Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6240786 | Journal of Cystic Fibrosis | 2013 | 4 Pages |
BackgroundMany infants with cystic fibrosis (CF) exhibit airway inflammation, gas trapping, bronchiectasis, and/or reduced flow, but by age 6 years have forced vital capacities (FVC) and expiratory volumes in 1 second (FEV1) within the variability range of the normal population. We sought evidence of diminished FVC and FEV1 in 6-year-olds with CF.MethodsGLI 2012 FVC and FEV1 Z-scores for 6-year-olds from the European CF Patient Registry were plotted against theoretical values from the Normal distribution.ResultsMean FVC and FEV1 Z-scores for 681 patients (322 females) were â 0.43 (SD = 1.41) and â 0.65 (1.40). Z-scores were consistently lower than expected for the normative population by quantile-quantile plot.ConclusionsDiminished FEV1, and to a lesser extent FVC, is found in a large majority of this population, consistent with an established body of evidence that loss of lung function begins early in life for most, if not all, children with CF.