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Published on: December 16, 2022
Fetal Heart Defects and Measures of Cerebral Size
Mette Høj Lauridsen1, Niels Uldbjerg2, Olav Bjørn Petersen2
1Department of Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Insights
Fetal brain size may be reduced in pregnancies with congenital heart defects (CHDs), indicating early developmental alterations. Neurodevelopmental follow-up is recommended for all infants with CHDs.
Area of Science:
- Perinatology
- Fetal Medicine
- Pediatric Cardiology
Background:
- Congenital heart defects (CHDs) are common birth anomalies.
- Early detection and understanding of associated conditions are crucial for improved outcomes.
Purpose of the Study:
- To investigate the association between fetal congenital heart defects (CHDs) and brain size measurements during pregnancy.
- To determine if brain size differences are detectable from the first trimester onwards.
Main Methods:
- A cohort study of 63,349 pregnancies in Western Denmark (2012-2013).
- Comparison of anthropometric measures (Z-scores) in fetuses with isolated CHDs versus controls.
- Analysis included biparietal diameter, head circumference, fetal weight, birthweight, and placental weight.
Main Results:
- No significant difference in first-trimester biparietal diameter Z-scores between groups.
- A statistically significant reduction in head circumference Z-scores was observed in the second trimester (-0.13) and at birth (-0.22) for fetuses with CHDs.
- Fetuses with univentricular physiology or tetralogy of Fallot showed the most significant reduction in cerebral size.
Conclusions:
- Brain alterations associated with CHDs appear to begin during pregnancy.
- The findings support the need for neurodevelopmental follow-up for all children diagnosed with CHDs.
- Specific CHDs, like univentricular physiology and tetralogy of Fallot, are linked to more pronounced cerebral size compromise.
Objectives:
To estimate the association between fetal congenital heart defects (CHDs) and measures of brain size throughout pregnancy, from the end of the first trimester to birth.
Study Design:
The cohort consisted of all fetuses scanned in Western Denmark in 2012 and 2013. Anthropometric measures in fetuses with isolated CHDs diagnosed within 12 months after birth were compared with those in the fetuses without CHDs. Z-scores standardized to gestational age were calculated for first trimester biparietal diameter, second trimester head circumference, fetal weight, birthweight, head circumference, and placental weight.
Results:
We obtained data from 63 349 pregnancies and identified 295 fetuses with isolated CHDs (major n = 145; minor n = 150). The first trimester mean biparietal diameter Z-scores were not different between those with and those without CHDs. The head circumference mean Z-score difference was -0.13 (95% CI, -0.24 to -0.01; P = .03) in the second trimester and -0.22 (95% CI, -0.35 to -0.09; P < .001) at birth. Fetuses with univentricular physiology or tetralogy of Fallot showed the most pronounced compromise in cerebral size.
Conclusions:
Our results suggest that the brain alterations inducing an increased risk of impaired neurodevelopment in children with CHDs begin during pregnancy. Although fetuses with univentricular physiology or tetralogy of Fallot exhibited the most pronounced compromise in cerebral size, we recommend neurodevelopmental follow-up for all children with CHDs.
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