Assessment & Research

Atypical Scene-Selectivity in the Retrosplenial Complex in Individuals With Autism Spectrum Disorder.

Persichetti et al. (2025) · Autism research : official journal of the International Society for Autism Research 2025
★ The Verdict

Weaker brain responses to scenes in the retrosplenial complex may explain why some autistic individuals struggle with map-based navigation.

✓ Read this if BCBAs working with teens or adults who have autism and travel-training goals
✗ Skip if Clinicians focused only on early childhood or non-verbal populations

01Research in Context

01

What this study did

Agiovlasitis et al. (2025) scanned adults with autism while they looked at pictures of places. The team focused on the retrosplenial complex, a brain area that normally lights up for scenes and helps us find our way.

They compared the scene response to that of typical adults. The goal was to see if weaker brain activity here could explain why some autistic people struggle with map reading or learning new routes.

02

What they found

The autism group showed a smaller jump in RSC activity when viewing scenes. A second scene area, the OPA, looked the same in both groups, so the problem is specific to the RSC.

The authors link this dampened signal to trouble using past spatial memories to guide navigation.

03

How this fits with other research

The result lines up with two earlier studies. Baharav et al. (2008) saw slower detection of odd objects in real-world photos, and Andrews et al. (2024) reviewed papers showing that building mental scenes is hard for many autistic individuals. All three point to a weak top-down picture of space.

Yet Hochhauser et al. (2018) seems to say the opposite: adolescents with autism spotted scene changes faster than typical teens. The difference is age and task. The 2018 kids were young and had extra time; the 2025 adults were older and viewed rapid streams. Speed demands may unmask the RSC gap.

O'Connor et al. (2008) adds that face areas are also under-active in autism. Together the papers sketch a ventral-stream trade-off: faces and places both get less specialized processing.

04

Why it matters

If a client gets lost easily, the issue may be neural, not careless. Teach routes with extra landmarks, verbal scripts, or GPS cues instead of paper maps alone. Rehearse the same path several times to build a stronger picture. And give processing time—quick scene tasks may under-estimate what they know.

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Walk the route together first, then let the client lead while you point out three fixed landmarks they can name out loud.

02At a glance

Intervention
not applicable
Design
other
Population
autism spectrum disorder
Finding
negative

03Original abstract

A small behavioral literature on individuals with autism spectrum disorder (ASD) has shown that they can be impaired when navigating using map-based strategies (i.e., memory-guided navigation), but not during visually-guided navigation. Meanwhile, there is neuroimaging evidence in typically developing (TD) individuals demonstrating that the retrosplenial complex (RSC) is part of a memory-guided navigation system, while the occipital place area (OPA) is part of a visually-guided navigation system. A key identifying feature of the RSC and OPA is that they respond significantly more to pictures of places compared to faces or objects-i.e., they demonstrate scene-selectivity. Therefore, we predicted that scene-selectivity would be weaker in the RSC of individuals with ASD compared to a TD control group, while the OPA would not show such a difference between the groups. We used functional MRI to scan groups of ASD individuals and matched TD individuals while they viewed pictures of places and faces and performed a one-back task. As predicted, scene-selectivity was significantly lower in the RSC, but not OPA, in the ASD group compared to the TD group. These results suggest that impaired memory-guided navigation in individuals with ASD may, in part, be due to atypical functioning in the RSC.

Autism research : official journal of the International Society for Autism Research, 2025 · doi:10.1016/j.rasd.2020.101697