Research Article
MEG detection of delayed auditory evoked responses in autism spectrum disorders: towards an imaging biomarker for autism
Article first published online: 8 JAN 2010
DOI: 10.1002/aur.111
Copyright © 2010, International Society for Autism Research, Wiley Periodicals, Inc.
Additional Information
How to Cite
Roberts, T. P., Khan, S. Y., Rey, M., Monroe, J. F., Cannon, K., Blaskey, L., Woldoff, S., Qasmieh, S., Gandal, M., Schmidt, G. L., Zarnow, D. M., Levy, S. E. and Edgar, J. C. (2010), MEG detection of delayed auditory evoked responses in autism spectrum disorders: towards an imaging biomarker for autism. Autism Research, 3: 8–18. doi: 10.1002/aur.111
Publication History
- Issue published online: 18 FEB 2010
- Article first published online: 8 JAN 2010
- Manuscript Accepted: 16 NOV 2009
- Manuscript Revised: 13 NOV 2009
- Manuscript Received: 13 JUL 2009
Funded by
- NIH. Grant Number: R01DC008871
- The Nancy Lurie Marks Family Foundation (NLMFF)
- Autism Speaks
- The Pennsylvania Department of Health
- Abstract
- Article
- References
- Cited By
Keywords:
- autism spectrum disorders;
- M50;
- M100;
- magnetoencephalography;
- language impairment;
- auditory evoked response
Abstract
Motivated by auditory and speech deficits in autism spectrum disorders (ASD), the frequency dependence of superior temporal gyrus (STG) 50 msec (M50) and 100 msec (M100) neuromagnetic auditory evoked field responses in children with ASD and typically developing controls were evaluated. Whole-cortex magnetoencephalography (MEG) was obtained from 17 typically developing children and 25 children with ASD. Subjects were presented tones with frequencies of 200, 300, 500, and 1,000 Hz, and left and right STG M50 and M100 STG activity was examined. No M50 latency or amplitude Group differences were observed. In the right hemisphere, a Group×Frequency ANOVA on M100 latency produced a main effect for Group (P=0.01), with an average M100 latency delay of 11 msec in children with ASD. In addition, only in the control group was the expected association of earlier M100 latencies in older than younger children observed. Group latency differences remained significant when hierarchical regression analyses partialed out M100 variance associated with age, IQ, and language ability (all P-values <0.05). Examining the right-hemisphere 500 Hz condition (where the largest latency differences were observed), a sensitivity of 75%, a specificity of 81%, and a positive predictive value (PPV) of 86% was obtained at a threshold of 116 msec. The M100 latency delay indicates disruption of encoding simple sensory information. Given similar findings in language impaired and nonlanguage impaired ASD subjects, a right-hemisphere M100 latency delay appears to be an electrophysiological endophenotype for autism.

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