International Meeting for Autism Research: Reduced Acetylcholinesterase Activity In the Fusiform Gyrus In Adults with Autism Spectrum Disorders

Reduced Acetylcholinesterase Activity In the Fusiform Gyrus In Adults with Autism Spectrum Disorders

Friday, May 13, 2011
Elizabeth Ballroom E-F and Lirenta Foyer Level 2 (Manchester Grand Hyatt)
11:00 AM
K. Nakamura1, K. Suzuki2, G. Sugihara2, Y. Ouchi3, M. Tsujii4, Y. Iwata1, K. Matsumoto2, K. Takebayashi2, T. Wakuda1, Y. Yoshihara1, S. Suda2, M. Kikuchi5, N. Takei2, T. Sugiyama6 and N. Mori1, (1)Psychiatry and Neurology, Hamamatsu University School of Medicine, Hamamatsu, Japan, (2)Research Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan, (3)Molecular Imaging Frontier Research Center, Hamamatsu University School of Medicine, Hamamatsu, Japan, (4)Department of Contemporary Sociology, Chukyo University, Nagoya, Japan, (5)Psychiatry and Neurobiology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan, (6)Child and Adolescent Psychiatry, Hamamatsu University School of Medicine, Hamamatsu, Japan
Background: Both neuropsychological and functional MRI 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 the central acetylcholinesterase (AChE) activity, a marker for the cholinergic system, is altered in ASD, and the alteration in the AChE activity, if any, is correlated with their social functioning.

Methods: Twenty adult subjects with ASD (14 male and 6 female; age range 18-33 years; mean [SD] IQ, 91.6 [4.3]) and 20 age-, sex-, and IQ-matched healthy comparison subjects were recruited from the community. Using positron emission tomography and a radiotracer N-[11C]methyl-4-piperidyl acetate ([11C]MP4A), regional cerebrocortical AChE activities were estimated by reference tissue-based linear least-squares analysis and were expressed in terms of the rate constant k3. Current and childhood autistic symptoms in the adult subjects with ASD were assessed by the Autism Diagnostic Observation Schedule (ADOS) and the Autism Diagnostic Interview-Revised (ADI-R), respectively. Voxel-based analyses as well as region-of-interest (ROI)-based methods were used for between-subject analysis and within-subject correlation analysis with respect to clinical variables. 

Results: Both voxel- and ROI-based analyses revealed significantly lower [11C]MP4A k3 values in the bilateral fusiform gyri in subjects with ASD than in those of controls (P < .05, corrected). The fusiform k3 values in subjects with ASD were negatively correlated with their social disabilities as assessed by ADOS as well as ADI-R.  

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 with not only current but also childhood impairment of social functioning.

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