| Literature DB >> 30977235 |
J Christopher Edgar1,2, Marissa Dipiero1, Emma McBride1, Heather L Green1, Jeffrey Berman1,2, Matthew Ku1, Song Liu1, Lisa Blaskey1,2,3, Emily Kuschner1,3,4, Megan Airey1, Judith L Ross5, Luke Bloy1, Mina Kim1, Simon Koppers6, William Gaetz1,2, Robert T Schultz3,4, Timothy P L Roberts1,2.
Abstract
Age-related changes in resting-state (RS) neural rhythms in typically developing children (TDC) but not children with autism spectrum disorder (ASD) suggest that RS measures may be of clinical use in ASD only for certain ages. The study examined this issue via assessing RS peak alpha frequency (PAF), a measure previous studies, have indicated as abnormal in ASD. RS magnetoencephalographic (MEG) data were obtained from 141 TDC (6.13-17.70 years) and 204 ASD (6.07-17.93 years). A source model with 15 regional sources projected the raw MEG surface data into brain source space. PAF was identified in each participant from the source showing the largest amplitude alpha activity (7-13 Hz). Given sex differences in PAF in TDC (females > males) and relatively few females in both groups, group comparisons were conducted examining only male TDC (N = 121) and ASD (N = 183). Regressions showed significant group slope differences, with an age-related increase in PAF in TDC (R2 = 0.32) but not ASD (R2 = 0.01). Analyses examining male children below or above 10-years-old (median split) indicated group effects only in the younger TDC (8.90 Hz) and ASD (9.84 Hz; Cohen's d = 1.05). In the older ASD, a higher nonverbal IQ was associated with a higher PAF. In the younger TDC, a faster speed of processing was associated with a higher PAF. PAF as a marker for ASD depends on age, with a RS alpha marker of more interest in younger versus older children with ASD. Associations between PAF and cognitive ability were also found to be age and group specific.Entities:
Keywords: alpha; autism spectrum disorders; magnetoencephalography; maturation; resting-state
Mesh:
Year: 2019 PMID: 30977235 PMCID: PMC6592733 DOI: 10.1002/hbm.24598
Source DB: PubMed Journal: Hum Brain Mapp ISSN: 1065-9471 Impact factor: 5.038