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dc.contributor.authorIturbe-Fernández D.
dc.contributor.authorPulito-Cueto V.
dc.contributor.authorMora-Cuesta V.M.
dc.contributor.authorRemuzgo-Martínez S.
dc.contributor.authorFerrer-Pargada D.J.
dc.contributor.authorGenre F.
dc.contributor.authorAlonso-Lecue P.
dc.contributor.authorLópez-Mejías R.
dc.contributor.authorAtienza-Mateo B.
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel 
dc.contributor.authorCifrián-Martínez J.M.
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-10-09T17:21:21Z
dc.date.available2024-10-09T17:21:21Z
dc.date.issued2024-05-16
dc.identifier.issn2227-9059
dc.identifier.urihttps://hdl.handle.net/10902/34194
dc.description.abstractOsteopontin (OPN) is a glycoprotein involved in Th1 and Th17 differentiation, and inflammation and tissue remodeling. OPN is a biomarker of disease activity in patients with autoimmune inflammatory conditions. This study aimed to assess the diagnostic and prognostic value of OPN in interstitial lung diseases (ILDs). Between May 2016 and October 2019, 344 patients with ILD were recruited at the Hospital Universitario Marqués de Valdecilla (Spain) and were prospectively followed-up. This study involved the determination of OPN serum levels by ELISA and OPN RNA expression quantified using qPCR. Six genetic polymorphisms in OPN (rs28357094, rs2853749, rs2853750, rs11728697, rs7695531, and rs1126616) were genotyped using TaqMan assays. OPN serum levels were also assessed in 140 healthy controls. OPN serum levels (median [interquartile range]) were significantly higher in ILD patients than in controls (1.05 [0.75-1.51] ng/mL versus 0.81 [0.65-0.98] ng/mL in healthy controls; p < 0.01). OPN serum levels were inversely correlated with the forced vital capacity. OPN serum levels were also higher in ILD patients who died or underwent lung transplantation when compared with the remaining ILD patients (1.15 [0.80-1.72] ng/mL versus 0.99 [0.66-1.32] ng/mL; p = 0.05). Survival worsened in ILD patients with OPN > 1.03 ng/mL at 1, 3, and 5 years. No statistically significant differences in the genetic frequencies of OPN polymorphisms or the RNA expression were found among the different ILD groups. Elevated levels of OPN in the serum may be a useful indicator in identifying patients with ILD who are more likely to experience poor outcomes.es_ES
dc.description.sponsorshipFunding: This study was financed by the SEPAR GEEPID-Roche 2017 grant, which was awarded to DIF. Writing and editorial assistance was funded by an unrestricted grant from Boehringer Ingelheim (BI) Spain. BI was given the opportunity to review the manuscript for medical and scientific accuracy, as well as intellectual property considerations. Acknowledgments: The authors wish to thank Content Ed Net and Carmen Acuña-Condal for their help in writing and editing the manuscript.es_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherMDPI AGes_ES
dc.rights© 2024 by the authors.Licensee MDPI, Basel, Switzerland.This article is an open access articledistributed under the terms andconditions of the Creative CommonsAttribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceBiomedicines, 2024, 12(5), 1108es_ES
dc.subject.otherInterstitial lung disease (ILD)es_ES
dc.subject.otherIdiopathic pulmonary fibrosises_ES
dc.subject.otherBiomarkerses_ES
dc.subject.otherOsteopontines_ES
dc.titleOsteopontin as a biomarker in interstitial lung diseaseses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/biomedicines12051108es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/biomedicines12051108
dc.type.versionpublishedVersiones_ES


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© 2024 by the authors.Licensee MDPI, Basel, Switzerland.This article is an open access articledistributed under the terms andconditions of the Creative CommonsAttribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).Excepto si se señala otra cosa, la licencia del ítem se describe como © 2024 by the authors.Licensee MDPI, Basel, Switzerland.This article is an open access articledistributed under the terms andconditions of the Creative CommonsAttribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).