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Robust disruptions in electroencephalogram cortical oscillations and large-scale functional networks in autism

Overview of attention for article published in BMC Neurology, June 2015
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Title
Robust disruptions in electroencephalogram cortical oscillations and large-scale functional networks in autism
Published in
BMC Neurology, June 2015
DOI 10.1186/s12883-015-0355-8
Pubmed ID
Authors

Sean Matlis, Katica Boric, Catherine J. Chu, Mark A. Kramer

Abstract

Autism spectrum disorders (ASD) are increasingly prevalent and have a significant impact on the lives of patients and their families. Currently, the diagnosis is determined by clinical judgment and no definitive physiological biomarker for ASD exists. Quantitative biomarkers obtainable from clinical neuroimaging data - such as the scalp electroencephalogram (EEG) - would provide an important aid to clinicians in the diagnosis of ASD. The interpretation of prior studies in this area has been limited by mixed results and the lack of validation procedures. Here we use retrospective clinical data from a well-characterized population of children with ASD to evaluate the rhythms and coupling patterns present in the EEG to develop and validate an electrophysiological biomarker of ASD. EEG data were acquired from a population of ASD (n = 27) and control (n = 55) children 4-8 years old. Data were divided into training (n = 13 ASD, n = 24 control) and validation (n = 14 ASD, n = 31 control) groups. Evaluation of spectral and functional network properties in the first group of patients motivated three biomarkers that were computed in the second group of age-matched patients for validation. Three biomarkers of ASD were identified in the first patient group: (1) reduced posterior/anterior power ratio in the alpha frequency range (8-14 Hz), which we label the "peak alpha ratio", (2) reduced global density in functional networks, and (3) a reduction in the mean connectivity strength of a subset of functional network edges. Of these three biomarkers, the first and third were validated in a second group of patients. Using the two validated biomarkers, we were able to classify ASD subjects with 83 % sensitivity and 68 % specificity in a post-hoc analysis. This study demonstrates that clinical EEG can provide quantitative biomarkers to assist diagnosis of autism. These results corroborate the general finding that ASD subjects have decreased alpha power gradients and network connectivities compared to control subjects. In addition, this study demonstrates the necessity of using statistical techniques to validate EEG biomarkers identified using exploratory methods.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 120 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 <1%
Israel 1 <1%
Mexico 1 <1%
Unknown 117 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 27 23%
Student > Ph. D. Student 22 18%
Student > Master 13 11%
Student > Bachelor 13 11%
Student > Doctoral Student 6 5%
Other 17 14%
Unknown 22 18%
Readers by discipline Count As %
Psychology 22 18%
Neuroscience 20 17%
Medicine and Dentistry 16 13%
Engineering 10 8%
Agricultural and Biological Sciences 9 8%
Other 20 17%
Unknown 23 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 27 June 2015.
All research outputs
#20,880,816
of 25,654,806 outputs
Outputs from BMC Neurology
#2,130
of 2,720 outputs
Outputs of similar age
#203,505
of 278,244 outputs
Outputs of similar age from BMC Neurology
#29
of 40 outputs
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