The predictive role of lung clearance index on FEV1 decline in cystic fibrosis

Turk J Pediatr. 2024 Jul 11;66(3):297-308. doi: 10.24953/turkjpediatr.2024.4516.

Abstract

Background: The lung clearance index (LCI) is a sensitive lung function index that is used to detect early lung disease changes in children with cystic fibrosis (CF). This study aimed to define the predictive role of baseline LCI, along with other potential factors on the change in forced expiratory volume in one second (FEV1) during one-year follow-up in CF patients who had a percent predicted (pp) FEV1≥80.

Methods: LCI was concurrently performed on 57 CF patients who had ppFEV1 ≥80 at month zero. The ppFEV1 decline was evaluated prospectively during the one year follow up. The primary outcome of ppFEV1 decline in the study group in one year was dichotomized according to the median value for the decline in ppFEV1, which was 3.7. The LCI value predicting ppFEV1 decline at the end of one year was calculated with receiver operating characteristic curve analysis. Regression analysis was performed. Furthermore, a decision tree was constructed using classification and regression tree methods to better define the potential effect of confounders on the ppFEV1 decline.

Results: The LCI value for predicting ppFEV1 decline >3.7% at the end of one year was 8.2 (area under the curve: 0.80) Multivariable regression analysis showed that the absence of the F508del mutation in at least one allele, LCI >8.2 and initial FEV1 z-score were predictors of a ppFEV1 decline >3.7 (p<0.001). Factors altering ppFEV1 decline>3.7% at the end of one-year evaluated by decision trees were as follows: initial FEV1 z-score, type of CFTR mutation, LCI value and initial weight-for-age z-score.

Conclusions: LCI is sensitive for predicting ppFEV1 decline in patients with ppFEV1 ≥80 along with the initial FEV1-z-score and type of CFTR mutation.

Keywords: FEV1 decline; cystic fibrosis; lung clearance index; multiple breath wash-out; spirometry.

MeSH terms

  • Adolescent
  • Child
  • Cystic Fibrosis* / genetics
  • Cystic Fibrosis* / physiopathology
  • Female
  • Forced Expiratory Volume
  • Humans
  • Lung / physiopathology
  • Male
  • Predictive Value of Tests
  • Prospective Studies
  • Respiratory Function Tests