Reduced exercise ventilatory efficiency in adults with cystic fibrosis and normal to moderately impaired lung function

Author:

Di Paolo Marcello12ORCID,Teopompi Elisabetta3,Savi Daniela14,Crisafulli Ernesto3,Longo Chiara3,Tzani Panagiota3,Longo Francesco3,Ielpo Antonella3,Pisi Giovanna5,Cimino Giuseppe6,Simmonds Nicholas J.27,Neder J. Alberto8,Chetta Alfredo3,Palange Paolo1

Affiliation:

1. Department of Public Health and Infectious Diseases, Adult Cystic Fibrosis Center, “Sapienza” University of Rome, Rome, Italy

2. Adult Cystic Fibrosis Center, Royal Brompton and Harefield National Health Service Foundation Trust, London, United Kingdom

3. Department of Medicine and Surgery, Respiratory Disease and Lung Function Unit, University Hospital of Parma, Parma, Italy

4. Cystic Fibrosis Unit, “Bambino Gesù” Children’s Hospital, Rome, Italy

5. Cystic Fibrosis Unit, University Hospital of Parma, Parma, Italy

6. Department of Pediatrics and Infantile Neuropsychiatry, Adult Cystic Fibrosis Center, “Sapienza” University of Rome, Rome, Italy

7. National Heart and Lung Institute, Imperial College London, London, United Kingdom

8. Respiratory Investigation Unit & Laboratory of Clinical Exercise Physiology, Queen's University and Kingston General Hospital, Kingston, Ontario, Canada

Abstract

Despite being a hallmark and an independent prognostic factor in several cardiopulmonary diseases, ventilatory efficiency—i.e., minute ventilation/carbon dioxide output relationship (V̇e/V̇co2)—has never been systematically explored in cystic fibrosis (CF). To provide a comprehensive frame of reference regarding measures of ventilatory efficiency in CF adults with normal to moderately impaired lung function and to confirm the hypothesis that V̇e/V̇co2 is a sensitive marker of early lung disease. CF patients were divided into three groups, according to their spirometry: normal (G1), mild impairment (G2), and moderate impairment (G3) in lung function. All participants underwent incremental cardiopulmonary exercise testing on a cycle ergometer. Lowest V̇e/V̇co2 ratio (nadir) and the slope and the intercept of the linear region of the V̇e/V̇co2 relationship were contrasted in a two-center retrospective analysis, involving 72 CF patients and 36 healthy controls (HC). Compared with HC, CF patients had significantly higher V̇e/V̇co2 nadir, slope, and intercept ( P < 0.001, P < 0.001, and P = 0.049, respectively). Subgroup analysis revealed significant differences in nadir ( P = 0.001) and slope ( P = 0.012) values even between HC and G1. Dynamic hyperinflation related negatively with slope ( P = 0.045) and positively with intercept ( P = 0.001), while no impact on nadir was observed. Ventilatory inefficiency is a clear feature of adults with CF, even among patients with normal spirometry. V̇e/V̇co2 nadir seems to be the most reliable metric to describe ventilatory efficiency in CF adults. Further prospective studies are needed to clarify whether V̇e/V̇co2 could represent a useful marker in the evaluation of early lung disease in CF. NEW & NOTEWORTHY This is the first study to investigate ventilatory efficiency in a cohort of adult cystic fibrosis (CF) patients with nonsevere lung disease. The finding of impaired ventilatory efficiency in patients with normal lung function confirms the higher sensitivity of exercise testing in detecting early lung disease compared with spirometry. Dynamic hyperinflation plays a significant role in determining the behavior of V̇e/V̇co2 slope and intercept values with increasing lung function impairment. Apparently free from interference from mechanical constraints, V̇e/V̇co2 nadir seems the most reliable parameter to evaluate ventilatory efficiency in CF adults.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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