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Artificial neural networks for non-linear age correction of diffusion metrics in the brain

Human aging is characterized by progressive loss of physiological functions. To assess changes in the brain that occur with increasing age, the concept of brain aging has gained momentum in neuroimaging with recent advancements in statistical regression and machine learning (ML). A common technique...

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Autores principales: Kocar, Thomas D., Behler, Anna, Leinert, Christoph, Denkinger, Michael, Ludolph, Albert C., Müller, Hans-Peter, Kassubek, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632350/
https://www.ncbi.nlm.nih.gov/pubmed/36337697
http://dx.doi.org/10.3389/fnagi.2022.999787
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author Kocar, Thomas D.
Behler, Anna
Leinert, Christoph
Denkinger, Michael
Ludolph, Albert C.
Müller, Hans-Peter
Kassubek, Jan
author_facet Kocar, Thomas D.
Behler, Anna
Leinert, Christoph
Denkinger, Michael
Ludolph, Albert C.
Müller, Hans-Peter
Kassubek, Jan
author_sort Kocar, Thomas D.
collection PubMed
description Human aging is characterized by progressive loss of physiological functions. To assess changes in the brain that occur with increasing age, the concept of brain aging has gained momentum in neuroimaging with recent advancements in statistical regression and machine learning (ML). A common technique to assess the brain age of a person is, first, fitting a regression model to neuroimaging data from a group of healthy subjects, and then, using the resulting model for age prediction. Although multiparametric MRI-based models generally perform best, models solely based on diffusion tensor imaging have achieved similar results, with the benefits of faster data acquisition and better replicability across scanners and field strengths. In the present study, we developed an artificial neural network (ANN) for brain age prediction based upon tract-based fractional anisotropy (FA). Consequently, we investigated if this age-prediction model could also be used for non-linear age correction of white matter diffusion metrics in healthy adults. The brain age prediction accuracy of the ANN (R(2) = 0.47) was similar to established multimodal models. The comparison of the ANN-based age-corrected FA with the tract-wise linear age-corrected FA resulted in an R(2) value of 0.90 [0.82; 0.93] and a mean difference of 0.00 [−0.04; 0.05] for all tract systems combined. In conclusion, this study demonstrated the applicability of complex ANN models to non-linear age correction of tract-based diffusion metrics as a proof of concept.
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spelling pubmed-96323502022-11-04 Artificial neural networks for non-linear age correction of diffusion metrics in the brain Kocar, Thomas D. Behler, Anna Leinert, Christoph Denkinger, Michael Ludolph, Albert C. Müller, Hans-Peter Kassubek, Jan Front Aging Neurosci Neuroscience Human aging is characterized by progressive loss of physiological functions. To assess changes in the brain that occur with increasing age, the concept of brain aging has gained momentum in neuroimaging with recent advancements in statistical regression and machine learning (ML). A common technique to assess the brain age of a person is, first, fitting a regression model to neuroimaging data from a group of healthy subjects, and then, using the resulting model for age prediction. Although multiparametric MRI-based models generally perform best, models solely based on diffusion tensor imaging have achieved similar results, with the benefits of faster data acquisition and better replicability across scanners and field strengths. In the present study, we developed an artificial neural network (ANN) for brain age prediction based upon tract-based fractional anisotropy (FA). Consequently, we investigated if this age-prediction model could also be used for non-linear age correction of white matter diffusion metrics in healthy adults. The brain age prediction accuracy of the ANN (R(2) = 0.47) was similar to established multimodal models. The comparison of the ANN-based age-corrected FA with the tract-wise linear age-corrected FA resulted in an R(2) value of 0.90 [0.82; 0.93] and a mean difference of 0.00 [−0.04; 0.05] for all tract systems combined. In conclusion, this study demonstrated the applicability of complex ANN models to non-linear age correction of tract-based diffusion metrics as a proof of concept. Frontiers Media S.A. 2022-10-20 /pmc/articles/PMC9632350/ /pubmed/36337697 http://dx.doi.org/10.3389/fnagi.2022.999787 Text en Copyright © 2022 Kocar, Behler, Leinert, Denkinger, Ludolph, Müller and Kassubek. 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
Kocar, Thomas D.
Behler, Anna
Leinert, Christoph
Denkinger, Michael
Ludolph, Albert C.
Müller, Hans-Peter
Kassubek, Jan
Artificial neural networks for non-linear age correction of diffusion metrics in the brain
title Artificial neural networks for non-linear age correction of diffusion metrics in the brain
title_full Artificial neural networks for non-linear age correction of diffusion metrics in the brain
title_fullStr Artificial neural networks for non-linear age correction of diffusion metrics in the brain
title_full_unstemmed Artificial neural networks for non-linear age correction of diffusion metrics in the brain
title_short Artificial neural networks for non-linear age correction of diffusion metrics in the brain
title_sort artificial neural networks for non-linear age correction of diffusion metrics in the brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632350/
https://www.ncbi.nlm.nih.gov/pubmed/36337697
http://dx.doi.org/10.3389/fnagi.2022.999787
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