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Deviation from normative brain development is associated with symptom severity in autism spectrum disorder.
Tunç, Birkan; Yankowitz, Lisa D; Parker, Drew; Alappatt, Jacob A; Pandey, Juhi; Schultz, Robert T; Verma, Ragini.
Afiliação
  • Tunç B; 1Center for Autism Research, The Children's Hospital of Philadelphia, Philadelphia, PA 19104 USA.
  • Yankowitz LD; 2Department of Biomedical and Health Informatics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104 USA.
  • Parker D; 3Department of Psychiatry, University of Pennsylvania, Philadelphia, PA 19104 USA.
  • Alappatt JA; 4Center for Biomedical Image Computing and Analytics, University of Pennsylvania, Philadelphia, PA 19104 USA.
  • Pandey J; 1Center for Autism Research, The Children's Hospital of Philadelphia, Philadelphia, PA 19104 USA.
  • Schultz RT; 5Department of Psychology, University of Pennsylvania, Philadelphia, PA 19104 USA.
  • Verma R; 6DiCIPHR (Diffusion and Connectomics in Precision Healthcare Research) Lab, Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104 USA.
Mol Autism ; 10: 46, 2019.
Article em En | MEDLINE | ID: mdl-31867092
ABSTRACT

Background:

Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental condition. The degree to which the brain development in ASD deviates from typical brain development, and how this deviation relates to observed behavioral outcomes at the individual level are not well-studied. We hypothesize that the degree of deviation from typical brain development of an individual with ASD would relate to observed symptom severity.

Methods:

The developmental changes in anatomical (cortical thickness, surface area, and volume) and diffusion metrics (fractional anisotropy and apparent diffusion coefficient) were compared between a sample of ASD (n = 247) and typically developing children (TDC) (n = 220) aged 6-25. Machine learning was used to predict age (brain age) from these metrics in the TDC sample, to define a normative model of brain development. This model was then used to compute brain age in the ASD sample. The difference between chronological age and brain age was considered a developmental deviation index (DDI), which was then correlated with ASD symptom severity.

Results:

Machine learning model trained on all five metrics accurately predicted age in the TDC (r = 0.88) and the ASD (r = 0.85) samples, with dominant contributions to the model from the diffusion metrics. Within the ASD group, the DDI derived from fractional anisotropy was correlated with ASD symptom severity (r = - 0.2), such that individuals with the most advanced brain age showing the lowest severity, and individuals with the most delayed brain age showing the highest severity.

Limitations:

This work investigated only linear relationships between five specific brain metrics and only one measure of ASD symptom severity in a limited age range. Reported effect sizes are moderate. Further work is needed to investigate developmental differences in other age ranges, other aspects of behavior, other neurobiological measures, and in an independent sample before results can be clinically applicable.

Conclusions:

Findings demonstrate that the degree of deviation from typical brain development relates to ASD symptom severity, partially accounting for the observed heterogeneity in ASD. Our approach enables characterization of each individual with reference to normative brain development and identification of distinct developmental subtypes, facilitating a better understanding of developmental heterogeneity in ASD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Encéfalo / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Encéfalo / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article