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Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data

The intervention at the stage of mild cognitive impairment (MCI) is promising for preventing Alzheimer’s disease (AD). This study aims to search for the optimal machine learning (ML) model to classify early and late MCI (EMCI and LMCI) subtypes using multimodal MRI data. First, the tract-based spati...

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Autores principales: Jitsuishi, Tatsuya, Yamaguchi, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917197/
https://www.ncbi.nlm.nih.gov/pubmed/35277565
http://dx.doi.org/10.1038/s41598-022-08231-y
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author Jitsuishi, Tatsuya
Yamaguchi, Atsushi
author_facet Jitsuishi, Tatsuya
Yamaguchi, Atsushi
author_sort Jitsuishi, Tatsuya
collection PubMed
description The intervention at the stage of mild cognitive impairment (MCI) is promising for preventing Alzheimer’s disease (AD). This study aims to search for the optimal machine learning (ML) model to classify early and late MCI (EMCI and LMCI) subtypes using multimodal MRI data. First, the tract-based spatial statistics (TBSS) analyses showed LMCI-related white matter changes in the Corpus Callosum. The ROI-based tractography addressed the connected cortical areas by affected callosal fibers. We then prepared two feature subsets for ML by measuring resting-state functional connectivity (TBSS-RSFC method) and graph theory metrics (TBSS-Graph method) in these cortical areas, respectively. We also prepared feature subsets of diffusion parameters in the regions of LMCI-related white matter alterations detected by TBSS analyses. Using these feature subsets, we trained and tested multiple ML models for EMCI/LMCI classification with cross-validation. Our results showed the ensemble ML model (AdaBoost) with feature subset of diffusion parameters achieved better performance of mean accuracy 70%. The useful brain regions for classification were those, including frontal, parietal lobe, Corpus Callosum, cingulate regions, insula, and thalamus regions. Our findings indicated the optimal ML model using diffusion parameters might be effective to distinguish LMCI from EMCI subjects at the prodromal stage of AD.
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spelling pubmed-89171972022-03-16 Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data Jitsuishi, Tatsuya Yamaguchi, Atsushi Sci Rep Article The intervention at the stage of mild cognitive impairment (MCI) is promising for preventing Alzheimer’s disease (AD). This study aims to search for the optimal machine learning (ML) model to classify early and late MCI (EMCI and LMCI) subtypes using multimodal MRI data. First, the tract-based spatial statistics (TBSS) analyses showed LMCI-related white matter changes in the Corpus Callosum. The ROI-based tractography addressed the connected cortical areas by affected callosal fibers. We then prepared two feature subsets for ML by measuring resting-state functional connectivity (TBSS-RSFC method) and graph theory metrics (TBSS-Graph method) in these cortical areas, respectively. We also prepared feature subsets of diffusion parameters in the regions of LMCI-related white matter alterations detected by TBSS analyses. Using these feature subsets, we trained and tested multiple ML models for EMCI/LMCI classification with cross-validation. Our results showed the ensemble ML model (AdaBoost) with feature subset of diffusion parameters achieved better performance of mean accuracy 70%. The useful brain regions for classification were those, including frontal, parietal lobe, Corpus Callosum, cingulate regions, insula, and thalamus regions. Our findings indicated the optimal ML model using diffusion parameters might be effective to distinguish LMCI from EMCI subjects at the prodromal stage of AD. Nature Publishing Group UK 2022-03-11 /pmc/articles/PMC8917197/ /pubmed/35277565 http://dx.doi.org/10.1038/s41598-022-08231-y 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
Jitsuishi, Tatsuya
Yamaguchi, Atsushi
Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data
title Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data
title_full Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data
title_fullStr Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data
title_full_unstemmed Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data
title_short Searching for optimal machine learning model to classify mild cognitive impairment (MCI) subtypes using multimodal MRI data
title_sort searching for optimal machine learning model to classify mild cognitive impairment (mci) subtypes using multimodal mri data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917197/
https://www.ncbi.nlm.nih.gov/pubmed/35277565
http://dx.doi.org/10.1038/s41598-022-08231-y
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