Moderate and late preterm birth: effect on brain size and maturation at term-equivalent age
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Published on: November 20, 2015
Jennifer M Walsh1, Lex W Doyle, Peter J Anderson
1From the Departments of Newborn Research and Neonatal Services (J.M.W., L.W.D., J.L.Y.C.), Royal Women's Hospital, 20 Flemington Rd, Parkville, VIC 3052, Australia; University of Melbourne, Melbourne, Australia (L.W.D., P.J.A., K.J.L., J.L.Y.C.); and Department of Victorian Infant Brain Studies, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Australia (J.M.W., L.W.D., P.J.A., K.J.L., J.L.Y.C.).
Insights
Moderate and late preterm infants show smaller brain size, delayed myelination, and immature gyral development compared to term-born infants. These brain differences may contribute to long-term neurodevelopmental issues in preterm children.
Area of Science:
- Neuroscience
- Developmental Biology
- Pediatric Imaging
Background:
- Moderate and late preterm (MLPT) birth is associated with increased risk of neurodevelopmental deficits.
- Understanding early brain development in MLPT infants is crucial for identifying potential causes of these deficits.
Purpose of the Study:
- To compare brain structure, myelination, gyral development, and injury evidence between MLPT and term-born infants at term-equivalent age.
- To investigate the impact of preterm birth on key aspects of brain maturation.
Main Methods:
- 3-T magnetic resonance (MR) imaging was performed on 199 MLPT and 50 term-born infants at 38-44 weeks corrected gestational age.
- T1- and T2-weighted MR images were analyzed for brain structure size, myelination, gyral maturation, and abnormalities by a blinded assessor.
- Statistical comparisons used linear and logistic regression, with reliability assessed by intraclass correlation coefficients.
Main Results:
- MLPT infants exhibited smaller brain biparietal diameter, corpus callosum, basal ganglia, thalami, and cerebellum compared to term infants.
- Less developed myelination of the posterior limb of the internal capsule and delayed gyral maturation were observed in MLPT infants.
- Extracerebral space was larger in MLPT infants; signal intensity abnormalities and cysts were uncommon in both groups.
Conclusions:
- MLPT birth is linked to reduced brain size, delayed myelination, and immature gyral folding compared to full-term birth.
- These observed brain alterations may underlie long-term neurodevelopmental challenges in MLPT children.
- The findings highlight critical developmental differences in the brains of MLPT infants.
Purpose:
To compare the size of multiple brain structures, maturation in terms of both brain myelination and gyral development, and evidence of brain injury between moderate and late preterm (MLPT) and term-born infants at term-equivalent age.
Materials And Methods:
The study was approved by the human research ethics committees of the participating hospitals, and informed parental consent was obtained for all infants. One hundred ninety-nine MLPT and 50 term-born infants underwent 3-T magnetic resonance (MR) imaging brain examinations at 38-44 weeks of corrected gestational age. T1- and T2-weighted MR images were compared between groups for size of multiple cerebral structures, degree of myelination in the posterior limb of the internal capsule, gyral maturation, signal intensity abnormalities, and presence of cysts by a single assessor who was blinded to the gestational group and perinatal course of the infants. Group differences were compared by using linear regression for continuous variables and logistic regression for categorical variables, and interrater and intrarater reliability was assessed by using intraclass correlation coefficients.
Results:
Compared with those in the term-born control group, measurements of brain biparietal diameter, corpus callosum, basal ganglia and thalami, and cerebellum were smaller in infants in the MLPT group (all P ≤ .01), while extracerebral space was larger (P < .0001). Myelination of the posterior limb of the internal capsule was less developed, and gyral maturation was delayed in the MLPT group (both P < .001). Signal intensity abnormalities and cysts were uncommon in both groups, with 13 (6.5%) MLPT infants and one (2%) term infant having abnormalities. Inter- and intrarater reliability was good for most measures, with intraclass correlation coefficients generally greater than 0.68.
Conclusion:
MLPT birth is associated with smaller brain size, less-developed myelination of the posterior limb of the internal capsule, and more immature gyral folding than those associated with full-term birth. These brain changes may form the basis of some of the long-term neurodevelopmental deficits observed in MLPT children. Online supplemental material is available for this article.
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