Publication:
Growth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia Cohort

dc.contributor.authorKARADAĞ, BÜLENT TANER
dc.contributor.authorsGoutaki, Myrofora; Halbeisen, Florian S.; Spycher, Ben D.; Maurer, Elisabeth; Belle, Fabien; Amirav, Israel; Behan, Laura; Boon, Mieke; Carr, Siobhan; Casaulta, Carmen; Clement, Annick; Crowley, Suzanne; Dell, Sharon; Ferkol, Thomas; Haarman, Eric G.; Karadag, Bulent; Knowles, Michael; Koerner-Rettberg, Cordula; Leigh, Margaret W.; Loebinger, Michael R.; Mazurek, Henryk; Morgan, Lucy; Nielsen, Kim G.; Phillipsen, Maria; Sagel, Scott D.; Santamaria, Francesca; Schwerk, Nicolaus; Yiallouros, Panayiotis; Lucas, Jane S.; Kuehni, Claudia E.
dc.date.accessioned2022-03-14T08:26:49Z
dc.date.accessioned2026-01-11T10:26:07Z
dc.date.available2022-03-14T08:26:49Z
dc.date.issued2017-12
dc.description.abstractChronic respiratory disease can affect growth and nutrition, which can influence lung function. We investigated height, body mass index (BMI), and lung function in patients with primary ciliary dyskinesia (PCD). In this study, based on the international PCD (iPCD) Cohort, we calculated z-scores for height and BMI using World Health Organization (WHO) and national growth references, and assessed associations with age, sex, country, diagnostic certainty, age at diagnosis, organ laterality and lung function in multilevel regression models that accounted for repeated measurements. We analysed 6402 measurements from 1609 iPCD Cohort patients. Height was reduced compared to WHO (z-score -0.12, 95% CI -0.17 to -0.06) and national references (z-score -0.27, 95% CI -0.33 to -0.21) in male and female patients in all age groups, with variation between countries. Height and BMI were higher in patients diagnosed earlier in life (p=0.026 and p<0.001, respectively) and closely associated with forced expiratory volume in 1 s and forced vital capacity z-scores (p<0.001). Our study indicates that both growth and nutrition are affected adversely in PCD patients from early life and are both strongly associated with lung function. If supported by longitudinal studies, these findings suggest that early diagnosis with multidisciplinary management and nutritional advice could improve growth and delay disease progression and lung function impairment in PCD.
dc.identifier.doi10.1183/13993003.01659-2017
dc.identifier.eissn1399-3003
dc.identifier.issn0903-1936
dc.identifier.pubmed29269581
dc.identifier.urihttps://hdl.handle.net/11424/241796
dc.identifier.wosWOS:000423716000014
dc.language.isoeng
dc.publisherEUROPEAN RESPIRATORY SOC JOURNALS LTD
dc.relation.ispartofEUROPEAN RESPIRATORY JOURNAL
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBODY-MASS INDEX
dc.subjectCYSTIC-FIBROSIS
dc.subjectCHILDHOOD ASTHMA
dc.subjectELECTRON-MICROSCOPY
dc.subjectEUROPEAN CHILDREN
dc.subjectDIAGNOSIS
dc.subjectRECOMMENDATIONS
dc.subjectSPIROMETRY
dc.subjectDISEASE
dc.subjectAGE
dc.titleGrowth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia Cohort
dc.typearticle
dspace.entity.typePublication
oaire.citation.issue6
oaire.citation.titleEUROPEAN RESPIRATORY JOURNAL
oaire.citation.volume50

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