• Amber L Nolan, Cathrine Petersen, Diego Iacono, Christine L Mac Donald, Pratik Mukherjee, Andre van der Kouwe, Sonia Jain, Allison Stevens, Bram R Diamond, Ruopeng Wang, Amy J Markowitz, Bruce Fischl, Daniel P Perl, Geoffrey T Manley, C Dirk Keene, Ramon Diaz-Arrastia, Brian L Edlow, and TRACK-TBI Investigators.
• Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
• J. Neurotrauma. 2021 Jun 15; 38 (12): 162016311620-1631.

AbstractDiffusion tractography magnetic resonance imaging (MRI) can infer changes in network connectivity in patients with traumatic brain injury (TBI), but the pathological substrates of disconnected tracts have not been well defined because of a lack of high-resolution imaging with histopathological validation. We developed an ex vivo MRI protocol to analyze tract terminations at 750-μm isotropic resolution, followed by histopathological evaluation of white matter pathology, and applied these methods to a 60-year-old man who died 26 days after TBI. Analysis of 74 cerebral hemispheric white matter regions revealed a heterogeneous distribution of tract disruptions. Associated histopathology identified variable white matter injury with patchy deposition of amyloid precursor protein (APP), loss of neurofilament-positive axonal processes, myelin dissolution, astrogliosis, microgliosis, and perivascular hemosiderin-laden macrophages. Multiple linear regression revealed that tract disruption strongly correlated with the density of APP-positive axonal swellings and neurofilament loss. Ex vivo diffusion MRI can detect tract disruptions in the human brain that reflect axonal injury.

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