Protocol and research program of the European registry and biobank for interstitial lung diseases (eurILDreg)

dc.contributor.authorKrauss, Ekaterina
dc.contributor.authorTello, Silke
dc.contributor.authorNaumann, Jennifer
dc.contributor.authorWobisch, Sandra
dc.contributor.authorRuppert, Clemens
dc.contributor.authorKuhn, Stefan
dc.contributor.authorMahavadi, Poornima
dc.contributor.authorMajeed, Raphael W.
dc.contributor.authorBonniaud, Philippe
dc.contributor.authorMolina-Molina, Maria
dc.contributor.authorWells, Athol
dc.contributor.authorHirani, Nik
dc.contributor.authorVancheri, Carlo
dc.contributor.authorWalsh, Simon
dc.contributor.authorGriese, Matthias
dc.contributor.authorCrestani, Bruno
dc.contributor.authorGuenther, Andreas
dc.contributor.authorBorie, Raphael
dc.contributor.authorKannengiesser, Caroline
dc.contributor.authorPoletti, Venerino
dc.contributor.authorBehr, Juergen
dc.contributor.authorDrakopanagiotakis, Fotios
dc.contributor.authorBastos, Helder
dc.contributor.authorRavaglia, Claudia
dc.contributor.authorHurley, Killian
dc.contributor.authorEils, Roland
dc.contributor.authorGut, Ivo
dc.contributor.authorHaick, Hossam
dc.contributor.authorBroza, Yoav Y.
dc.date.accessioned2025-11-06T10:38:14Z
dc.date.available2025-11-06T10:38:14Z
dc.date.issued2024
dc.description.abstractBackground and Aims: Interstitial lung diseases (ILDs), encompassing both pediatric and adult cases, present a diverse spectrum of chronic conditions with variable prognosis. Despite limited therapeutic options beyond antifibrotic drugs and immunosuppressants, accurate diagnosis is challenging, often necessitating invasive procedures that may not be feasible for certain patients. Drawn against this background, experts across pediatric and adult ILD fields have joined forces in the RARE-ILD initiative to pioneer novel non-invasive diagnostic algorithms and biomarkers. Collaborating with the RARE-ILD consortium, the eurILDreg aims to comprehensively describe different ILDs, analyze genetically defined forms across age groups, create innovative diagnostic and therapeutic biomarkers, and employ artificial intelligence for data analysis. Methods: The foundation of eurILDreg is built on a comprehensive parameter list developed and adopted by clinical experts, encompassing over 1,800 distinct parameters related to patient history, clinical examinations, diagnosis, lung function and biospecimen collection. This robust dataset is further enriched with daily assessments captured through the patientMpower app, including handheld spirometry and exercise tests, conducted on approximately 350 patients over the course of a year. This approach involves app-based daily assessments of quality of life, symptom tracking, handheld spirometry, saturation measurement, and the 1-min sit-to-stand test (1-STST). Additionally, pediatric data from the ChILD-EU registry will be integrated into the RARE-ILD Data Warehouse, with the ultimate goal of including a total of 4.000 ILD patients and over 100.000 biospecimen. Discussion: The collaborative efforts within the consortium are poised to streamline research endeavors significantly, promising to advance patient-centered care, foster innovation, and shape the future landscape of interstitial lung disease research and healthcare practices.en
dc.identifier.urihttps://jlupub.ub.uni-giessen.de/handle/jlupub/20919
dc.identifier.urihttps://doi.org/10.22029/jlupub-20270
dc.language.isoen
dc.rightsNamensnennung 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddcddc:610
dc.titleProtocol and research program of the European registry and biobank for interstitial lung diseases (eurILDreg)
dc.typearticle
local.affiliationFB 11 - Medizin
local.source.articlenumber572
local.source.epage8
local.source.journaltitleBMC pulmonary medicine
local.source.spage1
local.source.urihttps://doi.org/10.1186/s12890-024-03389-9
local.source.volume24

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