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Isolation and Characterization of Human Umbilical Cord-derived Mesenchymal Stem Cells from Preterm and Term Infants
Published on: January 26, 2019
Accelerated Small-World Property of Structural Brain Networks in Preterm Infants at Term-Equivalent Age
Joo Young Lee1, Hyun-Kyung Park1,2, Hyun Ju Lee3,4
1Department of Pediatrics, Hanyang University Hospital, Hanyang University College of Medicine, Seoul, Republic of Korea.
Insights
Preterm infants show altered brain network organization at term-equivalent age, with increased small worldness linked to lower gestational age. This suggests brain network reorganization may indicate resilience to prematurity.
Area of Science:
- Neuroscience
- Pediatrics
- Medical Imaging
Background:
- Predicting neurodevelopmental outcomes in preterm infants is a significant pediatric challenge.
- Understanding brain network development in preterm infants at term-equivalent age is limited.
- White matter connectivity analysis is a growing area of interest in infant brain development.
Purpose of the Study:
- To investigate the structural brain network in preterm infants at term-equivalent age using diffusion MRI.
- To compare brain networks of preterm infants with those of full-term infants.
- To explore the impact of gestational age and clinical factors on brain network structure.
Main Methods:
- Diffusion tensor imaging (DTI) data were collected from 55 preterm neonates and 21 full-term infants.
- Probabilistic white matter tractography and the Johns Hopkins University neonate atlas were used to create global structural brain networks.
- Connectivity between cortical regions was quantified.
Main Results:
- Preterm infants exhibited significantly lower global efficiency and increased small worldness compared to full-term infants.
- Increased small worldness in preterm infants correlated with lower gestational age.
- Chronic lung disease in preterm infants was associated with decreased clustering and local efficiency.
Conclusions:
- The accelerated small worldness in preterm infants suggests a reorganized structural brain network.
- This reorganization may represent a resilient adaptation to prematurity-associated pathology.
- Findings provide insights into brain network development following preterm birth.
Background:
The prediction of neurodevelopmental outcomes in preterm infants is one of the clinical challenges of pediatrics. Despite the recent interest in brain development and white matter connectivity using a network-based analysis, very little is known about the brain network of at term-equivalent age in preterm infants.
Objective:
We aimed to investigate the structural brain network using diffusion MRI following preterm delivery at term-equivalent age compared with term infants and explored the influence of gestational age (GA) and clinical factors.
Method:
Diffusion tensor imaging data were acquired prospectively from 55 preterm neonates without apparent brain abnormalities (mean gestational age: 29.43 weeks) and 21 full-term infants at term-equivalent age. The global structural brain networks were produced by probabilistic white matter tractography in combination with the Johns Hopkins University neonate atlas to quantify connectivity between different cortical regions.
Results:
Compared with full-term infants, preterm infants had significantly lower global efficiency (p = 0.048) and increased small worldness (p = 0.012) after correcting for sex and age at MRI scan. The increased small worldness in the brain network at term-equivalent age was significantly linearly correlated with lower GA after adjusting for sex and the effects of postmenstrual age at MRI scan on the data in preterm infants (β = -0.020, p = 0.037). In multivariate analysis, infants with chronic lung disease had significantly decreased changes in clustering (p = 0.014) and local efficiency (p = 0.027).
Conclusion:
The accelerated small worldness in preterm infants suggests that the structural brain network after preterm birth is reorganized in maximizing integrated and segregated processing, implying resilience against prematurity-associated pathology.
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