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Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males

BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental condition commonly studied in the context of early childhood. As ASD is a life-long condition, understanding the characteristics of brain microstructure from adolescence into adulthood and associations to clinical features is critica...

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Autores principales: DiPiero, Marissa, Cordash, Hassan, Prigge, Molly B., King, Carolyn K., Morgan, Jubel, Guerrero-Gonzalez, Jose, Adluru, Nagesh, King, Jace B., Lange, Nicholas, Bigler, Erin D., Zielinski, Brandon A., Alexander, Andrew L., Lainhart, Janet E., Dean, Douglas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565827/
https://www.ncbi.nlm.nih.gov/pubmed/37829720
http://dx.doi.org/10.3389/fnins.2023.1231719
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author DiPiero, Marissa
Cordash, Hassan
Prigge, Molly B.
King, Carolyn K.
Morgan, Jubel
Guerrero-Gonzalez, Jose
Adluru, Nagesh
King, Jace B.
Lange, Nicholas
Bigler, Erin D.
Zielinski, Brandon A.
Alexander, Andrew L.
Lainhart, Janet E.
Dean, Douglas C.
author_facet DiPiero, Marissa
Cordash, Hassan
Prigge, Molly B.
King, Carolyn K.
Morgan, Jubel
Guerrero-Gonzalez, Jose
Adluru, Nagesh
King, Jace B.
Lange, Nicholas
Bigler, Erin D.
Zielinski, Brandon A.
Alexander, Andrew L.
Lainhart, Janet E.
Dean, Douglas C.
author_sort DiPiero, Marissa
collection PubMed
description BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental condition commonly studied in the context of early childhood. As ASD is a life-long condition, understanding the characteristics of brain microstructure from adolescence into adulthood and associations to clinical features is critical for improving outcomes across the lifespan. In the current work, we utilized Tract Based Spatial Statistics (TBSS) and Gray Matter Based Spatial Statistics (GBSS) to examine the white matter (WM) and gray matter (GM) microstructure in neurotypical (NT) and autistic males. METHODS: Multi-shell diffusion MRI was acquired from 78 autistic and 81 NT males (12-to-46-years) and fit to the DTI and NODDI diffusion models. TBSS and GBSS were performed to analyze WM and GM microstructure, respectively. General linear models were used to investigate group and age-related group differences. Within the ASD group, relationships between WM and GM microstructure and measures of autistic symptoms were investigated. RESULTS: All dMRI measures were significantly associated with age across WM and GM. Significant group differences were observed across WM and GM. No significant age-by-group interactions were detected. Within the ASD group, positive relationships with WM microstructure were observed with ADOS-2 Calibrated Severity Scores. CONCLUSION: Using TBSS and GBSS our findings provide new insights into group differences of WM and GM microstructure in autistic males from adolescence into adulthood. Detection of microstructural differences across the lifespan as well as their relationship to the level of autistic symptoms will deepen to our understanding of brain-behavior relationships of ASD and may aid in the improvement of intervention options for autistic adults.
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spelling pubmed-105658272023-10-12 Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males DiPiero, Marissa Cordash, Hassan Prigge, Molly B. King, Carolyn K. Morgan, Jubel Guerrero-Gonzalez, Jose Adluru, Nagesh King, Jace B. Lange, Nicholas Bigler, Erin D. Zielinski, Brandon A. Alexander, Andrew L. Lainhart, Janet E. Dean, Douglas C. Front Neurosci Neuroscience BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental condition commonly studied in the context of early childhood. As ASD is a life-long condition, understanding the characteristics of brain microstructure from adolescence into adulthood and associations to clinical features is critical for improving outcomes across the lifespan. In the current work, we utilized Tract Based Spatial Statistics (TBSS) and Gray Matter Based Spatial Statistics (GBSS) to examine the white matter (WM) and gray matter (GM) microstructure in neurotypical (NT) and autistic males. METHODS: Multi-shell diffusion MRI was acquired from 78 autistic and 81 NT males (12-to-46-years) and fit to the DTI and NODDI diffusion models. TBSS and GBSS were performed to analyze WM and GM microstructure, respectively. General linear models were used to investigate group and age-related group differences. Within the ASD group, relationships between WM and GM microstructure and measures of autistic symptoms were investigated. RESULTS: All dMRI measures were significantly associated with age across WM and GM. Significant group differences were observed across WM and GM. No significant age-by-group interactions were detected. Within the ASD group, positive relationships with WM microstructure were observed with ADOS-2 Calibrated Severity Scores. CONCLUSION: Using TBSS and GBSS our findings provide new insights into group differences of WM and GM microstructure in autistic males from adolescence into adulthood. Detection of microstructural differences across the lifespan as well as their relationship to the level of autistic symptoms will deepen to our understanding of brain-behavior relationships of ASD and may aid in the improvement of intervention options for autistic adults. Frontiers Media S.A. 2023-09-27 /pmc/articles/PMC10565827/ /pubmed/37829720 http://dx.doi.org/10.3389/fnins.2023.1231719 Text en Copyright © 2023 DiPiero, Cordash, Prigge, King, Morgan, Guerrero-Gonzalez, Adluru, King, Lange, Bigler, Zielinski, Alexander, Lainhart and Dean. https://creativecommons.org/licenses/by/4.0/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) and the copyright owner(s) 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
DiPiero, Marissa
Cordash, Hassan
Prigge, Molly B.
King, Carolyn K.
Morgan, Jubel
Guerrero-Gonzalez, Jose
Adluru, Nagesh
King, Jace B.
Lange, Nicholas
Bigler, Erin D.
Zielinski, Brandon A.
Alexander, Andrew L.
Lainhart, Janet E.
Dean, Douglas C.
Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males
title Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males
title_full Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males
title_fullStr Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males
title_full_unstemmed Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males
title_short Tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males
title_sort tract- and gray matter- based spatial statistics show white matter and gray matter microstructural differences in autistic males
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565827/
https://www.ncbi.nlm.nih.gov/pubmed/37829720
http://dx.doi.org/10.3389/fnins.2023.1231719
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