Brain architecture-based vulnerability to traumatic injury

The white matter tracts forming the intricate wiring of the brain are subject-specific; this heterogeneity can complicate studies of brain function and disease. Here we collapse tractography data from the Human Connectome Project (HCP) into structural connectivity (SC) matrices and identify groups o...

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Main Authors: Jared A. Rifkin, Taotao Wu, Adam C. Rayfield, Erin D. Anderson, Matthew B. Panzer, David F. Meaney
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2022.936082/full
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author Jared A. Rifkin
Jared A. Rifkin
Taotao Wu
Adam C. Rayfield
Erin D. Anderson
Matthew B. Panzer
Matthew B. Panzer
David F. Meaney
David F. Meaney
author_facet Jared A. Rifkin
Jared A. Rifkin
Taotao Wu
Adam C. Rayfield
Erin D. Anderson
Matthew B. Panzer
Matthew B. Panzer
David F. Meaney
David F. Meaney
author_sort Jared A. Rifkin
collection DOAJ
description The white matter tracts forming the intricate wiring of the brain are subject-specific; this heterogeneity can complicate studies of brain function and disease. Here we collapse tractography data from the Human Connectome Project (HCP) into structural connectivity (SC) matrices and identify groups of similarly wired brains from both sexes. To characterize the significance of these architectural groupings, we examined how similarly wired brains led to distinct groupings of neural activity dynamics estimated with Kuramoto oscillator models (KMs). We then lesioned our networks to simulate traumatic brain injury (TBI) and finally we tested whether these distinct architecture groups’ dynamics exhibited differing responses to simulated TBI. At each of these levels we found that brain structure, simulated dynamics, and injury susceptibility were all related to brain grouping. We found four primary brain architecture groupings (two male and two female), with similar architectures appearing across both sexes. Among these groupings of brain structure, two architecture types were significantly more vulnerable than the remaining two architecture types to lesions. These groups suggest that mesoscale brain architecture types exist, and these architectural differences may contribute to differential risks to TBI and clinical outcomes across the population.
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spelling doaj.art-fc80eea7e0c7493a99ff8c9fe543adab2022-12-22T02:15:35ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852022-08-011010.3389/fbioe.2022.936082936082Brain architecture-based vulnerability to traumatic injuryJared A. Rifkin0Jared A. Rifkin1Taotao Wu2Adam C. Rayfield3Erin D. Anderson4Matthew B. Panzer5Matthew B. Panzer6David F. Meaney7David F. Meaney8Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, United StatesDepartment of Mechanical and Aerospace Engineering, University of Virginia, Charlottesville, VA, United StatesDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, United StatesDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, United StatesDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, United StatesDepartment of Mechanical and Aerospace Engineering, University of Virginia, Charlottesville, VA, United StatesDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, United StatesDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, United StatesDepartment of Neurosurgery, University of Pennsylvania, Philadelphia, PA, United StatesThe white matter tracts forming the intricate wiring of the brain are subject-specific; this heterogeneity can complicate studies of brain function and disease. Here we collapse tractography data from the Human Connectome Project (HCP) into structural connectivity (SC) matrices and identify groups of similarly wired brains from both sexes. To characterize the significance of these architectural groupings, we examined how similarly wired brains led to distinct groupings of neural activity dynamics estimated with Kuramoto oscillator models (KMs). We then lesioned our networks to simulate traumatic brain injury (TBI) and finally we tested whether these distinct architecture groups’ dynamics exhibited differing responses to simulated TBI. At each of these levels we found that brain structure, simulated dynamics, and injury susceptibility were all related to brain grouping. We found four primary brain architecture groupings (two male and two female), with similar architectures appearing across both sexes. Among these groupings of brain structure, two architecture types were significantly more vulnerable than the remaining two architecture types to lesions. These groups suggest that mesoscale brain architecture types exist, and these architectural differences may contribute to differential risks to TBI and clinical outcomes across the population.https://www.frontiersin.org/articles/10.3389/fbioe.2022.936082/fullKuramoto modelstructural connectivitybrain networkstraumatic brain injurylesions
spellingShingle Jared A. Rifkin
Jared A. Rifkin
Taotao Wu
Adam C. Rayfield
Erin D. Anderson
Matthew B. Panzer
Matthew B. Panzer
David F. Meaney
David F. Meaney
Brain architecture-based vulnerability to traumatic injury
Frontiers in Bioengineering and Biotechnology
Kuramoto model
structural connectivity
brain networks
traumatic brain injury
lesions
title Brain architecture-based vulnerability to traumatic injury
title_full Brain architecture-based vulnerability to traumatic injury
title_fullStr Brain architecture-based vulnerability to traumatic injury
title_full_unstemmed Brain architecture-based vulnerability to traumatic injury
title_short Brain architecture-based vulnerability to traumatic injury
title_sort brain architecture based vulnerability to traumatic injury
topic Kuramoto model
structural connectivity
brain networks
traumatic brain injury
lesions
url https://www.frontiersin.org/articles/10.3389/fbioe.2022.936082/full
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