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. 2021 Nov 30;13(1):57.
doi: 10.1186/s11689-021-09405-x.

Prediction of autism spectrum disorder diagnosis using nonlinear measures of language-related EEG at 6 and 12 months

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Prediction of autism spectrum disorder diagnosis using nonlinear measures of language-related EEG at 6 and 12 months

Fleming C Peck et al. J Neurodev Disord. .

Abstract

Background: Early identification of autism spectrum disorder (ASD) provides an opportunity for early intervention and improved developmental outcomes. The use of electroencephalography (EEG) in infancy has shown promise in predicting later ASD diagnoses and in identifying neural mechanisms underlying the disorder. Given the high co-morbidity with language impairment, we and others have speculated that infants who are later diagnosed with ASD have altered language learning, including phoneme discrimination. Phoneme learning occurs rapidly in infancy, so altered neural substrates during the first year of life may serve as early, accurate indicators of later autism diagnosis.

Methods: Using EEG data collected at two different ages during a passive phoneme task in infants with high familial risk for ASD, we compared the predictive accuracy of a combination of feature selection and machine learning models at 6 months (during native phoneme learning) and 12 months (after native phoneme learning), and we identified a single model with strong predictive accuracy (100%) for both ages. Samples at both ages were matched in size and diagnoses (n = 14 with later ASD; n = 40 without ASD). Features included a combination of power and nonlinear measures across the 10‑20 montage electrodes and 6 frequency bands. Predictive features at each age were compared both by feature characteristics and EEG scalp location. Additional prediction analyses were performed on all EEGs collected at 12 months; this larger sample included 67 HR infants (27 HR-ASD, 40 HR-noASD).

Results: Using a combination of Pearson correlation feature selection and support vector machine classifier, 100% predictive diagnostic accuracy was observed at both 6 and 12 months. Predictive features differed between the models trained on 6- versus 12-month data. At 6 months, predictive features were biased to measures from central electrodes, power measures, and frequencies in the alpha range. At 12 months, predictive features were more distributed between power and nonlinear measures, and biased toward frequencies in the beta range. However, diagnosis prediction accuracy substantially decreased in the larger, more behaviorally heterogeneous 12-month sample.

Conclusions: These results demonstrate that speech processing EEG measures can facilitate earlier identification of ASD but emphasize the need for age-specific predictive models with large sample sizes to develop clinically relevant classification algorithms.

Keywords: Autism; EEG; Infant; Language development; Machine learning; Sensitive period.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Two EEG nets were used in the study: the 128-channel EGI HydroCel Geodesic Sensor Net (version 1.0) presented on the left and the 64-channel EGI Geodesic Sensor Net (version 2.0) presented on the right. The 10-20 montage channels evaluated in this study are highlighted in blue, and HAPPE channels included in preprocessing steps are highlighted in yellow
Fig. 2
Fig. 2
Information about features most correlated with autism diagnostic outcome for nearly overlapping 6- and 12-month analyses (n = 54). The bottom row visualizes the values for the 12-month dataset (middle row) minus the 6-month dataset (top row). A, D, G Average number of features selected from each channel. Color indicates number of features selected from a given channel. B, E, H Average count of each EEG measure across iterations (orange) and percentage of iterations that each measure was selected at least once (blue). C, F, I Average count of each wavelet across iterations (orange) and percentage of iterations that each wavelet was selected at least once (blue)
Fig. 3
Fig. 3
Feature distributions for features most significantly different between the longitudinal 12-month classification analyses (n = 54). Features are listed and emboldened in Table 3. Kernel density estimates are color coded by group: blue for HR-noASD (n = 40); orange for longitudinal HR-ASD (n = 14); and green for cross sectional HR-ASD (n = 13)

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