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Age related changes in striatal resting state functional connectivity in autism

Characterizing the nature of developmental change is critical to understanding the mechanisms that are impaired in complex neurodevelopment disorders such as autism spectrum disorder (ASD) and, pragmatically, may allow us to pinpoint periods of plasticity when interventions are particularly useful....

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Autores principales: Padmanabhan, Aarthi, Lynn, Andrew, Foran, William, Luna, Beatriz, O'Hearn, Kirsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842522/
https://www.ncbi.nlm.nih.gov/pubmed/24348363
http://dx.doi.org/10.3389/fnhum.2013.00814
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author Padmanabhan, Aarthi
Lynn, Andrew
Foran, William
Luna, Beatriz
O'Hearn, Kirsten
author_facet Padmanabhan, Aarthi
Lynn, Andrew
Foran, William
Luna, Beatriz
O'Hearn, Kirsten
author_sort Padmanabhan, Aarthi
collection PubMed
description Characterizing the nature of developmental change is critical to understanding the mechanisms that are impaired in complex neurodevelopment disorders such as autism spectrum disorder (ASD) and, pragmatically, may allow us to pinpoint periods of plasticity when interventions are particularly useful. Although aberrant brain development has long been theorized as a characteristic feature of ASD, the neural substrates have been difficult to characterize, in part due to a lack of developmental data and to performance confounds. To address these issues, we examined the development of intrinsic functional connectivity, with resting state fMRI from late childhood to early adulthood (8–36 years), using a seed based functional connectivity method with the striatal regions. Overall, we found that both groups show decreases in cortico-striatal circuits over age. However, when controlling for age, ASD participants showed increased connectivity with parietal cortex and decreased connectivity with prefrontal cortex relative to typically developed (TD) participants. In addition, ASD participants showed aberrant age-related connectivity with anterior aspects of cerebellum, and posterior temporal regions (e.g., fusiform gyrus, inferior and superior temporal gyri). In sum, we found prominent differences in the development of striatal connectivity in ASD, most notably, atypical development of connectivity in striatal networks that may underlie cognitive and social reward processing. Our findings highlight the need to identify the biological mechanisms of perturbations in brain reorganization over development, which may also help clarify discrepant findings in the literature.
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spelling pubmed-38425222013-12-13 Age related changes in striatal resting state functional connectivity in autism Padmanabhan, Aarthi Lynn, Andrew Foran, William Luna, Beatriz O'Hearn, Kirsten Front Hum Neurosci Neuroscience Characterizing the nature of developmental change is critical to understanding the mechanisms that are impaired in complex neurodevelopment disorders such as autism spectrum disorder (ASD) and, pragmatically, may allow us to pinpoint periods of plasticity when interventions are particularly useful. Although aberrant brain development has long been theorized as a characteristic feature of ASD, the neural substrates have been difficult to characterize, in part due to a lack of developmental data and to performance confounds. To address these issues, we examined the development of intrinsic functional connectivity, with resting state fMRI from late childhood to early adulthood (8–36 years), using a seed based functional connectivity method with the striatal regions. Overall, we found that both groups show decreases in cortico-striatal circuits over age. However, when controlling for age, ASD participants showed increased connectivity with parietal cortex and decreased connectivity with prefrontal cortex relative to typically developed (TD) participants. In addition, ASD participants showed aberrant age-related connectivity with anterior aspects of cerebellum, and posterior temporal regions (e.g., fusiform gyrus, inferior and superior temporal gyri). In sum, we found prominent differences in the development of striatal connectivity in ASD, most notably, atypical development of connectivity in striatal networks that may underlie cognitive and social reward processing. Our findings highlight the need to identify the biological mechanisms of perturbations in brain reorganization over development, which may also help clarify discrepant findings in the literature. Frontiers Media S.A. 2013-11-28 /pmc/articles/PMC3842522/ /pubmed/24348363 http://dx.doi.org/10.3389/fnhum.2013.00814 Text en Copyright © 2013 Padmanabhan, Lynn, Foran, Luna and O'Hearn. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Padmanabhan, Aarthi
Lynn, Andrew
Foran, William
Luna, Beatriz
O'Hearn, Kirsten
Age related changes in striatal resting state functional connectivity in autism
title Age related changes in striatal resting state functional connectivity in autism
title_full Age related changes in striatal resting state functional connectivity in autism
title_fullStr Age related changes in striatal resting state functional connectivity in autism
title_full_unstemmed Age related changes in striatal resting state functional connectivity in autism
title_short Age related changes in striatal resting state functional connectivity in autism
title_sort age related changes in striatal resting state functional connectivity in autism
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842522/
https://www.ncbi.nlm.nih.gov/pubmed/24348363
http://dx.doi.org/10.3389/fnhum.2013.00814
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