POD13 White matter connectivity in semantic dementia

Semantic Dementia (SD) is known to be associated with grey matter atrophy of the anterior temporal lobes (ATL). The effect of the disease on white matter fibres has been less extensively studied. Semantic knowledge is thought to be organised in a widely distributed network throughout the brain conne...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.e45-e45
Hauptverfasser: Jones, M, Neary, D, Embleton, K, Snowden, J, Herholz, K
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e45
container_issue 11
container_start_page e45
container_title Journal of neurology, neurosurgery and psychiatry
container_volume 81
creator Jones, M
Neary, D
Embleton, K
Snowden, J
Herholz, K
description Semantic Dementia (SD) is known to be associated with grey matter atrophy of the anterior temporal lobes (ATL). The effect of the disease on white matter fibres has been less extensively studied. Semantic knowledge is thought to be organised in a widely distributed network throughout the brain connected by a number of white matter bundles. We explore the white matter connectivity of the semantic network in subjects with SD and healthy controls. Six subjects with SD and four healthy controls underwent diffusion weighted MR tractography imaging. Region of interest placement was performed to allow reconstruction of specific tracts thought to be involved in the semantic network and other classical language pathways. Tracts were assessed by visual inspection and quantitative atlas based region of interest analysis. SD subjects had a significantly reduced pattern of white matter connectivity from the left ATL. Specific tract reconstructions demonstrated significant reductions in connectivity in the left uncinate, inferior fronto-occipital fasciculi and anterior commissure tract in SD subjects. The arcuate fasciculi did not appear different between groups. The results demonstrate that in SD there is disruption of the semantic network extending beyond the boundaries of the ATLs and involving specific white matter pathways.
doi_str_mv 10.1136/jnnp.2010.226340.113
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1781244826</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4023878291</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1516-919f4e37210ae2ceef91bbf6703915c1b903d127a877ae31055f49ac69ed52083</originalsourceid><addsrcrecordid>eNqNUMtOwzAQtBBIlMIfcIjEOa3XTuz4iAIFpPI4lMLNctKNSCBJsV1Eb1z4Ub6EhCDO7GV3RzM72iHkGOgEgItp1TTrCaPdypjg0Q-6Q0YQiSTknD7ukhGljIWcxnSfHDhX0b4SNSLi7vYM-NfH58NT6TGojfdog7xtGsx9-Vb6bVA2gcPaNL7MgxXW2A3mkOwV5sXh0W8fk_vZ-SK9DOe3F1fp6TzMIAYRKlBFhFwyoAZZjlgoyLJCSMoVxDlkivIVMGkSKQ1yoHFcRMrkQuEqZjThY3Iy3F3b9nWDzuuq3dims9QgE2BRlHQfj0k0sHLbOmex0Gtb1sZuNVDdJ6T7hHSfkB4S6tFOFg6y0nl8_9MY-6yF5DLWN8tUL2dSXC9Yqucdfzrws7r6n8M31mV2og</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1781244826</pqid></control><display><type>article</type><title>POD13 White matter connectivity in semantic dementia</title><source>BMJ Journals - NESLi2</source><creator>Jones, M ; Neary, D ; Embleton, K ; Snowden, J ; Herholz, K</creator><creatorcontrib>Jones, M ; Neary, D ; Embleton, K ; Snowden, J ; Herholz, K</creatorcontrib><description>Semantic Dementia (SD) is known to be associated with grey matter atrophy of the anterior temporal lobes (ATL). The effect of the disease on white matter fibres has been less extensively studied. Semantic knowledge is thought to be organised in a widely distributed network throughout the brain connected by a number of white matter bundles. We explore the white matter connectivity of the semantic network in subjects with SD and healthy controls. Six subjects with SD and four healthy controls underwent diffusion weighted MR tractography imaging. Region of interest placement was performed to allow reconstruction of specific tracts thought to be involved in the semantic network and other classical language pathways. Tracts were assessed by visual inspection and quantitative atlas based region of interest analysis. SD subjects had a significantly reduced pattern of white matter connectivity from the left ATL. Specific tract reconstructions demonstrated significant reductions in connectivity in the left uncinate, inferior fronto-occipital fasciculi and anterior commissure tract in SD subjects. The arcuate fasciculi did not appear different between groups. The results demonstrate that in SD there is disruption of the semantic network extending beyond the boundaries of the ATLs and involving specific white matter pathways.</description><identifier>ISSN: 0022-3050</identifier><identifier>EISSN: 1468-330X</identifier><identifier>DOI: 10.1136/jnnp.2010.226340.113</identifier><identifier>CODEN: JNNPAU</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Dementia</subject><ispartof>Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.e45-e45</ispartof><rights>2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>Copyright: 2010 (c) 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jnnp.bmj.com/content/81/11/e45.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttps://jnnp.bmj.com/content/81/11/e45.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77343,77374</link.rule.ids></links><search><creatorcontrib>Jones, M</creatorcontrib><creatorcontrib>Neary, D</creatorcontrib><creatorcontrib>Embleton, K</creatorcontrib><creatorcontrib>Snowden, J</creatorcontrib><creatorcontrib>Herholz, K</creatorcontrib><title>POD13 White matter connectivity in semantic dementia</title><title>Journal of neurology, neurosurgery and psychiatry</title><addtitle>J Neurol Neurosurg Psychiatry</addtitle><description>Semantic Dementia (SD) is known to be associated with grey matter atrophy of the anterior temporal lobes (ATL). The effect of the disease on white matter fibres has been less extensively studied. Semantic knowledge is thought to be organised in a widely distributed network throughout the brain connected by a number of white matter bundles. We explore the white matter connectivity of the semantic network in subjects with SD and healthy controls. Six subjects with SD and four healthy controls underwent diffusion weighted MR tractography imaging. Region of interest placement was performed to allow reconstruction of specific tracts thought to be involved in the semantic network and other classical language pathways. Tracts were assessed by visual inspection and quantitative atlas based region of interest analysis. SD subjects had a significantly reduced pattern of white matter connectivity from the left ATL. Specific tract reconstructions demonstrated significant reductions in connectivity in the left uncinate, inferior fronto-occipital fasciculi and anterior commissure tract in SD subjects. The arcuate fasciculi did not appear different between groups. The results demonstrate that in SD there is disruption of the semantic network extending beyond the boundaries of the ATLs and involving specific white matter pathways.</description><subject>Dementia</subject><issn>0022-3050</issn><issn>1468-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqNUMtOwzAQtBBIlMIfcIjEOa3XTuz4iAIFpPI4lMLNctKNSCBJsV1Eb1z4Ub6EhCDO7GV3RzM72iHkGOgEgItp1TTrCaPdypjg0Q-6Q0YQiSTknD7ukhGljIWcxnSfHDhX0b4SNSLi7vYM-NfH58NT6TGojfdog7xtGsx9-Vb6bVA2gcPaNL7MgxXW2A3mkOwV5sXh0W8fk_vZ-SK9DOe3F1fp6TzMIAYRKlBFhFwyoAZZjlgoyLJCSMoVxDlkivIVMGkSKQ1yoHFcRMrkQuEqZjThY3Iy3F3b9nWDzuuq3dims9QgE2BRlHQfj0k0sHLbOmex0Gtb1sZuNVDdJ6T7hHSfkB4S6tFOFg6y0nl8_9MY-6yF5DLWN8tUL2dSXC9Yqucdfzrws7r6n8M31mV2og</recordid><startdate>201011</startdate><enddate>201011</enddate><creator>Jones, M</creator><creator>Neary, D</creator><creator>Embleton, K</creator><creator>Snowden, J</creator><creator>Herholz, K</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>201011</creationdate><title>POD13 White matter connectivity in semantic dementia</title><author>Jones, M ; Neary, D ; Embleton, K ; Snowden, J ; Herholz, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1516-919f4e37210ae2ceef91bbf6703915c1b903d127a877ae31055f49ac69ed52083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Dementia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jones, M</creatorcontrib><creatorcontrib>Neary, D</creatorcontrib><creatorcontrib>Embleton, K</creatorcontrib><creatorcontrib>Snowden, J</creatorcontrib><creatorcontrib>Herholz, K</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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>BMJ Journals</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>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Science Database</collection><collection>Nursing &amp; 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 Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jones, M</au><au>Neary, D</au><au>Embleton, K</au><au>Snowden, J</au><au>Herholz, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>POD13 White matter connectivity in semantic dementia</atitle><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle><addtitle>J Neurol Neurosurg Psychiatry</addtitle><date>2010-11</date><risdate>2010</risdate><volume>81</volume><issue>11</issue><spage>e45</spage><epage>e45</epage><pages>e45-e45</pages><issn>0022-3050</issn><eissn>1468-330X</eissn><coden>JNNPAU</coden><abstract>Semantic Dementia (SD) is known to be associated with grey matter atrophy of the anterior temporal lobes (ATL). The effect of the disease on white matter fibres has been less extensively studied. Semantic knowledge is thought to be organised in a widely distributed network throughout the brain connected by a number of white matter bundles. We explore the white matter connectivity of the semantic network in subjects with SD and healthy controls. Six subjects with SD and four healthy controls underwent diffusion weighted MR tractography imaging. Region of interest placement was performed to allow reconstruction of specific tracts thought to be involved in the semantic network and other classical language pathways. Tracts were assessed by visual inspection and quantitative atlas based region of interest analysis. SD subjects had a significantly reduced pattern of white matter connectivity from the left ATL. Specific tract reconstructions demonstrated significant reductions in connectivity in the left uncinate, inferior fronto-occipital fasciculi and anterior commissure tract in SD subjects. The arcuate fasciculi did not appear different between groups. The results demonstrate that in SD there is disruption of the semantic network extending beyond the boundaries of the ATLs and involving specific white matter pathways.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><doi>10.1136/jnnp.2010.226340.113</doi></addata></record>
fulltext fulltext
identifier ISSN: 0022-3050
ispartof Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.e45-e45
issn 0022-3050
1468-330X
language eng
recordid cdi_proquest_journals_1781244826
source BMJ Journals - NESLi2
subjects Dementia
title POD13 White matter connectivity in semantic dementia
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T19%3A17%3A27IST&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=POD13%E2%80%85White%20matter%20connectivity%20in%20semantic%20dementia&rft.jtitle=Journal%20of%20neurology,%20neurosurgery%20and%20psychiatry&rft.au=Jones,%20M&rft.date=2010-11&rft.volume=81&rft.issue=11&rft.spage=e45&rft.epage=e45&rft.pages=e45-e45&rft.issn=0022-3050&rft.eissn=1468-330X&rft.coden=JNNPAU&rft_id=info:doi/10.1136/jnnp.2010.226340.113&rft_dat=%3Cproquest_cross%3E4023878291%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=1781244826&rft_id=info:pmid/&rfr_iscdi=true