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Differential Effects of Brain Disorders on Structural and Functional Connectivity

Different measures of brain connectivity can be defined based on neuroimaging read-outs, including structural and functional connectivity. Neurological and psychiatric conditions are often associated with abnormal connectivity, but comparing the effects of the disease on different types of connectiv...

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Autores principales: Vega-Pons, Sandro, Olivetti, Emanuele, Avesani, Paolo, Dodero, Luca, Gozzi, Alessandro, Bifone, Angelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221415/
https://www.ncbi.nlm.nih.gov/pubmed/28119556
http://dx.doi.org/10.3389/fnins.2016.00605
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author Vega-Pons, Sandro
Olivetti, Emanuele
Avesani, Paolo
Dodero, Luca
Gozzi, Alessandro
Bifone, Angelo
author_facet Vega-Pons, Sandro
Olivetti, Emanuele
Avesani, Paolo
Dodero, Luca
Gozzi, Alessandro
Bifone, Angelo
author_sort Vega-Pons, Sandro
collection PubMed
description Different measures of brain connectivity can be defined based on neuroimaging read-outs, including structural and functional connectivity. Neurological and psychiatric conditions are often associated with abnormal connectivity, but comparing the effects of the disease on different types of connectivity remains a challenge. In this paper, we address the problem of quantifying the relative effects of brain disease on structural and functional connectivity at a group level. Within the framework of a graph representation of connectivity, we introduce a kernel two-sample test as an effective method to assess the difference between the patients and control group. Moreover, we propose a common representation space for structural and functional connectivity networks, and a novel test statistics to quantitatively assess differential effects of the disease on different types of connectivity. We apply this approach to a dataset from BTBR mice, a murine model of Agenesis of the Corpus Callosum (ACC), a congenital disorder characterized by the absence of the main bundle of fibers connecting the two hemispheres. We used normo-callosal mice (B6) as a comparator. The application of the proposed methods to this data-set shows that the two types of connectivity can be successfully used to discriminate between BTBR and B6, meaning that both types of connectivity are affected by ACC. However, our novel test statistics shows that structural connectivity is significantly more affected than functional connectivity, consistent with the idea that functional connectivity has a robust topology that can tolerate substantial alterations in its structural connectivity substrate.
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spelling pubmed-52214152017-01-24 Differential Effects of Brain Disorders on Structural and Functional Connectivity Vega-Pons, Sandro Olivetti, Emanuele Avesani, Paolo Dodero, Luca Gozzi, Alessandro Bifone, Angelo Front Neurosci Neuroscience Different measures of brain connectivity can be defined based on neuroimaging read-outs, including structural and functional connectivity. Neurological and psychiatric conditions are often associated with abnormal connectivity, but comparing the effects of the disease on different types of connectivity remains a challenge. In this paper, we address the problem of quantifying the relative effects of brain disease on structural and functional connectivity at a group level. Within the framework of a graph representation of connectivity, we introduce a kernel two-sample test as an effective method to assess the difference between the patients and control group. Moreover, we propose a common representation space for structural and functional connectivity networks, and a novel test statistics to quantitatively assess differential effects of the disease on different types of connectivity. We apply this approach to a dataset from BTBR mice, a murine model of Agenesis of the Corpus Callosum (ACC), a congenital disorder characterized by the absence of the main bundle of fibers connecting the two hemispheres. We used normo-callosal mice (B6) as a comparator. The application of the proposed methods to this data-set shows that the two types of connectivity can be successfully used to discriminate between BTBR and B6, meaning that both types of connectivity are affected by ACC. However, our novel test statistics shows that structural connectivity is significantly more affected than functional connectivity, consistent with the idea that functional connectivity has a robust topology that can tolerate substantial alterations in its structural connectivity substrate. Frontiers Media S.A. 2017-01-09 /pmc/articles/PMC5221415/ /pubmed/28119556 http://dx.doi.org/10.3389/fnins.2016.00605 Text en Copyright © 2017 Vega-Pons, Olivetti, Avesani, Dodero, Gozzi and Bifone. 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) or licensor 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
Vega-Pons, Sandro
Olivetti, Emanuele
Avesani, Paolo
Dodero, Luca
Gozzi, Alessandro
Bifone, Angelo
Differential Effects of Brain Disorders on Structural and Functional Connectivity
title Differential Effects of Brain Disorders on Structural and Functional Connectivity
title_full Differential Effects of Brain Disorders on Structural and Functional Connectivity
title_fullStr Differential Effects of Brain Disorders on Structural and Functional Connectivity
title_full_unstemmed Differential Effects of Brain Disorders on Structural and Functional Connectivity
title_short Differential Effects of Brain Disorders on Structural and Functional Connectivity
title_sort differential effects of brain disorders on structural and functional connectivity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221415/
https://www.ncbi.nlm.nih.gov/pubmed/28119556
http://dx.doi.org/10.3389/fnins.2016.00605
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