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Biomarkers and location of atherosclerosis: Matrix metalloproteinase-2 may be related to intracranial atherosclerosis

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dc.contributor.authorJeon, Sang-Beom-
dc.contributor.authorChun, Sail-
dc.contributor.authorChoi-Kwon, Smi-
dc.contributor.authorChi, Hyun-Sook-
dc.contributor.authorNah, Hyun-Wook-
dc.contributor.authorKwon, Sun U.-
dc.contributor.authorKim, Won-Ki-
dc.contributor.authorKim, Jong S.-
dc.date.accessioned2021-09-06T17:02:37Z-
dc.date.available2021-09-06T17:02:37Z-
dc.date.created2021-06-18-
dc.date.issued2012-08-
dc.identifier.issn0021-9150-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/107761-
dc.description.abstractBackground: Various biomarkers are linked with the pathophysiology of atherosclerosis. We hypothesized that these factors may be associated with the location and burden of cerebral atherosclerosis. Methods: We evaluated 177 consecutive patients with chronic (>6 months) ischemic stroke: 68 with small vessel occlusion (SVO) and 109 with large-artery atherosclerosis (LAA), with the latter further sub-classified into 80 patients with intracranial atherosclerosis (ICAS) and 29 with extracranial atherosclerosis (ECAS). The number of >= 50% steno-occlusions on magnetic resonance angiography was used to assess the burden of atherosclerosis. Serum concentrations of the biomarkers (matrix metalloproteinases (MMP)-2 and -9, homocysteine, interleukin (IL)-6, tumor necrosis factor-alpha, C-reactive protein, adiponectin, leptin, resistin, free fatty acid, and lipoprotein(a)) and the metabolic syndrome were measured in each study subject. Results: Decreased plasma concentrations of MMP-2 (p = 0.020) and homocysteine (p = 0.038) were more closely associated with ICAS than with ECAS, whereas increased IL-6 concentrations were related to severe (>= 4 steno-occlusions) atherosclerosis (p = 0.031). Multiple logistic regression analysis showed that the lowest tertile of MMP-2 was independently associated with ICAS (OR 4.84, 95% CI 1.29-18.19, p = 0.022). Conclusion: Low MMP-2 plasma levels are associated with intracranial location of cerebral atherosclerosis, suggesting that MMP-2 may play a role in the development of ICAS. (C) 2012 Elsevier Ireland Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectPLASMA HOMOCYST(E)INE-
dc.subjectISCHEMIC-STROKE-
dc.subjectCEREBRAL ATHEROSCLEROSIS-
dc.subjectHOMOCYSTEINE-
dc.subjectINFARCTION-
dc.subjectDISEASE-
dc.subjectLESIONS-
dc.subjectROLES-
dc.subjectRISK-
dc.titleBiomarkers and location of atherosclerosis: Matrix metalloproteinase-2 may be related to intracranial atherosclerosis-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Won-Ki-
dc.identifier.doi10.1016/j.atherosclerosis.2012.04.013-
dc.identifier.scopusid2-s2.0-84864762421-
dc.identifier.wosid000307239800031-
dc.identifier.bibliographicCitationATHEROSCLEROSIS, v.223, no.2, pp.442 - 447-
dc.relation.isPartOfATHEROSCLEROSIS-
dc.citation.titleATHEROSCLEROSIS-
dc.citation.volume223-
dc.citation.number2-
dc.citation.startPage442-
dc.citation.endPage447-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCardiovascular System & Cardiology-
dc.relation.journalWebOfScienceCategoryCardiac & Cardiovascular Systems-
dc.relation.journalWebOfScienceCategoryPeripheral Vascular Disease-
dc.subject.keywordPlusPLASMA HOMOCYST(E)INE-
dc.subject.keywordPlusISCHEMIC-STROKE-
dc.subject.keywordPlusCEREBRAL ATHEROSCLEROSIS-
dc.subject.keywordPlusHOMOCYSTEINE-
dc.subject.keywordPlusINFARCTION-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusLESIONS-
dc.subject.keywordPlusROLES-
dc.subject.keywordPlusRISK-
dc.subject.keywordAuthorAtherosclerosis-
dc.subject.keywordAuthorBiological markers-
dc.subject.keywordAuthorMatrix metalloproteinase-
dc.subject.keywordAuthorInterkeukin-6-
dc.subject.keywordAuthorHomocysteine-
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