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A Piglet Model of Neonatal Hypoxic-Ischemic Encephalopathy
Published on: May 16, 2015
Resting-state network complexity and magnitude changes in neonates with severe hypoxic ischemic encephalopathy
Hong-Xin Li1, Min Yu2, Ai-Bin Zheng3
1Department of Neonatology, Changzhou Children's Hospital, Changzhou, Jiangsu Province, China.
Insights
Severe hypoxic ischemic encephalopathy in infants disrupts brain network topology, impacting language and cognition. This finding may enable early predictions and interventions for affected newborns.
Area of Science:
- Neuroscience
- Developmental Neuroscience
- Medical Imaging
Background:
- Resting-state functional magnetic resonance imaging (rs-fMRI) reveals altered brain connectivity in older individuals with cerebral palsy.
- Understanding brain network disruptions in neonatal hypoxic-ischemic encephalopathy (HIE) is crucial for early intervention.
- Previous research has not fully elucidated the specific brain networks affected in neonatal HIE.
Purpose of the Study:
- To investigate the differences in resting-state functional brain network topology between infants with mild and severe hypoxic-ischemic encephalopathy (HIE).
- To identify specific brain regions and network properties associated with the severity of HIE in neonates.
- To explore the potential for early prediction of neurodevelopmental outcomes in infants with severe HIE.
Main Methods:
- Recruited 14 term-born infants with mild HIE and 14 with severe HIE from Changzhou Children's Hospital.
- Acquired resting-state functional magnetic resonance imaging (rs-fMRI) data from all participants.
- Analyzed whole-brain network organization, including small-world properties, local efficiency, clustering coefficient, and nodal efficiency.
Main Results:
- Both mild and severe HIE groups exhibited efficient small-world brain network organization.
- The severe HIE group showed significantly decreased local efficiency and a lower clustering coefficient compared to the mild HIE group.
- Reduced nodal efficiency was observed in key language and motor areas, including the left rolandic operculum, left supramarginal gyrus, bilateral superior temporal gyrus, and right middle temporal gyrus.
Conclusions:
- The topological structure of resting-state functional networks differs significantly between infants with severe and mild HIE.
- These network alterations in severe HIE are potentially linked to impaired language, motor, and cognitive functions.
- Findings suggest the possibility of early prediction of brain development in severe HIE, facilitating timely interventions.
Abstract:
Resting-state functional magnetic resonance imaging has revealed disrupted brain network connectivity in adults and teenagers with cerebral palsy. However, the specific brain networks implicated in neonatal cases remain poorly understood. In this study, we recruited 14 term-born infants with mild hypoxic ischemic encephalopathy and 14 term-born infants with severe hypoxic ischemic encephalopathy from Changzhou Children's Hospital, China. Resting-state functional magnetic resonance imaging data showed efficient small-world organization in whole-brain networks in both the mild and severe hypoxic ischemic encephalopathy groups. However, compared with the mild hypoxic ischemic encephalopathy group, the severe hypoxic ischemic encephalopathy group exhibited decreased local efficiency and a low clustering coefficient. The distribution of hub regions in the functional networks had fewer nodes in the severe hypoxic ischemic encephalopathy group compared with the mild hypoxic ischemic encephalopathy group. Moreover, nodal efficiency was reduced in the left rolandic operculum, left supramarginal gyrus, bilateral superior temporal gyrus, and right middle temporal gyrus. These results suggest that the topological structure of the resting state functional network in children with severe hypoxic ischemic encephalopathy is clearly distinct from that in children with mild hypoxic ischemic encephalopathy, and may be associated with impaired language, motion, and cognition. These data indicate that it may be possible to make early predictions regarding brain development in children with severe hypoxic ischemic encephalopathy, enabling early interventions targeting brain function. This study was approved by the Regional Ethics Review Boards of the Changzhou Children's Hospital (approval No. 2013-001) on January 31, 2013. Informed consent was obtained from the family members of the children. The trial was registered with the Chinese Clinical Trial Registry (registration number: ChiCTR1800016409) and the protocol version is 1.0.
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