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Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity

Microstructural abnormalities in white matter (WM) are often reported in Alzheimer's disease (AD) and may reflect primary or secondary circuitry degeneration (i.e., due to cortical atrophy). The interpretation of diffusion tensor imaging (DTI) eigenvectors, known as multiple indices, may provid...

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Autores principales: Alves, Gilberto Sousa, Oertel Knöchel, Viola, Knöchel, Christian, Carvalho, André Férrer, Pantel, Johannes, Engelhardt, Eliasz, Laks, Jerson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320890/
https://www.ncbi.nlm.nih.gov/pubmed/25685779
http://dx.doi.org/10.1155/2015/291658
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author Alves, Gilberto Sousa
Oertel Knöchel, Viola
Knöchel, Christian
Carvalho, André Férrer
Pantel, Johannes
Engelhardt, Eliasz
Laks, Jerson
author_facet Alves, Gilberto Sousa
Oertel Knöchel, Viola
Knöchel, Christian
Carvalho, André Férrer
Pantel, Johannes
Engelhardt, Eliasz
Laks, Jerson
author_sort Alves, Gilberto Sousa
collection PubMed
description Microstructural abnormalities in white matter (WM) are often reported in Alzheimer's disease (AD) and may reflect primary or secondary circuitry degeneration (i.e., due to cortical atrophy). The interpretation of diffusion tensor imaging (DTI) eigenvectors, known as multiple indices, may provide new insights into the main pathological models supporting primary or secondary patterns of WM disruption in AD, the retrogenesis, and Wallerian degeneration models, respectively. The aim of this review is to analyze the current literature on the contribution of DTI multiple indices to the understanding of AD neuropathology, taking the retrogenesis model as a reference for discussion. A systematic review using MEDLINE, EMBASE, and PUBMED was performed. Evidence suggests that AD evolves through distinct patterns of WM disruption, in which retrogenesis or, alternatively, the Wallerian degeneration may prevail. Distinct patterns of WM atrophy may be influenced by complex interactions which comprise disease status and progression, fiber localization, concurrent risk factors (i.e., vascular disease, gender), and cognitive reserve. The use of DTI multiple indices in addition to other standard multimodal methods in dementia research may help to determine the contribution of retrogenesis hypothesis to the understanding of neuropathological hallmarks that lead to AD.
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spelling pubmed-43208902015-02-15 Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity Alves, Gilberto Sousa Oertel Knöchel, Viola Knöchel, Christian Carvalho, André Férrer Pantel, Johannes Engelhardt, Eliasz Laks, Jerson Biomed Res Int Review Article Microstructural abnormalities in white matter (WM) are often reported in Alzheimer's disease (AD) and may reflect primary or secondary circuitry degeneration (i.e., due to cortical atrophy). The interpretation of diffusion tensor imaging (DTI) eigenvectors, known as multiple indices, may provide new insights into the main pathological models supporting primary or secondary patterns of WM disruption in AD, the retrogenesis, and Wallerian degeneration models, respectively. The aim of this review is to analyze the current literature on the contribution of DTI multiple indices to the understanding of AD neuropathology, taking the retrogenesis model as a reference for discussion. A systematic review using MEDLINE, EMBASE, and PUBMED was performed. Evidence suggests that AD evolves through distinct patterns of WM disruption, in which retrogenesis or, alternatively, the Wallerian degeneration may prevail. Distinct patterns of WM atrophy may be influenced by complex interactions which comprise disease status and progression, fiber localization, concurrent risk factors (i.e., vascular disease, gender), and cognitive reserve. The use of DTI multiple indices in addition to other standard multimodal methods in dementia research may help to determine the contribution of retrogenesis hypothesis to the understanding of neuropathological hallmarks that lead to AD. Hindawi Publishing Corporation 2015 2015-01-20 /pmc/articles/PMC4320890/ /pubmed/25685779 http://dx.doi.org/10.1155/2015/291658 Text en Copyright © 2015 Gilberto Sousa Alves et al. https://creativecommons.org/licenses/by/3.0/ 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 Review Article
Alves, Gilberto Sousa
Oertel Knöchel, Viola
Knöchel, Christian
Carvalho, André Férrer
Pantel, Johannes
Engelhardt, Eliasz
Laks, Jerson
Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity
title Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity
title_full Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity
title_fullStr Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity
title_full_unstemmed Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity
title_short Integrating Retrogenesis Theory to Alzheimer's Disease Pathology: Insight from DTI-TBSS Investigation of the White Matter Microstructural Integrity
title_sort integrating retrogenesis theory to alzheimer's disease pathology: insight from dti-tbss investigation of the white matter microstructural integrity
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320890/
https://www.ncbi.nlm.nih.gov/pubmed/25685779
http://dx.doi.org/10.1155/2015/291658
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