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Brain architecture-based vulnerability to traumatic injury.
Rifkin, Jared A; Wu, Taotao; Rayfield, Adam C; Anderson, Erin D; Panzer, Matthew B; Meaney, David F.
Afiliação
  • Rifkin JA; Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, United States.
  • Wu T; Department of Mechanical and Aerospace Engineering, University of Virginia, Charlottesville, VA, United States.
  • Rayfield AC; Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, United States.
  • Anderson ED; Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, United States.
  • Panzer MB; Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, United States.
  • Meaney DF; Department of Mechanical and Aerospace Engineering, University of Virginia, Charlottesville, VA, United States.
Front Bioeng Biotechnol ; 10: 936082, 2022.
Article em En | MEDLINE | ID: mdl-36091446
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Bioeng Biotechnol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Bioeng Biotechnol Ano de publicação: 2022 Tipo de documento: Article