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Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states
Accurate diagnosis of mild cognitive impairment (MCI) before conversion to Alzheimer’s disease (AD) is invaluable for patient treatment. Many works showed that MCI and AD affect functional and structural connections between brain regions as well as the shape of cortical regions. However, ‘shape conn...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841319/ https://www.ncbi.nlm.nih.gov/pubmed/29515158 http://dx.doi.org/10.1038/s41598-018-21568-7 |
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author | Mahjoub, Ines Mahjoub, Mohamed Ali Rekik, Islem |
author_facet | Mahjoub, Ines Mahjoub, Mohamed Ali Rekik, Islem |
author_sort | Mahjoub, Ines |
collection | PubMed |
description | Accurate diagnosis of mild cognitive impairment (MCI) before conversion to Alzheimer’s disease (AD) is invaluable for patient treatment. Many works showed that MCI and AD affect functional and structural connections between brain regions as well as the shape of cortical regions. However, ‘shape connections’ between brain regions are rarely investigated -e.g., how morphological attributes such as cortical thickness and sulcal depth of a specific brain region change in relation to morphological attributes in other regions. To fill this gap, we unprecedentedly design morphological brain multiplexes for late MCI/AD classification. Specifically, we use structural T1-w MRI to define morphological brain networks, each quantifying similarity in morphology between different cortical regions for a specific cortical attribute. Then, we define a brain multiplex where each intra-layer represents the morphological connectivity network of a specific cortical attribute, and each inter-layer encodes the similarity between two consecutive intra-layers. A significant performance gain is achieved when using the multiplex architecture in comparison to other conventional network analysis architectures. We also leverage this architecture to discover morphological connectional biomarkers fingerprinting the difference between late MCI and AD stages, which included the right entorhinal cortex and right caudal middle frontal gyrus. |
format | Online Article Text |
id | pubmed-5841319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58413192018-03-13 Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states Mahjoub, Ines Mahjoub, Mohamed Ali Rekik, Islem Sci Rep Article Accurate diagnosis of mild cognitive impairment (MCI) before conversion to Alzheimer’s disease (AD) is invaluable for patient treatment. Many works showed that MCI and AD affect functional and structural connections between brain regions as well as the shape of cortical regions. However, ‘shape connections’ between brain regions are rarely investigated -e.g., how morphological attributes such as cortical thickness and sulcal depth of a specific brain region change in relation to morphological attributes in other regions. To fill this gap, we unprecedentedly design morphological brain multiplexes for late MCI/AD classification. Specifically, we use structural T1-w MRI to define morphological brain networks, each quantifying similarity in morphology between different cortical regions for a specific cortical attribute. Then, we define a brain multiplex where each intra-layer represents the morphological connectivity network of a specific cortical attribute, and each inter-layer encodes the similarity between two consecutive intra-layers. A significant performance gain is achieved when using the multiplex architecture in comparison to other conventional network analysis architectures. We also leverage this architecture to discover morphological connectional biomarkers fingerprinting the difference between late MCI and AD stages, which included the right entorhinal cortex and right caudal middle frontal gyrus. Nature Publishing Group UK 2018-03-07 /pmc/articles/PMC5841319/ /pubmed/29515158 http://dx.doi.org/10.1038/s41598-018-21568-7 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mahjoub, Ines Mahjoub, Mohamed Ali Rekik, Islem Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states |
title | Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states |
title_full | Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states |
title_fullStr | Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states |
title_full_unstemmed | Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states |
title_short | Brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states |
title_sort | brain multiplexes reveal morphological connectional biomarkers fingerprinting late brain dementia states |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841319/ https://www.ncbi.nlm.nih.gov/pubmed/29515158 http://dx.doi.org/10.1038/s41598-018-21568-7 |
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