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dc.contributor.authorBalci, A.
dc.contributor.authorDuz, M. E.
dc.contributor.authorVurmaz, A.
dc.contributor.authorcilekar, S.
dc.contributor.authorKaya, F.
dc.date.accessioned2024-03-12T19:35:05Z
dc.date.available2024-03-12T19:35:05Z
dc.date.issued2023
dc.identifier.issn1128-3602
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2818
dc.description.abstractOBJECTIVE: Interstitial lung dis-eases (ILDs) are a group of diffuse parenchymal lung disorders that can be idiopathic [idiopath-ic pulmonary fibrosis (IPF)] or associated with other diseases and are characterized by varying degrees of inflammation and fibrosis with poor prognosis. Several indicators are essential in di-agnosing these individuals and differentiating between IPF and ILD. PATIENTS AND METHODS: The study in -volved 44 IPF patients, 22 ILD (non-IPF) patients, and 24 healthy people. We aimed to compare ILD (non-IPF) and IPF patient groups with each other and with healthy people in terms of interleukin (IL)-1, tumor necrosis factor-alpha (TNF-& alpha;), ma-trix metalloproteinase (MMP)-1, MMP-7, galec-tin (Gal)-3, IL-6, Krebs von den Lungen-6 (KL -6), total antioxidant status (TAS), total oxidant status (TOS), pyruvate kinase (PK), complete blood count (CBC), ferritin, erythrocyte sedi-mentation rate (ESR), and C-reactive protein (CRP) features. Furthermore, it was intended to assess the patient groups in terms of visu-al semi-quantitative score (VSQS) (IPF alone), respiratory function tests (RFT), and 6-minute walk test (6MWT), also potential correlations be-tween these tests and the previously indicated parameters.RESULTS: MMP-1, MMP-7, Gal-3, IL-6, KL-6, forced vital capacity (FVC), % FVC, forced expi-ratory volume in 1 second (FEV1), % FEV1, TAS, TOS, and PK values significantly elevated in IPF and ILD. Weight, IL-1, MMP-1, MMP-7, Gal-3, IL -6, KL-6, % FVC, FEV1, % FEV1, eosinophil count, and % red blood cell distribution width (RDW) val-ues differed between IPF and ILD. VSQS, 6MWT, and PK were substantially linked with MMP-1, MMP-7, Gal-3, IL-6, and KL-6 in IPF. CONCLUSIONS: The factors investigated can be helpful in the diagnosis and distinc-tion of IPF and ILD. In addition to focusing on the inflammatory environment in IPF and ILD patients, oxidant and antioxidant interactions must be studied.en_US
dc.language.isoengen_US
dc.publisherVerduci Publisheren_US
dc.relation.ispartofEuropean Review For Medical And Pharmacological Sciencesen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectInterstitial lung diseaseen_US
dc.subjectIdiopathic pulmonary fibrosisen_US
dc.subjectBiomarkersen_US
dc.subjectOxidative stressen_US
dc.subjectLung inflammationen_US
dc.titleComprehensive biomarker analysis of patients with idiopathic pulmonary fibrosis and interstitial lung disease with healthy individualsen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.identifier.volume27en_US
dc.identifier.issue12en_US
dc.identifier.startpage5468en_US
dc.identifier.endpage5479en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Balci, A.; Vurmaz, A.; cilekar, S.] Afyonkarahisar Univ, Med Fac, Dept Pulmonol, Afyon, Turkiye; [Duz, M. E.] Amasya Univ, Sabuncuoglu Serefeddin Training & Res Hosp, Dept Med Biochem, Amasya, Turkiye; [Kaya, F.] Afyonkarahisar Univ, Med Fac, Dept Radiol, Afyon, Turkiyeen_US
dc.identifier.wosWOS:001035764900015en_US
dc.identifier.pmid37401283en_US


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