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Randomized Controlled Trial
. 2014 Aug 22;9(8):e105609.
doi: 10.1371/journal.pone.0105609. eCollection 2014.

The effect of azithromycin in adults with stable neutrophilic COPD: a double blind randomised, placebo controlled trial

Affiliations
Randomized Controlled Trial

The effect of azithromycin in adults with stable neutrophilic COPD: a double blind randomised, placebo controlled trial

Jodie L Simpson et al. PLoS One. .

Abstract

Background: Chronic Obstructive Pulmonary Disease (COPD) is a progressive airway disease characterised by neutrophilic airway inflammation or bronchitis. Neutrophilic bronchitis is associated with both bacterial colonisation and lung function decline and is common in exacerbations of COPD. Despite current available therapies to control inflammation, neutrophilic bronchitis remains common. This study tested the hypothesis that azithromycin treatment, as an add-on to standard medication, would significantly reduce airway neutrophil and neutrophils chemokine (CXCL8) levels, as well as bacterial load. We conducted a randomised, double-blind, placebo-controlled study in COPD participants with stable neutrophilic bronchitis.

Methods: Eligible participants (n = 30) were randomised to azithromycin 250 mg daily or placebo for 12 weeks in addition to their standard respiratory medications. Sputum was induced at screening, randomisation and monthly for a 12 week treatment period and processed for differential cell counts, CXCL8 and neutrophil elastase assessment. Quantitative bacteriology was assessed in sputum samples at randomisation and the end of treatment visit. Severe exacerbations where symptoms increased requiring unscheduled treatment were recorded during the 12 week treatment period and for 14 weeks following treatment. A sub-group of participants underwent chest computed tomography scans (n = 15).

Results: Nine participants with neutrophilic bronchitis had a potentially pathogenic bacteria isolated and the median total bacterial load of all participants was 5.22×107 cfu/mL. Azithromycin treatment resulted in a non-significant reduction in sputum neutrophil proportion, CXCL8 levels and bacterial load. The mean severe exacerbation rate was 0.33 per person per 26 weeks in the azithromycin group compared to 0.93 exacerbations per person in the placebo group (incidence rate ratio (95%CI): 0.37 (0.11,1.21), p = 0.062). For participants who underwent chest CT scans, no alterations were observed.

Conclusions: In stable COPD with neutrophilic bronchitis, add-on azithromycin therapy showed a trend to reduced severe exacerbations sputum neutrophils, CXCL8 levels and bacterial load. Future studies with a larger sample size are warranted.

Trial registration: Australian New Zealand Clinical Trials Registry ACTRN12609000259246.

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Conflict of interest statement

Competing Interests: Research was funded by the National Health and Medical Research Council of Australia with project grant id 455508. JS salary is supported by the Australian Respiratory Council. KB salary is supported by the University of Newcastle. HO Coxson has received an honorarium for serving on the steering committee for the ECLIPSE project for GSK. In addition HC was the co-investigator on two multi-center studies sponsored by GSK and has received travel expenses to attend meetings related to the project. HC has a contract service agreement with Spiration Inc to measure changes in lung volume in subjects with severe emphysema. HC has received a fee for speaking at a conference and related travel expenses from AstraZeneca (Australia). There is no financial relationship between any industry and the current study. PGG reports grants from NHMRC, during the conduct of the study; personal fees from GlaxoSmithkline, AstraZeneca, Boerhinger Ingelheim, outside the submitted work. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.

Figures

Figure 1
Figure 1. Participant consort diagram.
Figure 2
Figure 2. Bar graphs showing the change in sputum neutrophil%, IL-8 ng/mL and total bacterial load following treatment with azithromycin (AZM) or placebo.
Figure 3
Figure 3. Kaplan-Meier curves showing the proportion of participants without a COPD exacerbation versus the days post randomisation visit (p = 0.100).

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References

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