Contribution of gene sequence variations of the hepatic cytochrome P450 3A4 enzyme to variability in individual responsiveness to clopidogrel Arterioscler Thromb Vasc Biol 26 1895-1900
[10]  
Donat F(2006)Increased risk of atherothrombotic events associated with cytochrome P450 3A5 polymorphism in patients taking clopidogrel CMAJ 174 1715-1722