Chronic Neurodegeneration After Traumatic Brain Injury: Alzheimer Disease, Chronic Traumatic Encephalopathy, or Persistent Neuroinflammation?

• Published in: Neurotherapeutics Vol. 12; no. 1; pp. 143 - 150
• Main Authors: Faden, Alan I., Loane, David J.
• Format: Journal Article
• Language: English
• Published: Boston Springer US 01.01.2015; Springer Nature B.V
• Subjects: Alzheimer Disease - etiology; Alzheimer Disease - pathology; Alzheimer's disease; Anesthesiology; Animals; Biomedical and Life Sciences; Biomedicine; Brain Injuries - complications; Brain Injury, Chronic - etiology; Brain Injury, Chronic - pathology; Chronic traumatic encephalopathy; Cohort analysis; Dementia; Encephalitis - etiology; Encephalitis - pathology; Football; Humans; Inflammation; Nerve Degeneration - etiology; Nerve Degeneration - pathology; Neurobiology; Neurodegeneration; Neurology; Neurosciences; Neurosurgery; Original; Original Article; Pathology; Risk factors; Traumatic brain injury; Traumatic brain injury; Concussion; Chronic traumatic encephalopathy; Neurodegeneration; Repetitive mild TBI; Alzheimer disease; Chronic traumatic brain inflammation; Microglial activation
• ISSN: 1933-7213; 1878-7479; 1878-7479
• DOI: 10.1007/s13311-014-0319-5

It has long been suggested that prior traumatic brain injury (TBI) increases the subsequent incidence of chronic neurodegenerative disorders, including Alzheimer disease, Parkinson disease, and amyotrophic lateral sclerosis. Among these, the association with Alzheimer disease has the strongest support. There is also a long-recognized association between repeated concussive insults and progressive cognitive decline or other neuropsychiatric abnormalities. The latter was first described in boxers as dementia pugilistica , and has received widespread recent attention in contact sports such as professional American football. The term chronic traumatic encephalopathy was coined to attempt to define a “specific” entity marked by neurobehavioral changes and the extensive deposition of phosphorylated tau protein. Nearly lost in the discussions of post-traumatic neurodegeneration after traumatic brain injury has been the role of sustained neuroinflammation, even though this association has been well established pathologically since the 1950s, and is strongly supported by subsequent preclinical and clinical studies. Manifested by extensive microglial and astroglial activation, such chronic traumatic brain inflammation may be the most important cause of post-traumatic neurodegeneration in terms of prevalence. Critically, emerging preclinical studies indicate that persistent neuroinflammation and associated neurodegeneration may be treatable long after the initiating insult(s).