Impact of Modulator Therapy on the Chronic Colonization of Lower Respiratory Tract Pathogens in Children: Data From Cystic Fibrosis Registry of Turkey

dc.contributor.authorSunman, Birce
dc.contributor.authorYalcin, Ebru
dc.contributor.authorErdal, Meltem Akgul
dc.contributor.authorSen, Velat
dc.contributor.authorBaskan, Azer Kilic
dc.contributor.authorKilinc, Ayse Ayzit
dc.contributor.authorDogru, Deniz
dc.date.accessioned2026-08-12T17:26:51Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstractBackground: Modulators have revolutionized cystic fibrosis (CF) management, but their effects on respiratory pathogens remain unclear. This study evaluated changes in lower respiratory tract pathogen detection after modulator therapy in children with CF, registered in the Cystic Fibrosis Registry of Turkey. Method: This retrospective, multicenter cohort study included children receiving modulator therapy between 2020 and 2022. Chronic respiratory tract colonization rates before and after therapy were compared, along with inhaler treatments, oral steroid, azithromycin use, pulmonary function tests, and hospitalizations for pulmonary exacerbations. The cohort was stratified by age, modulator type, and lung disease severity. Changes in microbiologic data over a 1-year period were also analyzed for children not receiving modulator therapy. Results: A total of 101 children (mean age 9.95 +/- 4.44 years) were included. Following modulator therapy, respiratory cultures of 57 (56.4%) were negative. Among 32 children with chronic Pseudomonas aeruginosa (P. aeruginosa) colonization, 14 (44%) showed negative respiratory cultures after receiving modulator therapy (p = 0.039). Conversion to culture-negative status was significant for methicillin-sensitive Staphylococcus aureus (MSSA) (p = 0.022) and methicillin-resistant Staphylococcus aureus (MRSA) (p = 0.034), with ETI therapy yielding the highest conversion rates. Inhaled antibiotic use for chronic respiratory pathogens decreased significantly (p = 0.039), and spirometry parameters improved (p < 0.001). Among 1232 children not receiving modulators, 180 (14.6%) had negative respiratory cultures when examined at 1-year interval. In the same group, intermittent/chronic P. aeruginosa colonization was negative in 58 cases, while 85 developed new growth, following modulator therapy, with positivity rates rising from 16.3% to 18.5% (p = 0.030). No significant changes in other pathogen detection were observed. Conclusion: Modulators, particularly ETI, reduced respiratory pathogen detection and improved lung function in children with CF.
dc.description.sponsorshipThe authors received no specific funding for this work.
dc.description.sponsorshipWe would like to thank the Cystic Fibrosis Registry of Turkey for supplying access to patient data and individual center representatives for allowing the use of data. This study was not previously presented or published anywhere.
dc.identifier.doi10.1002/ppul.71155
dc.identifier.issn8755-6863
dc.identifier.issn1099-0496
dc.identifier.issue6
dc.identifier.orcid0000-0002-7600-7909
dc.identifier.orcid0000-0002-7319-8535
dc.identifier.orcid0000-0001-6422-2639
dc.identifier.orcid0000-0002-7680-4000
dc.identifier.orcid0000-0002-0334-6336
dc.identifier.orcid0000-0002-2879-8910
dc.identifier.pmid40504038
dc.identifier.scopus2-s2.0-105007907934
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1002/ppul.71155
dc.identifier.urihttps://hdl.handle.net/11508/54981
dc.identifier.volume60
dc.identifier.wosWOS:001521291400032
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofPediatric Pulmonology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectCFTR modulator
dc.subjectcystic fibrosis
dc.subjectpathogen
dc.subjectPseudomonas
dc.titleImpact of Modulator Therapy on the Chronic Colonization of Lower Respiratory Tract Pathogens in Children: Data From Cystic Fibrosis Registry of Turkey
dc.typeArticle

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