TY - JOUR
T1 - Single Pulse Transcranial Magnetic Stimulation-Electroencephalogram Reveals No Electrophysiological Abnormality in Adults with High-Functioning Autism Spectrum Disorder
AU - Kirkovski, Melissa
AU - Rogasch, Nigel C.
AU - Saeki, Takashi
AU - Fitzgibbon, Bernadette M.
AU - Enticott, Peter G.
AU - Fitzgerald, Paul B.
N1 - Publisher Copyright:
© Mary Ann Liebert, Inc. 2016.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Objective: Neuroimaging and electrophysiological research have revealed a range of neural abnormalities in autism spectrum disorder (ASD), but a comprehensive understanding remains elusive. We utilized a novel methodology among individuals with ASD and matched controls, combining transcranial magnetic stimulation (TMS) with concurrent electroencephalogram (EEG) recording (TMS-EEG) to explore cortical function and connectivity in three sites implicated in the neuropathophysiology of ASD (dorsolateral prefrontal cortex, primary motor cortex, and temporoparietal junction). As there is evidence for neurobiological gender differences in ASD, we also examined the influence of biological sex. Methods: TMS pulses were applied to each of the three sites (right lateralized) during 20-channel EEG recording. Results: We did not identify any differences in the EEG response to TMS between ASD and control groups. This finding remained when data were stratified by sex. Nevertheless, traits and characteristics associated with ASD were correlated with the neurophysiological response to TMS. Conclusion: While TMS-EEG did not appear to clarify the neuropathophysiology of ASD, the relationships identified between the neurophysiological response to TMS and clinical characteristics warrant further investigation.
AB - Objective: Neuroimaging and electrophysiological research have revealed a range of neural abnormalities in autism spectrum disorder (ASD), but a comprehensive understanding remains elusive. We utilized a novel methodology among individuals with ASD and matched controls, combining transcranial magnetic stimulation (TMS) with concurrent electroencephalogram (EEG) recording (TMS-EEG) to explore cortical function and connectivity in three sites implicated in the neuropathophysiology of ASD (dorsolateral prefrontal cortex, primary motor cortex, and temporoparietal junction). As there is evidence for neurobiological gender differences in ASD, we also examined the influence of biological sex. Methods: TMS pulses were applied to each of the three sites (right lateralized) during 20-channel EEG recording. Results: We did not identify any differences in the EEG response to TMS between ASD and control groups. This finding remained when data were stratified by sex. Nevertheless, traits and characteristics associated with ASD were correlated with the neurophysiological response to TMS. Conclusion: While TMS-EEG did not appear to clarify the neuropathophysiology of ASD, the relationships identified between the neurophysiological response to TMS and clinical characteristics warrant further investigation.
UR - http://www.scopus.com/inward/record.url?scp=84988564524&partnerID=8YFLogxK
U2 - 10.1089/cap.2015.0181
DO - 10.1089/cap.2015.0181
M3 - Article
SN - 1044-5463
VL - 26
SP - 606
EP - 616
JO - Journal of Child and Adolescent Psychopharmacology
JF - Journal of Child and Adolescent Psychopharmacology
IS - 7
ER -