Pseudomonas aeruginosa, the type of mutation, lung function, and nutritional status in adults with cystic fibrosis

Abstract

ObjectiveThe aim of this study was to describe the relationship between the prevalence of Pseudomonas aeruginosa (PA) and lung function, as well as the nutritional status and type of gene mutation in adult patients with cystic fibrosis (CF). MethodsThis cross-sectional study evaluated 103 Polish adults with CF the following:• The occurrence of PA and the level of bacterial susceptibility to antibiotics;• Type of mutation in the CFTR gene;• Nutritional status assessed by body mass index (BMI), and• Lung function measured by forced expiratory volume in 1 s (FEV1%). ResultsThe absence or presence of PA and the level of bacterial resistance were significantly related to the type of gene mutation (P < 0.001). In patients with a severe mutation, PA more often was extensively drug resistant or pandrug resistant compared with Pseudomonas culture-negative patients or patients with mild or unclassified mutations on both alleles.Associations were found between the presence of PA and lower values of BMI (P < 0.001), and FEV1% (P < 0.001). The risk for PA occurrence and the development of bacterial resistance increased twice in the case of severe mutation (odds ratio [OR], 2.51; 95% confidence interval [CI], 1.62–3.89), four times when BMI decreased <18.5 (OR, 4.15; 95% CI, 1.43–10.08). and six times when FEV1% fell <40 (OR, 6.75; 95% CI, 3.11–14.64). ConclusionsThe presence of PA is associated with lower FEV1% and BMI values. Deterioration of lung function, undernutrition, and severe type of gene mutation are linked to a higher probability of PA acquisition and resistance to antibiotic treatment.