Transcranial magnetic stimulation in autism spectrum disorder: Challenges, promise, and roadmap for future research.

Published

Journal Article (Review)

Autism Spectrum Disorder (ASD) is a behaviorally defined complex neurodevelopmental syndrome characterized by impairments in social communication, by the presence of restricted and repetitive behaviors, interests and activities, and by abnormalities in sensory reactivity. Transcranial magnetic stimulation (TMS) is a promising, emerging tool for the study and potential treatment of ASD. Recent studies suggest that TMS measures provide rapid and noninvasive pathophysiological ASD biomarkers. Furthermore, repetitive TMS (rTMS) may represent a novel treatment strategy for reducing some of the core and associated ASD symptoms. However, the available literature on the TMS use in ASD is preliminary, composed of studies with methodological limitations. Thus, off-label clinical rTMS use for therapeutic interventions in ASD without an investigational device exemption and outside of an IRB approved research trial is premature pending further, adequately powered and controlled trials. Leaders in this field have gathered annually for a two-day conference (prior to the 2014 and 2015 International Meeting for Autism Research, IMFAR) to share recent progress, promote collaboration across laboratories, and establish consensus on protocols. Here we review the literature in the use of TMS in ASD in the context of the unique challenges required for the study and exploration of treatment strategies in this population. We also suggest future directions for this field of investigations. While its true potential in ASD has yet to be delineated, TMS represents an innovative research tool and a novel, possibly transformative approach to the treatment of neurodevelopmental disorders.

Full Text

Duke Authors

Cited Authors

  • Oberman, LM; Enticott, PG; Casanova, MF; Rotenberg, A; Pascual-Leone, A; McCracken, JT; TMS in ASD Consensus Group,

Published Date

  • February 2016

Published In

Volume / Issue

  • 9 / 2

Start / End Page

  • 184 - 203

PubMed ID

  • 26536383

Pubmed Central ID

  • 26536383

Electronic International Standard Serial Number (EISSN)

  • 1939-3806

Digital Object Identifier (DOI)

  • 10.1002/aur.1567

Language

  • eng

Conference Location

  • United States