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Updated: Apr 27, 2026

Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Infant antibiotic exposure and the development of childhood overweight and central adiposity
M B Azad1, S L Bridgman2, A B Becker3
11] Pediatrics, University of Alberta, Edmonton, Alberta, Canada [2] Pediatrics and Child Health, University of Manitoba, Winnipeg, Manitoba, Canada [3] Manitoba Institute of Child Health, Winnipeg, Manitoba, Canada.
Insights
Early-life antibiotic exposure is linked to increased childhood overweight and adiposity, particularly in boys. This highlights the importance of judicious antibiotic use in infancy to potentially mitigate long-term health risks.
Area of Science:
- Pediatric Health
- Microbiome Research
- Public Health
Background:
- Childhood obesity is a growing epidemic.
- Gut microbiota established in infancy is vulnerable to antibiotic disruption.
- Antibiotic use in early life may impact long-term health outcomes.
Purpose of the Study:
- To examine the association between antibiotic exposure in the first year of life and the development of overweight and central adiposity.
- To investigate potential gender-specific differences in this association.
Main Methods:
- Utilized Canadian longitudinal birth cohort data linked with provincial health records.
- Documented antibiotic exposure during infancy from prescription records.
- Assessed overweight and central adiposity using anthropometric measurements at ages 9 and 12.
- Employed multiple logistic regression for association analysis.
Main Results:
- Infants exposed to antibiotics in the first year were more likely to be overweight by age 12 (32.4% vs. 18.2%).
- This association persisted in boys after adjusting for confounders (aOR 5.35), but not in girls (aOR 1.13).
- Gender-specific associations were observed for overweight and central adiposity at ages 9 and 12.
Conclusions:
- Antibiotic exposure in infancy is associated with increased risk of overweight and central adiposity in preadolescent boys.
- Antibiotic stewardship during infancy is crucial.
- Further research is needed to understand mechanisms, long-term consequences, and mitigation strategies.
Background:
Obesity has been associated with disruption of the gut microbiota, which is established during infancy and vulnerable to disruption by antibiotics.
Objectives:
To investigate the association between early-life antibiotic exposure and subsequent development of overweight and central adiposity.
Methods:
Provincial health-care records were linked to clinical and survey data from a Canadian longitudinal birth cohort study. Antibiotic exposure during the first year of life was documented from prescription records. Overweight and central adiposity were determined from anthropometric measurements at ages 9 (n=616) and 12 (n=431). Associations were determined by multiple logistic regression.
Results:
Infants receiving antibiotics in the first year of life were more likely to be overweight later in childhood compared with those who were unexposed (32.4 versus 18.2% at age 12, P=0.002). Following adjustment for birth weight, breastfeeding, maternal overweight and other potential confounders, this association persisted in boys (aOR 5.35, 95% confidence interval (CI) 1.94-14.72) but not in girls (aOR 1.13, CI 0.46-2.81). Similar gender-specific associations were found for overweight at age 9 (aOR 2.19, CI 1.06-4.54 for boys; aOR 1.20, CI 0.53-2.70 for girls) and for high central adiposity at age 12 (aOR 2.85, CI 1.24-6.51 for boys; aOR 1.59, CI 0.68-3.68 for girls).
Conclusions:
Among boys, antibiotic exposure during the first year of life was associated with an increased risk of overweight and central adiposity in preadolescence, indicating that antibiotic stewardship is particularly important during infancy. Given the current epidemic of childhood obesity and the high prevalence of infant antibiotic exposure, further studies are necessary to determine the mechanisms underlying this association, to identify the long-term health consequences, and to develop strategies for mitigating these effects when antibiotic exposure cannot be avoided.
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