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Multivariate Neural Connectivity Patterns in Early Infancy Predict Later Autism Symptoms.
Dickinson, Abigail; Daniel, Manjari; Marin, Andrew; Gaonkar, Bilwaj; Dapretto, Mirella; McDonald, Nicole M; Jeste, Shafali.
Afiliación
  • Dickinson A; Semel Institute of Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, California. Electronic address: adickinson@mednet.ucla.edu.
  • Daniel M; Semel Institute of Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, California.
  • Marin A; Department of Psychology, University of California, San Diego, San Diego, California.
  • Gaonkar B; Department of Neurosurgery, Ronald Reagan UCLA Medical Center, University of California, Los Angeles, California.
  • Dapretto M; Ahmanson-Lovelace Brain Mapping Center, University of California, Los Angeles, Los Angeles, California.
  • McDonald NM; Semel Institute of Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, California.
  • Jeste S; Semel Institute of Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, California.
Article en En | MEDLINE | ID: mdl-32798139
ABSTRACT

BACKGROUND:

Functional brain connectivity is altered in children and adults with autism spectrum disorder (ASD). Functional disruption during infancy could provide earlier markers of ASD, thus providing a crucial opportunity to improve developmental outcomes. Using a whole-brain multivariate approach, we asked whether electroencephalography measures of neural connectivity at 3 months of age predict autism symptoms at 18 months.

METHODS:

Spontaneous electroencephalography data were collected from 65 infants with and without familial risk for ASD at 3 months of age. Neural connectivity patterns were quantified using phase coherence in the alpha range (6-12 Hz). Support vector regression analysis was used to predict ASD symptoms at age 18 months, with ASD symptoms quantified by the Toddler Module of the Autism Diagnostic Observation Schedule, Second Edition.

RESULTS:

Autism Diagnostic Observation Schedule scores predicted by support vector regression algorithms trained on 3-month electroencephalography data correlated highly with Autism Diagnostic Observation Schedule scores measured at 18 months (r = .76, p = .02, root-mean-square error = 2.38). Specifically, lower frontal connectivity and higher right temporoparietal connectivity at 3 months predicted higher ASD symptoms at 18 months. The support vector regression model did not predict cognitive abilities at 18 months (r = .15, p = .36), suggesting specificity of these brain patterns to ASD.

CONCLUSIONS:

Using a data-driven, unbiased analytic approach, neural connectivity across frontal and temporoparietal regions at 3 months predicted ASD symptoms at 18 months. Identifying early neural differences that precede an ASD diagnosis could promote closer monitoring of infants who show signs of neural risk and provide a crucial opportunity to mediate outcomes through early intervention.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans / Infant Idioma: En Revista: Biol Psychiatry Cogn Neurosci Neuroimaging Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans / Infant Idioma: En Revista: Biol Psychiatry Cogn Neurosci Neuroimaging Año: 2021 Tipo del documento: Article