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Published on: December 7, 2018
Anomalies in uncinate fasciculus development and social defects in preschoolers with autism spectrum disorder
Yun Li1, Zhengbing Zhou1, Chen Chang1
1Child Mental Health Research Center, Nanjing Brain Hospital affiliated to Nanjing Medical University, No.264 Guangzhou Road, Nanjing, 210029, Jiangsu, China.
Insights
Autism spectrum disorder (ASD) in young children shows faster uncinate fasciculus (UF) overgrowth, linked to worsening social deficits. This white matter development impacts socio-affective processing and emotional regulation.
Area of Science:
- Neuroscience
- Developmental Psychology
- Pediatrics
Background:
- Autism spectrum disorder (ASD) is characterized by social interaction deficits and emotional regulation difficulties.
- The uncinate fasciculus (UF), a white matter tract, is implicated in socio-affective processing, but its developmental trajectory in young children with ASD is unclear.
Purpose of the Study:
- To describe the developmental growth trajectory of the uncinate fasciculus (UF) in young children.
- To investigate the relationship between UF development and social deficits in autism spectrum disorder (ASD).
Main Methods:
- Diffusion tensor imaging (DTI)-based tractography was used to measure UF eigenvalues in 37 children with ASD and 27 with developmental delay (DD) aged 2-3 years.
- Measurements were taken at baseline and a 2-year follow-up.
- Growth rates were compared between groups, and associations with social deficit scores (ADI-R) were analyzed.
Main Results:
- At baseline, left UF axial diffusivity (AD) was higher in the ASD group.
- At follow-up, left UF fractional anisotropy (FA) was higher and radial diffusivity (RD) lower in the ASD group.
- UF growth rate was faster in children with ASD, with negative correlations between increased social deficits and UF RD/MD.
Conclusions:
- Young children with ASD exhibit UF overgrowth between ages 2-5 years.
- This white matter abnormality is directly associated with the progression of social deficits in ASD.
- Findings suggest UF maldevelopment contributes to socio-affective deficits in early childhood ASD.
Background:
Individuals with autism spectrum disorder (ASD) have social interaction deficits and difficulties in emotional regulation. The neural substrates for these socio-affective deficits are not yet clear, but one potential candidate is maldevelopment of the uncinate fasciculus (UF), a white matter tract thought to be involved in socio-affective processing. However, the developmental trajectory of the UF in young children with social interaction deficits has not been examined. The present study was designed to describe the developmental growth trajectory of the UF and the relationships between UF development and social deficits in ASD.
Methods:
Eigenvalues of the UF were measured by diffusion tensor imaging (DTI)-based tractography in 37 children with ASD and 27 matched 2-3-year-old subjects with developmental delay (DD) at baseline (time 1) and at 2-year follow-up (time 2). Growth rates of the UF were compared between groups and associations with social deficit scores according to the Autism Diagnostic Interview-Revised (ADI-R) analyzed by Pearson's correlations.
Results:
At time 1, axial diffusivity (AD) of the left UF was significantly larger in the ASD group than the DD group. At time 2, left UF fractional anisotropy (FA) was significantly higher and radial diffusivity (RD) significantly lower in the ASD group than the DD group. The rate of UF growth during this 2-year interval was faster in children with ASD than DD. Significant negative correlations were found between the rise in ADI-R social deficit measures and both right UF RD and left UF mean diffusivity (MD).
Conclusions:
Young children with ASD demonstrate UF overgrowth during the 2-year development period between 2 and 3 and 4-5 years of age, and this white matter abnormality is directly associated with the progression of social deficits.
Trial Registration:
World Health Organization class I registered international clinical trial platform, ChiCTR-ROC-17012877.
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