Published October 2021 | Version Supplemental Material
Journal Article Open

Associations between physiological and neural measures of sensory reactivity in youth with autism

  • 1. ROR icon University of California, Los Angeles
  • 2. ROR icon California Institute of Technology
  • 3. ROR icon University of Salzburg

Abstract

Background: Individuals with Autism Spectrum Disorder (ASD) commonly show sensory over‐responsivity (SOR), an impairing condition related to over‐reactive brain and behavioral responses to aversive stimuli. While individuals with ASD often show atypically high physiological arousal, it is unclear how this relates to sensory reactivity. We therefore investigated how physiological arousal relates to brain and behavioral indices of SOR, to inform understanding of the biological mechanisms underlying SOR and to determine whether physiological measures are associated with SOR‐related brain responses. Methods: Youth aged 8–18 (49 ASD; 30 age‐ and performance‐IQ‐matched typically developing (TD)) experienced mildly aversive tactile and auditory stimuli first during functional magnetic resonance imaging (N = 41 ASD, 26 TD) and then during skin conductance (SCR) (N = 48 ASD, 28 TD) and heart rate (HR) measurements (N = 48 ASD, 30 TD). Parents reported on their children's SOR severity. Results: Autism Spectrum Disorder youth overall displayed greater SCR to aversive sensory stimulation than TD youth and greater baseline HR. Within ASD, higher SOR was associated with higher mean HR across all stimuli after controlling for baseline HR. Furthermore, the ASD group overall, and the ASD‐high‐SOR group in particular, showed reduced HR deceleration/greater acceleration to sensory stimulation compared to the TD group. Both SCR and HR were associated with brain responses to sensory stimulation in regions previously associated with SOR and sensory regulation. Conclusions: Autism Spectrum Disorder youth displayed heightened physiological arousal to mildly aversive sensory stimulation, with HR responses in particular showing associations with brain and behavioral measures of SOR. These results have implications for using psychophysiological measures to assess SOR, particularly in individuals with ASD who cannot undergo MRI.

Additional Information

© 2021 Association for Child and Adolescent Mental Health. Issue Online: 29 September 2021; Version of Record online: 15 February 2021; Manuscript accepted: 18 December 2020; Manuscript revised: 17 December 2020; Manuscript received: 02 May 2020. Research funding: UCLA Friends of the Semel Institute (Scholar Grant); National Research Service Award postdoctoral fellowship. Grant Number: F32 MH105167; National Institute of Mental Health. Grant Numbers: K08 MH112871, R01MH100028; National Institute of Child Health and Human Development. Simons Foundation Autism Research Initiative. Grant Number: 345389. Conflict of interest statement: No conflicts declared.

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Additional details

Identifiers

Eprint ID
108146
Resolver ID
CaltechAUTHORS:20210222-125039388

Funding

UCLA
NIH Postdoctoral Fellowship
F32 MH105167
NIH
K08 MH112871
NIH
R01MH100028
NIH
P50 HD055784
Simons Foundation Autism Research Initiative
345389

Dates

Created
2021-02-22
Created from EPrint's datestamp field
Updated
2021-11-16
Created from EPrint's last_modified field