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Updated: Aug 14, 2025

A Murine Model of Fetal Exposure to Maternal Inflammation to Study the Effects of Acute Chorioamnionitis on Newborn Intestinal Development
Published on: June 24, 2020
In-utero antibiotic exposure and subsequent infections in infancy: a register-based cohort study with sibling
Aya O Nakitanda1, Helle Kieler2, Ingvild Odsbu3
1Centre for Pharmacoepidemiology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden (Drs Nakitanda, Kieler, Odsbu, and Pazzagli).
Insights
Prenatal antibiotic exposure slightly increased infant infection risk, but this association was largely explained by shared family factors and did not vary by antibiotic class.
Area of Science:
- Perinatal epidemiology
- Microbiome research
- Pediatric infectious diseases
Background:
- Maternal antibiotic use during pregnancy can alter the maternal microbiome, potentially impacting offspring's susceptibility to infections.
- Previous research suggests a link between prenatal antibiotic exposure and increased childhood infection risk, but infant-specific risks remain underexplored.
Purpose of the Study:
- To examine the association between in-utero antibiotic exposure and infant infections within the first year of life.
- To determine if infection risks differ based on the class of antibiotics used prenatally.
Main Methods:
- Utilized Swedish population-based registers to follow over 1.3 million live-born infants from birth to age one.
- Defined prenatal antibiotic exposure as maternal prescription fills between last menstrual period and delivery.
- Assessed infant outcomes including antimicrobial prescriptions, specialist-diagnosed infections, and infection-related mortality, employing regression analyses and sibling comparisons.
Main Results:
- Infants exposed to antibiotics in utero showed higher rates of antimicrobial prescriptions (aIRR 1.34) and specialist-diagnosed infections (aHR 1.28).
- Associations were consistent across most antibiotic classes but were attenuated in sibling analyses, suggesting a role for shared familial factors.
- No significant association was found between prenatal antibiotic exposure and infant mortality in the sibling cohort.
Conclusions:
- Minor associations between prenatal antibiotic exposure and infant infections are partly explained by shared familial factors.
- The risk of infant infection following in-utero antibiotic exposure does not significantly differ across commonly used antibiotic classes.
Background:
Prenatal antibiotic use, the ensuing maternal dysbiosis, and subsequent acquisition of altered microbiota in early life have been linked to the offspring's increased susceptibility to childhood infections. However, infection risks during the first year of life associated with in-utero antibiotic exposure have not been comprehensively explored.
Objective:
To investigate the associations between exposure to antibiotics in utero and subsequent infections during infancy and whether such associations differ by antibiotic class.
Study Design:
All data were retrieved from Swedish population-based registers. Singletons live-born between 2006 and 2018 were followed up from birth to their first birthday. Exposure was maternal filling of at least 1 antibiotic prescription between the last menstrual period and delivery. Outcomes were the infants' antimicrobial prescription fills, incident infections diagnosed in specialist care, and deaths with infections indicated as underlying or contributing causes ("infection-related deaths"). Birth year, birth season, maternal age, place of residence, parity, comorbidity indicator, body mass index, proxies for general health status, education level, and smoking status were considered covariates. Poisson regression was used to estimate crude and adjusted incidence rate ratios with 95% confidence intervals for the number of antimicrobial prescriptions filled to the infant. Cox regression was used to estimate crude and adjusted hazard ratios with 95% confidence intervals for incident infections diagnosed in specialist care and at death. Sibling analyses were used to account for shared familial factors. Sensitivity of the results to exposure definition and perinatal factors prognostic for the outcomes were assessed in supplementary analyses.
Results:
Of 1,347,018 infants in the full cohort, 294,657 (21.9%) were exposed to antibiotics in utero. There were 677,430 antimicrobial prescriptions filled (1.380 per 1000 person-days), 423,705 incident infections diagnosed in specialist care (0.870 per 1000 person-days), and 2800 infection-related deaths (0.006 deaths per 1000 person-days) during follow-up. Compared to unexposed, infants exposed to antibiotics in utero had higher rates of antimicrobial prescription fills (adjusted incidence rate ratio, 1.34; 95% confidence interval, 1.33-1.34), incident infections diagnosed in specialist care (adjusted hazard ratio, 1.28; 95% confidence interval, 1.27-1.29), and infection-related mortality (adjusted hazard ratio, 1.15; 95% confidence interval, 1.05-1.25). For antimicrobial prescriptions and infections diagnosed in specialist care, associations were consistent across most antibiotic classes but were attenuated in the sibling analyses: adjusted incidence rate ratio of 1.05 (95% confidence interval, 1.04-1.06) and adjusted hazard ratio of 1.05 (95% confidence interval, 1.03-1.07), respectively. No association with infant mortality was found in the sibling cohort (adjusted hazard ratio, 0.93; 95% confidence interval, 0.81-1.08).
Conclusion:
The minor associations between exposure to antibiotics in utero and infections during infancy were partly explained by shared familial factors and did not differ across frequently used antibiotic classes.
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