Macroscopic modelling of Alzheimer’s disease: difficulties and challenges
In the context of Alzheimer’s disease (AD), in silico research aims at giving complementary and better insight into the complex mechanisms which determine the development of AD. One of its important aspects is the construction of macroscopic mathematical models which are the basis for numerical simu...
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| Format: | Article |
| Language: | English |
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Elsevier
2021-01-01
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| Series: | Brain Multiphysics |
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| Online Access: | http://www.sciencedirect.com/science/article/pii/S2666522021000204 |
| _version_ | 1798026696268447744 |
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| author | Michiel Bertsch Bruno Franchi Ashish Raj Maria Carla Tesi |
| author_facet | Michiel Bertsch Bruno Franchi Ashish Raj Maria Carla Tesi |
| author_sort | Michiel Bertsch |
| collection | DOAJ |
| description | In the context of Alzheimer’s disease (AD), in silico research aims at giving complementary and better insight into the complex mechanisms which determine the development of AD. One of its important aspects is the construction of macroscopic mathematical models which are the basis for numerical simulations. In this paper we discuss some of the general and fundamental difficulties of macroscopic modelling of AD. In addition we formulate a mathematical model in the case of a specific problem in an early stage of AD, namely the propagation of pathological τ protein from the entorhinal cortex to the hippocampal region. The main feature of this model consists in the representation of the brain through two superposed finite graphs, which have the same vertices (that, roughly speaking, can be thought as parcels of a brain atlas), but different edges. We call these graphs “proximity graph” and “connectivity graph”, respectively. The edges of the first graph take into account the distances of the vertices and the heterogeneity of the cerebral parenchyma, whereas the edges of the second graph represent the connections by white-matter fiber pathways between different structures. The diffusion of the proteins Aβ and τ are described through the Laplace operators on the graphs, whereas the phenomenon of aggregation of the proteins leading ultimately to senile plaques and neuro-fibrillar tangles (as already observed by A. Alzheimer in 1907) is modelled by means of the classical Smoluchowski aggregation system. Statement of significance: Alzheimer’s disease is a neurodegenerative disease leading to dementia with huge economic and social costs. Despite a fast growing amount of clinical data, there is no widely accepted medical treatment to stop or slow down AD. It is generally accepted that two proteins, beta amyloid and tau, play a key role in the progression of the disease, and the edge of the current biomedical research focuses on the interactions of the two proteins also in the perspective of the production of new effective drugs. In this context, flexible mathematical models may give better and deeper insight by testing different clinical hypotheses. |
| first_indexed | 2024-04-11T18:39:35Z |
| format | Article |
| id | doaj.art-435fc8de1a1a4f25b234d084cac3d614 |
| institution | Directory Open Access Journal |
| issn | 2666-5220 |
| language | English |
| last_indexed | 2024-04-11T18:39:35Z |
| publishDate | 2021-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Brain Multiphysics |
| spelling | doaj.art-435fc8de1a1a4f25b234d084cac3d6142022-12-22T04:09:03ZengElsevierBrain Multiphysics2666-52202021-01-012100040Macroscopic modelling of Alzheimer’s disease: difficulties and challengesMichiel Bertsch0Bruno Franchi1Ashish Raj2Maria Carla Tesi3Corresponding author at: Department of Mathematics, University of Roma “Tor Vergata”, Roma, Italy.; Department of Mathematics, University of Roma “Tor Vergata”, Roma, Italy; Istituto per le Applicazioni del Calcolo “M. Picone”, Consiglio Nazionale delle Ricerche, Roma, ItalyDepartment of Mathematics, University of Bologna, Bologna, ItalyDepartment of Radiology and Biomedical Imaging, and Department of Bio-Engineering University of California at San Francisco, USADepartment of Mathematics, University of Bologna, Bologna, ItalyIn the context of Alzheimer’s disease (AD), in silico research aims at giving complementary and better insight into the complex mechanisms which determine the development of AD. One of its important aspects is the construction of macroscopic mathematical models which are the basis for numerical simulations. In this paper we discuss some of the general and fundamental difficulties of macroscopic modelling of AD. In addition we formulate a mathematical model in the case of a specific problem in an early stage of AD, namely the propagation of pathological τ protein from the entorhinal cortex to the hippocampal region. The main feature of this model consists in the representation of the brain through two superposed finite graphs, which have the same vertices (that, roughly speaking, can be thought as parcels of a brain atlas), but different edges. We call these graphs “proximity graph” and “connectivity graph”, respectively. The edges of the first graph take into account the distances of the vertices and the heterogeneity of the cerebral parenchyma, whereas the edges of the second graph represent the connections by white-matter fiber pathways between different structures. The diffusion of the proteins Aβ and τ are described through the Laplace operators on the graphs, whereas the phenomenon of aggregation of the proteins leading ultimately to senile plaques and neuro-fibrillar tangles (as already observed by A. Alzheimer in 1907) is modelled by means of the classical Smoluchowski aggregation system. Statement of significance: Alzheimer’s disease is a neurodegenerative disease leading to dementia with huge economic and social costs. Despite a fast growing amount of clinical data, there is no widely accepted medical treatment to stop or slow down AD. It is generally accepted that two proteins, beta amyloid and tau, play a key role in the progression of the disease, and the edge of the current biomedical research focuses on the interactions of the two proteins also in the perspective of the production of new effective drugs. In this context, flexible mathematical models may give better and deeper insight by testing different clinical hypotheses.http://www.sciencedirect.com/science/article/pii/S2666522021000204Alzheimer’s diseaseAβ proteinτ ProteinGraphsSmoluchowski equation |
| spellingShingle | Michiel Bertsch Bruno Franchi Ashish Raj Maria Carla Tesi Macroscopic modelling of Alzheimer’s disease: difficulties and challenges Brain Multiphysics Alzheimer’s disease Aβ protein τ Protein Graphs Smoluchowski equation |
| title | Macroscopic modelling of Alzheimer’s disease: difficulties and challenges |
| title_full | Macroscopic modelling of Alzheimer’s disease: difficulties and challenges |
| title_fullStr | Macroscopic modelling of Alzheimer’s disease: difficulties and challenges |
| title_full_unstemmed | Macroscopic modelling of Alzheimer’s disease: difficulties and challenges |
| title_short | Macroscopic modelling of Alzheimer’s disease: difficulties and challenges |
| title_sort | macroscopic modelling of alzheimer s disease difficulties and challenges |
| topic | Alzheimer’s disease Aβ protein τ Protein Graphs Smoluchowski equation |
| url | http://www.sciencedirect.com/science/article/pii/S2666522021000204 |
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