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Background And Objectives: We determined whether white matter injury (WMI) severity and location on early-life vs term-equivalent age (TEA) brain MRI were more strongly associated with 36-month neurodevelopment.
Methods: Very preterm infants were recruited across 3 tertiary NICUs and underwent early-life and TEA MRI. Moderate-severe WMI severity and anterior or posterior location were scored. 36-month neurodevelopmental assessments were completed with Bayley Scales of Infant Development, Third Edition; delay was defined as a composite score <85 points. Multivariable logistic regressions adjusting for birth gestational age, site, infection, retinopathy of prematurity, moderate-severe intraventricular hemorrhage, and antenatal magnesium sulfate were used to determine associations of WMI severity and location at each scan with neurodevelopment.
Results: A total of 393 neonates (postmenstrual age median 27.6, SD 2.3 weeks, 47% female) completed early-life and TEA MRI scans. Cognitive delay was associated with early-life moderate-severe (OR 3.82, 95% CI 1.17-9.14) and anterior (OR 5.47, 95% CI 1.72-17.29) WMI. Motor delay was associated with early-life anterior WMI (OR 3.02, 95% CI 1.12-8.2). These associations were not observed at TEA in multivariable logistic regressions.
Discussion: Moderate-severe and anterior WMI on early-life, but not TEA, MRI were associated with neurodevelopmental outcomes. Early-life MRI may represent a more optimal time point for assessing WMI in very preterm infants.
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http://dx.doi.org/10.1212/WNL.0000000000214016 | DOI Listing |
Neurology
September 2025
Pediatrics, University of British Columbia and BC Children's Hospital Research Institute, Vancouver, BC, Canada.
Background And Objectives: We determined whether white matter injury (WMI) severity and location on early-life vs term-equivalent age (TEA) brain MRI were more strongly associated with 36-month neurodevelopment.
Methods: Very preterm infants were recruited across 3 tertiary NICUs and underwent early-life and TEA MRI. Moderate-severe WMI severity and anterior or posterior location were scored.
medRxiv
June 2025
Centre for Reproductive Health, Institute for Regeneration and Repair, University of Edinburgh, UK.
Background: Preterm birth and socioeconomic status (SES) are associated with brain development in early life, but the contribution of each over time is uncertain. We examined the effects of gestational age (GA) and SES on white matter microstructure in the neonatal period and at five years.
Methods: Participants included preterm and term children.
Biol Psychiatry
June 2025
Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada. Electronic address:
Background: Children born very preterm (≤32 weeks gestational age) display altered neonatal brain maturation and physiological stress regulation that may be related to executive function difficulties. Supportive parent behaviors are related to better neurodevelopment, but children may vary in their susceptibility to such behaviors. We investigated whether supportive parenting during toddlerhood (1.
View Article and Find Full Text PDFAnn Neurol
August 2025
Liggins Institute, University of Auckland, Auckland, New Zealand.
Objective: Moderate-to-late preterm (MLP) infants contribute to the greatest proportion of preterm children with neurodevelopmental impairments. White matter injury (WMI) is common and predicts adverse outcomes in very preterm (VP) infants. However, little is known about white matter abnormality (WMA) in MLP infants.
View Article and Find Full Text PDFJ Pediatr Gastroenterol Nutr
July 2025
Department of Pediatrics and Neonatology, North West Clinics, Alkmaar, the Netherlands.
Objectives: Long-term neurodevelopment of moderate and late preterm infants (MLPTI; gestational age [GA] 32 0/7 weeks to 36 6/7 weeks) is at a lower level than that of those at term age. Increased protein and energy intakes in the first week of life have been associated with better neurodevelopment early in life, in very preterm infants. This study aimed to evaluate the neurodevelopmental outcome of MLPTI at 2 years corrected age (CA) for prematurity (i.
View Article and Find Full Text PDF