4.3 Article

Post-traumatic neurodegeneration and chronic traumatic encephalopathy

期刊

MOLECULAR AND CELLULAR NEUROSCIENCE
卷 66, 期 -, 页码 81-90

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.mcn.2015.03.007

关键词

Traumatic brain injury; Chronic traumatic encephalopathy; Axonal injury; Brain trauma; Posttraumatic neurodegeneration; Motor neuron disease; Tau protein; Concussion; Blast and impact neurotrauma

资金

  1. Department of Veterans Affairs
  2. Veterans Affairs Biorepository [CSP 501]
  3. Translational Research Center for Traumatic Brain Injury and Stress Disorders (TRACTS) Veterans Affairs Rehabilitation Research and Development Traumatic Brain Injury Center of Excellence [B6796-C]
  4. National Institute of Neurological Diseases and Stroke [1U01NS086659-01]
  5. National Institute of Aging Boston University Alzheimer's Disease Center [P30AG13846, 0572063345-5]
  6. National Institute of Aging Boston University Framingham Heart Study [R01 [AG1649]]
  7. Sports Legacy Institute
  8. National Operating Committee on Standards for Athletic Equipment
  9. National Football League
  10. Andlinger Foundation
  11. WWE

向作者/读者索取更多资源

Traumatic brain injury (TBI) is a leading cause of mortality and morbidity around the world. Concussive and subconcussive forms of closed-head injury due to impact or blast neurotrauma represent the most common types of TBI in civilian and military settings. It is becoming increasingly evident that TBI can lead to persistent, long-term debilitating effects, and in some cases, progressive neurodegeneration and chronic traumatic encephalopathy (CTE). The epidemiological literature suggests that a single moderate-to-severe TBI may be associated with accelerated neurodegeneration and increased risk of Alzheimer's disease, Parkinson's disease, or motor neuron disease. However, the pathologic phenotype of these post-traumatic neurodegenerations is largely unknown and there may be pathobiological differences between post-traumatic disease and the corresponding sporadic disorder. By contrast, the pathology of CTE is increasingly well known and is characterized by a distinctive pattern of progressive brain atrophy and accumulation of hyperphosphorylated tau neurofibrillary and glial tangles, dystrophic neurites, 43 kDa TAR DNA-binding protein (TDP-43) neuronal and glial aggregates, microvasculopathy, myelinated axonopathy, neuroinflammation, and white matter degeneration. Clinically, CTE is associated with behavioral changes, executive dysfunction, memory deficits, and cognitive impairments that begin insidiously and most often progress slowly over decades. Although research on the long-term effects of TBI is advancing quickly, the incidence and prevalence of post-traumatic neurodegeneration and CTE are unknown. Critical knowledge gaps include elucidation of pathogenic mechanisms, identification of genetic risk factors, and clarification of relevant variables-including age at exposure to trauma, history of prior and subsequent head trauma, substance use, gender, stress, and comorbidities-all of which may contribute to risk profiles and the development of post-traumatic neurodegeneration and CTE. This article is part of a Special Issue entitled 'Traumatic Brain Injury'. Published by Elsevier Inc.

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