Cited by 36Traumatic Brain Injury ResearchDementia and Cognitive Impairment ResearchAlzheimer's disease research and treatments

Psychiatric phenotypes in chronic traumatic encephalopathy

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Mahar, Ian, Alosco, Michael L., McKee, Ann C.·2017·Neuroscience & Biobehavioral Reviews

Abstract

Chronic traumatic encephalopathy (CTE) is a neurodegenerative disorder involving cognitive, motor, and psychiatrically-relevant symptoms resulting from repetitive head impacts. Psychiatric phenotypes of CTE, including depression and suicidality, present particular challenges for CTE research, given that the diagnosis requires postmortem neuropathological examination. The pathognomonic lesion of CTE is the perivascular accumulation of hyperphosphorylated tau (ptau) protein at the depths of cortical sulci. These lesions are found in the earliest disease stages, and with advancing pathological severity, ptau deposition occurs in widespread brain regions in a four-stage scheme of severity. We review the psychiatric phenotypes of individuals neuropathologically diagnosed with CTE, and suggest that earlier CTE stages hold particular interest for psychiatric CTE research. In the early CTE stages, there is ptau pathology in frontal cortex and axonal loss in the frontal white matter, followed by progressive ptau neurofibrillary degeneration in the amygdala and hippocampus. Neuropathological changes in the frontal and medial temporal lobes may underlie psychiatric phenotypes. Additional insight into the association between CTE pathology and psychiatric sequelae may come from advancements in in vivo methods of CTE detection. Further epidemiological, clinical, and postmortem studies are needed to validate the nature of psychiatric sequelae in CTE.

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Crossref · 10.1016/j.neubiorev.2017.08.023

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  • CTE is described clinically by a set of non-specific but severe symptoms including depression, anxiety, motor dysfunction, aggression, irritability, memory loss, and suicidality.

    “However, CTE is described clinically by a set of non-specific but yet severe symptoms including depression, anxiety, motor dysfunction, aggression, irritability, memory loss, and suicidality [4, 68, 94].”

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References 109 · Cited by 36

Authors
Mahar, I., Alosco, M. L., & McKee, A. C.
Affiliations
Boston University (US)
Corresponding author
McKee, Ann C.
Venue
Neuroscience & Biobehavioral Reviews
Publisher
Elsevier BV
Published
2017-12
Volume
83
Pages
622-630
ISSN
0149-7634 (ISSN-L)
OpenAlex
W2751183703
Cited by
36
References
109
Citations by year
2026: 1 · 2025: 2 · 2024: 5 · 2023: 1 · 2022: 4 · 2021: 3 · 2020: 6 · 2019: 9 · 2018: 5
FWCI
0.72
Type
journal article
Language
en
Open access
Locations
  • Neuroscience & Biobehavioral Reviews (acceptedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (F32NS096803-01)
  • Department of Veterans Affairs
  • Veterans Health Administration
  • Clinical Sciences Research and Development Merit Award (I01-CX001038)
  • Alzheimer’s Association (NIRG-305779)
  • National Institute of Aging (1RF1AG054156-01)
  • National Institute of Neurological Disorders and Stroke
  • National Institute of Biomedical Imaging and Bioengineering (U01NS086659-01)
  • National Institute of Aging Boston University AD Center (P30AG13846, 0572063345-5)
  • Department of Defense Peer Reviewed Alzheimer’s Research Program (#13267017)
  • National Heart, Lung, and Blood Institute, Framingham Heart Study (#N01-HC-25195, R01AG08122)
  • NINDS (1F32NS096803-01)
  • Concussion Legacy Foundation
  • Andlinger Foundation
  • National Football League
  • WWE
Topics
  • Health Sciences › Medicine › Epidemiology › Traumatic Brain Injury Research
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
Keywords
chronic traumatic encephalopathy, psychiatric phenotypes, depression, suicidality, hyperphosphorylated tau, neurofibrillary degeneration, repetitive head impacts, frontal cortex, amygdala, hippocampus, medial temporal lobe, axonal loss
MeSH terms
Chronic Traumatic Encephalopathy, Brain, Humans, Phenotype, Psychotic Disorders, Suicide, Neurofibrillary Tangles, tau Proteins

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