Post-traumatic neurodegeneration and chronic traumatic encephalopathy
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...
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Veröffentlicht in: | Molecular and cellular neuroscience 2015-05, Vol.66 (Pt B), p.81-90 |
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description | 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, 43kDa 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'. |
doi_str_mv | 10.1016/j.mcn.2015.03.007 |
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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, 43kDa 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'.</description><identifier>ISSN: 1044-7431</identifier><identifier>EISSN: 1095-9327</identifier><identifier>DOI: 10.1016/j.mcn.2015.03.007</identifier><identifier>PMID: 25758552</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Axonal injury ; Behavior - physiology ; Blast and impact neurotrauma ; Brain - metabolism ; Brain - pathology ; Brain Injury, Chronic - metabolism ; Brain Injury, Chronic - physiopathology ; Brain trauma ; Chronic traumatic encephalopathy ; Concussion ; DNA-Binding Proteins - metabolism ; Humans ; Motor neuron disease ; Neurodegenerative Diseases - etiology ; Neurodegenerative Diseases - metabolism ; Neurodegenerative Diseases - physiopathology ; Neurons - metabolism ; Posttraumatic neurodegeneration ; Tau protein ; Traumatic brain injury</subject><ispartof>Molecular and cellular neuroscience, 2015-05, Vol.66 (Pt B), p.81-90</ispartof><rights>2015</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-dadc3a2ba7575c7a12607611638ea1035ae2deded715339e54f68cf9a288831f3</citedby><cites>FETCH-LOGICAL-c423t-dadc3a2ba7575c7a12607611638ea1035ae2deded715339e54f68cf9a288831f3</cites><orcidid>0000-0003-3691-9513 ; 0000-0001-6954-4477</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1044743115000366$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25758552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Daneshvar, Daniel H.</creatorcontrib><creatorcontrib>Goldstein, Lee E.</creatorcontrib><creatorcontrib>Kiernan, Patrick T.</creatorcontrib><creatorcontrib>Stein, Thor D.</creatorcontrib><creatorcontrib>McKee, Ann C.</creatorcontrib><title>Post-traumatic neurodegeneration and chronic traumatic encephalopathy</title><title>Molecular and cellular neuroscience</title><addtitle>Mol Cell Neurosci</addtitle><description>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, 43kDa 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'.</description><subject>Animals</subject><subject>Axonal injury</subject><subject>Behavior - physiology</subject><subject>Blast and impact neurotrauma</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Brain Injury, Chronic - metabolism</subject><subject>Brain Injury, Chronic - physiopathology</subject><subject>Brain trauma</subject><subject>Chronic traumatic encephalopathy</subject><subject>Concussion</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Humans</subject><subject>Motor neuron disease</subject><subject>Neurodegenerative Diseases - etiology</subject><subject>Neurodegenerative Diseases - metabolism</subject><subject>Neurodegenerative Diseases - physiopathology</subject><subject>Neurons - metabolism</subject><subject>Posttraumatic neurodegeneration</subject><subject>Tau protein</subject><subject>Traumatic brain injury</subject><issn>1044-7431</issn><issn>1095-9327</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQhi0EolD4ASyoI0uCP2I7EROqyodUCQaYLde-0FSJXewEqf8eRy2wIQ9n-Z57T34QuiI4J5iI203eGZdTTHiOWY6xPEJnBFc8qxiVx-O9KDJZMDJB5zFuMMacVuwUTSiXvOScnqHFq4991gc9dLpvzMzBELyFD3AQ0oN3M-3szKyDd6n7x4EzsF3r1m91v95doJNatxEuD3WK3h8Wb_OnbPny-Dy_X2amoKzPrLaGabrSMu03UhMqsBSECFaCJphxDdRCOpJwxirgRS1KU1ealmXJSM2m6Gafuw3-c4DYq66JBtpWO_BDVERiKjgTpUgo2aMm-BgD1Gobmk6HnSJYjfbURiV7arSnMFPJXpq5PsQPqw7s78SPrgTc7QFIn_xqIKhomlGFbQKYXlnf_BP_DabbgHQ</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Daneshvar, Daniel H.</creator><creator>Goldstein, Lee E.</creator><creator>Kiernan, Patrick T.</creator><creator>Stein, Thor D.</creator><creator>McKee, Ann C.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3691-9513</orcidid><orcidid>https://orcid.org/0000-0001-6954-4477</orcidid></search><sort><creationdate>20150501</creationdate><title>Post-traumatic neurodegeneration and chronic traumatic encephalopathy</title><author>Daneshvar, Daniel H. ; Goldstein, Lee E. ; Kiernan, Patrick T. ; Stein, Thor D. ; McKee, Ann C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-dadc3a2ba7575c7a12607611638ea1035ae2deded715339e54f68cf9a288831f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Axonal injury</topic><topic>Behavior - physiology</topic><topic>Blast and impact neurotrauma</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Brain Injury, Chronic - metabolism</topic><topic>Brain Injury, Chronic - physiopathology</topic><topic>Brain trauma</topic><topic>Chronic traumatic encephalopathy</topic><topic>Concussion</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Humans</topic><topic>Motor neuron disease</topic><topic>Neurodegenerative Diseases - etiology</topic><topic>Neurodegenerative Diseases - metabolism</topic><topic>Neurodegenerative Diseases - physiopathology</topic><topic>Neurons - metabolism</topic><topic>Posttraumatic neurodegeneration</topic><topic>Tau protein</topic><topic>Traumatic brain injury</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Daneshvar, Daniel H.</creatorcontrib><creatorcontrib>Goldstein, Lee E.</creatorcontrib><creatorcontrib>Kiernan, Patrick T.</creatorcontrib><creatorcontrib>Stein, Thor D.</creatorcontrib><creatorcontrib>McKee, Ann C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Daneshvar, Daniel H.</au><au>Goldstein, Lee E.</au><au>Kiernan, Patrick T.</au><au>Stein, Thor D.</au><au>McKee, Ann C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Post-traumatic neurodegeneration and chronic traumatic encephalopathy</atitle><jtitle>Molecular and cellular neuroscience</jtitle><addtitle>Mol Cell Neurosci</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>66</volume><issue>Pt B</issue><spage>81</spage><epage>90</epage><pages>81-90</pages><issn>1044-7431</issn><eissn>1095-9327</eissn><abstract>Traumatic brain injury (TBI) is a leading cause of mortality and morbidity around the world. 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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, 43kDa 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. 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subjects | Animals Axonal injury Behavior - physiology Blast and impact neurotrauma Brain - metabolism Brain - pathology Brain Injury, Chronic - metabolism Brain Injury, Chronic - physiopathology Brain trauma Chronic traumatic encephalopathy Concussion DNA-Binding Proteins - metabolism Humans Motor neuron disease Neurodegenerative Diseases - etiology Neurodegenerative Diseases - metabolism Neurodegenerative Diseases - physiopathology Neurons - metabolism Posttraumatic neurodegeneration Tau protein Traumatic brain injury |
title | Post-traumatic neurodegeneration and chronic traumatic encephalopathy |
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