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Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning

Autism spectrum disorder (ASD) is the fourth most common neurodevelopmental disorder, with a prevalence of 1 in 160 children. Accurate diagnosis relies on experts, but such individuals are scarce. This has led to increasing interest in the development of machine learning (ML) models that can integra...

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Autores principales: Mellema, Cooper J., Nguyen, Kevin P., Treacher, Alex, Montillo, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866395/
https://www.ncbi.nlm.nih.gov/pubmed/35197468
http://dx.doi.org/10.1038/s41598-022-06459-2
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author Mellema, Cooper J.
Nguyen, Kevin P.
Treacher, Alex
Montillo, Albert
author_facet Mellema, Cooper J.
Nguyen, Kevin P.
Treacher, Alex
Montillo, Albert
author_sort Mellema, Cooper J.
collection PubMed
description Autism spectrum disorder (ASD) is the fourth most common neurodevelopmental disorder, with a prevalence of 1 in 160 children. Accurate diagnosis relies on experts, but such individuals are scarce. This has led to increasing interest in the development of machine learning (ML) models that can integrate neuroimaging features from functional and structural MRI (fMRI and sMRI) to help reveal central nervous system alterations characteristic of ASD. We optimized and compared the performance of 12 of the most popular and powerful ML models. Each was separately trained using 15 different combinations of fMRI and sMRI features and optimized with an unbiased model search. Deep learning models predicted ASD with the highest diagnostic accuracy and generalized well to other MRI datasets. Our model achieves state-of-the-art 80% area under the ROC curve (AUROC) in diagnosis on test data from the IMPAC dataset; and 86% and 79% AUROC on the external ABIDE I and ABIDE II datasets (with further improvement to 93% and 90% after supervised domain adaptation). The highest performing models identified reproducible putative biomarkers for accurate ASD diagnosis in accord with known ASD markers as well as novel cerebellar biomarkers. Such reproducibility lends credence to their tremendous potential for defining and using a set of truly generalizable ASD biomarkers that will advance scientific understanding of neuronal changes in ASD.
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spelling pubmed-88663952022-02-25 Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning Mellema, Cooper J. Nguyen, Kevin P. Treacher, Alex Montillo, Albert Sci Rep Article Autism spectrum disorder (ASD) is the fourth most common neurodevelopmental disorder, with a prevalence of 1 in 160 children. Accurate diagnosis relies on experts, but such individuals are scarce. This has led to increasing interest in the development of machine learning (ML) models that can integrate neuroimaging features from functional and structural MRI (fMRI and sMRI) to help reveal central nervous system alterations characteristic of ASD. We optimized and compared the performance of 12 of the most popular and powerful ML models. Each was separately trained using 15 different combinations of fMRI and sMRI features and optimized with an unbiased model search. Deep learning models predicted ASD with the highest diagnostic accuracy and generalized well to other MRI datasets. Our model achieves state-of-the-art 80% area under the ROC curve (AUROC) in diagnosis on test data from the IMPAC dataset; and 86% and 79% AUROC on the external ABIDE I and ABIDE II datasets (with further improvement to 93% and 90% after supervised domain adaptation). The highest performing models identified reproducible putative biomarkers for accurate ASD diagnosis in accord with known ASD markers as well as novel cerebellar biomarkers. Such reproducibility lends credence to their tremendous potential for defining and using a set of truly generalizable ASD biomarkers that will advance scientific understanding of neuronal changes in ASD. Nature Publishing Group UK 2022-02-23 /pmc/articles/PMC8866395/ /pubmed/35197468 http://dx.doi.org/10.1038/s41598-022-06459-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mellema, Cooper J.
Nguyen, Kevin P.
Treacher, Alex
Montillo, Albert
Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning
title Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning
title_full Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning
title_fullStr Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning
title_full_unstemmed Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning
title_short Reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning
title_sort reproducible neuroimaging features for diagnosis of autism spectrum disorder with machine learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866395/
https://www.ncbi.nlm.nih.gov/pubmed/35197468
http://dx.doi.org/10.1038/s41598-022-06459-2
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