Impact of azithromycin on serum inflammatory markers in children with cystic fibrosis and new Pseudomonas

Jessica E. Pittman, Michelle S. Skalland, Scott D. Sagel, Bonnie W. Ramsey, Nicole Mayer-Hamblett, George Z. Retsch-Bogart

Research output: Contribution to journalArticlepeer-review

Abstract

Chronic azithromycin improves outcomes in cystic fibrosis (CF), but its mechanism of action is unclear. The OPTIMIZE trial demonstrated improvement in time to first pulmonary exacerbation in children with new Pseudomonas treated with azithromycin. Azithromycin effect on systemic markers of inflammation over 18 months was assessed by change from baseline for high-sensitivity C-reactive protein, myeloperoxidase, calprotectin and absolute neutrophil count in the OPTIMIZE population. Subjects treated with chronic azithromycin or placebo had samples collected at baseline, 39 and 78 weeks of treatment. In 129 subjects, a significant decrease in high-sensitivity C-reactive protein was present at 39 weeks in the azithromycin group compared to placebo, but no significant difference between the groups at 78 weeks. No differences in change from baseline in myeloperoxidase, calprotectin or absolute neutrophil count were present at either time point. This supports the concept of a transient immunomodulatory effect for chronic azithromycin therapy in children with CF.

Original languageEnglish
JournalJournal of Cystic Fibrosis
DOIs
StateAccepted/In press - 2022

Keywords

  • Azithromycin
  • Cystic fibrosis
  • Inflammatory markers
  • Pseudomonas

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