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Published on: June 24, 2020
Risk of immune-related diseases in childhood after intrapartum antibiotic exposure
Sofia Ainonen1, Eveliina Ronkainen2, Mikael Hakkola1
1Research Unit of Clinical Medicine, University of Oulu, Oulu, Finland.
Insights
Intrapartum antibiotic exposure in newborns is linked to a higher risk of childhood autoimmune diseases. This association highlights the need for targeted group B streptococcus prevention strategies.
Area of Science:
- Pediatric immunology
- Microbiome research
- Public health
Background:
- Intrapartum antibiotic prophylaxis prevents early-onset group B streptococcal disease.
- Antibiotic use during childbirth impacts infant gut microbiota development.
- Gut microbiota composition is linked to childhood immune-related diseases.
Purpose of the Study:
- To investigate the hypothesis that intrapartum antibiotic exposure is associated with immune-related diseases in childhood.
- To analyze the relationship between antibiotic exposure and autoimmune, allergic, and obstructive airway diseases.
Main Methods:
- Population-based cohort study of vaginally delivered children.
- Data on intrapartum antibiotic exposure extracted from electronic medical records.
- Childhood disease outcomes obtained from national registers; Cox regression analysis used.
Main Results:
- A total of 45,575 children were included; 21% received intrapartum antibiotics.
- Intrapartum antibiotic exposure showed an association with autoimmune disease diagnosis (aHR, 1.28).
- No significant association was found between antibiotic exposure and allergic or obstructive airway diseases.
Conclusions:
- Intrapartum antibiotic exposure may increase the risk of autoimmune diseases in childhood.
- Findings support the development of more specific prevention strategies for group B streptococcal disease.
- Further research into the mechanisms linking antibiotics, microbiota, and immune development is warranted.
Background:
Intrapartum antibiotic prophylaxis is effective in preventing early-onset group B streptococcal disease in newborn infants, but it influences gut microbiota development. Gut microbiota composition is, in turn, associated with immune-related diseases in childhood.
Objective:
This study hypothesized that intrapartum antibiotic exposure is associated with immune-related diseases in childhood.
Study Design:
We conducted a population-based cohort study of vaginally delivered children. We retrieved data on intrapartum antibiotic exposure from structured electronic medical records and obtained outcome data on childhood autoimmune, allergic, and obstructive airway diseases from comprehensive national registers. We used Cox regression analysis with adjustment for maternal and neonatal covariates and regarded death as a competing risk in the analyses.
Results:
The study population comprised 45,575 vaginally born children of whom 9733 (21%) had been exposed to intrapartum antibiotics. Intrapartum antibiotic exposure was associated with an autoimmune disease diagnosis (adjusted hazard ratio, 1.28; 95% confidence interval, 1.02-1.62), which corresponds to 22% (95% confidence interval, 6-39) as a theoretical population-attributable fraction. Intrapartum antibiotic exposure was not associated with diagnoses of allergic (adjusted hazard ratio, 1.08; 95% confidence interval, 0.97-1.20) or obstructive airway diseases (adjusted hazard ratio, 1.04; 95% confidence interval, 0.96-1.14).
Conclusion:
Intrapartum antibiotic exposure may be associated with an increased risk for autoimmune diseases in childhood. This finding supports the efforts to develop more specific group B streptococcal disease prevention strategies in the future.
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