The Effect of Cilostazol on Carotid Intima-Media Thickness Progression in Patients with Symptomatic Intracranial Atherosclerotic Stenosis

被引:5
|
作者
Kim, Bum Joon [1 ]
Rha, Joung-Ho [2 ]
Kim, Seong Rae [2 ]
Kim, Dong-Eog [3 ]
Kim, Hahn Young [4 ]
Lee, Ju-Hun [5 ]
Bae, Hee-Joon [6 ]
Han, Moon-Ku [6 ]
Kang, Dong-Wha [1 ]
Ratanakorn, Disya [7 ]
Kim, Jong S. [1 ]
Kwon, Sun U. [1 ]
机构
[1] Univ Ulsan, Dept Neurol, Asan Med Ctr, Seoul 138736, South Korea
[2] Inha Univ Hosp, Dept Neurol, Inchon, South Korea
[3] Dong Guk Univ Hosp, Dept Neurol, Ilsan, South Korea
[4] Keonguk Univ Hosp, Dept Neurol, Seoul, South Korea
[5] Kangdong Sacred Heart Hosp, Dept Neurol, Seoul, South Korea
[6] Seoul Natl Univ, Bundang Hosp, Dept Neurol, Songnam, South Korea
[7] Mahidol Univ, Ramathibodi Hosp, Dept Med, Div Neurol, Bangkok 10700, Thailand
来源
关键词
Intracranial arterial stenosis; intima; media thickness; atherosclerosis; antiplatelets; RANDOMIZED CONTROLLED-TRIALS; TYPE-2; DIABETES-MELLITUS; ARTERY INTIMA; STROKE; COMMON; RISK; METAANALYSIS; INFARCTION; INHIBITOR;
D O I
10.1016/j.jstrokecerebrovasdis.2013.10.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: The progression of carotid intima- media thickness (CIMT) is closely associated with ischemic stroke recurrence. However, the efficacy of cilostazol on preventing CIMT progression in stroke patients has never been investigated properly by a prospective trial. Methods: This study is a part of '' Trial of Cilostazol in Symptomatic Intracranial Arterial Stenosis- 2.'' Six centers that are available to measure CIMT according to the protocol participated in this substudy. After 7 months of randomization, the changes of CIMT were compared between cilostazol group and clopidogrel group. CIMT was measured by a semiautomated software (Intimascope) and was presented as the mean of maximum (CIMT- max) and average (CIMT- ave) of both common carotid arteries. Linear logistic regression analysis and analysis of covariance were performed to verify the independent factors associated with CIMT progression. Results: Among the 85 patients, 39 subjects were assigned to cilostazol group and 46 subjects to clopidogrel group. Follow- up CIMT significantly decreased in cilostazol group (CIMT-max: -.03 +/- .11 and CIMT-ave: -.02 +/- .08) compared with the increase in clopidogrel group (CIMT-max: .04 +/- .20 and CIMT-ave: .04 +/- .11; P = .05 and P = .04, respectively). Female, diabetes, and smoking were independently associated with the progression of CIMT, whereas the use of cilostazol was against CIMT progression from the results of linear regression analysis (P = .03 for both CIMT-max and CIMT-ave). The use of cilostazol also well predicted less progression of CIMT at follow-up after adjusting for baseline CIMT values and conventional risk factors (CIMT-max: P = .04 and CIMT-ave: P = .03). Conclusion: Cilostazol has a beneficial effect in preventing the progression of CIMT in ischemic stroke patients.
引用
收藏
页码:1164 / 1170
页数:7
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