Plasma endocan levels associate with inflammation, vascular abnormalities, cardiovascular events, and survival in chronic kidney disease
| dc.authorid | 0000-0003-0592-7828 | |
| dc.authorid | 0009-0008-8303-1318 | |
| dc.contributor.author | Yilmaz, Mahmut I. | |
| dc.contributor.author | Siriopol, Dimitrie | |
| dc.contributor.author | Saglam, Mutlu | |
| dc.contributor.author | Kurt, Yasemin G. | |
| dc.contributor.author | Unal, Hilmi U. | |
| dc.contributor.author | Eyileten, Tayfun | |
| dc.contributor.author | Gok, Mahmut | |
| dc.date.accessioned | 2025-05-10T19:44:12Z | |
| dc.date.issued | 2014 | |
| dc.department | İstanbul Medeniyet Üniversitesi | |
| dc.description.abstract | Plasma endocan levels are elevated in a large number of diseases, and may reflect endothelial cell dysfunction. There are currently no data on endocan in patients with chronic kidney disease (CKD). Therefore, we measured plasma endocan in 251 patients with CKD (stage 1-5) and 60 control individuals. Plasma endocan concentrations correlated with estimated glomerular filtration rate (eGFR), different markers of inflammation (pentraxin 3 and high-sensitivity C-reactive protein), and vascular abnormalities (flow-mediated vasodilation (FMV) and carotid intima media thickness (CIMT)). All-cause mortality and cardiovascular events (CVE) were also analyzed with respect to plasma endocan. Patients with CKD showed significantly increased plasma endocan (4.7 [IQR 1.9-9.4] compared with controls [IQR 1.1-1.5] ng/ml), with values progressively higher across stages of CKD. On univariate analysis, plasma endocan concentrations correlated negatively with eGFR and FMV, but positively with both markers of inflammation and CIMT. However, on multivariate analysis only high-sensitivity C-reactive protein, FMV, and CIMT remained significantly associated with plasma endocan. On Cox survival analysis, endocan levels were associated with all-cause mortality and CVE in these patients. Thus, plasma endocan increases in the presence of decreasing eGFR and influences all-cause mortality and CVE in patients with CKD independent of traditional and nontraditional risk factors. | |
| dc.description.sponsorship | University of Medicine and Pharmacy, Iasi [1640/01.02.2013, IDEI-PCE 2011, PN-II-ID-PCE-2011-3-0637] | |
| dc.description.sponsorship | We thank the patients and personnel involved in the creation of this patient material. The authors express their sincere appreciation to FAVOR (FMF Arthritis Vasculitis and Orphan Diseases Research/www.favor.org.tr) web registries at Gulhane Medical Academy, Institute of Health Sciences for their supports in epidemiological and statistical advisory and invaluable guidance for the preparation of the manuscript. Part of this study was funded by grant numbers 1640/01.02.2013 and IDEI-PCE 2011, PN-II-ID-PCE-2011-3-0637 from the University of Medicine and Pharmacy, Iasi. | |
| dc.identifier.doi | 10.1038/ki.2014.227 | |
| dc.identifier.endpage | 1220 | |
| dc.identifier.issn | 0085-2538 | |
| dc.identifier.issn | 1523-1755 | |
| dc.identifier.issue | 6 | |
| dc.identifier.pmid | 24988065 | |
| dc.identifier.scopus | 2-s2.0-84926167129 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 1213 | |
| dc.identifier.uri | https://doi.org/10.1038/ki.2014.227 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14730/10869 | |
| dc.identifier.volume | 86 | |
| dc.identifier.wos | WOS:000345616900020 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Science Inc | |
| dc.relation.ispartof | Kidney International | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WOS_20250302 | |
| dc.subject | cardiovascular disease | |
| dc.subject | chronic kidney disease | |
| dc.subject | endocan | |
| dc.subject | inflammation | |
| dc.title | Plasma endocan levels associate with inflammation, vascular abnormalities, cardiovascular events, and survival in chronic kidney disease | |
| dc.type | Article |
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