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Bronchopulmonary Dysplasia Is Associated with Altered Brain Volumes and White Matter Microstructure in Preterm
Jong-Min Lee1, Yong-Ho Choi1, Jinwoo Hong1
1Department of Biomedical Engineering, Hanyang University, Seoul, Republic of Korea.
Insights
Bronchopulmonary dysplasia (BPD) impairs white matter development in preterm infants. This condition is linked to reduced brain volumes and altered white matter microstructure, impacting neurodevelopmental outcomes.
Area of Science:
- Neonatal neuroscience
- Pediatric neurology
- Developmental biology
Background:
- Bronchopulmonary dysplasia (BPD) is an inflammatory lung disease affecting preterm infants.
- BPD is associated with adverse neurodevelopmental outcomes.
Purpose of the Study:
- To investigate brain volume and white matter (WM) microstructure in preterm infants with and without BPD.
- To assess the impact of BPD on brain development at term-equivalent age.
Main Methods:
- Studied 56 preterm infants (33 with BPD, 23 without) and 22 healthy term infants.
- Utilized advanced MRI segmentation and diffusion tensor imaging for quantitative analysis.
- Employed atlas-based analysis using the JHU neonatal template.
Main Results:
- Preterm infants with BPD had significantly smaller cerebral WM volumes compared to those without BPD.
- Infants with BPD showed reduced fractional anisotropy in the corpus callosum, corticospinal tract, and superior cerebellar peduncle.
- These findings were independent of confounding factors like sex and gestational age.
Conclusions:
- BPD negatively influences WM and cerebellar development in preterm infants.
- These brain alterations suggest clinical significance for the neurodevelopmental trajectory of infants with BPD.
Background:
Bronchopulmonary dysplasia (BPD), an inflammatory disease involving disrupted lung development, is associated with neurodevelopmental outcome in preterm infants.
Objective:
This study examined the brain volume and white matter (WM) microstructure in preterm infants at term-equivalent age and explored the effects of BPD on brain development.
Method:
We studied 56 preterm infants (33 with BPD and 23 without BPD) with no evidence of focal abnormalities on conventional magnetic resonance imaging (MRI) at term-equivalent age. Regional brain volumes and diffusion tensor images were examined using advanced segmentation techniques to acquire quantitative volume measurements, and the JHU neonatal template was used for the atlas-based analysis. We compared these infants with 22 healthy term infants of a similar postmenstrual age.
Results:
The preterm infants with BPD had smaller cerebral WM (p = 0.005) volumes than the preterm infants without BPD, independent of sex, gestational age, age at MRI scan, and total intracranial volume. Independent of sex, gestational age, and age at MRI scan, the preterm infants with BPD exhibited marked reductions in fractional anisotropy in the corpus callosum (p = 0.006), corticospinal tract (p = 0.003), and superior cerebellar peduncle (p = 0.002) compared with the infants with no BPD, with a significance level of p ≤ 0.008 as a Bonferroni correction for multiple comparisons.
Conclusion:
Our study highlights the potential impairing influence of BPD on WM and cerebellar development in preterm infants compared with those without BPD at term-equivalent age, suggesting its clinical significance for neurodevelopment in BPD infants.
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