Brain chains as topological signatures for Alzheimer’s disease

Topology is providing new insights for neuroscience. For instance, graphs, simplicial complexes, directed graphs, flag complexes, persistent homology and convex covers have been used to study functional brain networks, synaptic connectivity, and hippocampal place cell codes. We propose a topological...

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Main Authors: Goodbrake, C, Beers, D, Thompson, TB, Harrington, HA, Goriely, A
格式: Journal article
語言:English
出版: Springer 2024
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author Goodbrake, C
Beers, D
Thompson, TB
Harrington, HA
Goriely, A
author_facet Goodbrake, C
Beers, D
Thompson, TB
Harrington, HA
Goriely, A
author_sort Goodbrake, C
collection OXFORD
description Topology is providing new insights for neuroscience. For instance, graphs, simplicial complexes, directed graphs, flag complexes, persistent homology and convex covers have been used to study functional brain networks, synaptic connectivity, and hippocampal place cell codes. We propose a topological framework to study the evolution of Alzheimer’s disease, the most common neurodegenerative disease. The modeling of this disease starts with the representation of the brain connectivity as a graph and the seeding of a toxic protein in a specific region represented by a vertex. Over time, the accumulation of toxic proteins at vertices and their propagation along edges are modeled by a dynamical system on this graph. These dynamics provide an order on the edges of the graph according to the damage created by high concentrations of proteins. This sequence of edges defines a filtration of the graph. We consider different filtrations given by different disease seeding locations. To study these filtrations we propose a new combinatorial and topological method. A filtration defines a maximal chain in the partially ordered set of spanning subgraphs ordered by inclusion. To identify similar graphs, and define a topological signature, we quotient this poset by graph homotopy equivalence, which gives maximal chains in a smaller poset. We provide an algorithm to compute this direct quotient without computing all subgraphs and then propose bounds on the total number of graphs up to homotopy equivalence. To compare the maximal chains generated by this method, we extend Kendall’s <i>d<sub>K</sub></i> metric for permutations to more general graded posets and establish bounds for this metric. We then demonstrate the utility of this framework on actual brain graphs by studying the dynamics of tau proteins on the structural connectome. We show that the proposed topological brain chain equivalence classes distinguish different simulated subtypes of Alzheimer’s disease.
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spelling oxford-uuid:29cd801d-9e47-4526-b3ed-65e5d690fe112024-11-20T09:27:10ZBrain chains as topological signatures for Alzheimer’s diseaseJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:29cd801d-9e47-4526-b3ed-65e5d690fe11EnglishSymplectic ElementsSpringer2024Goodbrake, CBeers, DThompson, TBHarrington, HAGoriely, ATopology is providing new insights for neuroscience. For instance, graphs, simplicial complexes, directed graphs, flag complexes, persistent homology and convex covers have been used to study functional brain networks, synaptic connectivity, and hippocampal place cell codes. We propose a topological framework to study the evolution of Alzheimer’s disease, the most common neurodegenerative disease. The modeling of this disease starts with the representation of the brain connectivity as a graph and the seeding of a toxic protein in a specific region represented by a vertex. Over time, the accumulation of toxic proteins at vertices and their propagation along edges are modeled by a dynamical system on this graph. These dynamics provide an order on the edges of the graph according to the damage created by high concentrations of proteins. This sequence of edges defines a filtration of the graph. We consider different filtrations given by different disease seeding locations. To study these filtrations we propose a new combinatorial and topological method. A filtration defines a maximal chain in the partially ordered set of spanning subgraphs ordered by inclusion. To identify similar graphs, and define a topological signature, we quotient this poset by graph homotopy equivalence, which gives maximal chains in a smaller poset. We provide an algorithm to compute this direct quotient without computing all subgraphs and then propose bounds on the total number of graphs up to homotopy equivalence. To compare the maximal chains generated by this method, we extend Kendall’s <i>d<sub>K</sub></i> metric for permutations to more general graded posets and establish bounds for this metric. We then demonstrate the utility of this framework on actual brain graphs by studying the dynamics of tau proteins on the structural connectome. We show that the proposed topological brain chain equivalence classes distinguish different simulated subtypes of Alzheimer’s disease.
spellingShingle Goodbrake, C
Beers, D
Thompson, TB
Harrington, HA
Goriely, A
Brain chains as topological signatures for Alzheimer’s disease
title Brain chains as topological signatures for Alzheimer’s disease
title_full Brain chains as topological signatures for Alzheimer’s disease
title_fullStr Brain chains as topological signatures for Alzheimer’s disease
title_full_unstemmed Brain chains as topological signatures for Alzheimer’s disease
title_short Brain chains as topological signatures for Alzheimer’s disease
title_sort brain chains as topological signatures for alzheimer s disease
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AT beersd brainchainsastopologicalsignaturesforalzheimersdisease
AT thompsontb brainchainsastopologicalsignaturesforalzheimersdisease
AT harringtonha brainchainsastopologicalsignaturesforalzheimersdisease
AT gorielya brainchainsastopologicalsignaturesforalzheimersdisease