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

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 whe...

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Autores principales: Doan, Thuy, Hinterwirth, Armin, Arzika, Ahmed M, Cotter, Sun Y, Ray, Kathryn J, O’Brien, Kieran S, Zhong, Lina, Chow, Eric D, Zhou, Zhaoxia, Cummings, Susie L, Fry, Dionna, Oldenburg, Catherine E, Worden, Lee, Porco, Travis C, Keenan, Jeremy D, Lietman, Thomas M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101535/
https://www.ncbi.nlm.nih.gov/pubmed/30151409
http://dx.doi.org/10.1093/ofid/ofy182
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author Doan, Thuy
Hinterwirth, Armin
Arzika, Ahmed M
Cotter, Sun Y
Ray, Kathryn J
O’Brien, Kieran S
Zhong, Lina
Chow, Eric D
Zhou, Zhaoxia
Cummings, Susie L
Fry, Dionna
Oldenburg, Catherine E
Worden, Lee
Porco, Travis C
Keenan, Jeremy D
Lietman, Thomas M
author_facet Doan, Thuy
Hinterwirth, Armin
Arzika, Ahmed M
Cotter, Sun Y
Ray, Kathryn J
O’Brien, Kieran S
Zhong, Lina
Chow, Eric D
Zhou, Zhaoxia
Cummings, Susie L
Fry, Dionna
Oldenburg, Catherine E
Worden, Lee
Porco, Travis C
Keenan, Jeremy D
Lietman, Thomas M
author_sort Doan, Thuy
collection PubMed
description 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.
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spelling pubmed-61015352018-08-27 Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial Doan, Thuy Hinterwirth, Armin Arzika, Ahmed M Cotter, Sun Y Ray, Kathryn J O’Brien, Kieran S Zhong, Lina Chow, Eric D Zhou, Zhaoxia Cummings, Susie L Fry, Dionna Oldenburg, Catherine E Worden, Lee Porco, Travis C Keenan, Jeremy D Lietman, Thomas M Open Forum Infect Dis Major Article 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. Oxford University Press 2018-07-24 /pmc/articles/PMC6101535/ /pubmed/30151409 http://dx.doi.org/10.1093/ofid/ofy182 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Doan, Thuy
Hinterwirth, Armin
Arzika, Ahmed M
Cotter, Sun Y
Ray, Kathryn J
O’Brien, Kieran S
Zhong, Lina
Chow, Eric D
Zhou, Zhaoxia
Cummings, Susie L
Fry, Dionna
Oldenburg, Catherine E
Worden, Lee
Porco, Travis C
Keenan, Jeremy D
Lietman, Thomas M
Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial
title Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial
title_full Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial
title_fullStr Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial
title_full_unstemmed Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial
title_short Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial
title_sort mass azithromycin distribution and community microbiome: a cluster-randomized trial
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101535/
https://www.ncbi.nlm.nih.gov/pubmed/30151409
http://dx.doi.org/10.1093/ofid/ofy182
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