Related Experiment Video
Updated: Jun 4, 2025

Probing the Brain in Autism Using fMRI and Diffusion Tensor Imaging
Published on: September 12, 2011
Aberrant brain structural-functional coupling and structural/functional network topology explain developmental delays
Zhongxin Huang1,2, Helin Zheng3,4, Longlun Wang3,4
1Department of Radiology, Women and Children's Hospital of Chongqing Medical University, Chongqing, 401147, China.
Insights
Children with Prader-Willi syndrome (PWS) show reduced brain structural-functional coupling and altered network properties. These neuroimaging findings may explain early developmental delays in PWS.
Area of Science:
- Neuroimaging
- Developmental Neuroscience
- Systems Neuroscience
Background:
- Prader-Willi syndrome (PWS) is a neurodevelopmental disorder linked to brain network abnormalities.
- Understanding structural-functional coupling and network topology in PWS is crucial for early diagnosis.
Purpose of the Study:
- To investigate structural-functional coupling and network topological properties in children with PWS.
- To correlate these neuroimaging findings with developmental scales.
Main Methods:
- Diffusion tensor imaging (DTI) and resting-state functional magnetic resonance imaging (rs-fMRI) were used.
- Structural and functional brain networks were constructed and analyzed for global and nodal properties.
- Partial correlations with developmental scales were assessed.
Main Results:
- Children with PWS exhibited decreased structural-functional coupling.
- Global network properties showed higher characteristic path length and lower global efficiency in the structural network.
- Nodal properties were altered in both structural (decreased) and functional (increased) networks.
- Functional network alterations significantly correlated with developmental scales.
Conclusions:
- Structural-functional decoupling and altered network topology are key neuroimaging features in PWS.
- These findings may elucidate mechanisms of early neurodevelopmental delays in PWS.
- Network properties could serve as potential biomarkers for assessing developmental backwardness.
Abstract:
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder characterized by dysplasia in early life. Psychoradiology studies have suggested that mental and behavioral deficits in individuals with PWS are linked to abnormalities in brain structural and functional networks. However, little is known about changes in network-based structural-functional coupling and structural/functional topological properties and their correlations with developmental scales in children with PWS. Here, we acquired diffusion tensor imaging and resting-state functional magnetic resonance imaging data from 25 children with PWS and 28 age- and sex-matched healthy controls, constructed structural and functional networks, examined intergroup differences in structural-functional coupling and structural/functional topological properties (both global and nodal), and tested their partial correlations with developmental scales. We found that children with PWS exhibited (1) decreased structural-functional coupling, (2) a higher characteristic path length and lower global efficiency in the structural network in terms of global properties, (3) alterations in classical cortical and subcortical networks in terms of nodal properties, with the structural network dominated by decreases and the functional network dominated by increases, and (4) partial correlation with developmental scales, especially for functional networks. These findings suggest that structural-functional decoupling and abundant structural/functional network topological properties may reveal the mechanism of early neurodevelopmental delays in PWS from a neuroimaging perspective and might serve as potential markers to assess early neurodevelopmental backwardness in PWS.
More Related Videos
09:01A Method for Investigating Age-related Differences in the Functional Connectivity of Cognitive Control Networks Associated with Dimensional Change Card Sort Performance
Published on: May 7, 2014
10:47Rapid Detection of Neurodevelopmental Phenotypes in Human Neural Precursor Cells NPCs
Published on: March 2, 2018
Related Concept Videos
Biological Causes of Schizophrenia
Genetic Factors in Schizophrenia
The genetic basis of schizophrenia is strongly supported by family and twin...
Attention-Deficit/Hyperactivity Disorder
Diagnostic Criteria and Symptoms
To diagnose ADHD, symptoms must manifest before age 12 and be evident across multiple settings....
Psychosis: Pathophysiology of Schizophrenia and Other Psychotic Disorders
Researchers have identified genetic factors that increase susceptibility to schizophrenia, underscoring the intricate interplay between genetics and environment in disease development. At the core of schizophrenia's pathophysiology is excessive dopaminergic neurotransmission within...
Autism Spectrum Disorder
These core symptoms manifest differently among individuals, ranging from mild to severe. The disorder's complexity extends beyond its clinical presentation, encompassing a diverse range of biological, cognitive, and sociocultural influences.
Neuroplasticity