Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial

Author:

Doan Thuy12,Hinterwirth Armin1,Arzika Ahmed M3,Cotter Sun Y1,Ray Kathryn J14,O’Brien Kieran S1,Zhong Lina1,Chow Eric D5,Zhou Zhaoxia1,Cummings Susie L1,Fry Dionna1,Oldenburg Catherine E12,Worden Lee14,Porco Travis C14,Keenan Jeremy D12,Lietman Thomas M124

Affiliation:

1. Francis I. Proctor Foundation, San Francisco, California

2. Department of Ophthalmology, University of California San Francisco, San Francisco, California

3. The Carter Center Niger, Republique du Niger, Niger

4. Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California

5. Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, California

Abstract

Abstract Background Mass distributions of oral azithromycin have long been used to eliminate trachoma, and they are now being proposed to reduce childhood mortality. The observed benefit appears to be augmented with each additional treatment, suggesting a possible community-level effect. Here, we assess whether 2 biannual mass treatments of preschool children affect the community’s gut microbiome at 6 months after the last distribution. Methods In this cluster-randomized controlled trial, children aged 1–60 months in the Dossa region of Niger were randomized at the village level to receive a single dose of azithromycin or placebo every 6 months. Fecal samples were collected 6 months after the second treatment for metagenomic deep sequencing. The prespecified primary outcome was the Euclidean PERMANOVA of the gut microbiome, or effectively the distance between the genus-level centroid at the community level, with the secondary outcome being the Simpson’s α diversity. Results In the azithromycin arm, the gut microbial structures were significantly different than in the placebo arm (Euclidean PERMANOVA, P < .001). Further, the diversity of the gut microbiome in the azithromycin arm was significantly lower than in the placebo arm (inverse Simpson’s index, P = .005). Conclusions Two mass azithromycin administrations, 6 months apart, in preschool children led to long-term alterations of the gut microbiome structure and community diversity. Here, long-term microbial alterations in the community did not imply disease but were associated with an improvement in childhood mortality. Clinical Trials Registration NCT02048007.

Funder

Bill and Melinda Gates Foundation

National Eye Institute

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

Reference29 articles.

1. Prescribing azithromycin;McMullan;Aust Prescr,2015

2. A cluster-randomized trial to assess the efficacy of targeting trachoma treatment to children;Amza;Clin Infect Dis,2017

3. Trachoma: an update on prevention, diagnosis, and treatment;Bhosai;Curr Opin Ophthalmol,2012

4. Effect of mass distribution of azithromycin for trachoma control on overall mortality in Ethiopian children: a randomized trial;Porco;JAMA,2009

5. Azithromycin to reduce childhood mortality in Sub-Saharan Africa;Keenan;N Engl J Med,2018

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