International Meeting for Autism Research: Low-Frequency Repetitive Transcranial Magnetic Stimulation (rTMS) Modulates Evoked-Gamma Frequency Oscillations In Autism Spectrum Disorder (ASD)

Low-Frequency Repetitive Transcranial Magnetic Stimulation (rTMS) Modulates Evoked-Gamma Frequency Oscillations In Autism Spectrum Disorder (ASD)

Thursday, May 12, 2011
Elizabeth Ballroom E-F and Lirenta Foyer Level 2 (Manchester Grand Hyatt)
1:00 PM
M. F. Casanova1, J. M. Baruth2, A. S. El-Baz3, L. L. Sears4 and E. M. Sokhadze1, (1)Psychiatry & Behavioral Sciences, University of Louisville, Louisville, KY, (2)Anatomical Sciences & Neurobiology, University of Louisville, Louisville, KY, (3)Bioengineering, University of Louisville, Louisville, KY, (4)Pediatrics, University of Louisville, Louisville, KY
Background:  It has been reported that individuals with Autism Spectrum Disorder (ASD) have both abnormal reactions to the sensory environment and visuo-perceptual abnormalities. Electrophysiological research has provided evidence that gamma band activity (30-80 Hz) is a physiological indicator of the co-activation of cortical cells engaged in processing visual stimuli and integrating different features of a stimulus. A number of studies have found augmented and indiscriminative gamma band power at early stages of visual processing in ASD; this may be related to decreased inhibitory processing and an increase in the ratio of cortical excitation to inhibition. Low frequency or 'slow' (≤1HZ) repetitive transcranial magnetic stimulation (rTMS) has been shown to increase inhibition of stimulated cortex by the activation of inhibitory circuits.

Objectives:  We wanted to test the hypothesis of gamma band abnormalities at early stages of visual processing in ASD by investigating relative evoked (i.e. ~ 100 ms) gamma power in individuals with ASD and controls. Additionally, we wanted to assess the effects of 12 sessions of bilateral 'slow' rTMS to the dorsolateral prefrontal cortex (DLPFC) on evoked gamma activity.

Methods:  We recruited 25 subjects with ASD and 20 age-matched controls and assessed evoked gamma activity using Kanizsa illusory figures at baseline and after 12 sessions of bilateral 'slow' rTMS using a randomized controlled design.

Results:  In individuals with ASD evoked gamma activity was not discriminative of stimulus type, whereas in controls early gamma power differences between target and non-target stimuli were highly significant. Following rTMS individuals with ASD showed significant improvement in discriminatory gamma activity between relevant and irrelevant visual stimuli. We also found significant improvement in the responses on behavioral questionnaires (i.e., irritability, repetitive behavior) as a result of rTMS.

Conclusions:  We proposed that 'slow' rTMS may have increased cortical inhibitory tone which improved discriminatory gamma activity at early stages of visual processing. rTMS has the potential to become an important therapeutic tool in ASD treatment and has shown significant benefits in treating core symptoms of ASD with few, if any side effects.

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