Adhesion molecules as diagnostic and severity biomarkers in pediatric community-acquired pneumonia

dc.contributor.authorTanir Basaranoglu, Sevgen
dc.contributor.authorOzsurekci, Yasemin
dc.contributor.authorAykac, Kubra
dc.contributor.authorIyigun, Irem
dc.contributor.authorSatirer, Ozlem
dc.contributor.authorAkin, Mustafa Senol
dc.contributor.authorCeyhan, Mehmet
dc.date.accessioned2026-08-12T17:35:50Z
dc.date.issued2021
dc.departmentFırat Üniversitesi
dc.description.abstractBackground Discrimination of the cases with severe and mild pneumonia is crucial due to the requirement of hospitalization, additional management, and treatment protocols. We aimed to analyze the role of IL6 (Interleukin), IL8, IL10, VCAM-1 (soluble Vascular Cell Adhesion Molecule), and sSELE (soluble E-selectin) in the diagnosis and prognostic evaluation of community-acquired pneumonia (CAP). Methods Pediatric patients with severe pneumonia (SP) were hospitalized and patients with mild disease (MP) were treated in the community. IL6, IL8, IL10, VCAM-1, and sSELE levels of the patients were investigated and compared with the age- and gender-matched healthy subjects. Results A total of 113 patients fulfilling the criteria for a diagnosis of CAP were enrolled in the study, 62 (54.8%) of which had SP and 51 (45%) had MP. MP and SP groups were significantly different in terms of IL8, IL10, and sSELE levels. Patients with SP and MP had significantly different WBC, ESR, and CRP values, as well. Conclusions Besides classical acute phase parameters, inflammatory response parameters such as IL6 and VCAM-1 levels may be helpful in diagnosis of pneumonia. In terms of determination of disease severity in pediatric CAP, systemic inflammatory markers like IL8 and IL10 and adhesion molecules like sSELE seem useful in clinical settings.
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK) [216S316]
dc.description.sponsorshipThis work was funded by the Scientific and Technological Research Council of Turkey (TUBITAK) (3001 - Initial R&D Projects Support Program-Grant no: 216S316)
dc.identifier.doi10.1111/crj.13334
dc.identifier.endpage529
dc.identifier.issn1752-6981
dc.identifier.issn1752-699X
dc.identifier.issue5
dc.identifier.orcid0000-0001-7583-389X
dc.identifier.orcid0000-0003-0055-8277
dc.identifier.orcid0000-0002-0974-4765
dc.identifier.pmid33484111
dc.identifier.scopus2-s2.0-85100490469
dc.identifier.scopusqualityQ2
dc.identifier.startpage522
dc.identifier.urihttps://doi.org/10.1111/crj.13334
dc.identifier.urihttps://hdl.handle.net/11508/57697
dc.identifier.volume15
dc.identifier.wosWOS:000615695600001
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.subjectadhesion molecules
dc.subjectcommunity? acquired pneumonia
dc.subjectdiagnosis of pneumonia
dc.subjectpediatric
dc.titleAdhesion molecules as diagnostic and severity biomarkers in pediatric community-acquired pneumonia
dc.typeArticle

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