Serum KL-6 as a biomarker to predict progression at one year in interstitial lung disease

dc.contributor.authorBonella, Francesco
dc.contributor.authorVegas Sánchez, M.C.
dc.contributor.authorAlessandro, M. d'
dc.contributor.authorMillan Billi, P.
dc.contributor.authorSantos, R.F.
dc.contributor.authorSchröder, N.
dc.contributor.authorBastos, H. N.
dc.contributor.authorMolina Molina, M.
dc.contributor.authorSánchez Pernaute, O.
dc.contributor.authorCastillo Villegas, D.
dc.contributor.authorBargagli, E.
dc.date.accessioned2025-11-13T08:34:29Z
dc.date.available2025-11-13T08:34:29Z
dc.date.issued2025-10-09
dc.date.updated2025-10-31T10:37:54Z
dc.description.abstractAbout one third of non-IPF ILD patients progresses over time. Serum KL-6, a lung epithelial mucin type 1, is an established marker to assess disease severity in ILD but its ability to predict progression needs to be further explored. To investigate whether serum KL-6 is of additional value to stratify the patients for the risk of developing clinical or functional progression at one year. ILD patients from 6 European centers were retrospectively enrolled. Disease progression was defined as relative decline >= 10% in FVC or >= 15% in DLco from baseline. Serum KL-6 was measured using a full-automated chemiluminescent immunoassay (Fujirebio). Comparative logistic regression was used to identify predictors of progression at one year. 303 patients were included. 37% developed progression after one year from KL-6 measurement. A stepwise selection was used to identify and include five predictors of progression in a risk score: age, gender, BMI, FVC, and KL-6. The final model was superior to KL-6 alone to predict progression at one year, with 55% sensitivity, 73% specificity and 67% accuracy at a cut-off of 5. Patients were stratified in low and high risk of progression at one year based on the cut-off of 5, with a similar accuracy for IIP 0.687 and CTD-ILD 0.720 but not for HP. Serum KL-6 levels, included in a risk score with other clinical and functional variables, may help to better stratify patients for the risk of disease progression at one year, compared to any individual predictor.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/2445/224335
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41598-025-22483-4
dc.relation.ispartofScientific Reports, 2025, vol. 15, 35243
dc.relation.urihttps://doi.org/10.1038/s41598-025-22483-4
dc.rightscc-by (c) Bonella, Francesco et al., 2025
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationDiagnòstic immunohistoquímic
dc.subject.classificationMarcadors tumorals
dc.subject.classificationFibrosi pulmonar
dc.subject.otherDiagnostic immunohistochemistry
dc.subject.otherTumor markers
dc.subject.otherPulmonary fibrosis
dc.titleSerum KL-6 as a biomarker to predict progression at one year in interstitial lung disease
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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