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

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dc.contributor.authorKim, Bum Joon-
dc.contributor.authorRha, Joung-Ho-
dc.contributor.authorKim, Seong Rae-
dc.contributor.authorKim, Dong-Eog-
dc.contributor.authorKim, Hahn Young-
dc.contributor.authorLee, Ju-Hun-
dc.contributor.authorBae, Hee-Joon-
dc.contributor.authorHan, Moon-Ku-
dc.contributor.authorKang, Dong-Wha-
dc.contributor.authorRatanakorn, Disya-
dc.contributor.authorKim, Jong S.-
dc.contributor.authorKwon, Sun U.-
dc.date.accessioned2024-08-08T05:01:36Z-
dc.date.available2024-08-08T05:01:36Z-
dc.date.issued2014-05-
dc.identifier.issn1052-3057-
dc.identifier.issn1532-8511-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/18483-
dc.description.abstractBackground: 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.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titleThe Effect of Cilostazol on Carotid Intima-Media Thickness Progression in Patients with Symptomatic Intracranial Atherosclerotic Stenosis-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.jstrokecerebrovasdis.2013.10.007-
dc.identifier.scopusid2-s2.0-84901368491-
dc.identifier.wosid000336482000068-
dc.identifier.bibliographicCitationJOURNAL OF STROKE & CEREBROVASCULAR DISEASES, v.23, no.5, pp 1164 - 1170-
dc.citation.titleJOURNAL OF STROKE & CEREBROVASCULAR DISEASES-
dc.citation.volume23-
dc.citation.number5-
dc.citation.startPage1164-
dc.citation.endPage1170-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaCardiovascular System & Cardiology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalWebOfScienceCategoryPeripheral Vascular Disease-
dc.subject.keywordPlusRANDOMIZED CONTROLLED-TRIALS-
dc.subject.keywordPlusTYPE-2 DIABETES-MELLITUS-
dc.subject.keywordPlusARTERY INTIMA-
dc.subject.keywordPlusSTROKE-
dc.subject.keywordPlusCOMMON-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusMETAANALYSIS-
dc.subject.keywordPlusINFARCTION-
dc.subject.keywordPlusINHIBITOR-
dc.subject.keywordAuthorIntracranial arterial stenosis-
dc.subject.keywordAuthorintima-
dc.subject.keywordAuthormedia thickness-
dc.subject.keywordAuthoratherosclerosis-
dc.subject.keywordAuthorantiplatelets-
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