Lung Function in Children with Primary Ciliary Dyskinesia.
Valentina Agnese FerraroRaimondo Junior CastaldoValentina TonazzoStefania ZanconatoSilvia CarraroPublished in: Children (Basel, Switzerland) (2023)
The majority of recent published studies showed normal spirometric values in PCD children, even if some authors described a pulmonary impairment. Together with spirometry, Lung Clearance Index has been applied for detecting peripheral airway disease, and it might have a role in early mild lung disease assessment. Studies on lung function trajectories after PCD diagnosis showed a significant heterogeneity, with some patients maintaining reasonably good lung function, whereas others showing a decline. Further studies are needed to analyze lung function prospectively from childhood into adulthood, and to evaluate whether lung function trajectories are affected by PCD clinical phenotype, ultrastructural ciliary defect or genetic background.
Keyphrases
- lung function
- cystic fibrosis
- chronic obstructive pulmonary disease
- air pollution
- depressive symptoms
- end stage renal disease
- young adults
- case control
- newly diagnosed
- ejection fraction
- chronic kidney disease
- pulmonary hypertension
- prognostic factors
- peritoneal dialysis
- randomized controlled trial
- gene expression
- early life
- copy number
- dna methylation
- single cell
- patient reported outcomes