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A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment
OBJECTIVE: Glucose-based positron emission tomography (PET) imaging has been widely used to predict the progression of mild cognitive impairment (MCI) into Alzheimer's disease (AD) clinically. However, existing discriminant methods are unsubtle to reveal pathophysiological changes. Therefore, w...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450311/ https://www.ncbi.nlm.nih.gov/pubmed/32908613 http://dx.doi.org/10.1155/2020/2825037 |
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author | Wang, Min Yan, Zhuangzhi Xiao, Shu-yun Zuo, Chuantao Jiang, Jiehui |
author_facet | Wang, Min Yan, Zhuangzhi Xiao, Shu-yun Zuo, Chuantao Jiang, Jiehui |
author_sort | Wang, Min |
collection | PubMed |
description | OBJECTIVE: Glucose-based positron emission tomography (PET) imaging has been widely used to predict the progression of mild cognitive impairment (MCI) into Alzheimer's disease (AD) clinically. However, existing discriminant methods are unsubtle to reveal pathophysiological changes. Therefore, we present a novel metabolic connectome-based predictive modeling to predict progression from MCI to AD accurately. METHODS: In this study, we acquired fluorodeoxyglucose PET images and clinical assessments from 420 MCI patients with 36 months follow-up. Individual metabolic network based on connectome analysis was constructed, and the metabolic connectivity in this network was extracted as predictive features. Three different classification strategies were implemented to interrogate the predictive performance. To verify the effectivity of selected features, specific brain regions associated with MCI conversion were identified based on these features and compared with prior knowledge. RESULTS: As a result, 4005 connectome features were obtained, and 153 in which were selected as efficient features. Our proposed feature extraction method had achieved 85.2% accuracy for MCI conversion prediction (sensitivity: 88.1%; specificity: 81.2%; and AUC: 0.933). The discriminative brain regions associated with MCI conversion were mainly located in the precentral gyrus, precuneus, lingual, and inferior frontal gyrus. CONCLUSION: Overall, the results suggest that our proposed individual metabolic connectome method has great potential to predict whether MCI patients will progress to AD. The metabolic connectome may help to identify brain metabolic dysfunction and build a clinically applicable biomarker to predict the MCI progression. |
format | Online Article Text |
id | pubmed-7450311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-74503112020-09-08 A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment Wang, Min Yan, Zhuangzhi Xiao, Shu-yun Zuo, Chuantao Jiang, Jiehui Behav Neurol Research Article OBJECTIVE: Glucose-based positron emission tomography (PET) imaging has been widely used to predict the progression of mild cognitive impairment (MCI) into Alzheimer's disease (AD) clinically. However, existing discriminant methods are unsubtle to reveal pathophysiological changes. Therefore, we present a novel metabolic connectome-based predictive modeling to predict progression from MCI to AD accurately. METHODS: In this study, we acquired fluorodeoxyglucose PET images and clinical assessments from 420 MCI patients with 36 months follow-up. Individual metabolic network based on connectome analysis was constructed, and the metabolic connectivity in this network was extracted as predictive features. Three different classification strategies were implemented to interrogate the predictive performance. To verify the effectivity of selected features, specific brain regions associated with MCI conversion were identified based on these features and compared with prior knowledge. RESULTS: As a result, 4005 connectome features were obtained, and 153 in which were selected as efficient features. Our proposed feature extraction method had achieved 85.2% accuracy for MCI conversion prediction (sensitivity: 88.1%; specificity: 81.2%; and AUC: 0.933). The discriminative brain regions associated with MCI conversion were mainly located in the precentral gyrus, precuneus, lingual, and inferior frontal gyrus. CONCLUSION: Overall, the results suggest that our proposed individual metabolic connectome method has great potential to predict whether MCI patients will progress to AD. The metabolic connectome may help to identify brain metabolic dysfunction and build a clinically applicable biomarker to predict the MCI progression. Hindawi 2020-08-18 /pmc/articles/PMC7450311/ /pubmed/32908613 http://dx.doi.org/10.1155/2020/2825037 Text en Copyright © 2020 Min Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Min Yan, Zhuangzhi Xiao, Shu-yun Zuo, Chuantao Jiang, Jiehui A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment |
title | A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment |
title_full | A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment |
title_fullStr | A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment |
title_full_unstemmed | A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment |
title_short | A Novel Metabolic Connectome Method to Predict Progression to Mild Cognitive Impairment |
title_sort | novel metabolic connectome method to predict progression to mild cognitive impairment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450311/ https://www.ncbi.nlm.nih.gov/pubmed/32908613 http://dx.doi.org/10.1155/2020/2825037 |
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