Loading…

Distinct loci of lexical and semantic access deficits in aphasia: Evidence from voxel-based lesion-symptom mapping and diffusion tensor imaging

Naming pictures and matching words to pictures belonging to the same semantic category negatively affects language production and comprehension. By most accounts, semantic interference arises when accessing lexical representations in naming (e.g., Damian, Vigliocco, & Levelt, 2001) and semantic...

Full description

Saved in:
Bibliographic Details
Published in:Cortex 2015-06, Vol.67 (Jun), p.37-58
Main Authors: Harvey, Denise Y., Schnur, Tatiana T.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c441t-627c22e666a682f6979e0f4a867875d99fb07f7bdcb74db4374b01ca5bf845c33
cites cdi_FETCH-LOGICAL-c441t-627c22e666a682f6979e0f4a867875d99fb07f7bdcb74db4374b01ca5bf845c33
container_end_page 58
container_issue Jun
container_start_page 37
container_title Cortex
container_volume 67
creator Harvey, Denise Y.
Schnur, Tatiana T.
description Naming pictures and matching words to pictures belonging to the same semantic category negatively affects language production and comprehension. By most accounts, semantic interference arises when accessing lexical representations in naming (e.g., Damian, Vigliocco, & Levelt, 2001) and semantic representations in comprehension (e.g., Forde & Humphreys, 1997). Further, damage to the left inferior frontal gyrus (LIFG), a region implicated in cognitive control, results in increasing semantic interference when items repeat across cycles in both language production and comprehension (Jefferies, Baker, Doran, & Lambon Ralph, 2007). This generates the prediction that the LIFG via white matter connections supports resolution of semantic interference arising from different loci (lexical vs semantic) in the temporal lobe. However, it remains unclear whether the cognitive and neural mechanisms that resolve semantic interference are the same across tasks. Thus, we examined which gray matter structures [using whole brain and region of interest (ROI) approaches] and white matter connections (using deterministic tractography) when damaged impact semantic interference and its increase across cycles when repeatedly producing and understanding words in 15 speakers with varying lexical-semantic deficits from left hemisphere stroke. We found that damage to distinct brain regions, the posterior versus anterior temporal lobe, was associated with semantic interference (collapsed across cycles) in naming and comprehension, respectively. Further, those with LIFG damage compared to those without exhibited marginally larger increases in semantic interference across cycles in naming but not comprehension. Lastly, the inferior fronto-occipital fasciculus, connecting the LIFG with posterior temporal lobe, related to semantic interference in naming, whereas the inferior longitudinal fasciculus (ILF), connecting posterior with anterior temporal regions related to semantic interference in comprehension. These neuroanatomical-behavioral findings have implications for models of the lexical-semantic language network by demonstrating that semantic interference in language production and comprehension involves different representations which differentially recruit a cognitive control mechanism for interference resolution.
doi_str_mv 10.1016/j.cortex.2015.03.004
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1738472748</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0010945215000829</els_id><sourcerecordid>1738472748</sourcerecordid><originalsourceid>FETCH-LOGICAL-c441t-627c22e666a682f6979e0f4a867875d99fb07f7bdcb74db4374b01ca5bf845c33</originalsourceid><addsrcrecordid>eNqFkc2OFCEURonROO3oGxjD0k21QEFBuTAx4_iTTOJG14SCy0inqii5dKfnKeaVrbZHl7pi8Z373XAPIS8523LGuze7rc-lwnErGFdb1m4Zk4_Ihve6bQxn4jHZMMZZ00slLsgzxB1jghmlnpILoYxhulcbcv8hYU2zr3TMPtEc6QjH5N1I3RwowuTmmjx13gMiDRCTTxVpmqlbfjhM7i29PqQAswcaS57oIR9hbAaHENYqTHlu8G5a6hpNblnSfPu7OaQY96eUVpgxF5omd7uGz8mT6EaEFw_vJfn-8frb1efm5uunL1fvbxovJa9NJ7QXArquc50Rset1DyxKZzpttAp9Hwemox6CH7QMg2y1HBj3Tg3RSOXb9pK8PvcuJf_cA1Y7JfQwjm6GvEfLdWukFlqa_6OdUVoqrfWKyjPqS0YsEO1S1o-VO8uZPVmzO3u2Zk_WLGvtam0de_WwYT9MEP4O_dG0Au_OAKwnOSQoFn063TykAr7akNO_N_wCL4es4w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1685745777</pqid></control><display><type>article</type><title>Distinct loci of lexical and semantic access deficits in aphasia: Evidence from voxel-based lesion-symptom mapping and diffusion tensor imaging</title><source>ScienceDirect Freedom Collection</source><source>Linguistics and Language Behavior Abstracts (LLBA)</source><creator>Harvey, Denise Y. ; Schnur, Tatiana T.</creator><creatorcontrib>Harvey, Denise Y. ; Schnur, Tatiana T.</creatorcontrib><description>Naming pictures and matching words to pictures belonging to the same semantic category negatively affects language production and comprehension. By most accounts, semantic interference arises when accessing lexical representations in naming (e.g., Damian, Vigliocco, &amp; Levelt, 2001) and semantic representations in comprehension (e.g., Forde &amp; Humphreys, 1997). Further, damage to the left inferior frontal gyrus (LIFG), a region implicated in cognitive control, results in increasing semantic interference when items repeat across cycles in both language production and comprehension (Jefferies, Baker, Doran, &amp; Lambon Ralph, 2007). This generates the prediction that the LIFG via white matter connections supports resolution of semantic interference arising from different loci (lexical vs semantic) in the temporal lobe. However, it remains unclear whether the cognitive and neural mechanisms that resolve semantic interference are the same across tasks. Thus, we examined which gray matter structures [using whole brain and region of interest (ROI) approaches] and white matter connections (using deterministic tractography) when damaged impact semantic interference and its increase across cycles when repeatedly producing and understanding words in 15 speakers with varying lexical-semantic deficits from left hemisphere stroke. We found that damage to distinct brain regions, the posterior versus anterior temporal lobe, was associated with semantic interference (collapsed across cycles) in naming and comprehension, respectively. Further, those with LIFG damage compared to those without exhibited marginally larger increases in semantic interference across cycles in naming but not comprehension. Lastly, the inferior fronto-occipital fasciculus, connecting the LIFG with posterior temporal lobe, related to semantic interference in naming, whereas the inferior longitudinal fasciculus (ILF), connecting posterior with anterior temporal regions related to semantic interference in comprehension. These neuroanatomical-behavioral findings have implications for models of the lexical-semantic language network by demonstrating that semantic interference in language production and comprehension involves different representations which differentially recruit a cognitive control mechanism for interference resolution.</description><identifier>ISSN: 0010-9452</identifier><identifier>EISSN: 1973-8102</identifier><identifier>DOI: 10.1016/j.cortex.2015.03.004</identifier><identifier>PMID: 25880795</identifier><language>eng</language><publisher>Italy: Elsevier Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Aphasia - etiology ; Aphasia - pathology ; Aphasia - physiopathology ; Brain - pathology ; Brain - physiopathology ; Brain Mapping ; Comprehension ; Diffusion Tensor Imaging ; Female ; Humans ; Language ; Language production and comprehension ; Lesion-symptom mapping ; Lexical-semantic deficits ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Neural Pathways ; Neuropsychological Tests ; Prefrontal Cortex - pathology ; Prefrontal Cortex - physiopathology ; Semantic interference ; Semantics ; Stroke - complications ; Stroke - pathology ; Stroke - physiopathology ; Temporal Lobe - pathology ; Temporal Lobe - physiopathology</subject><ispartof>Cortex, 2015-06, Vol.67 (Jun), p.37-58</ispartof><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-627c22e666a682f6979e0f4a867875d99fb07f7bdcb74db4374b01ca5bf845c33</citedby><cites>FETCH-LOGICAL-c441t-627c22e666a682f6979e0f4a867875d99fb07f7bdcb74db4374b01ca5bf845c33</cites><orcidid>0000-0002-4312-9512 ; 0000-0002-4651-7721</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,31270</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25880795$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harvey, Denise Y.</creatorcontrib><creatorcontrib>Schnur, Tatiana T.</creatorcontrib><title>Distinct loci of lexical and semantic access deficits in aphasia: Evidence from voxel-based lesion-symptom mapping and diffusion tensor imaging</title><title>Cortex</title><addtitle>Cortex</addtitle><description>Naming pictures and matching words to pictures belonging to the same semantic category negatively affects language production and comprehension. By most accounts, semantic interference arises when accessing lexical representations in naming (e.g., Damian, Vigliocco, &amp; Levelt, 2001) and semantic representations in comprehension (e.g., Forde &amp; Humphreys, 1997). Further, damage to the left inferior frontal gyrus (LIFG), a region implicated in cognitive control, results in increasing semantic interference when items repeat across cycles in both language production and comprehension (Jefferies, Baker, Doran, &amp; Lambon Ralph, 2007). This generates the prediction that the LIFG via white matter connections supports resolution of semantic interference arising from different loci (lexical vs semantic) in the temporal lobe. However, it remains unclear whether the cognitive and neural mechanisms that resolve semantic interference are the same across tasks. Thus, we examined which gray matter structures [using whole brain and region of interest (ROI) approaches] and white matter connections (using deterministic tractography) when damaged impact semantic interference and its increase across cycles when repeatedly producing and understanding words in 15 speakers with varying lexical-semantic deficits from left hemisphere stroke. We found that damage to distinct brain regions, the posterior versus anterior temporal lobe, was associated with semantic interference (collapsed across cycles) in naming and comprehension, respectively. Further, those with LIFG damage compared to those without exhibited marginally larger increases in semantic interference across cycles in naming but not comprehension. Lastly, the inferior fronto-occipital fasciculus, connecting the LIFG with posterior temporal lobe, related to semantic interference in naming, whereas the inferior longitudinal fasciculus (ILF), connecting posterior with anterior temporal regions related to semantic interference in comprehension. These neuroanatomical-behavioral findings have implications for models of the lexical-semantic language network by demonstrating that semantic interference in language production and comprehension involves different representations which differentially recruit a cognitive control mechanism for interference resolution.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aphasia - etiology</subject><subject>Aphasia - pathology</subject><subject>Aphasia - physiopathology</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Brain Mapping</subject><subject>Comprehension</subject><subject>Diffusion Tensor Imaging</subject><subject>Female</subject><subject>Humans</subject><subject>Language</subject><subject>Language production and comprehension</subject><subject>Lesion-symptom mapping</subject><subject>Lexical-semantic deficits</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neural Pathways</subject><subject>Neuropsychological Tests</subject><subject>Prefrontal Cortex - pathology</subject><subject>Prefrontal Cortex - physiopathology</subject><subject>Semantic interference</subject><subject>Semantics</subject><subject>Stroke - complications</subject><subject>Stroke - pathology</subject><subject>Stroke - physiopathology</subject><subject>Temporal Lobe - pathology</subject><subject>Temporal Lobe - physiopathology</subject><issn>0010-9452</issn><issn>1973-8102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>7T9</sourceid><recordid>eNqFkc2OFCEURonROO3oGxjD0k21QEFBuTAx4_iTTOJG14SCy0inqii5dKfnKeaVrbZHl7pi8Z373XAPIS8523LGuze7rc-lwnErGFdb1m4Zk4_Ihve6bQxn4jHZMMZZ00slLsgzxB1jghmlnpILoYxhulcbcv8hYU2zr3TMPtEc6QjH5N1I3RwowuTmmjx13gMiDRCTTxVpmqlbfjhM7i29PqQAswcaS57oIR9hbAaHENYqTHlu8G5a6hpNblnSfPu7OaQY96eUVpgxF5omd7uGz8mT6EaEFw_vJfn-8frb1efm5uunL1fvbxovJa9NJ7QXArquc50Rset1DyxKZzpttAp9Hwemox6CH7QMg2y1HBj3Tg3RSOXb9pK8PvcuJf_cA1Y7JfQwjm6GvEfLdWukFlqa_6OdUVoqrfWKyjPqS0YsEO1S1o-VO8uZPVmzO3u2Zk_WLGvtam0de_WwYT9MEP4O_dG0Au_OAKwnOSQoFn063TykAr7akNO_N_wCL4es4w</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Harvey, Denise Y.</creator><creator>Schnur, Tatiana T.</creator><general>Elsevier Ltd</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><scope>7T9</scope><orcidid>https://orcid.org/0000-0002-4312-9512</orcidid><orcidid>https://orcid.org/0000-0002-4651-7721</orcidid></search><sort><creationdate>201506</creationdate><title>Distinct loci of lexical and semantic access deficits in aphasia: Evidence from voxel-based lesion-symptom mapping and diffusion tensor imaging</title><author>Harvey, Denise Y. ; Schnur, Tatiana T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-627c22e666a682f6979e0f4a867875d99fb07f7bdcb74db4374b01ca5bf845c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aphasia - etiology</topic><topic>Aphasia - pathology</topic><topic>Aphasia - physiopathology</topic><topic>Brain - pathology</topic><topic>Brain - physiopathology</topic><topic>Brain Mapping</topic><topic>Comprehension</topic><topic>Diffusion Tensor Imaging</topic><topic>Female</topic><topic>Humans</topic><topic>Language</topic><topic>Language production and comprehension</topic><topic>Lesion-symptom mapping</topic><topic>Lexical-semantic deficits</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neural Pathways</topic><topic>Neuropsychological Tests</topic><topic>Prefrontal Cortex - pathology</topic><topic>Prefrontal Cortex - physiopathology</topic><topic>Semantic interference</topic><topic>Semantics</topic><topic>Stroke - complications</topic><topic>Stroke - pathology</topic><topic>Stroke - physiopathology</topic><topic>Temporal Lobe - pathology</topic><topic>Temporal Lobe - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harvey, Denise Y.</creatorcontrib><creatorcontrib>Schnur, Tatiana T.</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><collection>Linguistics and Language Behavior Abstracts (LLBA)</collection><jtitle>Cortex</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harvey, Denise Y.</au><au>Schnur, Tatiana T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct loci of lexical and semantic access deficits in aphasia: Evidence from voxel-based lesion-symptom mapping and diffusion tensor imaging</atitle><jtitle>Cortex</jtitle><addtitle>Cortex</addtitle><date>2015-06</date><risdate>2015</risdate><volume>67</volume><issue>Jun</issue><spage>37</spage><epage>58</epage><pages>37-58</pages><issn>0010-9452</issn><eissn>1973-8102</eissn><abstract>Naming pictures and matching words to pictures belonging to the same semantic category negatively affects language production and comprehension. By most accounts, semantic interference arises when accessing lexical representations in naming (e.g., Damian, Vigliocco, &amp; Levelt, 2001) and semantic representations in comprehension (e.g., Forde &amp; Humphreys, 1997). Further, damage to the left inferior frontal gyrus (LIFG), a region implicated in cognitive control, results in increasing semantic interference when items repeat across cycles in both language production and comprehension (Jefferies, Baker, Doran, &amp; Lambon Ralph, 2007). This generates the prediction that the LIFG via white matter connections supports resolution of semantic interference arising from different loci (lexical vs semantic) in the temporal lobe. However, it remains unclear whether the cognitive and neural mechanisms that resolve semantic interference are the same across tasks. Thus, we examined which gray matter structures [using whole brain and region of interest (ROI) approaches] and white matter connections (using deterministic tractography) when damaged impact semantic interference and its increase across cycles when repeatedly producing and understanding words in 15 speakers with varying lexical-semantic deficits from left hemisphere stroke. We found that damage to distinct brain regions, the posterior versus anterior temporal lobe, was associated with semantic interference (collapsed across cycles) in naming and comprehension, respectively. Further, those with LIFG damage compared to those without exhibited marginally larger increases in semantic interference across cycles in naming but not comprehension. Lastly, the inferior fronto-occipital fasciculus, connecting the LIFG with posterior temporal lobe, related to semantic interference in naming, whereas the inferior longitudinal fasciculus (ILF), connecting posterior with anterior temporal regions related to semantic interference in comprehension. These neuroanatomical-behavioral findings have implications for models of the lexical-semantic language network by demonstrating that semantic interference in language production and comprehension involves different representations which differentially recruit a cognitive control mechanism for interference resolution.</abstract><cop>Italy</cop><pub>Elsevier Ltd</pub><pmid>25880795</pmid><doi>10.1016/j.cortex.2015.03.004</doi><tpages>22</tpages><orcidid>https://orcid.org/0000-0002-4312-9512</orcidid><orcidid>https://orcid.org/0000-0002-4651-7721</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0010-9452
ispartof Cortex, 2015-06, Vol.67 (Jun), p.37-58
issn 0010-9452
1973-8102
language eng
recordid cdi_proquest_miscellaneous_1738472748
source ScienceDirect Freedom Collection; Linguistics and Language Behavior Abstracts (LLBA)
subjects Adult
Aged
Aged, 80 and over
Aphasia - etiology
Aphasia - pathology
Aphasia - physiopathology
Brain - pathology
Brain - physiopathology
Brain Mapping
Comprehension
Diffusion Tensor Imaging
Female
Humans
Language
Language production and comprehension
Lesion-symptom mapping
Lexical-semantic deficits
Magnetic Resonance Imaging
Male
Middle Aged
Neural Pathways
Neuropsychological Tests
Prefrontal Cortex - pathology
Prefrontal Cortex - physiopathology
Semantic interference
Semantics
Stroke - complications
Stroke - pathology
Stroke - physiopathology
Temporal Lobe - pathology
Temporal Lobe - physiopathology
title Distinct loci of lexical and semantic access deficits in aphasia: Evidence from voxel-based lesion-symptom mapping and diffusion tensor imaging
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T22%3A18%3A55IST&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=Distinct%20loci%20of%20lexical%20and%20semantic%20access%20deficits%20in%20aphasia:%20Evidence%20from%20voxel-based%20lesion-symptom%20mapping%20and%20diffusion%20tensor%20imaging&rft.jtitle=Cortex&rft.au=Harvey,%20Denise%20Y.&rft.date=2015-06&rft.volume=67&rft.issue=Jun&rft.spage=37&rft.epage=58&rft.pages=37-58&rft.issn=0010-9452&rft.eissn=1973-8102&rft_id=info:doi/10.1016/j.cortex.2015.03.004&rft_dat=%3Cproquest_cross%3E1738472748%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c441t-627c22e666a682f6979e0f4a867875d99fb07f7bdcb74db4374b01ca5bf845c33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1685745777&rft_id=info:pmid/25880795&rfr_iscdi=true