» Articles » PMID: 24117888

Maternal Infections During Pregnancy and Cerebral Palsy: a Population-based Cohort Study

Abstract

Background: Cerebral palsy (CP) is a common motor disability in childhood. We examined the association between maternal infections during pregnancy and the risk of congenital CP in the child.

Methods: Liveborn singletons in Denmark between 1997 and 2003 were identified from the Danish National Birth Registry and followed from 1 year of life until 2008. Redemption of antibiotics from the National Register of Medicinal Product Statistics and maternal infections reported by the National Hospital Register were used as markers of maternal infection during pregnancy. CP diagnoses were obtained from the Danish Cerebral Palsy Registry. Adjusted hazard ratio (HR) and 95% confidence interval (CI) were estimated by Cox proportional hazard models.

Results: Of the 440 564 singletons with follow-up data, 840 were diagnosed with congenital CP. Maternal genito-urinary tract infections (HR 2.1, 95% CI 1.4, 3.2) were associated with CP in all births, in term births (HR 1.9, 95% CI 1.1, 3.2), in children with spastic CP (HR 2.1, 95% CI 1.4, 3.3), and among first-born children (HR 1.9, 95% CI 1.4, 3.3). Overall, we found associations between redeemed nitrofurantoin (HR 1.7, 95% CI 1.1, 2.8) and CP. Among trimester-specific exposures, CP risk was associated with prescriptions redeemed in the first trimester for any antibacterials, beta-lactam antibacterials, and nitrofurantoin, an antibiotic commonly used to treat lower urinary tract infection, and genito-urinary tract infections in the third trimester.

Conclusion: Genito-urinary tract infections and antibiotic use during pregnancy were associated with increased risks of CP, indicating that some maternal infections or causes of maternal infections present in prenatal life may be part of a causal pathway leading to CP.

Citing Articles

Ambient Toxic Air Contaminants in the Maternal Residential Area during Pregnancy and Cerebral Palsy in the Offspring.

Zhuo H, Ritz B, Warren J, Pollitt K, Liew Z Environ Health Perspect. 2025; 133(1):17008.

PMID: 39853265 PMC: 11758984. DOI: 10.1289/EHP14742.


A nationwide longitudinal investigation on the role of prenatal exposure to infectious diseases on the onset of chronic conditions in children and adolescents in Brazil.

Paixao E, Cerqueira-Silva T, Florentino P, Carroll O, Clemente N, Lawlor D Wellcome Open Res. 2024; 9:320.

PMID: 39429627 PMC: 11489840. DOI: 10.12688/wellcomeopenres.22430.2.


Genetic pathways in cerebral palsy: a review of the implications for precision diagnosis and understanding disease mechanisms.

Xu Y, Li Y, Richard S, Sun Y, Zhu C Neural Regen Res. 2023; 19(7):1499-1508.

PMID: 38051892 PMC: 10883492. DOI: 10.4103/1673-5374.385855.


Season of Conception and Risk of Cerebral Palsy.

Zhuo H, Ritz B, Warren J, Liew Z JAMA Netw Open. 2023; 6(9):e2335164.

PMID: 37738049 PMC: 10517373. DOI: 10.1001/jamanetworkopen.2023.35164.


Beyond TORCH: A narrative review of the impact of antenatal and perinatal infections on the risk of disability.

Devaraju M, Li A, Ha S, Li M, Shivakumar M, Li H Neurosci Biobehav Rev. 2023; 153:105390.

PMID: 37708918 PMC: 10617835. DOI: 10.1016/j.neubiorev.2023.105390.


References
1.
Hallas J . Conducting pharmacoepidemiologic research in Denmark. Pharmacoepidemiol Drug Saf. 2002; 10(7):619-23. DOI: 10.1002/pds.638. View

2.
Olsen J . Options in making use of pregnancy history in planning and analysing studies of reproductive failure. J Epidemiol Community Health. 1994; 48(2):171-4. PMC: 1059928. DOI: 10.1136/jech.48.2.171. View

3.
Nelson K, Willoughby R . Infection, inflammation and the risk of cerebral palsy. Curr Opin Neurol. 2000; 13(2):133-9. DOI: 10.1097/00019052-200004000-00004. View

4.
Yoon B, Park C, Chaiworapongsa T . Intrauterine infection and the development of cerebral palsy. BJOG. 2003; 110 Suppl 20:124-7. DOI: 10.1016/s1470-0328(03)00063-6. View

5.
Wu Y, Colford Jr J . Chorioamnionitis as a risk factor for cerebral palsy: A meta-analysis. JAMA. 2000; 284(11):1417-24. DOI: 10.1001/jama.284.11.1417. View