4.4 Article

Impact of Antibiotics on the Lung Microbiome and Lung Function in Children With Cystic Fibrosis 1 Year After Hospitalization for an Initial Pulmonary Exacerbation

Journal

OPEN FORUM INFECTIOUS DISEASES
Volume 9, Issue 9, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/ofid/ofac466

Keywords

antibiotics; cystic fibrosis; microbiome; pulmonary exacerbations

Funding

  1. Infectious Diseases Society of America's Grants for Emerging Researchers/Clinicians Mentorship Award
  2. Margaret Q. Landenberger Foundation [BBH20170207]
  3. Harry Shwachman Clinical Investigator Award by the Cystic Fibrosis Foundation [HAHN18A0-Q]
  4. NIH NCATS [UL1TR001876]

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In CF patients, despite an increase in recurrent exacerbations and antibiotic treatments, PEx events did not lead to changes in microbial diversity but were associated with changes in lung function. Specifically, over time, microbial diversity increased in the lung microbiome, while bacterial richness remained stable.
Background. Cystic fibrosis (CF) is characterized by recurrent pulmonary exacerbations (PEx) and lung function decline. PEx are frequently treated with antibiotics. However, little is known about the effects of antibiotics on the airway microbiome of persons with CF over time. The purpose of this study was to evaluate changes in the microbiome and lung function in persons with CF over 1 year following an initial study pulmonary exacerbation (iPEx). Methods. Twenty children aged <= 18 years with CF were enrolled in the study, which occurred prior to the routine administration of highly effective modulator therapy. Respiratory samples and spirometry were obtained at a minimum of quarterly visits and up to 1 year after an iPEx. Metagenomic sequencing was performed, and bacterial taxa were assigned using MetaPhlAn 2.0. Paired t test, analysis of variance, and generalized least squares regression were used to compare outcome variables. Results. The mean age of study participants at the time of the iPEx was 10.6 years. There were 31.6 PEx treated with antibiotics per person during the study period. Bacterial richness was similar at 1 year compared to iPEx (40.3 vs 39.3, P=.852), whereas the mean Shannon diversity index was significantly higher at 1 year (2.84 vs 1.62, P<.001). The number of PEx treated with antibiotics was not associated with changes in microbial diversity but was associated with changes in lung function. Conclusions. In our 1-year prospective study, we found that microbial diversity increased despite decreases in lung function associated with repeated PEx events requiring antibiotic therapy.

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