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Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET

Neurodegenerative dementia often has multiple types of underlying pathology, for example, beta-amyloid, misfolded tau, chronic neuroinflammation and neurodegeneration may coexist in Alzheimer’s disease. However, the relationship between them is often unclear, in other words, whether one pathology is...

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Autores principales: Su, Li, Huang, Yujing, Wang, Yi, Rowe, James, O’Brien, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187250/
https://www.ncbi.nlm.nih.gov/pubmed/30349473
http://dx.doi.org/10.3389/fnagi.2018.00306
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author Su, Li
Huang, Yujing
Wang, Yi
Rowe, James
O’Brien, John
author_facet Su, Li
Huang, Yujing
Wang, Yi
Rowe, James
O’Brien, John
author_sort Su, Li
collection PubMed
description Neurodegenerative dementia often has multiple types of underlying pathology, for example, beta-amyloid, misfolded tau, chronic neuroinflammation and neurodegeneration may coexist in Alzheimer’s disease. However, the relationship between them is often unclear, in other words, whether one pathology is upstream or downstream of others can be very difficult to investigate directly. This is partly because the underlying pathology in dementia may precede detectable symptoms by several years if not decades. The time scale associated with disease progression in dementia generally exceeds that in conventional longitudinal imaging studies in humans, so it is difficult to directly observe the temporal ordering of different pathologies. Also, animal studies are not always transferable to patients due to obvious differences between the two systems. To investigate the disease progression and relationships among underlying pathological changes, we propose a novel computational modeling approach for multimodal MRI and PET inspired by reaction rate equation in chemical kinetics. We also discuss the possibility and prerequisites to use cross-sectional data to generate preliminary hypothesis for future longitudinal studies. It has been shown that the rate of change in some biomarkers can be approximated by the average trajectory across patients at different stages of disease severity in cross-sectional studies. The relationship modeled in our approach is akin to that in the control theory, and can be assessed by demonstrating that the presence of one disease related biomarker predicts dynamics in another. We argue that the proposed framework has important implications for trials targeting different pathologies in dementia.
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spelling pubmed-61872502018-10-22 Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET Su, Li Huang, Yujing Wang, Yi Rowe, James O’Brien, John Front Aging Neurosci Neuroscience Neurodegenerative dementia often has multiple types of underlying pathology, for example, beta-amyloid, misfolded tau, chronic neuroinflammation and neurodegeneration may coexist in Alzheimer’s disease. However, the relationship between them is often unclear, in other words, whether one pathology is upstream or downstream of others can be very difficult to investigate directly. This is partly because the underlying pathology in dementia may precede detectable symptoms by several years if not decades. The time scale associated with disease progression in dementia generally exceeds that in conventional longitudinal imaging studies in humans, so it is difficult to directly observe the temporal ordering of different pathologies. Also, animal studies are not always transferable to patients due to obvious differences between the two systems. To investigate the disease progression and relationships among underlying pathological changes, we propose a novel computational modeling approach for multimodal MRI and PET inspired by reaction rate equation in chemical kinetics. We also discuss the possibility and prerequisites to use cross-sectional data to generate preliminary hypothesis for future longitudinal studies. It has been shown that the rate of change in some biomarkers can be approximated by the average trajectory across patients at different stages of disease severity in cross-sectional studies. The relationship modeled in our approach is akin to that in the control theory, and can be assessed by demonstrating that the presence of one disease related biomarker predicts dynamics in another. We argue that the proposed framework has important implications for trials targeting different pathologies in dementia. Frontiers Media S.A. 2018-10-08 /pmc/articles/PMC6187250/ /pubmed/30349473 http://dx.doi.org/10.3389/fnagi.2018.00306 Text en Copyright © 2018 Su, Huang, Wang, Rowe and O’Brien. 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 Neuroscience
Su, Li
Huang, Yujing
Wang, Yi
Rowe, James
O’Brien, John
Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET
title Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET
title_full Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET
title_fullStr Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET
title_full_unstemmed Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET
title_short Predict Disease Progression With Reaction Rate Equation Modeling of Multimodal MRI and PET
title_sort predict disease progression with reaction rate equation modeling of multimodal mri and pet
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187250/
https://www.ncbi.nlm.nih.gov/pubmed/30349473
http://dx.doi.org/10.3389/fnagi.2018.00306
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