Deviation from normative brain development is associated with symptom severity in autism spectrum disorder

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. W...

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Main Authors: Birkan Tunç, Lisa D. Yankowitz, Drew Parker, Jacob A. Alappatt, Juhi Pandey, Robert T. Schultz, Ragini Verma
Format: Article
Language:English
Published: BMC 2019-12-01
Series:Molecular Autism
Subjects:
Online Access:https://doi.org/10.1186/s13229-019-0301-5
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spelling doaj-493a341fccb041d29376d4d1cfb977422020-12-13T12:17:58ZengBMCMolecular Autism2040-23922019-12-0110111410.1186/s13229-019-0301-5Deviation from normative brain development is associated with symptom severity in autism spectrum disorderBirkan Tunç0Lisa D. Yankowitz1Drew Parker2Jacob A. Alappatt3Juhi Pandey4Robert T. Schultz5Ragini Verma6Center for Autism Research, The Children’s Hospital of PhiladelphiaCenter for Autism Research, The Children’s Hospital of PhiladelphiaDiCIPHR (Diffusion and Connectomics in Precision Healthcare Research) Lab, Department of Radiology, University of PennsylvaniaDiCIPHR (Diffusion and Connectomics in Precision Healthcare Research) Lab, Department of Radiology, University of PennsylvaniaCenter for Autism Research, The Children’s Hospital of PhiladelphiaCenter for Autism Research, The Children’s Hospital of PhiladelphiaCenter for Biomedical Image Computing and Analytics, University of PennsylvaniaAbstract 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.https://doi.org/10.1186/s13229-019-0301-5AutismBrain developmentHeterogeneitySymptom severityMachine learningNormative modeling
collection DOAJ
language English
format Article
sources DOAJ
author Birkan Tunç
Lisa D. Yankowitz
Drew Parker
Jacob A. Alappatt
Juhi Pandey
Robert T. Schultz
Ragini Verma
spellingShingle Birkan Tunç
Lisa D. Yankowitz
Drew Parker
Jacob A. Alappatt
Juhi Pandey
Robert T. Schultz
Ragini Verma
Deviation from normative brain development is associated with symptom severity in autism spectrum disorder
Molecular Autism
Autism
Brain development
Heterogeneity
Symptom severity
Machine learning
Normative modeling
author_facet Birkan Tunç
Lisa D. Yankowitz
Drew Parker
Jacob A. Alappatt
Juhi Pandey
Robert T. Schultz
Ragini Verma
author_sort Birkan Tunç
title Deviation from normative brain development is associated with symptom severity in autism spectrum disorder
title_short Deviation from normative brain development is associated with symptom severity in autism spectrum disorder
title_full Deviation from normative brain development is associated with symptom severity in autism spectrum disorder
title_fullStr Deviation from normative brain development is associated with symptom severity in autism spectrum disorder
title_full_unstemmed Deviation from normative brain development is associated with symptom severity in autism spectrum disorder
title_sort deviation from normative brain development is associated with symptom severity in autism spectrum disorder
publisher BMC
series Molecular Autism
issn 2040-2392
publishDate 2019-12-01
description 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.
topic Autism
Brain development
Heterogeneity
Symptom severity
Machine learning
Normative modeling
url https://doi.org/10.1186/s13229-019-0301-5
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