Anatomical evidence of an indirect pathway for word repetition
OBJECTIVETo combine MRI-based cortical morphometry and diffusion white matter tractography to describe the anatomical correlates of repetition deficits in patients with primary progressive aphasia (PPA). METHODSThe traditional anatomical model of language identifies a network for word repetition tha...
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creator | Forkel, Stephanie J. Rogalski, Emily Drossinos Sancho, Niki D'Anna, Lucio Luque Laguna, Pedro Sridhar, Jaiashre Dell'Acqua, Flavio Weintraub, Sandra Thompson, Cynthia Mesulam, M.-Marsel Catani, Marco |
description | OBJECTIVETo combine MRI-based cortical morphometry and diffusion white matter tractography to describe the anatomical correlates of repetition deficits in patients with primary progressive aphasia (PPA).
METHODSThe traditional anatomical model of language identifies a network for word repetition that includes Wernicke and Broca regions directly connected via the arcuate fasciculus. Recent tractography findings of an indirect pathway between Wernicke and Broca regions suggest a critical role of the inferior parietal lobe for repetition. To test whether repetition deficits are associated with damage to the direct or indirect pathway between both regions, tractography analysis was performed in 30 patients with PPA (64.27 ± 8.51 years) and 22 healthy controls. Cortical volume measurements were also extracted from 8 perisylvian language areas connected by the direct and indirect pathways.
RESULTSCompared to healthy controls, patients with PPA presented with reduced performance in repetition tasks and increased damage to most of the perisylvian cortical regions and their connections through the indirect pathway. Repetition deficits were prominent in patients with cortical atrophy of the temporo-parietal region with volumetric reductions of the indirect pathway.
CONCLUSIONSThe results suggest that in PPA, deficits in repetition are due to damage to the temporo-parietal cortex and its connections to Wernicke and Broca regions. We therefore propose a revised language model that also includes an indirect pathway for repetition, which has important clinical implications for the functional mapping and treatment of neurologic patients. |
doi_str_mv | 10.1212/WNL.0000000000008746 |
format | Article |
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METHODSThe traditional anatomical model of language identifies a network for word repetition that includes Wernicke and Broca regions directly connected via the arcuate fasciculus. Recent tractography findings of an indirect pathway between Wernicke and Broca regions suggest a critical role of the inferior parietal lobe for repetition. To test whether repetition deficits are associated with damage to the direct or indirect pathway between both regions, tractography analysis was performed in 30 patients with PPA (64.27 ± 8.51 years) and 22 healthy controls. Cortical volume measurements were also extracted from 8 perisylvian language areas connected by the direct and indirect pathways.
RESULTSCompared to healthy controls, patients with PPA presented with reduced performance in repetition tasks and increased damage to most of the perisylvian cortical regions and their connections through the indirect pathway. Repetition deficits were prominent in patients with cortical atrophy of the temporo-parietal region with volumetric reductions of the indirect pathway.
CONCLUSIONSThe results suggest that in PPA, deficits in repetition are due to damage to the temporo-parietal cortex and its connections to Wernicke and Broca regions. We therefore propose a revised language model that also includes an indirect pathway for repetition, which has important clinical implications for the functional mapping and treatment of neurologic patients.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/WNL.0000000000008746</identifier><identifier>PMID: 31996450</identifier><language>eng</language><publisher>PHILADELPHIA: American Academy of Neurology</publisher><subject>Aged ; Aphasia, Primary Progressive - diagnostic imaging ; Aphasia, Primary Progressive - physiopathology ; Broca Area - diagnostic imaging ; Broca Area - physiopathology ; Case-Control Studies ; Cerebral Cortex - diagnostic imaging ; Cerebral Cortex - pathology ; Cerebral Cortex - physiopathology ; Clinical Neurology ; Diffusion Tensor Imaging ; Female ; Gray Matter - diagnostic imaging ; Humans ; Life Sciences & Biomedicine ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Neural Pathways - diagnostic imaging ; Neurosciences & Neurology ; Organ Size ; Parietal Lobe - diagnostic imaging ; Parietal Lobe - physiopathology ; Science & Technology ; Wernicke Area - diagnostic imaging ; Wernicke Area - physiopathology ; White Matter - diagnostic imaging</subject><ispartof>Neurology, 2020-02, Vol.94 (6), p.e594-e606</ispartof><rights>American Academy of Neurology</rights><rights>2020 American Academy of Neurology</rights><rights>Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.</rights><rights>Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. 2020 American Academy of Neurology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>54</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000530106000013</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c6196-84f1b1855a71442a5d5ab7d7b9820e05906b786dea5fdc987427406d1b0506293</citedby><cites>FETCH-LOGICAL-c6196-84f1b1855a71442a5d5ab7d7b9820e05906b786dea5fdc987427406d1b0506293</cites><orcidid>0000-0003-0493-0283 ; 0000-0001-5313-5476 ; 0000-0002-6472-1363 ; 0000-0001-5731-851X ; 0000-0002-5488-6463 ; 0000-0003-3718-7545 ; 0000-0003-2605-5205 ; 0000-0002-9191-7409</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27929,27930,28253,28254</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31996450$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Forkel, Stephanie J.</creatorcontrib><creatorcontrib>Rogalski, Emily</creatorcontrib><creatorcontrib>Drossinos Sancho, Niki</creatorcontrib><creatorcontrib>D'Anna, Lucio</creatorcontrib><creatorcontrib>Luque Laguna, Pedro</creatorcontrib><creatorcontrib>Sridhar, Jaiashre</creatorcontrib><creatorcontrib>Dell'Acqua, Flavio</creatorcontrib><creatorcontrib>Weintraub, Sandra</creatorcontrib><creatorcontrib>Thompson, Cynthia</creatorcontrib><creatorcontrib>Mesulam, M.-Marsel</creatorcontrib><creatorcontrib>Catani, Marco</creatorcontrib><title>Anatomical evidence of an indirect pathway for word repetition</title><title>Neurology</title><addtitle>NEUROLOGY</addtitle><addtitle>Neurology</addtitle><description>OBJECTIVETo combine MRI-based cortical morphometry and diffusion white matter tractography to describe the anatomical correlates of repetition deficits in patients with primary progressive aphasia (PPA).
METHODSThe traditional anatomical model of language identifies a network for word repetition that includes Wernicke and Broca regions directly connected via the arcuate fasciculus. Recent tractography findings of an indirect pathway between Wernicke and Broca regions suggest a critical role of the inferior parietal lobe for repetition. To test whether repetition deficits are associated with damage to the direct or indirect pathway between both regions, tractography analysis was performed in 30 patients with PPA (64.27 ± 8.51 years) and 22 healthy controls. Cortical volume measurements were also extracted from 8 perisylvian language areas connected by the direct and indirect pathways.
RESULTSCompared to healthy controls, patients with PPA presented with reduced performance in repetition tasks and increased damage to most of the perisylvian cortical regions and their connections through the indirect pathway. Repetition deficits were prominent in patients with cortical atrophy of the temporo-parietal region with volumetric reductions of the indirect pathway.
CONCLUSIONSThe results suggest that in PPA, deficits in repetition are due to damage to the temporo-parietal cortex and its connections to Wernicke and Broca regions. We therefore propose a revised language model that also includes an indirect pathway for repetition, which has important clinical implications for the functional mapping and treatment of neurologic patients.</description><subject>Aged</subject><subject>Aphasia, Primary Progressive - diagnostic imaging</subject><subject>Aphasia, Primary Progressive - physiopathology</subject><subject>Broca Area - diagnostic imaging</subject><subject>Broca Area - physiopathology</subject><subject>Case-Control Studies</subject><subject>Cerebral Cortex - diagnostic imaging</subject><subject>Cerebral Cortex - pathology</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Clinical Neurology</subject><subject>Diffusion Tensor Imaging</subject><subject>Female</subject><subject>Gray Matter - diagnostic imaging</subject><subject>Humans</subject><subject>Life Sciences & Biomedicine</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neural Pathways - diagnostic imaging</subject><subject>Neurosciences & Neurology</subject><subject>Organ Size</subject><subject>Parietal Lobe - diagnostic imaging</subject><subject>Parietal Lobe - physiopathology</subject><subject>Science & Technology</subject><subject>Wernicke Area - diagnostic imaging</subject><subject>Wernicke Area - physiopathology</subject><subject>White Matter - diagnostic imaging</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>ARHDP</sourceid><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhi0EokvhHyCUIxJKmfFXnEulalU-pFV7AcHNchKHNWTjxXa66r_H6ZbVlgMwlznM-77jeWRCXiKcIUX69svV6gyOSlVcPiILFFSWktGvj8kCgKqSqUqdkGcxfgfIw6p-Sk4Y1rXkAhbk_GI0yW9ca4bC3rjOjq0tfF-YsXBj54JtU7E1ab0zt0XvQ7HzoSuC3drkkvPjc_KkN0O0L-77Kfn87vLT8kO5un7_cXmxKluJtSwV77FBJYSpkHNqRCdMU3VVUysKFkQNsqmU7KwRfdfW-RRacZAdNiBA0pqdkvN97nZqNrZr7ZiCGfQ2uI0Jt9obpx9ORrfW3_yNrpBJkDIHvL4PCP7nZGPSGxdbOwxmtH6KmjKuFCAFlqV8L22DjzHY_rAGQc_odUav_0Sfba-On3gw_WadBWov2NnG97F1M-uDLMcIBghyDkS2dMnMgJd-GlO2vvl_69EiPyQb4o9h2tmg19YMaf2vI_hfrLNMIvKSAs1_CxHKOyf7BcGxv_k</recordid><startdate>20200211</startdate><enddate>20200211</enddate><creator>Forkel, Stephanie J.</creator><creator>Rogalski, Emily</creator><creator>Drossinos Sancho, Niki</creator><creator>D'Anna, Lucio</creator><creator>Luque Laguna, Pedro</creator><creator>Sridhar, Jaiashre</creator><creator>Dell'Acqua, Flavio</creator><creator>Weintraub, Sandra</creator><creator>Thompson, Cynthia</creator><creator>Mesulam, M.-Marsel</creator><creator>Catani, Marco</creator><general>American Academy of Neurology</general><general>Lippincott Williams & Wilkins</general><scope>17B</scope><scope>AOWDO</scope><scope>ARHDP</scope><scope>BLEPL</scope><scope>DTL</scope><scope>DVR</scope><scope>EGQ</scope><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>5PM</scope><orcidid>https://orcid.org/0000-0003-0493-0283</orcidid><orcidid>https://orcid.org/0000-0001-5313-5476</orcidid><orcidid>https://orcid.org/0000-0002-6472-1363</orcidid><orcidid>https://orcid.org/0000-0001-5731-851X</orcidid><orcidid>https://orcid.org/0000-0002-5488-6463</orcidid><orcidid>https://orcid.org/0000-0003-3718-7545</orcidid><orcidid>https://orcid.org/0000-0003-2605-5205</orcidid><orcidid>https://orcid.org/0000-0002-9191-7409</orcidid></search><sort><creationdate>20200211</creationdate><title>Anatomical evidence of an indirect pathway for word repetition</title><author>Forkel, Stephanie J. ; Rogalski, Emily ; Drossinos Sancho, Niki ; D'Anna, Lucio ; Luque Laguna, Pedro ; Sridhar, Jaiashre ; Dell'Acqua, Flavio ; Weintraub, Sandra ; Thompson, Cynthia ; Mesulam, M.-Marsel ; Catani, Marco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6196-84f1b1855a71442a5d5ab7d7b9820e05906b786dea5fdc987427406d1b0506293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Aphasia, Primary Progressive - diagnostic imaging</topic><topic>Aphasia, Primary Progressive - physiopathology</topic><topic>Broca Area - diagnostic imaging</topic><topic>Broca Area - physiopathology</topic><topic>Case-Control Studies</topic><topic>Cerebral Cortex - diagnostic imaging</topic><topic>Cerebral Cortex - pathology</topic><topic>Cerebral Cortex - physiopathology</topic><topic>Clinical Neurology</topic><topic>Diffusion Tensor Imaging</topic><topic>Female</topic><topic>Gray Matter - diagnostic imaging</topic><topic>Humans</topic><topic>Life Sciences & Biomedicine</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neural Pathways - diagnostic imaging</topic><topic>Neurosciences & Neurology</topic><topic>Organ Size</topic><topic>Parietal Lobe - diagnostic imaging</topic><topic>Parietal Lobe - physiopathology</topic><topic>Science & Technology</topic><topic>Wernicke Area - diagnostic imaging</topic><topic>Wernicke Area - physiopathology</topic><topic>White Matter - diagnostic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Forkel, Stephanie J.</creatorcontrib><creatorcontrib>Rogalski, Emily</creatorcontrib><creatorcontrib>Drossinos Sancho, Niki</creatorcontrib><creatorcontrib>D'Anna, Lucio</creatorcontrib><creatorcontrib>Luque Laguna, Pedro</creatorcontrib><creatorcontrib>Sridhar, Jaiashre</creatorcontrib><creatorcontrib>Dell'Acqua, Flavio</creatorcontrib><creatorcontrib>Weintraub, Sandra</creatorcontrib><creatorcontrib>Thompson, Cynthia</creatorcontrib><creatorcontrib>Mesulam, M.-Marsel</creatorcontrib><creatorcontrib>Catani, Marco</creatorcontrib><collection>Web of Knowledge</collection><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science - Social Sciences Citation Index – 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Social Sciences Citation Index</collection><collection>Web of Science Primary (SCIE, SSCI & AHCI)</collection><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>PubMed Central (Full Participant titles)</collection><jtitle>Neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Forkel, Stephanie J.</au><au>Rogalski, Emily</au><au>Drossinos Sancho, Niki</au><au>D'Anna, Lucio</au><au>Luque Laguna, Pedro</au><au>Sridhar, Jaiashre</au><au>Dell'Acqua, Flavio</au><au>Weintraub, Sandra</au><au>Thompson, Cynthia</au><au>Mesulam, M.-Marsel</au><au>Catani, Marco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anatomical evidence of an indirect pathway for word repetition</atitle><jtitle>Neurology</jtitle><stitle>NEUROLOGY</stitle><addtitle>Neurology</addtitle><date>2020-02-11</date><risdate>2020</risdate><volume>94</volume><issue>6</issue><spage>e594</spage><epage>e606</epage><pages>e594-e606</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><abstract>OBJECTIVETo combine MRI-based cortical morphometry and diffusion white matter tractography to describe the anatomical correlates of repetition deficits in patients with primary progressive aphasia (PPA).
METHODSThe traditional anatomical model of language identifies a network for word repetition that includes Wernicke and Broca regions directly connected via the arcuate fasciculus. Recent tractography findings of an indirect pathway between Wernicke and Broca regions suggest a critical role of the inferior parietal lobe for repetition. To test whether repetition deficits are associated with damage to the direct or indirect pathway between both regions, tractography analysis was performed in 30 patients with PPA (64.27 ± 8.51 years) and 22 healthy controls. Cortical volume measurements were also extracted from 8 perisylvian language areas connected by the direct and indirect pathways.
RESULTSCompared to healthy controls, patients with PPA presented with reduced performance in repetition tasks and increased damage to most of the perisylvian cortical regions and their connections through the indirect pathway. Repetition deficits were prominent in patients with cortical atrophy of the temporo-parietal region with volumetric reductions of the indirect pathway.
CONCLUSIONSThe results suggest that in PPA, deficits in repetition are due to damage to the temporo-parietal cortex and its connections to Wernicke and Broca regions. We therefore propose a revised language model that also includes an indirect pathway for repetition, which has important clinical implications for the functional mapping and treatment of neurologic patients.</abstract><cop>PHILADELPHIA</cop><pub>American Academy of Neurology</pub><pmid>31996450</pmid><doi>10.1212/WNL.0000000000008746</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-0493-0283</orcidid><orcidid>https://orcid.org/0000-0001-5313-5476</orcidid><orcidid>https://orcid.org/0000-0002-6472-1363</orcidid><orcidid>https://orcid.org/0000-0001-5731-851X</orcidid><orcidid>https://orcid.org/0000-0002-5488-6463</orcidid><orcidid>https://orcid.org/0000-0003-3718-7545</orcidid><orcidid>https://orcid.org/0000-0003-2605-5205</orcidid><orcidid>https://orcid.org/0000-0002-9191-7409</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aphasia, Primary Progressive - diagnostic imaging Aphasia, Primary Progressive - physiopathology Broca Area - diagnostic imaging Broca Area - physiopathology Case-Control Studies Cerebral Cortex - diagnostic imaging Cerebral Cortex - pathology Cerebral Cortex - physiopathology Clinical Neurology Diffusion Tensor Imaging Female Gray Matter - diagnostic imaging Humans Life Sciences & Biomedicine Magnetic Resonance Imaging Male Middle Aged Neural Pathways - diagnostic imaging Neurosciences & Neurology Organ Size Parietal Lobe - diagnostic imaging Parietal Lobe - physiopathology Science & Technology Wernicke Area - diagnostic imaging Wernicke Area - physiopathology White Matter - diagnostic imaging |
title | Anatomical evidence of an indirect pathway for word repetition |
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