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Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework
Alzheimer’s disease (AD) is a complex neurodegenerative disease involving a variety of pathogenic factors, and the etiology detection of this disease has been a major concern of researchers. Neuroimaging is a basic and important means to explore the problem. It is the main current scientific researc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795747/ https://www.ncbi.nlm.nih.gov/pubmed/31649738 http://dx.doi.org/10.3389/fgene.2019.00976 |
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author | Bi, Xia-an Cai, Ruipeng Wang, Yang Liu, Yingchao |
author_facet | Bi, Xia-an Cai, Ruipeng Wang, Yang Liu, Yingchao |
author_sort | Bi, Xia-an |
collection | PubMed |
description | Alzheimer’s disease (AD) is a complex neurodegenerative disease involving a variety of pathogenic factors, and the etiology detection of this disease has been a major concern of researchers. Neuroimaging is a basic and important means to explore the problem. It is the main current scientific research direction for combining neuroimaging with other modal data to dig deep into the potential information of AD through the complementarities among multiple data points. Machine learning methods possess great potentiality and have reached some achievements in this research area. A few studies have proposed some solutions to the effects of multimodal data fusion, however, the overall analytical framework for data fusion and fusion result analysis has thus far been ignored. In this paper, we first put forward a novel multimodal data fusion method, and further present a new machine learning framework of data fusion, classification, feature selection, and disease-causing factor extraction. The real dataset of 37 AD patients and 35 normal controls (NC) with functional magnetic resonance imaging (fMRI) and genetic data was used to verify the effectiveness of the framework, which was more accurate in classification and optimal feature extraction than other methods. Furthermore, we revealed disease-causing brain regions and genes, such as the olfactory cortex, insula, posterior cingulate gyrus, lingual gyrus, CNTNAP2, LRP1B, FRMD4A, and DAB1. The results show that the machine learning framework could effectively perform multimodal data fusion analysis, providing new insights and perspectives for the diagnosis of Alzheimer’s disease. |
format | Online Article Text |
id | pubmed-6795747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67957472019-10-24 Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework Bi, Xia-an Cai, Ruipeng Wang, Yang Liu, Yingchao Front Genet Genetics Alzheimer’s disease (AD) is a complex neurodegenerative disease involving a variety of pathogenic factors, and the etiology detection of this disease has been a major concern of researchers. Neuroimaging is a basic and important means to explore the problem. It is the main current scientific research direction for combining neuroimaging with other modal data to dig deep into the potential information of AD through the complementarities among multiple data points. Machine learning methods possess great potentiality and have reached some achievements in this research area. A few studies have proposed some solutions to the effects of multimodal data fusion, however, the overall analytical framework for data fusion and fusion result analysis has thus far been ignored. In this paper, we first put forward a novel multimodal data fusion method, and further present a new machine learning framework of data fusion, classification, feature selection, and disease-causing factor extraction. The real dataset of 37 AD patients and 35 normal controls (NC) with functional magnetic resonance imaging (fMRI) and genetic data was used to verify the effectiveness of the framework, which was more accurate in classification and optimal feature extraction than other methods. Furthermore, we revealed disease-causing brain regions and genes, such as the olfactory cortex, insula, posterior cingulate gyrus, lingual gyrus, CNTNAP2, LRP1B, FRMD4A, and DAB1. The results show that the machine learning framework could effectively perform multimodal data fusion analysis, providing new insights and perspectives for the diagnosis of Alzheimer’s disease. Frontiers Media S.A. 2019-10-10 /pmc/articles/PMC6795747/ /pubmed/31649738 http://dx.doi.org/10.3389/fgene.2019.00976 Text en Copyright © 2019 Bi, Cai, Wang and Liu http://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 | Genetics Bi, Xia-an Cai, Ruipeng Wang, Yang Liu, Yingchao Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework |
title | Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework |
title_full | Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework |
title_fullStr | Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework |
title_full_unstemmed | Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework |
title_short | Effective Diagnosis of Alzheimer’s Disease via Multimodal Fusion Analysis Framework |
title_sort | effective diagnosis of alzheimer’s disease via multimodal fusion analysis framework |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795747/ https://www.ncbi.nlm.nih.gov/pubmed/31649738 http://dx.doi.org/10.3389/fgene.2019.00976 |
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