Endocan as a potential biomarker of disease severity and exacerbations in COPD

dc.contributor.authorIn, Erdal
dc.contributor.authorKuluozturk, Mutlu
dc.contributor.authorTurgut, Teyfik
dc.contributor.authorGeckil, Aysegul Altintop
dc.contributor.authorIlhan, Nevin
dc.date.accessioned2026-08-12T17:35:47Z
dc.date.issued2021
dc.departmentFırat Üniversitesi
dc.description.abstractIntroduction: Endocan is a proteoglycan that is regarded as a novel marker of endothelial dysfunction. Endothelial dysfunction in pulmonary vascular bed is known to play an important role for the pathogenesis of COPD. Objective: This study aimed to determine serum endocan levels in patients with stable COPD and acute exacerbation of COPD (AECOPD) and to test the relationship between serum endocan levels and exacerbations. Methods: This study enrolled a total of 55 COPD patients, 24 of which had AECOPD and 31 had stable COPD. All patients' basic demographic and clinical data were recorded and blood samples were collected. Results: Serum endocan levels were significantly higher in the AECOPD group compared to the stable COPD and control groups (for both p < 0.001) and stable COPD group had higher levels than the control group (p < 0.005). Additionally, serum endocan levels were negatively correlated with FVC, FEV1, partial oxygen pressure and oxygen saturation (r = -0.30, p = 0.03; r = -0.34, p = 0.01; r = -0.34, p = 0.01 and r = -0.36, p = 0.007 respectively), and positively correlated with disease duration and systolic pulmonary artery pressure (r = 0.47, p < 0.001; r = 0.31, p = 0.02 respectively). A cut-off value of 434.29 pg/ml for endocan predicted exacerbation with a sensitivity of 79% and a specificity of 84% (AUC: 0.778, 95% Cl 0.648-0.909; p < 0.001). Logistic regression analysis revealed that increased endocan levels was independent predictor of COPD exacerbation (OR = 9.32, 95%CI, 1.64-52.95; p = 0.01). Conclusion: Endocan may be a novel biomarker for detection of endothelial dysfunction and prediction of exacerbations in patients with COPD.
dc.identifier.doi10.1111/crj.13320
dc.identifier.endpage453
dc.identifier.issn1752-6981
dc.identifier.issn1752-699X
dc.identifier.issue4
dc.identifier.orcid0000-0002-8807-5853
dc.identifier.orcid0000-0002-0208-8929
dc.identifier.pmid33319462
dc.identifier.scopus2-s2.0-85098120541
dc.identifier.scopusqualityQ2
dc.identifier.startpage445
dc.identifier.urihttps://doi.org/10.1111/crj.13320
dc.identifier.urihttps://hdl.handle.net/11508/57664
dc.identifier.volume15
dc.identifier.wosWOS:000605362000001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofClinical Respiratory Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectchronic obstructive pulmonary disease
dc.subjectendocan
dc.subjectendothelial cell specific molecule-1
dc.subjectendothelial dysfunction
dc.subjectsystemic inflammation
dc.titleEndocan as a potential biomarker of disease severity and exacerbations in COPD
dc.typeArticle

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