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Novel ThickNet features for the discrimination of amnestic MCI subtypes
BACKGROUND: Amnestic mild cognitive impairment (aMCI) is considered to be a transitional stage between healthy aging and Alzheimer's disease (AD), and consists of two subtypes: single-domain aMCI (sd-aMCI) and multi-domain aMCI (md-aMCI). Individuals with md-aMCI are found to exhibit higher ris...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215394/ https://www.ncbi.nlm.nih.gov/pubmed/25379441 http://dx.doi.org/10.1016/j.nicl.2014.09.005 |
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author | Raamana, Pradeep Reddy Wen, Wei Kochan, Nicole A. Brodaty, Henry Sachdev, Perminder S. Wang, Lei Beg, Mirza Faisal |
author_facet | Raamana, Pradeep Reddy Wen, Wei Kochan, Nicole A. Brodaty, Henry Sachdev, Perminder S. Wang, Lei Beg, Mirza Faisal |
author_sort | Raamana, Pradeep Reddy |
collection | PubMed |
description | BACKGROUND: Amnestic mild cognitive impairment (aMCI) is considered to be a transitional stage between healthy aging and Alzheimer's disease (AD), and consists of two subtypes: single-domain aMCI (sd-aMCI) and multi-domain aMCI (md-aMCI). Individuals with md-aMCI are found to exhibit higher risk of conversion to AD. Accurate discrimination among aMCI subtypes (sd- or md-aMCI) and controls could assist in predicting future decline. METHODS: We apply our novel thickness network (ThickNet) features to discriminate md-aMCI from healthy controls (NC). ThickNet features are extracted from the properties of a graph constructed from inter-regional co-variation of cortical thickness. We fuse these ThickNet features using multiple kernel learning to form a composite classifier. We apply the proposed ThickNet classifier to discriminate between md-aMCI and NC, sd-aMCI and NC and; and also between sd-aMCI and md-aMCI, using baseline T1 MR scans from the Sydney Memory and Ageing Study. RESULTS: ThickNet classifier achieved an area under curve (AUC) of 0.74, with 70% sensitivity and 69% specificity in discriminating md-aMCI from healthy controls. The same classifier resulted in AUC = 0.67 and 0.67 for sd-aMCI/NC and sd-aMCI/md-aMCI classification experiments respectively. CONCLUSIONS: The proposed ThickNet classifier demonstrated potential for discriminating md-aMCI from controls, and in discriminating sd-aMCI from md-aMCI, using cortical features from baseline MRI scan alone. Use of the proposed novel ThickNet features demonstrates significant improvements over previous experiments using cortical thickness alone. This result may offer the possibility of early detection of Alzheimer's disease via improved discrimination of aMCI subtypes. |
format | Online Article Text |
id | pubmed-4215394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-42153942014-11-06 Novel ThickNet features for the discrimination of amnestic MCI subtypes Raamana, Pradeep Reddy Wen, Wei Kochan, Nicole A. Brodaty, Henry Sachdev, Perminder S. Wang, Lei Beg, Mirza Faisal Neuroimage Clin Article BACKGROUND: Amnestic mild cognitive impairment (aMCI) is considered to be a transitional stage between healthy aging and Alzheimer's disease (AD), and consists of two subtypes: single-domain aMCI (sd-aMCI) and multi-domain aMCI (md-aMCI). Individuals with md-aMCI are found to exhibit higher risk of conversion to AD. Accurate discrimination among aMCI subtypes (sd- or md-aMCI) and controls could assist in predicting future decline. METHODS: We apply our novel thickness network (ThickNet) features to discriminate md-aMCI from healthy controls (NC). ThickNet features are extracted from the properties of a graph constructed from inter-regional co-variation of cortical thickness. We fuse these ThickNet features using multiple kernel learning to form a composite classifier. We apply the proposed ThickNet classifier to discriminate between md-aMCI and NC, sd-aMCI and NC and; and also between sd-aMCI and md-aMCI, using baseline T1 MR scans from the Sydney Memory and Ageing Study. RESULTS: ThickNet classifier achieved an area under curve (AUC) of 0.74, with 70% sensitivity and 69% specificity in discriminating md-aMCI from healthy controls. The same classifier resulted in AUC = 0.67 and 0.67 for sd-aMCI/NC and sd-aMCI/md-aMCI classification experiments respectively. CONCLUSIONS: The proposed ThickNet classifier demonstrated potential for discriminating md-aMCI from controls, and in discriminating sd-aMCI from md-aMCI, using cortical features from baseline MRI scan alone. Use of the proposed novel ThickNet features demonstrates significant improvements over previous experiments using cortical thickness alone. This result may offer the possibility of early detection of Alzheimer's disease via improved discrimination of aMCI subtypes. Elsevier 2014-09-16 /pmc/articles/PMC4215394/ /pubmed/25379441 http://dx.doi.org/10.1016/j.nicl.2014.09.005 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Raamana, Pradeep Reddy Wen, Wei Kochan, Nicole A. Brodaty, Henry Sachdev, Perminder S. Wang, Lei Beg, Mirza Faisal Novel ThickNet features for the discrimination of amnestic MCI subtypes |
title | Novel ThickNet features for the discrimination of amnestic MCI subtypes |
title_full | Novel ThickNet features for the discrimination of amnestic MCI subtypes |
title_fullStr | Novel ThickNet features for the discrimination of amnestic MCI subtypes |
title_full_unstemmed | Novel ThickNet features for the discrimination of amnestic MCI subtypes |
title_short | Novel ThickNet features for the discrimination of amnestic MCI subtypes |
title_sort | novel thicknet features for the discrimination of amnestic mci subtypes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215394/ https://www.ncbi.nlm.nih.gov/pubmed/25379441 http://dx.doi.org/10.1016/j.nicl.2014.09.005 |
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