The association of vascular endothelial growth factor, metalloproteinases and their tissue inhibitors with cardiovascular risk factors in the metabolic syndrome

dc.authorid0000-0003-4121-5107
dc.authorid0000-0003-3343-8650
dc.authorid0000-0002-1347-8498
dc.contributor.authorErman, H.
dc.contributor.authorGelisgen, R.
dc.contributor.authorCengiz, M.
dc.contributor.authorTabak, O.
dc.contributor.authorErdenen, F.
dc.contributor.authorUzun, H.
dc.date.accessioned2025-05-10T19:28:40Z
dc.date.issued2016
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractOBJECTIVE: The present study was proposed to examine the matrix metalloproteinases (MMPs), tissue inhibitors of metalloproteinases (TIMPs) and vascular endothelial growth factor (VEGF) in patients with metabolic syndrome (MetS), and to compare these parameters with healthy controls. We also compared the possible association of the circulating levels of MMP-2, MMP-9, TIMP-1, TIMP-2, and VEGF with cardiovascular risk factors in patients with MetS. We also compared the possible association of the circulating levels of MMP-2, MMP-9, TIMP-1, TIMP-2, and VEGF with cardiovascular risk factors in patients with MetS. PATIENTS AND METHODS: A total of 45 patients with MetS and 17 healthy controls with a body mass index (BMI) less than 25 kg/m(2) were enrolled in the study. Plasma MMP-2, MMP-9, TIMP-1, TIMP-2, and VEGF levels were determined using ELISA. RESULTS: TIMP-1,-2, MMP-2,-9 levels were significantly higher in patients with MetS compared with healthy controls (p < 0.001). Carotid intima-media thickness and serum VEGF levels were found to be significantly increased (p < 0.01, p < 0.05 respectively) in MetS compared with healthy controls. According to the ROC curves, TIMP-1 levels were both sensitive (93.3%) and specific (81.2%). CONCLUSIONS: We observed that the patients with MetS have increased circulating concentrations of MMP-9, MMP-2, and TIMP-1, TIMP-2 that are associated with increased concentrations of VEGF. These findings suggest that MMP-2 may have a role in the increased cardiovascular risk of MetS patients.
dc.identifier.endpage1022
dc.identifier.issn1128-3602
dc.identifier.issue6
dc.identifier.pmid27049251
dc.identifier.scopus2-s2.0-85017183688
dc.identifier.scopusqualityQ2
dc.identifier.startpage1015
dc.identifier.urihttps://hdl.handle.net/20.500.14730/7433
dc.identifier.volume20
dc.identifier.wosWOS:000376901700005
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherVerduci Publisher
dc.relation.ispartofEuropean Review For Medical and Pharmacological Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectMetabolic syndrome
dc.subjectMatrix metalloproteinases
dc.subjectTissue inhibitors of metalloproteinases
dc.subjectVascular endothelial growth factor
dc.subjectCarotid Intima-Media Thickness
dc.titleThe association of vascular endothelial growth factor, metalloproteinases and their tissue inhibitors with cardiovascular risk factors in the metabolic syndrome
dc.typeArticle

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