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2026journaloriginal-researcheLife

Pregistered movie-fMRI analyses reveal altered visual feature encoding in autism in pSTS

Jeff Mentch, Yibei Chen, Tamara Vanderwal, Satrajit S Ghosh

Identifiers and access

DOI
10.7554/elife.111008

Key findings

Preregistered stacked-encoding analyses of naturalistic movie-fMRI (Healthy Brain Network) show autism is not linked to enhanced low-level sensory encoding; instead, autistic children/adolescents show reduced high-level visual representations and a shift toward low-level encoding in integrative/social regions (notably pSTS), where the high-low weighting tracks Social Responsiveness Scale scores - favoring weak-central-coherence over early-sensory-enhancement accounts.

Abstract

Source: crossref

Sensory-perceptual differences are widely reported in autism, yet their underlying mechanisms remain unclear. We tested preregistered hypotheses using stacked encoding models applied to naturalistic movie-viewing fMRI from children and adolescents with and without an autism diagnosis from the Healthy Brain Network. We mapped cortical responsiveness to low- and high-level auditory and visual feature spaces. Contrary to enhanced perceptual functioning predictions, autism was not associated with increased low-level encoding in primary sensory cortices. Instead, autistic children and adolescents had reduced high-level visual representations and a relative shift toward low-level over high-level feature encoding in integration and social brain regions including the pSTS and adjacent face/social areas. In pSTS, this high-low weighting tracked Social Responsiveness Scale (SRS) scores. By contrast, audio-visual modality preference and sensory dominance were broadly conserved across groups. Developmentally, encoding exhibited strong, lateralized, modality-congruent age effects. Together, these findings favor weak central coherence accounts over early sensory enhancement.

Topics

  • brain-dynamics-naturalistic
  • child-development-education
  • neuroimaging-methods

Preprint precursor

Earlier versions of this work that have been superseded by the published record above.

  • bioRxiv202610.64898/2026.03.23.713749

Lab authors

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