Single-slice Alzheimer's disease classification and disease regional analysis with Supervised Switching Autoencoders
Alzheimer's disease (AD) is a difficult to diagnose pathology of the brain that progressively impairs cognitive functions. Computer-assisted diagnosis of AD based on image analysis is an emerging tool to support AD diagnosis. In this article, we explore the application of Supervised Switching A...
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description | Alzheimer's disease (AD) is a difficult to diagnose pathology of the brain that progressively impairs cognitive functions. Computer-assisted diagnosis of AD based on image analysis is an emerging tool to support AD diagnosis. In this article, we explore the application of Supervised Switching Autoencoders (SSAs) to perform AD classification using only one structural Magnetic Resonance Imaging (sMRI) slice. SSAs are revised supervised autoencoder architectures, combining unsupervised representation and supervised classification as one unified model. In this work, we study the capabilities of SSAs to capture complex visual neurodegeneration patterns, and fuse disease semantics simultaneously. We also examine how regions associated to disease state can be discovered by SSAs following a local patch-based approach.
Patch-based SSAs models are trained on individual patches extracted from a single 2D slice, independently for Axial, Coronal, and Sagittal anatomical planes of the brain at selected informative locations, exploring different patch sizes and network parameterizations. Then, models perform binary class prediction - healthy (CDR = 0) or AD-demented (CDR > 0) - on test data at patch level. The final subject classification is performed employing a majority rule from the ensemble of patch predictions. In addition, relevant regions are identified, by computing accuracy densities from patch-level predictions, and analyzed, supported by Atlas-based regional definitions.
Our experiments employing a single 2D T1-w sMRI slice per subject show that SSAs perform similarly to previous proposals that rely on full volumetric information and feature-engineered representations. SSAs classification accuracy on slices extracted along the Axial, Coronal, and Sagittal anatomical planes from a balanced cohort of 40 independent test subjects was 87.5%, 90.0%, and 90.0%, respectively. A top sensitivity of 95.0% on both Coronal and Sagittal planes was also obtained.
SSAs provided well-ranked accuracy performance among previous classification proposals, including feature-engineered and feature learning based methods, using only one scan slice per subject, instead of the whole 3D volume, as it is conventionally done. In addition, regions identified as relevant by SSAs’ were, in most part, coherent or partially coherent in regard to relevant regions reported on previous works. These regions were also associated with findings from medical knowledge, which gives value to our method |
doi_str_mv | 10.1016/j.compbiomed.2019.103527 |
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Patch-based SSAs models are trained on individual patches extracted from a single 2D slice, independently for Axial, Coronal, and Sagittal anatomical planes of the brain at selected informative locations, exploring different patch sizes and network parameterizations. Then, models perform binary class prediction - healthy (CDR = 0) or AD-demented (CDR > 0) - on test data at patch level. The final subject classification is performed employing a majority rule from the ensemble of patch predictions. In addition, relevant regions are identified, by computing accuracy densities from patch-level predictions, and analyzed, supported by Atlas-based regional definitions.
Our experiments employing a single 2D T1-w sMRI slice per subject show that SSAs perform similarly to previous proposals that rely on full volumetric information and feature-engineered representations. SSAs classification accuracy on slices extracted along the Axial, Coronal, and Sagittal anatomical planes from a balanced cohort of 40 independent test subjects was 87.5%, 90.0%, and 90.0%, respectively. A top sensitivity of 95.0% on both Coronal and Sagittal planes was also obtained.
SSAs provided well-ranked accuracy performance among previous classification proposals, including feature-engineered and feature learning based methods, using only one scan slice per subject, instead of the whole 3D volume, as it is conventionally done. In addition, regions identified as relevant by SSAs’ were, in most part, coherent or partially coherent in regard to relevant regions reported on previous works. These regions were also associated with findings from medical knowledge, which gives value to our methodology as a potential analytical aid for disease understanding.
•Introduces a new method for single slice Alzheimer's disease identification merging unsupervised and supervised learning.•Proposes a new supervised autoencoder architecture to learn label-enriched visual representations and classification models.•Presents a novel image analysis approach to identify Alzheimer's disease relevant regions from autoencoder reconstructions.•Evaluates the association between identified relevant regions and current medical knowledge, finding them markedly coherent.</description><identifier>ISSN: 0010-4825</identifier><identifier>EISSN: 1879-0534</identifier><identifier>DOI: 10.1016/j.compbiomed.2019.103527</identifier><identifier>PMID: 31765915</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Accuracy ; Adolescent ; Adult ; Aged ; Aged, 80 and over ; Alzheimer disease ; Alzheimer Disease - diagnostic imaging ; Alzheimer's disease ; Artificial Intelligence ; Brain ; Brain - diagnostic imaging ; Brain slice preparation ; Classification ; Cognitive ability ; Computer Science ; Convolutional neural networks ; Dementia ; Diagnosis ; Engineering ; Engineering Sciences ; Feature extraction ; Female ; Humans ; Image analysis ; Image Interpretation, Computer-Assisted - methods ; Image Processing ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Middle Aged ; Neural and Evolutionary Computing ; Neural networks ; Neural Networks, Computer ; Neurodegeneration ; Neurodegenerative diseases ; Neuroimaging ; Planes ; Proposals ; Regional analysis ; Regional planning ; Representation learning ; Representations ; Semantics ; Signal and Image processing ; Supervised autoencoder ; Supervised Machine Learning ; Supervised switching autoencoder ; Switching ; Two dimensional models ; Young Adult</subject><ispartof>Computers in biology and medicine, 2020-01, Vol.116, p.103527-103527, Article 103527</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><rights>2019. Elsevier Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-80bd6210a5441c9d7f939ca4d1c6c52e3526814b504c6ebc6522c497bd4620d93</citedby><cites>FETCH-LOGICAL-c436t-80bd6210a5441c9d7f939ca4d1c6c52e3526814b504c6ebc6522c497bd4620d93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2344190264?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31765915$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02430191$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Mendoza-Léon, Ricardo</creatorcontrib><creatorcontrib>Puentes, John</creatorcontrib><creatorcontrib>Uriza, Luis Felipe</creatorcontrib><creatorcontrib>Hernández Hoyos, Marcela</creatorcontrib><title>Single-slice Alzheimer's disease classification and disease regional analysis with Supervised Switching Autoencoders</title><title>Computers in biology and medicine</title><addtitle>Comput Biol Med</addtitle><description>Alzheimer's disease (AD) is a difficult to diagnose pathology of the brain that progressively impairs cognitive functions. Computer-assisted diagnosis of AD based on image analysis is an emerging tool to support AD diagnosis. In this article, we explore the application of Supervised Switching Autoencoders (SSAs) to perform AD classification using only one structural Magnetic Resonance Imaging (sMRI) slice. SSAs are revised supervised autoencoder architectures, combining unsupervised representation and supervised classification as one unified model. In this work, we study the capabilities of SSAs to capture complex visual neurodegeneration patterns, and fuse disease semantics simultaneously. We also examine how regions associated to disease state can be discovered by SSAs following a local patch-based approach.
Patch-based SSAs models are trained on individual patches extracted from a single 2D slice, independently for Axial, Coronal, and Sagittal anatomical planes of the brain at selected informative locations, exploring different patch sizes and network parameterizations. Then, models perform binary class prediction - healthy (CDR = 0) or AD-demented (CDR > 0) - on test data at patch level. The final subject classification is performed employing a majority rule from the ensemble of patch predictions. In addition, relevant regions are identified, by computing accuracy densities from patch-level predictions, and analyzed, supported by Atlas-based regional definitions.
Our experiments employing a single 2D T1-w sMRI slice per subject show that SSAs perform similarly to previous proposals that rely on full volumetric information and feature-engineered representations. SSAs classification accuracy on slices extracted along the Axial, Coronal, and Sagittal anatomical planes from a balanced cohort of 40 independent test subjects was 87.5%, 90.0%, and 90.0%, respectively. A top sensitivity of 95.0% on both Coronal and Sagittal planes was also obtained.
SSAs provided well-ranked accuracy performance among previous classification proposals, including feature-engineered and feature learning based methods, using only one scan slice per subject, instead of the whole 3D volume, as it is conventionally done. In addition, regions identified as relevant by SSAs’ were, in most part, coherent or partially coherent in regard to relevant regions reported on previous works. These regions were also associated with findings from medical knowledge, which gives value to our methodology as a potential analytical aid for disease understanding.
•Introduces a new method for single slice Alzheimer's disease identification merging unsupervised and supervised learning.•Proposes a new supervised autoencoder architecture to learn label-enriched visual representations and classification models.•Presents a novel image analysis approach to identify Alzheimer's disease relevant regions from autoencoder reconstructions.•Evaluates the association between identified relevant regions and current medical knowledge, finding them markedly coherent.</description><subject>Accuracy</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer disease</subject><subject>Alzheimer Disease - diagnostic imaging</subject><subject>Alzheimer's disease</subject><subject>Artificial Intelligence</subject><subject>Brain</subject><subject>Brain - diagnostic imaging</subject><subject>Brain slice preparation</subject><subject>Classification</subject><subject>Cognitive ability</subject><subject>Computer Science</subject><subject>Convolutional neural networks</subject><subject>Dementia</subject><subject>Diagnosis</subject><subject>Engineering</subject><subject>Engineering Sciences</subject><subject>Feature extraction</subject><subject>Female</subject><subject>Humans</subject><subject>Image analysis</subject><subject>Image Interpretation, Computer-Assisted - 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diagnostic imaging</topic><topic>Alzheimer's disease</topic><topic>Artificial Intelligence</topic><topic>Brain</topic><topic>Brain - diagnostic imaging</topic><topic>Brain slice preparation</topic><topic>Classification</topic><topic>Cognitive ability</topic><topic>Computer Science</topic><topic>Convolutional neural networks</topic><topic>Dementia</topic><topic>Diagnosis</topic><topic>Engineering</topic><topic>Engineering Sciences</topic><topic>Feature extraction</topic><topic>Female</topic><topic>Humans</topic><topic>Image analysis</topic><topic>Image Interpretation, Computer-Assisted - methods</topic><topic>Image Processing</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neural and Evolutionary Computing</topic><topic>Neural networks</topic><topic>Neural Networks, Computer</topic><topic>Neurodegeneration</topic><topic>Neurodegenerative diseases</topic><topic>Neuroimaging</topic><topic>Planes</topic><topic>Proposals</topic><topic>Regional analysis</topic><topic>Regional planning</topic><topic>Representation learning</topic><topic>Representations</topic><topic>Semantics</topic><topic>Signal and Image processing</topic><topic>Supervised autoencoder</topic><topic>Supervised Machine Learning</topic><topic>Supervised switching autoencoder</topic><topic>Switching</topic><topic>Two dimensional models</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mendoza-Léon, Ricardo</creatorcontrib><creatorcontrib>Puentes, John</creatorcontrib><creatorcontrib>Uriza, Luis Felipe</creatorcontrib><creatorcontrib>Hernández Hoyos, Marcela</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Computing Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Computer Science Collection</collection><collection>Computer Science Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Computing Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Computers in biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mendoza-Léon, Ricardo</au><au>Puentes, John</au><au>Uriza, Luis Felipe</au><au>Hernández Hoyos, Marcela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-slice Alzheimer's disease classification and disease regional analysis with Supervised Switching Autoencoders</atitle><jtitle>Computers in biology and medicine</jtitle><addtitle>Comput Biol Med</addtitle><date>2020-01</date><risdate>2020</risdate><volume>116</volume><spage>103527</spage><epage>103527</epage><pages>103527-103527</pages><artnum>103527</artnum><issn>0010-4825</issn><eissn>1879-0534</eissn><abstract>Alzheimer's disease (AD) is a difficult to diagnose pathology of the brain that progressively impairs cognitive functions. Computer-assisted diagnosis of AD based on image analysis is an emerging tool to support AD diagnosis. In this article, we explore the application of Supervised Switching Autoencoders (SSAs) to perform AD classification using only one structural Magnetic Resonance Imaging (sMRI) slice. SSAs are revised supervised autoencoder architectures, combining unsupervised representation and supervised classification as one unified model. In this work, we study the capabilities of SSAs to capture complex visual neurodegeneration patterns, and fuse disease semantics simultaneously. We also examine how regions associated to disease state can be discovered by SSAs following a local patch-based approach.
Patch-based SSAs models are trained on individual patches extracted from a single 2D slice, independently for Axial, Coronal, and Sagittal anatomical planes of the brain at selected informative locations, exploring different patch sizes and network parameterizations. Then, models perform binary class prediction - healthy (CDR = 0) or AD-demented (CDR > 0) - on test data at patch level. The final subject classification is performed employing a majority rule from the ensemble of patch predictions. In addition, relevant regions are identified, by computing accuracy densities from patch-level predictions, and analyzed, supported by Atlas-based regional definitions.
Our experiments employing a single 2D T1-w sMRI slice per subject show that SSAs perform similarly to previous proposals that rely on full volumetric information and feature-engineered representations. SSAs classification accuracy on slices extracted along the Axial, Coronal, and Sagittal anatomical planes from a balanced cohort of 40 independent test subjects was 87.5%, 90.0%, and 90.0%, respectively. A top sensitivity of 95.0% on both Coronal and Sagittal planes was also obtained.
SSAs provided well-ranked accuracy performance among previous classification proposals, including feature-engineered and feature learning based methods, using only one scan slice per subject, instead of the whole 3D volume, as it is conventionally done. In addition, regions identified as relevant by SSAs’ were, in most part, coherent or partially coherent in regard to relevant regions reported on previous works. These regions were also associated with findings from medical knowledge, which gives value to our methodology as a potential analytical aid for disease understanding.
•Introduces a new method for single slice Alzheimer's disease identification merging unsupervised and supervised learning.•Proposes a new supervised autoencoder architecture to learn label-enriched visual representations and classification models.•Presents a novel image analysis approach to identify Alzheimer's disease relevant regions from autoencoder reconstructions.•Evaluates the association between identified relevant regions and current medical knowledge, finding them markedly coherent.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>31765915</pmid><doi>10.1016/j.compbiomed.2019.103527</doi><tpages>1</tpages></addata></record> |
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subjects | Accuracy Adolescent Adult Aged Aged, 80 and over Alzheimer disease Alzheimer Disease - diagnostic imaging Alzheimer's disease Artificial Intelligence Brain Brain - diagnostic imaging Brain slice preparation Classification Cognitive ability Computer Science Convolutional neural networks Dementia Diagnosis Engineering Engineering Sciences Feature extraction Female Humans Image analysis Image Interpretation, Computer-Assisted - methods Image Processing Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Middle Aged Neural and Evolutionary Computing Neural networks Neural Networks, Computer Neurodegeneration Neurodegenerative diseases Neuroimaging Planes Proposals Regional analysis Regional planning Representation learning Representations Semantics Signal and Image processing Supervised autoencoder Supervised Machine Learning Supervised switching autoencoder Switching Two dimensional models Young Adult |
title | Single-slice Alzheimer's disease classification and disease regional analysis with Supervised Switching Autoencoders |
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