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Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort

Introduction: Early-life antibiotic exposure is common and impacts the development of the child’s microbiome and immune system. Information on the impacts of early-life antibiotics exposure on childhood asthma is lacking. Methods: This study examined associations between early-life (0–24 months) ant...

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Autores principales: Lu, Yankun, Wang, Yichao, Wang, Jing, Lowe, Adrian J., Grzeskowiak, Luke E., Hu, Yanhong J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952656/
https://www.ncbi.nlm.nih.gov/pubmed/36830225
http://dx.doi.org/10.3390/antibiotics12020314
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author Lu, Yankun
Wang, Yichao
Wang, Jing
Lowe, Adrian J.
Grzeskowiak, Luke E.
Hu, Yanhong J.
author_facet Lu, Yankun
Wang, Yichao
Wang, Jing
Lowe, Adrian J.
Grzeskowiak, Luke E.
Hu, Yanhong J.
author_sort Lu, Yankun
collection PubMed
description Introduction: Early-life antibiotic exposure is common and impacts the development of the child’s microbiome and immune system. Information on the impacts of early-life antibiotics exposure on childhood asthma is lacking. Methods: This study examined associations between early-life (0–24 months) antibiotics exposure with childhood (6–15 years) asthma trajectories through the Australian Longitudinal Study of Australian Children (LSAC) and their linked data from the Pharmaceutical Benefits Scheme. Asthma phenotypes were derived by group-based trajectory modeling. Results: Of 5107 LSAC participants, 4318 were included in the final analyses (84.6% retention). Four asthma phenotypes were identified: Always-low-risk (79.0%), early-resolving asthma (7.1%), early-persistent asthma (7.9%), and late-onset asthma (6.0%). Any early-life antibiotic exposure increased risk 2.3-fold (95% CI: 1.47–3.67; p < 0.001) for early-persistent asthma among all children. In subgroup analyses, early-persistent asthma risk increased by 2.7-fold with any second-generation cephalosporin exposure, and by 2-fold with any β-lactam other than cephalosporin or macrolide exposure. Conclusion: We concluded that early-life antibiotic exposure is associated with an increased risk of early-persistent childhood asthma. This reinforces scrutiny of early-life antibiotic use, particularly for common viral infections where no antibiotics are required.
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spelling pubmed-99526562023-02-25 Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort Lu, Yankun Wang, Yichao Wang, Jing Lowe, Adrian J. Grzeskowiak, Luke E. Hu, Yanhong J. Antibiotics (Basel) Article Introduction: Early-life antibiotic exposure is common and impacts the development of the child’s microbiome and immune system. Information on the impacts of early-life antibiotics exposure on childhood asthma is lacking. Methods: This study examined associations between early-life (0–24 months) antibiotics exposure with childhood (6–15 years) asthma trajectories through the Australian Longitudinal Study of Australian Children (LSAC) and their linked data from the Pharmaceutical Benefits Scheme. Asthma phenotypes were derived by group-based trajectory modeling. Results: Of 5107 LSAC participants, 4318 were included in the final analyses (84.6% retention). Four asthma phenotypes were identified: Always-low-risk (79.0%), early-resolving asthma (7.1%), early-persistent asthma (7.9%), and late-onset asthma (6.0%). Any early-life antibiotic exposure increased risk 2.3-fold (95% CI: 1.47–3.67; p < 0.001) for early-persistent asthma among all children. In subgroup analyses, early-persistent asthma risk increased by 2.7-fold with any second-generation cephalosporin exposure, and by 2-fold with any β-lactam other than cephalosporin or macrolide exposure. Conclusion: We concluded that early-life antibiotic exposure is associated with an increased risk of early-persistent childhood asthma. This reinforces scrutiny of early-life antibiotic use, particularly for common viral infections where no antibiotics are required. MDPI 2023-02-03 /pmc/articles/PMC9952656/ /pubmed/36830225 http://dx.doi.org/10.3390/antibiotics12020314 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lu, Yankun
Wang, Yichao
Wang, Jing
Lowe, Adrian J.
Grzeskowiak, Luke E.
Hu, Yanhong J.
Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort
title Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort
title_full Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort
title_fullStr Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort
title_full_unstemmed Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort
title_short Early-Life Antibiotic Exposure and Childhood Asthma Trajectories: A National Population-Based Birth Cohort
title_sort early-life antibiotic exposure and childhood asthma trajectories: a national population-based birth cohort
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952656/
https://www.ncbi.nlm.nih.gov/pubmed/36830225
http://dx.doi.org/10.3390/antibiotics12020314
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