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Prenatal maternal C-reactive protein prospectively predicts child executive functioning at ages 4-6 years
Julia E Morgan1,2, Steve S Lee1, Nicole E Mahrer1
1Department of Psychology, University of California, Los Angeles, CA, USA.
Insights
Maternal inflammation, indicated by C-reactive protein (CRP), during the third trimester predicts lower child cognitive flexibility. This finding highlights the impact of prenatal inflammation on early childhood executive functions.
Area of Science:
- Neuroscience
- Developmental Psychology
- Reproductive Medicine
Background:
- Childhood executive functioning (EF) is crucial for development.
- Maternal health during pregnancy can impact child neurodevelopment.
- Previous research has explored links between maternal factors and child EF, but timing and specific biomarkers require further investigation.
Purpose of the Study:
- To prospectively examine maternal preconception and prenatal biomarkers as predictors of child executive functioning (EF).
- To investigate the specific timing of maternal biomarker exposure (e.g., C-reactive protein, HbA1C, blood pressure) in relation to child cognitive flexibility and response inhibition.
Main Methods:
- Prospective longitudinal study of 100 mother-child dyads.
- Assayed maternal glycated hemoglobin (HbA1C), C-reactive protein (CRP), and blood pressure (BP) preconceptionally and during prenatal trimesters.
- Assessed child EF (cognitive flexibility, response inhibition) at ages 4-6 years.
Main Results:
- Higher third-trimester maternal CRP uniquely predicted poorer child cognitive flexibility, independent of other maternal biomarkers and covariates.
- Maternal HbA1C and blood pressure did not predict child EF.
- Child response inhibition was not associated with any maternal biomarkers.
Conclusions:
- Maternal inflammation during the third trimester is a significant predictor of deficits in child cognitive flexibility.
- The timing of maternal inflammation exposure is critical for its impact on child EF.
- These findings underscore the importance of monitoring maternal inflammation during pregnancy for child neurodevelopmental outcomes.
Abstract:
This prospective longitudinal study evaluated multiple maternal biomarkers from the preconception and prenatal periods as time-sensitive predictors of child executive functioning (EF) in 100 mother-child dyads. Maternal glycated hemoglobin (HbA1C ), C-reactive protein (CRP), and blood pressure (BP) were assayed before pregnancy and during the second and third trimesters. Subsequently, children were followed from birth and assessed for EF (i.e. cognitive flexibility, response inhibition) at ages 4-6 years. Perinatal data were also extracted from neonatal records. Higher maternal CRP, but not maternal HbA1C or BP, uniquely predicted poorer child cognitive flexibility, even with control of maternal HbA1C and BP, relevant demographic factors, and multiple prenatal/perinatal covariates (i.e. preconception maternal body mass index, maternal depression, maternal age at birth, child birth weight, child birth order, child gestational age, and child birth/neonatal complications). Predictions from maternal CRP were specific to the third trimester, and third trimester maternal CRP robustly predicted child cognitive flexibility independently of preconception and second trimester CRP. Child response inhibition was unrelated to maternal biomarkers from all time points. These findings provide novel, prospective evidence that maternal inflammation uniquely predicts child cognitive flexibility deficits, and that these associations depend on the timing of exposure before or during pregnancy.
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