Literature DB >> 31943945

Exercise capacity and ventilation inhomogeneity in cystic fibrosis: A cross-sectional study.

Simone Gambazza1,2,3, Riccardo Guarise1, Federica Carta1,3, Federico Ambrogi2, Marina Mirabella3, Anna Brivio1,3, Carla Colombo1,4.   

Abstract

BACKGROUND: Lung clearance index (LCI2.5 ) is a marker of overall lung ventilation inhomogeneity and has proven to be able to detect early peripheral damage in subjects with cystic fibrosis (CF), with greater sensitivity than conventional spirometry. Combining its sensitivity with the output of an incremental exercise testing, we hypothesized that any sign of ventilation inhomogeneity in subjects without severe airflow obstruction and with a normal exercise tolerance could be relevant for the CF team, tracking early lung disease and potential exercise limiting factors.
METHODS: Patients with CF in clinical stable conditions were recruited between 2015 and 2017. Available spirometry, nitrogen multiple-breath washout test and symptoms-limited exercise testing performed as parts of patients' annual routine evaluation were considered for this cross-sectional study. To describe the relationship between exercise intensity and ventilation inhomogeneity, a linear regression analysis was performed using backward elimination based on Akaike information criteria.
RESULTS: Seventy-seven patients (38 females) were included. Sacin and LCI2.5 were significantly higher in patients with an overall reduced exercise tolerance. Peak work developed during exercise was associated with body mass index (b = 5.25; 95% confidence interval [CI] = 1.53-8.98), forced expiratory volume in 1 second (FEV1 ; b = 3.71; 95% CI = 1.96-5.46), Pseudomonas aeruginosa chronic infection (b = -8.84; 95% CI = -15.84 to -1.84) but not with LCI2.5 .
CONCLUSION: Exercise capacity and airflow obstruction are associated in this Italian CF cohort. Considering the greater discriminatory power of LCI2.5 over FEV1 and peak work, the Godfrey protocol without gas analysis cannot provide detailed information about lung function or efficiency. However, this incremental protocol without gas exchange measures can still provide the CF team with information about exercise tolerance and disability.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  cystic fibrosis; exercise tolerance; lung clearance index; multiple breath washout; ventilation inhomogeneity

Year:  2020        PMID: 31943945     DOI: 10.1002/ppul.24525

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  3 in total

1.  Time Free From Hospitalization in Children and Adolescents With Cystic Fibrosis: Findings From FEV1, Lung Clearance Index and Peak Work Rate.

Authors:  Simone Gambazza; Alessandra Mariani; Anna Brivio; Federica Carta; Chiara Blardone; Saba Lisiero; Maria Russo; Carla Colombo
Journal:  Front Pediatr       Date:  2022-06-22       Impact factor: 3.569

Review 2.  Toward the Establishment of New Clinical Endpoints for Cystic Fibrosis: The Role of Lung Clearance Index and Cardiopulmonary Exercise Testing.

Authors:  Elpis Hatziagorou; Asterios Kampouras; Vasiliki Avramidou; Ilektra Toulia; Elisavet-Anna Chrysochoou; Maria Galogavrou; Fotios Kirvassilis; John Tsanakas
Journal:  Front Pediatr       Date:  2021-02-25       Impact factor: 3.418

3.  Cystic Fibrosis, New Frontier: Exploring the Functional Connectivity of the Brain Default Mode Network. Comment on Elce et al. Impact of Physical Activity on Cognitive Functions: A New Field for Research and Management of Cystic Fibrosis. Diagnostics 2020, 10, 489.

Authors:  Simone Gambazza; Rita Maria Nobili; Riccardo Biffi; Paul Eugene Summers; Carla Colombo; Antonella Costa
Journal:  Diagnostics (Basel)       Date:  2021-05-31
  3 in total

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