Abstract

Traumatic brain injury (TBI) has been increasingly accepted as a major external risk factor for neurodegenerative morbidity and mortality. Recent evidence indicates that the resultant chronic neurobiological sequelae following head trauma may, at least in part, contribute to a pathologically distinct disease known as Chronic Traumatic Encephalopathy (CTE). The clinical manifestation of CTE is variable, but the symptoms of this progressive disease include impaired memory and cognition, affective disorders (i.e., impulsivity, aggression, depression, suicidality, etc.), and diminished motor control. Notably, mounting evidence suggests that the pathology contributing to CTE may be caused by repetitive exposure to subconcussive hits to the head, even in those with no history of a clinically evident head injury. Given the millions of athletes and military personnel with potential exposure to repetitive subconcussive insults and TBI, CTE represents an important public health issue. However, the incidence rates and pathological mechanisms are still largely unknown, primarily due to the fact that there is no in vivo diagnostic tool. The primary objective of this manuscript is to address this limitation and discuss potential neuroimaging modalities that may be capable of diagnosing CTE in vivo through the detection of tau and other known pathological features. Additionally, we will discuss the challenges of TBI research, outline the known pathology of CTE (with an emphasis on Tau), review current neuroimaging modalities to assess the potential routes for in vivo diagnosis, and discuss the future directions of CTE research.

Highlights

  • There has been a recent explosion of research focused on improving the diagnosis and treatment of Traumatic Brain Injury (TBI)

  • 11C-Pittsburgh Compound B (PiB) stayed at the control level, but there was increased retention of 11C-PBB3 in the basal ganglia. This indicates that 11C-PBB3 is specific to Tau, but it might bind to conformations other than what is expected in Chronic Traumatic Encephalopathy (CTE) and Alzheimer’s disease (AD) populations (Maruyama et al, 2013)

  • When a reliable and effective radiopharmaceutical is available for P-Tau, Positron Emission Tomography (PET) will be a vital tool for researchers to uncover the underlying pathological processes of CTE

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Summary

Introduction

There has been a recent explosion of research focused on improving the diagnosis and treatment of Traumatic Brain Injury (TBI). This Tau distribution in CTE may match the biomechanics of head injuries since there is speculation that the depths of the sulci are areas of stress concentration for shear forces given that athletes of contact sports experience frequent high-intensity impacts on the crown of their helmets, which corresponds to pathological findings in the superior and dorsal-lateral frontal lobes (Hof et al, 1992; Cloots et al, 2013; McKee et al, 2014) This region is one in which functional impairments were observed via fMRI in a group of football players (Talavage et al, 2014). This indicates that 11C-PBB3 is specific to Tau, but it might bind to conformations other than what is expected in CTE and AD populations (Maruyama et al, 2013)

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