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A voxel-wise assessment of growth differences in infants developing autism spectrum disorder
Autism Spectrum Disorder (ASD) is a phenotypically and etiologically heterogeneous developmental disorder typically diagnosed around 4 years of age. The development of biomarkers to help in earlier, presymptomatic diagnosis could facilitate earlier identification and therefore earlier intervention a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806791/ https://www.ncbi.nlm.nih.gov/pubmed/33421871 http://dx.doi.org/10.1016/j.nicl.2020.102551 |
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author | Cárdenas-de-la-Parra, A. Lewis, J.D. Fonov, V.S. Botteron, K.N. McKinstry, R.C. Gerig, G. Pruett, J.R. Dager, S.R. Elison, J.T. Styner, M.A. Evans, A.C. Piven, J. Collins, D.L |
author_facet | Cárdenas-de-la-Parra, A. Lewis, J.D. Fonov, V.S. Botteron, K.N. McKinstry, R.C. Gerig, G. Pruett, J.R. Dager, S.R. Elison, J.T. Styner, M.A. Evans, A.C. Piven, J. Collins, D.L |
author_sort | Cárdenas-de-la-Parra, A. |
collection | PubMed |
description | Autism Spectrum Disorder (ASD) is a phenotypically and etiologically heterogeneous developmental disorder typically diagnosed around 4 years of age. The development of biomarkers to help in earlier, presymptomatic diagnosis could facilitate earlier identification and therefore earlier intervention and may lead to better outcomes, as well as providing information to help better understand the underlying mechanisms of ASD. In this study, magnetic resonance imaging (MRI) scans of infants at high familial risk, from the Infant Brain Imaging Study (IBIS), at 6, 12 and 24 months of age were included in a morphological analysis, fitting a mixed-effects model to Tensor Based Morphometry (TBM) results to obtain voxel-wise growth trajectories. Subjects were grouped by familial risk and clinical diagnosis at 2 years of age. Several regions, including the posterior cingulate gyrus, the cingulum, the fusiform gyrus, and the precentral gyrus, showed a significant effect for the interaction of group and age associated with ASD, either as an increased or a decreased growth rate of the cerebrum. In general, our results showed increased growth rate within white matter with decreased growth rate found mostly in grey matter. Overall, the regions showing increased growth rate were larger and more numerous than those with decreased growth rate. These results detail, at the voxel level, differences in brain growth trajectories in ASD during the first years of life, previously reported in terms of overall brain volume and surface area. |
format | Online Article Text |
id | pubmed-7806791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78067912021-01-22 A voxel-wise assessment of growth differences in infants developing autism spectrum disorder Cárdenas-de-la-Parra, A. Lewis, J.D. Fonov, V.S. Botteron, K.N. McKinstry, R.C. Gerig, G. Pruett, J.R. Dager, S.R. Elison, J.T. Styner, M.A. Evans, A.C. Piven, J. Collins, D.L Neuroimage Clin Regular Article Autism Spectrum Disorder (ASD) is a phenotypically and etiologically heterogeneous developmental disorder typically diagnosed around 4 years of age. The development of biomarkers to help in earlier, presymptomatic diagnosis could facilitate earlier identification and therefore earlier intervention and may lead to better outcomes, as well as providing information to help better understand the underlying mechanisms of ASD. In this study, magnetic resonance imaging (MRI) scans of infants at high familial risk, from the Infant Brain Imaging Study (IBIS), at 6, 12 and 24 months of age were included in a morphological analysis, fitting a mixed-effects model to Tensor Based Morphometry (TBM) results to obtain voxel-wise growth trajectories. Subjects were grouped by familial risk and clinical diagnosis at 2 years of age. Several regions, including the posterior cingulate gyrus, the cingulum, the fusiform gyrus, and the precentral gyrus, showed a significant effect for the interaction of group and age associated with ASD, either as an increased or a decreased growth rate of the cerebrum. In general, our results showed increased growth rate within white matter with decreased growth rate found mostly in grey matter. Overall, the regions showing increased growth rate were larger and more numerous than those with decreased growth rate. These results detail, at the voxel level, differences in brain growth trajectories in ASD during the first years of life, previously reported in terms of overall brain volume and surface area. Elsevier 2020-12-29 /pmc/articles/PMC7806791/ /pubmed/33421871 http://dx.doi.org/10.1016/j.nicl.2020.102551 Text en © 2021 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Regular Article Cárdenas-de-la-Parra, A. Lewis, J.D. Fonov, V.S. Botteron, K.N. McKinstry, R.C. Gerig, G. Pruett, J.R. Dager, S.R. Elison, J.T. Styner, M.A. Evans, A.C. Piven, J. Collins, D.L A voxel-wise assessment of growth differences in infants developing autism spectrum disorder |
title | A voxel-wise assessment of growth differences in infants developing autism spectrum disorder |
title_full | A voxel-wise assessment of growth differences in infants developing autism spectrum disorder |
title_fullStr | A voxel-wise assessment of growth differences in infants developing autism spectrum disorder |
title_full_unstemmed | A voxel-wise assessment of growth differences in infants developing autism spectrum disorder |
title_short | A voxel-wise assessment of growth differences in infants developing autism spectrum disorder |
title_sort | voxel-wise assessment of growth differences in infants developing autism spectrum disorder |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806791/ https://www.ncbi.nlm.nih.gov/pubmed/33421871 http://dx.doi.org/10.1016/j.nicl.2020.102551 |
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