Prenatal paracetamol exposure and child neurodevelopment: a sibling-controlled cohort study
- PMID: 24163279
- PMCID: PMC3887567
- DOI: 10.1093/ije/dyt183
Prenatal paracetamol exposure and child neurodevelopment: a sibling-controlled cohort study
Abstract
Background: Paracetamol is used extensively during pregnancy, but studies regarding the potential neurodevelopmental sequelae of foetal paracetamol exposure are lacking. Method Between 1999 and 2008 all pregnant Norwegian women were eligible for recruitment into the prospective Norwegian Mother and Child Cohort Study. The mothers were asked to report on their use of paracetamol at gestational weeks 17 and 30 and at 6 months postpartum. We used data on 48 631 children whose mothers returned the 3-year follow-up questionnaire by May 2011. Within this sample were 2919 same-sex sibling pairs who were used to adjust for familial and genetic factors. We modelled psychomotor development (communication, fine and gross motor development), externalizing and internalizing behaviour problems, and temperament (emotionality, activity, sociability and shyness) based on prenatal paracetamol exposure using generalized linear regression, adjusting for a number of factors, including febrile illness, infections and co-medication use during pregnancy.
Results: The sibling-control analysis revealed that children exposed to prenatal paracetamol for more than 28 days had poorer gross motor development [β 0.24, 95% confidence interval (CI) 0.12-0.51], communication (β 0.20, 95% CI 0.01-0.39), externalizing behaviour (β 0.28, 95% CI 0.15-0.42), internalizing behaviour (β 0.14, 95% CI 0.01-0.28), and higher activity levels (β 0.24, 95% CI 0.11-0.38). Children exposed prenatally to short-term use of paracetamol (1-27 days) also had poorer gross motor outcomes (β 0.10, 95% CI 0.02-0.19), but the effects were smaller than with long-term use. Ibuprofen exposure was not associated with neurodevelopmental outcomes.
Conclusion: Children exposed to long-term use of paracetamol during pregnancy had substantially adverse developmental outcomes at 3 years of age.
Keywords: MoBa; Norwegian Mother and Child Cohort Study; Paracetamol; acetaminophen; ibuprofen; neurodevelopment; sibling design.
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Comment in
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Paracetamol, oxidative stress, vitamin D and autism spectrum disorders.Int J Epidemiol. 2014 Jun;43(3):974-5. doi: 10.1093/ije/dyu004. Epub 2014 Feb 11. Int J Epidemiol. 2014. PMID: 24518930 No abstract available.
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Authors' Response: More research on paracetamol is required.Int J Epidemiol. 2014 Jun;43(3):975-6. doi: 10.1093/ije/dyu015. Epub 2014 Feb 11. Int J Epidemiol. 2014. PMID: 24518931 No abstract available.
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Annotations and reflections: pregnancy and paracetamol: methodological considerations on the study of associations between in utero exposure to drugs and childhood neurodevelopment.Basic Clin Pharmacol Toxicol. 2015 Jan;116(1):2-5. doi: 10.1111/bcpt.12322. Epub 2014 Oct 28. Basic Clin Pharmacol Toxicol. 2015. PMID: 25224918 No abstract available.
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Annotations and reflections: response to "Pregnancy and paracetamol: methodological considerations on the study of associations between in utero exposure to drugs and childhood neurodevelopment".Basic Clin Pharmacol Toxicol. 2015 Jan;116(1):6-8. doi: 10.1111/bcpt.12339. Epub 2014 Nov 8. Basic Clin Pharmacol Toxicol. 2015. PMID: 25308892 No abstract available.
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