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Reduced acetylcholinesterase activity in the fusiform gyrus in adults with autism spectrum disorders. | LitMetric

AI Article Synopsis

  • Studies indicate that individuals with autism spectrum disorders (ASD) show impairments in face perception linked to the function of the fusiform gyrus, a critical brain area for recognizing faces.
  • The research aimed to examine whether acetylcholinesterase activity, which is connected to the cholinergic system, is altered in adults with ASD and if such changes relate to their social skills.
  • Results demonstrated lower acetylcholinesterase activity in the fusiform gyri of ASD subjects compared to controls, and this reduction was associated with greater social disabilities as evaluated through specific autism assessment tools.*

Article Abstract

Context: Both neuropsychological and functional magnetic resonance imaging studies have shown deficiencies in face perception in subjects with autism spectrum disorders (ASD). The fusiform gyrus has been regarded as the key structure in face perception. The cholinergic system is known to regulate the function of the visual pathway, including the fusiform gyrus.

Objectives: To determine whether central acetylcholinesterase activity, a marker for the cholinergic system, is altered in ASD and whether the alteration in acetylcholinesterase activity, if any, is correlated with their social functioning.

Design: Using positron emission tomography and a radiotracer, N-[(11)C]methyl-4-piperidyl acetate ([(11)C]MP4A), regional cerebrocortical acetylcholinesterase activities were estimated by reference tissue-based linear least-squares analysis and expressed in terms of the rate constant k(3). Current and childhood autism symptoms in the adult subjects with ASD were assessed by the Autism Diagnostic Observation Schedule and the Autism Diagnostic Interview-Revised, respectively. Voxel-based analyses as well as region of interest-based methods were used for between-subject analysis and within-subject correlation analysis with respect to clinical variables.

Setting: Participants recruited from the community.

Participants: Twenty adult subjects with ASD (14 male and 6 female; age range, 18-33 years; mean [SD] intelligence quotient, 91.6 [4.3]) and 20 age-, sex-, and intelligence quotient-matched healthy controls.

Results: Both voxel- and region of interest-based analyses revealed significantly lower [(11)C]MP4A k(3) values in the bilateral fusiform gyri of subjects with ASD than in those of controls (P < .05, corrected). The fusiform k(3) values in subjects with ASD were negatively correlated with their social disabilities as assessed by Autism Diagnostic Observation Schedule as well as Autism Diagnostic Interview-Revised.

Conclusions: The results suggest that a deficit in cholinergic innervations of the fusiform gyrus, which can be observed in adults with ASD, may be related to not only current but also childhood impairment of social functioning.

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Source
http://dx.doi.org/10.1001/archgenpsychiatry.2011.4DOI Listing

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