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Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder

Inconsistencies across studies investigating subcortical correlates of autism spectrum disorder (ASD) may stem from small sample size, sample heterogeneity, and omitting or linearly adjusting for total brain volume (TBV). To properly adjust for TBV, brain allometry—the nonlinear scaling relationship...

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Autores principales: Williams, Camille Michèle, Peyre, Hugo, Toro, Roberto, Beggiato, Anita, Ramus, Franck
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555078/
https://www.ncbi.nlm.nih.gov/pubmed/32729664
http://dx.doi.org/10.1002/hbm.25145
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author Williams, Camille Michèle
Peyre, Hugo
Toro, Roberto
Beggiato, Anita
Ramus, Franck
author_facet Williams, Camille Michèle
Peyre, Hugo
Toro, Roberto
Beggiato, Anita
Ramus, Franck
author_sort Williams, Camille Michèle
collection PubMed
description Inconsistencies across studies investigating subcortical correlates of autism spectrum disorder (ASD) may stem from small sample size, sample heterogeneity, and omitting or linearly adjusting for total brain volume (TBV). To properly adjust for TBV, brain allometry—the nonlinear scaling relationship between regional volumes and TBV—was considered when examining subcortical volumetric differences between typically developing (TD) and ASD individuals. Autism Brain Imaging Data Exchange I (ABIDE I; N = 654) data was analyzed with two methodological approaches: univariate linear mixed effects models and multivariate multiple group confirmatory factor analyses. Analyses were conducted on the entire sample and in subsamples based on age, sex, and full scale intelligence quotient (FSIQ). A similar ABIDE I study was replicated and the impact of different TBV adjustments on neuroanatomical group differences was investigated. No robust subcortical allometric or volumetric group differences were observed in the entire sample across methods. Exploratory analyses suggested that allometric scaling and volume group differences may exist in certain subgroups defined by age, sex, and/or FSIQ. The type of TBV adjustment influenced some reported volumetric and scaling group differences. This study supports the absence of robust volumetric differences between ASD and TD individuals in the investigated volumes when adjusting for brain allometry, expands the literature by finding no group difference in allometric scaling, and further suggests that differing TBV adjustments contribute to the variability of reported neuroanatomical differences in ASD.
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spelling pubmed-75550782020-10-19 Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder Williams, Camille Michèle Peyre, Hugo Toro, Roberto Beggiato, Anita Ramus, Franck Hum Brain Mapp Research Articles Inconsistencies across studies investigating subcortical correlates of autism spectrum disorder (ASD) may stem from small sample size, sample heterogeneity, and omitting or linearly adjusting for total brain volume (TBV). To properly adjust for TBV, brain allometry—the nonlinear scaling relationship between regional volumes and TBV—was considered when examining subcortical volumetric differences between typically developing (TD) and ASD individuals. Autism Brain Imaging Data Exchange I (ABIDE I; N = 654) data was analyzed with two methodological approaches: univariate linear mixed effects models and multivariate multiple group confirmatory factor analyses. Analyses were conducted on the entire sample and in subsamples based on age, sex, and full scale intelligence quotient (FSIQ). A similar ABIDE I study was replicated and the impact of different TBV adjustments on neuroanatomical group differences was investigated. No robust subcortical allometric or volumetric group differences were observed in the entire sample across methods. Exploratory analyses suggested that allometric scaling and volume group differences may exist in certain subgroups defined by age, sex, and/or FSIQ. The type of TBV adjustment influenced some reported volumetric and scaling group differences. This study supports the absence of robust volumetric differences between ASD and TD individuals in the investigated volumes when adjusting for brain allometry, expands the literature by finding no group difference in allometric scaling, and further suggests that differing TBV adjustments contribute to the variability of reported neuroanatomical differences in ASD. John Wiley & Sons, Inc. 2020-07-30 /pmc/articles/PMC7555078/ /pubmed/32729664 http://dx.doi.org/10.1002/hbm.25145 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Williams, Camille Michèle
Peyre, Hugo
Toro, Roberto
Beggiato, Anita
Ramus, Franck
Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder
title Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder
title_full Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder
title_fullStr Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder
title_full_unstemmed Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder
title_short Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder
title_sort adjusting for allometric scaling in abide i challenges subcortical volume differences in autism spectrum disorder
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555078/
https://www.ncbi.nlm.nih.gov/pubmed/32729664
http://dx.doi.org/10.1002/hbm.25145
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