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Comprehensive biomarker analysis of patients with idiopathic pulmonary fibrosis and interstitial lung disease with healthy individuals

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info:eu-repo/semantics/closedAccess

Date

2023

Author

Balci, A.
Duz, M. E.
Vurmaz, A.
cilekar, S.
Kaya, F.

Metadata

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Abstract

OBJECTIVE: 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.

Volume

27

Issue

12

URI

https://hdl.handle.net/20.500.12450/2818

Collections

  • PubMed İndeksli Yayınlar Koleksiyonu [458]
  • WoS İndeksli Yayınlar Koleksiyonu [2182]



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