机构:[1]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China.重点科室诊疗科室神经病学中心神经病学中心首都医科大学附属天坛医院[2]China National Clinical Research Center for Neurological Diseases, China.[3]Center of Stroke, Beijing Institute for Brain Disorders, China.[4]Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease, China.
ObjectiveTo determine the relationship of high-sensitive C-reactive protein (hsCRP) and the efficacy and safety of dual antiplatelet therapy in patients with and without intracranial arterial stenosis (ICAS) in the Clopidogrel in High-Risk Patients with Acute Non-disabling Cerebrovascular Events (CHANCE) trial.MethodsA subgroup of 807 patients with both magnetic resonance angiography images and hsCRP measurement was analyzed. Cox proportional hazards models were used to assess the interaction of hsCRP levels with the effects of dual and single antiplatelet therapy.ResultsA total of 358 (44.4%) patients had ICAS and 449 (55.6%) did not. The proportion of patients with elevated hsCRP levels was higher in the ICAS group than in the non-ICAS group (40.2% vs 30.1%, p = 0.003). There was significant interaction between hsCRP and the 2 antiplatelet therapy groups in their effects on recurrent stroke after adjustment for confounding factors in the patients with ICAS (p = 0.012), but not in those without (p = 0.256). Compared with aspirin alone, clopidogrel plus aspirin significantly reduced the risk of recurrent stroke only in the patients with ICAS and nonelevated hsCRP levels (adjusted hazard ratio 0.27; 95% confidence interval 0.11 to 0.69; p = 0.006). Similar results were observed for composite vascular events. No significant difference in bleeding was found.ConclusionsPresence of both ICAS and nonelevated hsCRP levels may predict better response to dual antiplatelet therapy in reducing new stroke and composite vascular events in minor stroke or high-risk TIA patients. Further large-scale randomized and controlled clinical trials are needed to confirm this finding.
基金:
Ministry of Science and Technology of the People's Republic of ChinaMinistry of Science and Technology, China [2013BAI09B03, 2013BAI09B14, 2015BAI12B04, 2015BAI12B02, 2016YFC0901000, 2016YFC0901001, 2016YFC0901002]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China [81671128, 81471211]; Beijing Biobank of Cerebral Vascular Disease [D131100005313003]; Beijing Institute for Brain Disorders [1152130306]; Beijing Municipal Science and Technology CommissionBeijing Municipal Science & Technology Commission [D131100002313002, D151100002015001, D151100002015002, D151100002015003, Z15110200390000, Z151100003915117]; Beijing Municipal Commission of Health and Family Planning [2016-1-2041, SML20150502]
第一作者机构:[1]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China.[2]China National Clinical Research Center for Neurological Diseases, China.[3]Center of Stroke, Beijing Institute for Brain Disorders, China.[4]Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease, China.
通讯作者:
通讯机构:[1]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China.[2]China National Clinical Research Center for Neurological Diseases, China.[3]Center of Stroke, Beijing Institute for Brain Disorders, China.[4]Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease, China.
推荐引用方式(GB/T 7714):
Jiejie Li,Anxin Wang,Xingquan Zhao,et al.High-sensitive C-reactive protein and dual antiplatelet in intracranial arterial stenosis[J].NEUROLOGY.2018,90(6):E447-E454.doi:10.1212/WNL.0000000000004928.
APA:
Jiejie Li,Anxin Wang,Xingquan Zhao,Liping Liu,Xia Meng...&Yongjun Wang.(2018).High-sensitive C-reactive protein and dual antiplatelet in intracranial arterial stenosis.NEUROLOGY,90,(6)
MLA:
Jiejie Li,et al."High-sensitive C-reactive protein and dual antiplatelet in intracranial arterial stenosis".NEUROLOGY 90..6(2018):E447-E454