Increased resting-state thalamocortical functional connectivity in children and young adults with autism spectrum disorder
Document Type
Article
Publication Date
12-22-2022
Institution/Department
MaineHealth Institute for Research; Pediatrics; Neurology & Neuroscience
Journal Title
Autism Research : Official Journal of the International Society for Autism Research
Abstract
There is converging evidence that abnormal thalamocortical interactions contribute to attention deficits and sensory sensitivities in autism spectrum disorder (ASD). However, previous functional MRI studies of thalamocortical connectivity in ASD have produced inconsistent findings in terms of both the direction (hyper vs. hypoconnectivity) and location of group differences. This may reflect, in part, the confounding effects of head motion during scans. In the present study, we investigated resting-state thalamocortical functional connectivity in 8-25 year-olds with ASD and their typically developing (TD) peers. We used pre-scan training, on-line motion correction, and rigorous data quality assurance protocols to minimize motion confounds. ASD participants showed increased thalamic connectivity with temporal cortex relative to TD. Both groups showed similar age-related decreases in thalamic connectivity with occipital cortex, consistent with a process of circuit refinement. Findings of thalamocortical hyperconnectivity in ASD are consistent with other evidence that decreased thalamic inhibition leads to increase and less filtered sensory information reaching the cortex where it disrupts attention and contributes to sensory sensitivity. This literature motivates studies of mechanisms, functional consequences, and treatment of thalamocortical circuit dysfunction in ASD.
Recommended Citation
Baran B, Nguyen QTH, Mylonas D, Santangelo SL, Manoach DS. Increased resting-state thalamocortical functional connectivity in children and young adults with autism spectrum disorder [published online ahead of print, 2022 Dec 22]. Autism Res. 2022;10.1002/aur.2875. doi:10.1002/aur.2875