The Effect of Cilostazol on Carotid Intima-Media Thickness Progression in Patients with Symptomatic Intracranial Atherosclerotic Stenosisopen access
- Authors
- Kim, Bum Joon; Rha, Joung-Ho; Kim, Seong Rae; Kim, Dong-Eog; Kim, Hahn Young; Lee, Ju-Hun; Bae, Hee-Joon; Han, Moon-Ku; Kang, Dong-Wha; Ratanakorn, Disya; Kim, Jong S.; Kwon, Sun U.
- Issue Date
- May-2014
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- Intracranial arterial stenosis; intima; media thickness; atherosclerosis; antiplatelets
- Citation
- JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, v.23, no.5, pp 1164 - 1170
- Pages
- 7
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF STROKE & CEREBROVASCULAR DISEASES
- Volume
- 23
- Number
- 5
- Start Page
- 1164
- End Page
- 1170
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/18483
- DOI
- 10.1016/j.jstrokecerebrovasdis.2013.10.007
- ISSN
- 1052-3057
1532-8511
- Abstract
- 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.
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Collections - Graduate School > Department of Medicine > 1. Journal Articles

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