Association of glial tau pathology and LATE-NC in the ageing brain

Ageing-related pathologies of the brain include neurofibrillary tangles, argyrophilic grains, ageing-related tau astrogliopathy (ARTAG), limbic-predominant age-related TDP-43 encephalopathy-neuropathological change (LATE-NC), vascular pathology and corpora amylacea. This study used an unbiased appro...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurobiology of aging 2022-11, Vol.119, p.77-88
Hauptverfasser: Forrest, Shelley L., Wagner, Stephanie, Kim, Ain, Kovacs, Gabor G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 88
container_issue
container_start_page 77
container_title Neurobiology of aging
container_volume 119
creator Forrest, Shelley L.
Wagner, Stephanie
Kim, Ain
Kovacs, Gabor G.
description Ageing-related pathologies of the brain include neurofibrillary tangles, argyrophilic grains, ageing-related tau astrogliopathy (ARTAG), limbic-predominant age-related TDP-43 encephalopathy-neuropathological change (LATE-NC), vascular pathology and corpora amylacea. This study used an unbiased approach to evaluate a broad range of pathologies in an unselected European community-dwelling ageing cohort of 101 individuals (77–90 years). Pathological alterations observed included neurofibrillary tangles and corpora amylacea in all cases, ARTAG (79%), Thal amyloid−β phase >1 (60%), cerebral amyloid angiopathy (39%), Lewy bodies (22%), LATE-NC (21%), oligodendroglial tau-positive coiled bodies (33%), and argyrophilic grains (15%). We demonstrate association of LATE-NC with the previously unappreciated age-related tau oligodendrogliopathy (ARTOG) and highlight the association of LATE-NC with various ARTAG types pointing toward common pathogenic aspects. Only neurofibrillary tangles and LATE-NC were associated with cognitive decline. This study broadens the spectrum of age-related brain pathologies and highlights a novel ageing-related tau pathology in oligodendroglia. Results from this study suggest overlapping pathogenic mechanisms between LATE-NC and glial tau pathologies in the medial temporal lobe.
doi_str_mv 10.1016/j.neurobiolaging.2022.07.010
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2703986149</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S019745802200166X</els_id><sourcerecordid>2703986149</sourcerecordid><originalsourceid>FETCH-LOGICAL-c363t-6a855449591e1f586f0b23ffb38026171faf734843eb52768948fc9a4bb5659b3</originalsourceid><addsrcrecordid>eNqNkLtOwzAARS0EEqXwDx4YWBLs-BmJpVQtIFWwlNmyXTt1lcbFTpD696QqCxvTXe5D9wBwj1GJEeaPu7JzQ4omxFY3oWvKClVViUSJMLoAE8yYLDCtxSWYIFyLgjKJrsFNzjuEkKCCT8DzLOdog-5D7GD0sGmDbmGvB3jQ_Ta2sTlC3W3garZeFO9zGDrYbx3UjRv3oEk6dLfgyus2u7tfnYLP5WI9fy1WHy9v89mqsISTvuBaMkZpzWrssGeSe2Qq4r0hElUcC-y1F4RKSpxhleCyptLbWlNjGGe1IVPwcO49pPg1uNyrfcjWta3uXByyqgQiteTj4dH6dLbaFHNOzqtDCnudjgojdUKnduovOnVCp5BQI7oxvjzH3XjnO7iksg2us24TkrO92sTwv6IfJjl-Wg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2703986149</pqid></control><display><type>article</type><title>Association of glial tau pathology and LATE-NC in the ageing brain</title><source>Elsevier ScienceDirect Journals</source><creator>Forrest, Shelley L. ; Wagner, Stephanie ; Kim, Ain ; Kovacs, Gabor G.</creator><creatorcontrib>Forrest, Shelley L. ; Wagner, Stephanie ; Kim, Ain ; Kovacs, Gabor G.</creatorcontrib><description>Ageing-related pathologies of the brain include neurofibrillary tangles, argyrophilic grains, ageing-related tau astrogliopathy (ARTAG), limbic-predominant age-related TDP-43 encephalopathy-neuropathological change (LATE-NC), vascular pathology and corpora amylacea. This study used an unbiased approach to evaluate a broad range of pathologies in an unselected European community-dwelling ageing cohort of 101 individuals (77–90 years). Pathological alterations observed included neurofibrillary tangles and corpora amylacea in all cases, ARTAG (79%), Thal amyloid−β phase &gt;1 (60%), cerebral amyloid angiopathy (39%), Lewy bodies (22%), LATE-NC (21%), oligodendroglial tau-positive coiled bodies (33%), and argyrophilic grains (15%). We demonstrate association of LATE-NC with the previously unappreciated age-related tau oligodendrogliopathy (ARTOG) and highlight the association of LATE-NC with various ARTAG types pointing toward common pathogenic aspects. Only neurofibrillary tangles and LATE-NC were associated with cognitive decline. This study broadens the spectrum of age-related brain pathologies and highlights a novel ageing-related tau pathology in oligodendroglia. Results from this study suggest overlapping pathogenic mechanisms between LATE-NC and glial tau pathologies in the medial temporal lobe.</description><identifier>ISSN: 0197-4580</identifier><identifier>EISSN: 1558-1497</identifier><identifier>DOI: 10.1016/j.neurobiolaging.2022.07.010</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>Ageing ; ARTAG ; Limbic Age-related TDP-43 Encephalopathy-neuropathological change ; Mixed pathology ; Oligodendroglia ; Tau</subject><ispartof>Neurobiology of aging, 2022-11, Vol.119, p.77-88</ispartof><rights>2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-6a855449591e1f586f0b23ffb38026171faf734843eb52768948fc9a4bb5659b3</citedby><cites>FETCH-LOGICAL-c363t-6a855449591e1f586f0b23ffb38026171faf734843eb52768948fc9a4bb5659b3</cites><orcidid>0000-0003-3841-5511</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S019745802200166X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids></links><search><creatorcontrib>Forrest, Shelley L.</creatorcontrib><creatorcontrib>Wagner, Stephanie</creatorcontrib><creatorcontrib>Kim, Ain</creatorcontrib><creatorcontrib>Kovacs, Gabor G.</creatorcontrib><title>Association of glial tau pathology and LATE-NC in the ageing brain</title><title>Neurobiology of aging</title><description>Ageing-related pathologies of the brain include neurofibrillary tangles, argyrophilic grains, ageing-related tau astrogliopathy (ARTAG), limbic-predominant age-related TDP-43 encephalopathy-neuropathological change (LATE-NC), vascular pathology and corpora amylacea. This study used an unbiased approach to evaluate a broad range of pathologies in an unselected European community-dwelling ageing cohort of 101 individuals (77–90 years). Pathological alterations observed included neurofibrillary tangles and corpora amylacea in all cases, ARTAG (79%), Thal amyloid−β phase &gt;1 (60%), cerebral amyloid angiopathy (39%), Lewy bodies (22%), LATE-NC (21%), oligodendroglial tau-positive coiled bodies (33%), and argyrophilic grains (15%). We demonstrate association of LATE-NC with the previously unappreciated age-related tau oligodendrogliopathy (ARTOG) and highlight the association of LATE-NC with various ARTAG types pointing toward common pathogenic aspects. Only neurofibrillary tangles and LATE-NC were associated with cognitive decline. This study broadens the spectrum of age-related brain pathologies and highlights a novel ageing-related tau pathology in oligodendroglia. Results from this study suggest overlapping pathogenic mechanisms between LATE-NC and glial tau pathologies in the medial temporal lobe.</description><subject>Ageing</subject><subject>ARTAG</subject><subject>Limbic Age-related TDP-43 Encephalopathy-neuropathological change</subject><subject>Mixed pathology</subject><subject>Oligodendroglia</subject><subject>Tau</subject><issn>0197-4580</issn><issn>1558-1497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqNkLtOwzAARS0EEqXwDx4YWBLs-BmJpVQtIFWwlNmyXTt1lcbFTpD696QqCxvTXe5D9wBwj1GJEeaPu7JzQ4omxFY3oWvKClVViUSJMLoAE8yYLDCtxSWYIFyLgjKJrsFNzjuEkKCCT8DzLOdog-5D7GD0sGmDbmGvB3jQ_Ta2sTlC3W3garZeFO9zGDrYbx3UjRv3oEk6dLfgyus2u7tfnYLP5WI9fy1WHy9v89mqsISTvuBaMkZpzWrssGeSe2Qq4r0hElUcC-y1F4RKSpxhleCyptLbWlNjGGe1IVPwcO49pPg1uNyrfcjWta3uXByyqgQiteTj4dH6dLbaFHNOzqtDCnudjgojdUKnduovOnVCp5BQI7oxvjzH3XjnO7iksg2us24TkrO92sTwv6IfJjl-Wg</recordid><startdate>202211</startdate><enddate>202211</enddate><creator>Forrest, Shelley L.</creator><creator>Wagner, Stephanie</creator><creator>Kim, Ain</creator><creator>Kovacs, Gabor G.</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3841-5511</orcidid></search><sort><creationdate>202211</creationdate><title>Association of glial tau pathology and LATE-NC in the ageing brain</title><author>Forrest, Shelley L. ; Wagner, Stephanie ; Kim, Ain ; Kovacs, Gabor G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-6a855449591e1f586f0b23ffb38026171faf734843eb52768948fc9a4bb5659b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Ageing</topic><topic>ARTAG</topic><topic>Limbic Age-related TDP-43 Encephalopathy-neuropathological change</topic><topic>Mixed pathology</topic><topic>Oligodendroglia</topic><topic>Tau</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Forrest, Shelley L.</creatorcontrib><creatorcontrib>Wagner, Stephanie</creatorcontrib><creatorcontrib>Kim, Ain</creatorcontrib><creatorcontrib>Kovacs, Gabor G.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neurobiology of aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Forrest, Shelley L.</au><au>Wagner, Stephanie</au><au>Kim, Ain</au><au>Kovacs, Gabor G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of glial tau pathology and LATE-NC in the ageing brain</atitle><jtitle>Neurobiology of aging</jtitle><date>2022-11</date><risdate>2022</risdate><volume>119</volume><spage>77</spage><epage>88</epage><pages>77-88</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><abstract>Ageing-related pathologies of the brain include neurofibrillary tangles, argyrophilic grains, ageing-related tau astrogliopathy (ARTAG), limbic-predominant age-related TDP-43 encephalopathy-neuropathological change (LATE-NC), vascular pathology and corpora amylacea. This study used an unbiased approach to evaluate a broad range of pathologies in an unselected European community-dwelling ageing cohort of 101 individuals (77–90 years). Pathological alterations observed included neurofibrillary tangles and corpora amylacea in all cases, ARTAG (79%), Thal amyloid−β phase &gt;1 (60%), cerebral amyloid angiopathy (39%), Lewy bodies (22%), LATE-NC (21%), oligodendroglial tau-positive coiled bodies (33%), and argyrophilic grains (15%). We demonstrate association of LATE-NC with the previously unappreciated age-related tau oligodendrogliopathy (ARTOG) and highlight the association of LATE-NC with various ARTAG types pointing toward common pathogenic aspects. Only neurofibrillary tangles and LATE-NC were associated with cognitive decline. This study broadens the spectrum of age-related brain pathologies and highlights a novel ageing-related tau pathology in oligodendroglia. Results from this study suggest overlapping pathogenic mechanisms between LATE-NC and glial tau pathologies in the medial temporal lobe.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.neurobiolaging.2022.07.010</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-3841-5511</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0197-4580
ispartof Neurobiology of aging, 2022-11, Vol.119, p.77-88
issn 0197-4580
1558-1497
language eng
recordid cdi_proquest_miscellaneous_2703986149
source Elsevier ScienceDirect Journals
subjects Ageing
ARTAG
Limbic Age-related TDP-43 Encephalopathy-neuropathological change
Mixed pathology
Oligodendroglia
Tau
title Association of glial tau pathology and LATE-NC in the ageing brain
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T16%3A30%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Association%20of%20glial%20tau%20pathology%20and%20LATE-NC%20in%20the%20ageing%20brain&rft.jtitle=Neurobiology%20of%20aging&rft.au=Forrest,%20Shelley%20L.&rft.date=2022-11&rft.volume=119&rft.spage=77&rft.epage=88&rft.pages=77-88&rft.issn=0197-4580&rft.eissn=1558-1497&rft_id=info:doi/10.1016/j.neurobiolaging.2022.07.010&rft_dat=%3Cproquest_cross%3E2703986149%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2703986149&rft_id=info:pmid/&rft_els_id=S019745802200166X&rfr_iscdi=true