Effects of Inhaled Corticosteroid/Long-Acting β<sub>2</sub>-Agonist Combination on the Airway Microbiome of Patients with Chronic Obstructive Pulmonary Disease: A Randomized Controlled Clinical Trial (DISARM).

Leitao Filho, Fernando Sergio; Takiguchi, Hiroto; Akata, Kentaro; Ra, Seung Won; Moon, Ji-Yong; Kim, Hyun Kuk; Cho, Yuji; Yamasaki, Kei et al. · Am J Respir Crit Care Med · 2021

rct · Level II

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Abstract

<b>Rationale:</b> Inhaled corticosteroids (ICS) are commonly prescribed with long-acting β<sub>2</sub>-agonists (LABA) in chronic obstructive pulmonary disease (COPD). To date, the effects of ICS therapy on the airway microbiome in COPD are unknown. <b>Objectives:</b> To determine the effects of ICS/LABA on the airway microbiome of patients with COPD. <b>Methods:</b> Clinically stable patients with COPD were enrolled into a 4-week run-in period during which ICS was discontinued and all participants were placed on formoterol (Form) 12 μg twice daily (BID). The participants were then randomized to budesonide/formoterol (Bud + Form; 400/12 μg BID), fluticasone/salmeterol (Flu + Salm; 250/50 μg BID), or formoterol only (12 μg BID) for 12 weeks. Participants underwent bronchoscopy before and after the 12-week treatment period. The primary endpoint was the comparison of changes in the airway microbiome over the trial period between the ICS/LABA and LABA-only groups. <b>Measurements and Main Results:</b> Sixty-three participants underwent randomization: Bud + Form (<i>n</i> = 20), Flu + Salm (<i>n</i> = 22), and Form (<i>n</i> = 21) groups; 56 subjects completed all visits. After the treatment period, changes in α-diversity were significantly different across groups, especially between Flu + Salm and Form groups (Δrichness: <i>P</i> = 0.02; ΔShannon index: <i>P</i> = 0.03). Longitudinal differential abundance analyses revealed more pronounced microbial shifts from baseline in the fluticasone (vs. budesonide or formoterol only) group. <b>Conclusions:</b> Fluticasone-based ICS/LABA therapy modifies the airway microbiome in COPD, leading to a relative reduction in α-diversity and a greater number of bacterial taxa changes. These data may have implications in patients who develop pneumonia on ICS. Clinical trial registered with www.clinicaltrials.gov (NCT02833480).

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