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Updated: Mar 21, 2026

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Neonatal brain abnormalities predict preschool executive functioning performance in children born very preterm
Leanne Tamm1, Ellie Thoma1, Beth M Kline-Fath2
1Department of Pediatrics, Cincinnati Children's Hospital Medical Center.
Insights
Brain abnormalities in very preterm infants are linked to later executive functioning (EF) deficits. Early MRI scans can help identify children at risk for poorer performance on EF tasks.
Area of Science:
- Neuroscience
- Developmental Psychology
- Pediatrics
Background:
- Premature birth is associated with executive functioning (EF) deficits in children.
- Early EF development is crucial for neurodevelopmental and behavioral outcomes.
- Understanding risk factors for EF deficits in very preterm children is essential.
Purpose of the Study:
- To investigate the association between brain abnormalities and EF measures in very preterm children.
- To determine if global and regional brain abnormalities predict EF performance and caregiver ratings at 5-year corrected age.
Main Methods:
- Longitudinal prospective cohort study of 314 very preterm children (≤32 weeks gestation).
- Magnetic resonance imaging (MRI) at term-equivalent age to assess global and regional brain abnormalities.
- Regression analyses to evaluate associations with EF performance and caregiver ratings at 5-year corrected age.
Main Results:
- A global brain abnormality score predicted poorer performance-based EF, but not caregiver-rated EF.
- Cerebellar abnormalities were linked to deficits in working memory, inhibition, cognitive flexibility, and spatial working memory.
- White matter abnormalities were associated with poorer planning abilities.
Conclusions:
- Brain abnormalities in very preterm infants consistently predict poorer performance-based executive functioning.
- Conventional MRI at term-equivalent age can aid in identifying at-risk children.
- Interpretation of MRI findings should consider other influences on child EF, such as social factors.
Abstract:
Children born prematurely consistently exhibit deficits on performance-based and caregiver-report measures of executive functioning (EF). As early EF may mediate premature childbirth's impact on neurodevelopmental and behavioral outcomes, it is important to understand risk factors for EF deficits. Data from a longitudinal prospective cohort study were used to explore the association of brain abnormalities with EF measures in very preterm children (≤32 weeks of age). Participants included 314 very preterm children (M = 69.5, SD = 2.0 months of age; 51.9% male; 71.3% White). Regression analyses evaluated whether the global brain abnormality composite score on magnetic resonance imaging at term-equivalent age was associated with EF performance and caregiver ratings at 5-year corrected age, as well as which specific aspects of regional abnormalities (i.e., white matter, grey matter, cerebellar, and deep nuclear grey matter abnormalities) predicted EF. The global brain abnormality score significantly predicted poorer EF performance but not caregiver-rated EF, independent of known confounders (sex, gestational age, birthweight, social risk, chorioamnionitis, hypertensive disorders, bronchopulmonary dysplasia, retinopathy of pre-maturity, and global developmental delay). Exploratory analyses revealed that cerebellar abnormalities were associated with poorer working memory, inhibition, and cognitive flexibility and spatial working memory, and white matter abnormalities were associated with poorer planning. This study adds to the research showing that brain abnormalities associated with premature birth consistently predict poorer scores on performance-based measures of EF. Conventional magnetic resonance imaging at term-equivalent age may assist with identifying at-risk children when interpreted in the context of other influences on child EF such as family social circumstances and functioning. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
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