Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30261
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dc.date.accessioned2023-01-04T13:31:11Z-
dc.date.available2023-01-04T13:31:11Z-
dc.date.issued2017-
dc.identifier.citationDilektaşlı, A. G. vd. (2017). ''Serum CCL-18 level is a risk factor for COPD exacerbations requiring hospitalization''. International Journal of COPD, 12, 199-208.en_US
dc.identifier.issn1178-2005-
dc.identifier.urihttps://www.dovepress.com/getfile.php?fileID=34330-
dc.identifier.urihttps://doi.org/10.2147/COPD.S118424-
dc.identifier.urihttp://hdl.handle.net/11452/30261-
dc.description.abstractIntroduction: Chemokine (C-C motif) ligand 18 (CCL-18) has been shown to be elevated in chronic obstructive pulmonary disease (COPD) patients. This study primarily aimed to evaluate whether the serum CCL-18 level differentiates the frequent exacerbator COPD phenotype from infrequent exacerbators. The secondary aim was to investigate whether serum CCL-18 level is a risk factor for exacerbations requiring hospitalization. Materials and methods: Clinically stable COPD patients and participants with smoking history but normal spirometry (NSp) were recruited for the study. Modified Medical Research Council Dyspnea Scale, COPD Assessment Test, spirometry, and 6-min walking test were performed. Serum CCL-18 levels were measured with a commercial ELISA Kit. Results: Sixty COPD patients and 20 NSp patients were recruited. Serum CCL-18 levels were higher in COPD patients than those in NSp patients (169 vs 94 ng/mL, P, 0.0001). CCL-18 level was significantly correlated with the number of exacerbations (r=0.30, P=0.026), although a difference in CCL-18 values between infrequent and frequent exacerbator COPD (168 vs 196 ng/mL) subgroups did not achieve statistical significance (P=0.09). Serum CCL-18 levels were significantly higher in COPD patients who had experienced at least one exacerbation during the previous 12 months. Overall, ROC analysis revealed that a serum CCL-18 level of 181.71 ng/mL could differentiate COPD patients with hospitalized exacerbations from those who were not hospitalized with a 88% sensitivity and 88.2% specificity (area under curve: 0.92). Serum CCL-18 level had a strong correlation with the frequency of exacerbations requiring hospitalization (r=0.68, P, 0.0001) and was found to be an independent risk factor for hospitalized exacerbations in the multivariable analysis. Conclusion: CCL-18 is a promising biomarker in COPD, as it is associated with frequency of exacerbations, particularly with severe COPD exacerbations requiring hospitalization, as well as with functional parameters and symptom scores.en_US
dc.language.isoenen_US
dc.publisherDove Medicalen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectRespiratory systemen_US
dc.subjectCOPDen_US
dc.subjectFrequent exacerbatoren_US
dc.subjectHospitalized exacerbationen_US
dc.subjectPARC/(CCL-18)en_US
dc.subjectObstructive pulmonary-diseaseen_US
dc.subjectSystemic inflammationen_US
dc.subjectLung-functionen_US
dc.subjectBiomarkersen_US
dc.subjectFrequencyen_US
dc.subjectCCL18en_US
dc.subjectMacrophagesen_US
dc.subjectValidationen_US
dc.subjectPhenotypesen_US
dc.subjectDyspneaen_US
dc.subject.meshAgeden_US
dc.subject.meshBiomarkersen_US
dc.subject.meshCase-control studiesen_US
dc.subject.meshChemokines, CCen_US
dc.subject.meshCross-sectional studiesen_US
dc.subject.meshDisease progressionen_US
dc.subject.meshEnzyme-linked immunosorbent assayen_US
dc.subject.meshExercise toleranceen_US
dc.subject.meshFemaleen_US
dc.subject.meshHospitalizationen_US
dc.subject.meshHumansen_US
dc.subject.meshLungen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshPhenotypeen_US
dc.subject.meshPulmonary disease, chronic obstructiveen_US
dc.subject.meshRisk factorsen_US
dc.subject.meshSpirometryen_US
dc.subject.meshSurveys and questionnairesen_US
dc.subject.meshUp-regulationen_US
dc.subject.meshWalk testen_US
dc.titleSerum CCL-18 level is a risk factor for COPD exacerbations requiring hospitalizationen_US
dc.typeArticleen_US
dc.identifier.wos000391200500001tr_TR
dc.identifier.scopus2-s2.0-85009465893tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Akciğer Hastalıkları Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyoistatistik Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0003-3604-8826tr_TR
dc.identifier.startpage199tr_TR
dc.identifier.endpage208tr_TR
dc.identifier.volume12tr_TR
dc.relation.journalInternational Journal of COPDen_US
dc.contributor.buuauthorDilektaşlı, Aslı Görek-
dc.contributor.buuauthorÇetinoğlu, Ezgi Demirdoğen-
dc.contributor.buuauthorUzaslan, Esra-
dc.contributor.buuauthorBudak, Ferah-
dc.contributor.buuauthorCoşkun, Funda-
dc.contributor.buuauthorUrsavaş, Ahmet-
dc.contributor.buuauthorErcan, İlker-
dc.contributor.buuauthorEge, Ercüment-
dc.contributor.researcheridAAD-1271-2019tr_TR
dc.contributor.researcheridF-4657-2014tr_TR
dc.contributor.researcheridAAI-3169-2021tr_TR
dc.contributor.researcheridAAI-1004-2021tr_TR
dc.contributor.researcheridABF-2367-2020tr_TR
dc.identifier.pubmed28115842tr_TR
dc.subject.wosRespiratory systemen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid36466376600tr_TR
dc.contributor.scopusid57189524206tr_TR
dc.contributor.scopusid8761653500tr_TR
dc.contributor.scopusid6701913697tr_TR
dc.contributor.scopusid21734137500tr_TR
dc.contributor.scopusid8329319900tr_TR
dc.contributor.scopusid6603789069tr_TR
dc.contributor.scopusid6701341320tr_TR
dc.subject.scopusUndifferentiated Connective Tissue Diseases; Adrenal Cortex Hormone; Global Initiativesen_US
dc.subject.emtreeBiological markeren_US
dc.subject.emtreeCC chemokine ligand 18en_US
dc.subject.emtreeChemokineen_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeBeta chemokineen_US
dc.subject.emtreeBiological markeren_US
dc.subject.emtreeCCL18 protein, humanen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeArea under the curveen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeChronic obstructive lung diseaseen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCOPD assessment testen_US
dc.subject.emtreeDiagnostic test accuracy studyen_US
dc.subject.emtreeDisease associationen_US
dc.subject.emtreeDisease exacerbationen_US
dc.subject.emtreeDisease severityen_US
dc.subject.emtreeELISA kiten_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHospitalizationen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeModified medical research council dyspnea scaleen_US
dc.subject.emtreePhenotypeen_US
dc.subject.emtreePredictive valueen_US
dc.subject.emtreeProtein blood levelen_US
dc.subject.emtreeReceiver operating characteristicen_US
dc.subject.emtreeRespiratory tract disease assessmenten_US
dc.subject.emtreeRisk factoren_US
dc.subject.emtreeSensitivity and specificityen_US
dc.subject.emtreeSix minute walk testen_US
dc.subject.emtreeSpirometryen_US
dc.subject.emtreeUpregulationen_US
dc.subject.emtreeBlooden_US
dc.subject.emtreeCase control studyen_US
dc.subject.emtreeCross-sectional studyen_US
dc.subject.emtreeDisease courseen_US
dc.subject.emtreeEnzyme linked immunosorbent assayen_US
dc.subject.emtreeExercise toleranceen_US
dc.subject.emtreeLungen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreePathophysiologyen_US
dc.subject.emtreePulmonary disease, chronic obstructiveen_US
dc.subject.emtreeQuestionnaireen_US
dc.subject.emtreeRisk factoren_US
dc.subject.emtreeWalk testen_US
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