Factors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort study

dc.contributor.authorEmiralioglu, Nagehan
dc.contributor.authorCakir, Banu
dc.contributor.authorSertcelik, Ahmet
dc.contributor.authorYalcin, Ebru
dc.contributor.authorKiper, Nural
dc.contributor.authorSen, Velat
dc.contributor.authorDogru, Deniz
dc.date.accessioned2026-08-12T17:39:03Z
dc.date.issued2024
dc.departmentFırat Üniversitesi
dc.description.abstractBackground: The decline in pulmonary function is a predictor of disease progression in patients with cystic fibrosis (CF). This study aimed to determine the decline rate of percent predicted forced expiratory volume in 1 s (ppFEV1) based on the data of the CF Registry of Turkey. The secondary aim was to investigate the risk factors related to the decline in ppFEV1. Methods: A retrospective cohort study of CF patients over 6 years old, with pulmonary function data over at least 2 years of follow-up was extracted from the national CF registry for years 2017-2019. Patients were classified according to disease severity and age groups. Multivariate analysis was used to predict the decline in ppFEV1 and to investigate the associated risk factors. Results: A total of 1722 pulmonary function test results were available from 574 patients over the study period. Mean diagnostic age was older and weight for age, height for age, and body mass index z scores were significantly lower in the group of ppFEV1 < 40, while chronic Pseudomonas aeruginosa (p < .001) and mucoid P. aeruginosa colonization (p < .001) were significantly higher in this group (p < .001). Overall mean annual ppFEV1 decline was -0.97% (95% confidence interval [CI] = -0.02 to -1.92%). The mean change of ppFEV1 was significantly higher in the group with ppFEV1 >= 70 compared with the other (ppFEV1 < 40 and ppFEV1: 40-69) two groups (p = .004). Chronic P. aeruginosa colonization (odds ratio [OR] = 1.79 95% CI = 1.26-2.54; p = .01) and initial ppFEV1 >= 70 (OR = 2.98 95% CI = 1.06-8.36), p = .038) were associated with significant ppFEV1 decline in the whole cohort. Conclusions: This data analysis recommends close follow-up of patients with normal initial ppFEV1 levels at baseline; advocates for early interventions for P. aeruginosa; and underlines the importance of nutritional interventions to slow down lung disease progression.
dc.description.sponsorshipThe authors have no funding to report.
dc.identifier.doi10.1002/ppul.27165
dc.identifier.endpage2966
dc.identifier.issn8755-6863
dc.identifier.issn1099-0496
dc.identifier.issue11
dc.identifier.orcid0000-0002-1438-7854
dc.identifier.orcid0000-0001-6422-2639
dc.identifier.orcid0000-0003-1378-9250
dc.identifier.orcid0000-0002-7680-4000
dc.identifier.orcid0000-0002-0793-9710
dc.identifier.orcid0000-0002-2879-8910
dc.identifier.orcid0000-0003-4301-0586
dc.identifier.pmid38980199
dc.identifier.scopus2-s2.0-85197756695
dc.identifier.scopusqualityQ1
dc.identifier.startpage2956
dc.identifier.urihttps://doi.org/10.1002/ppul.27165
dc.identifier.urihttps://hdl.handle.net/11508/58675
dc.identifier.volume59
dc.identifier.wosWOS:001268137200001
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/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectcystic fibrosis
dc.subjectFEV1
dc.subjectpulmonary function test
dc.subjectPseudomonas aeruginosa
dc.titleFactors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort study
dc.typeArticle

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