Effects of anterior cingulate fissurization on cognitive control during stroop interference
Identifieur interne : 001827 ( Istex/Corpus ); précédent : 001826; suivant : 001828Effects of anterior cingulate fissurization on cognitive control during stroop interference
Auteurs : Rene J. Huster ; Carsten Wolters ; Andreas Wollbrink ; Elisabeth Schweiger ; Werner Wittling ; Christo Pantev ; Markus JunghoferSource :
- Human Brain Mapping [ 1065-9471 ] ; 2009-04.
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Abstract
The midcingulate cortex, as part of the more anteriorly located cingulate regions, is thought to play a major role in cognitive processes like conflict monitoring or response selection. Regarding midcingulate fissurization, the occurrence of a second or paracingulate sulcus is more common in the left than in the right hemisphere and has been shown to be associated with an advantageous performance on tests of executive functions. However, the cognitive mechanisms underlying such behavioral differences are completely unknown. The current study addressed this issue by comparing subjects with a low and a high degree of left hemispheric midcingulate fissurization while collecting behavioral as well as electrophysiological correlates of Stroop interference. A high degree of fissurization was associated with decreased behavioral Stroop interference accompanied by a stronger and prolonged frontal negative potential to incongruent trials starting around 320 ms. This increased frontal negativity is assumed to reflect an enhanced activity of a conflict monitoring system located in the midcingulate cortex. In contrast and starting around 400 ms, subjects with low fissurization revealed an increased positivity over parieto‐occipital regions suggesting a compensatory need for enhanced effortful cognitive control in this group. These results contribute to the understanding of the neuronal implementation of individual differences regarding attentional mechanisms. Hum Brain Mapp 2009. © 2008 Wiley‐Liss, Inc.
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DOI: 10.1002/hbm.20594
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Huster</name><affiliation><mods:affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Psychiatry and Psychotherapy and Interdisciplinary Center for Clinical Research (IZKF), University of Münster, Münster, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, Malmedyweg 15, 48149 Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wolters, Carsten" sort="Wolters, Carsten" uniqKey="Wolters C" first="Carsten" last="Wolters">Carsten Wolters</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wollbrink, Andreas" sort="Wollbrink, Andreas" uniqKey="Wollbrink A" first="Andreas" last="Wollbrink">Andreas Wollbrink</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Schweiger, Elisabeth" sort="Schweiger, Elisabeth" uniqKey="Schweiger E" first="Elisabeth" last="Schweiger">Elisabeth Schweiger</name><affiliation><mods:affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wittling, Werner" sort="Wittling, Werner" uniqKey="Wittling W" first="Werner" last="Wittling">Werner Wittling</name><affiliation><mods:affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Pantev, Christo" sort="Pantev, Christo" uniqKey="Pantev C" first="Christo" last="Pantev">Christo Pantev</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Junghofer, Markus" sort="Junghofer, Markus" uniqKey="Junghofer M" first="Markus" last="Junghofer">Markus Junghofer</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:CD899C82257B109E3670A6560CFE681534698BF9</idno><date when="2009" year="2009">2009</date><idno type="doi">10.1002/hbm.20594</idno><idno type="url">https://api.istex.fr/document/CD899C82257B109E3670A6560CFE681534698BF9/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">001827</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001827</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Effects of anterior cingulate fissurization on cognitive control during stroop interference</title><author><name sortKey="Huster, Rene J" sort="Huster, Rene J" uniqKey="Huster R" first="Rene J." last="Huster">Rene J. Huster</name><affiliation><mods:affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Psychiatry and Psychotherapy and Interdisciplinary Center for Clinical Research (IZKF), University of Münster, Münster, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, Malmedyweg 15, 48149 Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wolters, Carsten" sort="Wolters, Carsten" uniqKey="Wolters C" first="Carsten" last="Wolters">Carsten Wolters</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wollbrink, Andreas" sort="Wollbrink, Andreas" uniqKey="Wollbrink A" first="Andreas" last="Wollbrink">Andreas Wollbrink</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Schweiger, Elisabeth" sort="Schweiger, Elisabeth" uniqKey="Schweiger E" first="Elisabeth" last="Schweiger">Elisabeth Schweiger</name><affiliation><mods:affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wittling, Werner" sort="Wittling, Werner" uniqKey="Wittling W" first="Werner" last="Wittling">Werner Wittling</name><affiliation><mods:affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Pantev, Christo" sort="Pantev, Christo" uniqKey="Pantev C" first="Christo" last="Pantev">Christo Pantev</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author><author><name sortKey="Junghofer, Markus" sort="Junghofer, Markus" uniqKey="Junghofer M" first="Markus" last="Junghofer">Markus Junghofer</name><affiliation><mods:affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Human Brain Mapping</title><title level="j" type="abbrev">Hum. Brain Mapp.</title><idno type="ISSN">1065-9471</idno><idno type="eISSN">1097-0193</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2009-04">2009-04</date><biblScope unit="volume">30</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="1279">1279</biblScope><biblScope unit="page" to="1289">1289</biblScope></imprint><idno type="ISSN">1065-9471</idno></series><idno type="istex">CD899C82257B109E3670A6560CFE681534698BF9</idno><idno type="DOI">10.1002/hbm.20594</idno><idno type="ArticleID">HBM20594</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">1065-9471</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>cognitive control</term><term>conflict monitoring</term><term>dACC</term><term>fissurization</term><term>paracingulate</term><term>stroop</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The midcingulate cortex, as part of the more anteriorly located cingulate regions, is thought to play a major role in cognitive processes like conflict monitoring or response selection. Regarding midcingulate fissurization, the occurrence of a second or paracingulate sulcus is more common in the left than in the right hemisphere and has been shown to be associated with an advantageous performance on tests of executive functions. However, the cognitive mechanisms underlying such behavioral differences are completely unknown. The current study addressed this issue by comparing subjects with a low and a high degree of left hemispheric midcingulate fissurization while collecting behavioral as well as electrophysiological correlates of Stroop interference. A high degree of fissurization was associated with decreased behavioral Stroop interference accompanied by a stronger and prolonged frontal negative potential to incongruent trials starting around 320 ms. This increased frontal negativity is assumed to reflect an enhanced activity of a conflict monitoring system located in the midcingulate cortex. In contrast and starting around 400 ms, subjects with low fissurization revealed an increased positivity over parieto‐occipital regions suggesting a compensatory need for enhanced effortful cognitive control in this group. These results contribute to the understanding of the neuronal implementation of individual differences regarding attentional mechanisms. Hum Brain Mapp 2009. © 2008 Wiley‐Liss, Inc.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Rene J. Huster</name><affiliations><json:string>Center for Neuropsychological Research, University of Trier, Trier, Germany</json:string><json:string>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</json:string><json:string>Department of Psychiatry and Psychotherapy and Interdisciplinary Center for Clinical Research (IZKF), University of Münster, Münster, Germany</json:string><json:string>Institute for Biomagnetism and Biosignalanalysis, Malmedyweg 15, 48149 Münster, Germany</json:string></affiliations></json:item><json:item><name>Carsten Wolters</name><affiliations><json:string>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</json:string></affiliations></json:item><json:item><name>Andreas Wollbrink</name><affiliations><json:string>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</json:string></affiliations></json:item><json:item><name>Elisabeth Schweiger</name><affiliations><json:string>Center for Neuropsychological Research, University of Trier, Trier, Germany</json:string></affiliations></json:item><json:item><name>Werner Wittling</name><affiliations><json:string>Center for Neuropsychological Research, University of Trier, Trier, Germany</json:string></affiliations></json:item><json:item><name>Christo Pantev</name><affiliations><json:string>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</json:string></affiliations></json:item><json:item><name>Markus Junghofer</name><affiliations><json:string>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>dACC</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>stroop</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>paracingulate</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>conflict monitoring</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>cognitive control</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>fissurization</value></json:item></subject><articleId><json:string>HBM20594</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>The midcingulate cortex, as part of the more anteriorly located cingulate regions, is thought to play a major role in cognitive processes like conflict monitoring or response selection. Regarding midcingulate fissurization, the occurrence of a second or paracingulate sulcus is more common in the left than in the right hemisphere and has been shown to be associated with an advantageous performance on tests of executive functions. However, the cognitive mechanisms underlying such behavioral differences are completely unknown. The current study addressed this issue by comparing subjects with a low and a high degree of left hemispheric midcingulate fissurization while collecting behavioral as well as electrophysiological correlates of Stroop interference. A high degree of fissurization was associated with decreased behavioral Stroop interference accompanied by a stronger and prolonged frontal negative potential to incongruent trials starting around 320 ms. This increased frontal negativity is assumed to reflect an enhanced activity of a conflict monitoring system located in the midcingulate cortex. In contrast and starting around 400 ms, subjects with low fissurization revealed an increased positivity over parieto‐occipital regions suggesting a compensatory need for enhanced effortful cognitive control in this group. These results contribute to the understanding of the neuronal implementation of individual differences regarding attentional mechanisms. 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In contrast and starting around 400 ms, subjects with low fissurization revealed an increased positivity over parieto‐occipital regions suggesting a compensatory need for enhanced effortful cognitive control in this group. These results contribute to the understanding of the neuronal implementation of individual differences regarding attentional mechanisms. 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anteriorly located cingulate regions, is thought to play a major role in cognitive processes like conflict monitoring or response selection. Regarding midcingulate fissurization, the occurrence of a second or paracingulate sulcus is more common in the left than in the right hemisphere and has been shown to be associated with an advantageous performance on tests of executive functions. However, the cognitive mechanisms underlying such behavioral differences are completely unknown. The current study addressed this issue by comparing subjects with a low and a high degree of left hemispheric midcingulate fissurization while collecting behavioral as well as electrophysiological correlates of Stroop interference. A high degree of fissurization was associated with decreased behavioral Stroop interference accompanied by a stronger and prolonged frontal negative potential to incongruent trials starting around 320 ms. This increased frontal negativity is assumed to reflect an enhanced activity of a conflict monitoring system located in the midcingulate cortex. In contrast and starting around 400 ms, subjects with low fissurization revealed an increased positivity over parieto‐occipital regions suggesting a compensatory need for enhanced effortful cognitive control in this group. These results contribute to the understanding of the neuronal implementation of individual differences regarding attentional mechanisms. Hum Brain Mapp 2009. © 2008 Wiley‐Liss, Inc.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Effects of anterior cingulate fissurization on cognitive control during stroop interference</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Effects of Anterior Cingulate Fissurization</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Effects of anterior cingulate fissurization on cognitive control during stroop interference</title></titleInfo><name type="personal"><namePart type="given">Rene J.</namePart><namePart type="family">Huster</namePart><affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</affiliation><affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</affiliation><affiliation>Department of Psychiatry and Psychotherapy and Interdisciplinary Center for Clinical Research (IZKF), University of Münster, Münster, Germany</affiliation><affiliation>Institute for Biomagnetism and Biosignalanalysis, Malmedyweg 15, 48149 Münster, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Carsten</namePart><namePart type="family">Wolters</namePart><affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Andreas</namePart><namePart type="family">Wollbrink</namePart><affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Elisabeth</namePart><namePart type="family">Schweiger</namePart><affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Werner</namePart><namePart type="family">Wittling</namePart><affiliation>Center for Neuropsychological Research, University of Trier, Trier, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christo</namePart><namePart type="family">Pantev</namePart><affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Markus</namePart><namePart type="family">Junghofer</namePart><affiliation>Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2009-04</dateIssued><dateCaptured encoding="w3cdtf">2007-10-15</dateCaptured><dateValid encoding="w3cdtf">2008-03-21</dateValid><copyrightDate encoding="w3cdtf">2009</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">6</extent><extent unit="references">38</extent><extent unit="words">7658</extent></physicalDescription><abstract lang="en">The midcingulate cortex, as part of the more anteriorly located cingulate regions, is thought to play a major role in cognitive processes like conflict monitoring or response selection. Regarding midcingulate fissurization, the occurrence of a second or paracingulate sulcus is more common in the left than in the right hemisphere and has been shown to be associated with an advantageous performance on tests of executive functions. However, the cognitive mechanisms underlying such behavioral differences are completely unknown. The current study addressed this issue by comparing subjects with a low and a high degree of left hemispheric midcingulate fissurization while collecting behavioral as well as electrophysiological correlates of Stroop interference. A high degree of fissurization was associated with decreased behavioral Stroop interference accompanied by a stronger and prolonged frontal negative potential to incongruent trials starting around 320 ms. This increased frontal negativity is assumed to reflect an enhanced activity of a conflict monitoring system located in the midcingulate cortex. In contrast and starting around 400 ms, subjects with low fissurization revealed an increased positivity over parieto‐occipital regions suggesting a compensatory need for enhanced effortful cognitive control in this group. These results contribute to the understanding of the neuronal implementation of individual differences regarding attentional mechanisms. Hum Brain Mapp 2009. © 2008 Wiley‐Liss, Inc.</abstract><subject lang="en"><genre>keywords</genre><topic>dACC</topic><topic>stroop</topic><topic>paracingulate</topic><topic>conflict monitoring</topic><topic>cognitive control</topic><topic>fissurization</topic></subject><relatedItem type="host"><titleInfo><title>Human Brain Mapping</title></titleInfo><titleInfo type="abbreviated"><title>Hum. 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