Peer-reviewed article
Maternal congenital heart disease and risk of child developmental vulnerability in early school age: A population-based cohort study.
Hossin MZ, Gadermann A, Nagy E, Gill R, Petteni MG et al. ·
Summary
Written by AI, not yet AICS's view · claude-haiku-4-5-20251001This Canadian population study of 256,629 children found that those exposed to maternal congenital heart disease in the womb had a 28% higher risk of developmental vulnerability at school entry (age 5-6 years) compared to unexposed children. The risk was highest for children whose mothers had severe heart disease. The increased vulnerability was seen across multiple developmental areas including physical health, social competence, language and cognitive development. While the study could not fully explain the cause of this link, it suggests that women with congenital heart disease may benefit from enhanced clinical support during pregnancy.
Key points
- 25.2% of children exposed to maternal CHD showed developmental vulnerability versus 16.6% in unexposed children
- Maternal CHD was associated with 28% higher adjusted risk of developmental vulnerability (aRR 1.28; 95% CI [1.11, 1.48])
- Increased risk observed across physical health, social competence, language and cognitive development, and communication domains
- Severe maternal CHD showed stronger association (aRR 1.98) compared to mild CHD (aRR 1.19)
- Preterm birth explained only about 8% of the association, suggesting other mechanisms are at play
Limitations
The study could not separate in-utero effects from genetic inheritance or postnatal family influences on child development. Some misclassification of maternal CHD diagnoses may have occurred, which would likely underestimate the true association.
Abstract
Background While maternal congenital heart disease (CHD) is associated with increased risks of adverse pregnancy outcomes, its impact on long-term child development remains unknown. This study aimed to investigate if in-utero exposure to maternal CHD is associated with child developmental vulnerability at school entry. Methods and findings This population-based cohort study included 256,629 singleton offspring born in British Columbia, Canada between January 1, 1995 and December 31, 2016, with follow up through linkage to teacher-rated Early Development Instrument (EDI) surveys administered in kindergarten around 5-6 years of age. Over 90% children enrolled in participating schools completed the questionnaire. Developmental vulnerability was defined as a score <10th percentile in any two of the five EDI domains: physical health and wellbeing, social competence, emotional maturity, language and cognitive development, and communication and general knowledge. The association between maternal CHD and child developmental vulnerability was examined using modified Poisson regression models, adjusted for maternal age at delivery, parity, country of birth, marital status, neighborhood income quintiles, preexisting psychiatric disorders, and pre-gestational diabetes. A counterfactual four-way decomposition method was used to quantify potential mediation and moderation by preterm birth. Of the 256,629 children (51.4% female) included in the analysis, 456 (0.2%) were exposed to maternal CHD. Developmental vulnerability was identified among 25.2% children exposed to maternal CHD compared with 16.6% among the unexposed. In the adjusted model, maternal CHD was associated with 28% higher risk of developmental vulnerability (aRR 1.28; 95% CI [1.11, 1.48]) compared with no maternal CHD. The increased risk was observed across multiple developmental domains related to physical health and wellbeing (aRR 1.31; 95% CI [1.11, 1.54]), social competence (aRR 1.22; 95% CI [1.02, 1.45]), language and cognitive development (aRR 1.39; 95% CI [1.13, 1.70]), and communication and general knowledge (aRR 1.33; 95% CI [1.09, 1.63]). Preterm birth mediated only about 8% of the overall association. Severe CHD was more strongly associated with developmental vulnerability (aRR 1.98; 95% CI [1.31, 3.00]) compared to mild CHD (aRR 1.19; 95% CI [1.00, 1.42]). However, the study had limited capacity to separate intrauterine effects from potential genetic and postnatal familial influences. Some degree of CHD misclassification is possible, which would likely bias the association toward the null. Conclusions In this population-based study, maternal CHD was associated with child developmental vulnerability at school entry. While further research is required to elucidate the mechanisms, enhanced clinical monitoring and tailored support to reproductive age women with CHD may help reduce the risk of developmental vulnerability in their children.