Chronic Neurodegeneration After Traumatic Brain Injury: Alzheimer Disease, Chronic Traumatic Encephalopathy, or Persistent Neuroinflammation?
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 suppo...
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description | 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). |
doi_str_mv | 10.1007/s13311-014-0319-5 |
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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).</description><identifier>ISSN: 1933-7213</identifier><identifier>ISSN: 1878-7479</identifier><identifier>EISSN: 1878-7479</identifier><identifier>DOI: 10.1007/s13311-014-0319-5</identifier><identifier>PMID: 25421001</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>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</subject><ispartof>Neurotherapeutics, 2015-01, Vol.12 (1), p.143-150</ispartof><rights>The American Society for Experimental NeuroTherapeutics, Inc. 2014</rights><rights>The American Society for Experimental NeuroTherapeutics, Inc. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-4a162ec95aee694bd9737ef89cf588e24a7639144bf39e709995e643e4ebfb813</citedby><cites>FETCH-LOGICAL-c540t-4a162ec95aee694bd9737ef89cf588e24a7639144bf39e709995e643e4ebfb813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322076/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322076/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25421001$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Faden, Alan I.</creatorcontrib><creatorcontrib>Loane, David J.</creatorcontrib><title>Chronic Neurodegeneration After Traumatic Brain Injury: Alzheimer Disease, Chronic Traumatic Encephalopathy, or Persistent Neuroinflammation?</title><title>Neurotherapeutics</title><addtitle>Neurotherapeutics</addtitle><addtitle>Neurotherapeutics</addtitle><description>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).</description><subject>Alzheimer Disease - etiology</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Anesthesiology</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain Injuries - complications</subject><subject>Brain Injury, Chronic - etiology</subject><subject>Brain Injury, Chronic - pathology</subject><subject>Chronic traumatic encephalopathy</subject><subject>Cohort analysis</subject><subject>Dementia</subject><subject>Encephalitis - etiology</subject><subject>Encephalitis - pathology</subject><subject>Football</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Nerve Degeneration - etiology</subject><subject>Nerve Degeneration - pathology</subject><subject>Neurobiology</subject><subject>Neurodegeneration</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><subject>Original</subject><subject>Original Article</subject><subject>Pathology</subject><subject>Risk factors</subject><subject>Traumatic brain injury</subject><issn>1933-7213</issn><issn>1878-7479</issn><issn>1878-7479</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kc9u1DAQxi0Eou3CA3BBkbhwaMB_45gDaLsUqFQBh3K2HO9k41Vib-0EaXkH3hkvaUtB4uSR5zffN6MPoWcEvyIYy9eJMEZIiQkvMSOqFA_QMallXUou1cNcK8ZKSQk7QicpbTEWjKn6MTqigtOsQI7Rz1UXg3e2-AxTDGvYgIdoRhd8sWxHiMVVNNOQP2xxFo3zxYXfTnH_plj2PzpwQybeuwQmwWlxK_Vn5Nxb2HWmDzszdvvTIsTiK8Tk0gh-nC2db3szDL8t3z1Bj1rTJ3h68y7Qtw_nV6tP5eWXjxer5WVpBcdjyQ2pKFglDECleLNWkkloa2VbUddAuZEVU4TzpmUKJFZKCag4Aw5N29SELdDbWXc3NQOsbd4mml7vohtM3OtgnP67412nN-G75oxSnMUX6OWNQAzXE6RRDy5Z6HvjIUxJk0pwiXFVqYy--Afdhin6fN6BohWnmOFMkZmyMaQUob1bhmB9CFvPYesctj6ErUWeeX7_iruJ23QzQGcg5ZbfQLxn_V_VX9fQt8U</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Faden, Alan I.</creator><creator>Loane, David J.</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>Chronic Neurodegeneration After Traumatic Brain Injury: Alzheimer Disease, Chronic Traumatic Encephalopathy, or Persistent Neuroinflammation?</title><author>Faden, Alan I. ; Loane, David J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-4a162ec95aee694bd9737ef89cf588e24a7639144bf39e709995e643e4ebfb813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alzheimer Disease - etiology</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer's disease</topic><topic>Anesthesiology</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain Injuries - complications</topic><topic>Brain Injury, Chronic - etiology</topic><topic>Brain Injury, Chronic - pathology</topic><topic>Chronic traumatic encephalopathy</topic><topic>Cohort analysis</topic><topic>Dementia</topic><topic>Encephalitis - etiology</topic><topic>Encephalitis - pathology</topic><topic>Football</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Nerve Degeneration - etiology</topic><topic>Nerve Degeneration - pathology</topic><topic>Neurobiology</topic><topic>Neurodegeneration</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><topic>Original</topic><topic>Original Article</topic><topic>Pathology</topic><topic>Risk factors</topic><topic>Traumatic brain injury</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Faden, Alan I.</creatorcontrib><creatorcontrib>Loane, David J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurotherapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Faden, Alan I.</au><au>Loane, David J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic Neurodegeneration After Traumatic Brain Injury: Alzheimer Disease, Chronic Traumatic Encephalopathy, or Persistent Neuroinflammation?</atitle><jtitle>Neurotherapeutics</jtitle><stitle>Neurotherapeutics</stitle><addtitle>Neurotherapeutics</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>12</volume><issue>1</issue><spage>143</spage><epage>150</epage><pages>143-150</pages><issn>1933-7213</issn><issn>1878-7479</issn><eissn>1878-7479</eissn><abstract>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).</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>25421001</pmid><doi>10.1007/s13311-014-0319-5</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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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 |
title | Chronic Neurodegeneration After Traumatic Brain Injury: Alzheimer Disease, Chronic Traumatic Encephalopathy, or Persistent Neuroinflammation? |
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