Abstract

Sensory processing disorders (SPDs) affect up to 16% of school-aged children, and contribute to cognitive and behavioral deficits impacting affected individuals and their families. While sensory processing differences are now widely recognized in children with autism, children with sensory-based dysfunction who do not meet autism criteria based on social communication deficits remain virtually unstudied. In a previous pilot diffusion tensor imaging (DTI) study, we demonstrated that boys with SPD have altered white matter microstructure primarily affecting the posterior cerebral tracts, which subserve sensory processing and integration. This disrupted microstructural integrity, measured as reduced white matter fractional anisotropy (FA), correlated with parent report measures of atypical sensory behavior. In this present study, we investigate white matter microstructure as it relates to tactile and auditory function in depth with a larger, mixed-gender cohort of children 8–12 years of age. We continue to find robust alterations of posterior white matter microstructure in children with SPD relative to typically developing children (TDC), along with more spatially distributed alterations. We find strong correlations of FA with both parent report and direct measures of tactile and auditory processing across children, with the direct assessment measures of tactile and auditory processing showing a stronger and more continuous mapping to the underlying white matter integrity than the corresponding parent report measures. Based on these findings of microstructure as a neural correlate of sensory processing ability, diffusion MRI merits further investigation as a tool to find biomarkers for diagnosis, prognosis and treatment response in children with SPD. To our knowledge, this work is the first to demonstrate associations of directly measured tactile and non-linguistic auditory function with white matter microstructural integrity – not just in children with SPD, but also in TDC.

Highlights

  • Hypo-and/or hyper responsiveness to sensory stimulation is estimated to occur in 5–16% of children within the general population, and 40–80% of children with neurodevelopmental disorders (Ahn et al, 2004)

  • Visual reference with the Johns Hopkins University (JHU) white matter atlas reveals that the differences in FA are primarily localized to the bilateral posterior thalamic radiations (PTR), the splenium of the corpus callosum (SCC), and the right RLIC

  • A ceiling effect of the dichotic digits and temporal patterning tasks can be observed from these plots, limiting the range of sensory function that can be differentiated between subjects, in the TDC cohort. These findings corroborate and generalize our previous work demonstrating the role of disrupted posterior white matter microstructure in Sensory processing disorder (SPD)

Read more

Summary

Introduction

Hypo-and/or hyper responsiveness to sensory stimulation is estimated to occur in 5–16% of children within the general population, and 40–80% of children with neurodevelopmental disorders (Ahn et al, 2004). The Diagnostic Classification of Mental Health and Developmental Disorders in Infancy and Early Childhood includes a diagnostic label for Regulation Disorders of Sensory Processing (Zero to Three, 2005), but the Diagnostic and Statistical Manual 5 (DSM-V) does not include SPDs as a standalone category. They do include hyper- or hyporeactivity to sensory input or unusual interest in sensory aspects of the environment in their revised ASD criteria. These sensory processing differences are being increasingly investigated in the field of autism research and recognized as a core and critical clinical feature—children with SPD who do not have social communication deficits that meet ASD criteria can provide insight into the neural underpinnings of sensory processing in particular

Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.