Connected speech production in three variants of primary progressive aphasia
Primary progressive aphasia is a clinical syndrome defined by progressive deficits isolated to speech and/or language, and can be classified into non-fluent, semantic and logopenic variants based on motor speech, linguistic and cognitive features. The connected speech of patients with primary progre...
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description | Primary progressive aphasia is a clinical syndrome defined by progressive deficits isolated to speech and/or language, and can be classified into non-fluent, semantic and logopenic variants based on motor speech, linguistic and cognitive features. The connected speech of patients with primary progressive aphasia has often been dichotomized simply as ‘fluent’ or ‘non-fluent’, however fluency is a multidimensional construct that encompasses features such as speech rate, phrase length, articulatory agility and syntactic structure, which are not always impacted in parallel. In this study, our first objective was to improve the characterization of connected speech production in each variant of primary progressive aphasia, by quantifying speech output along a number of motor speech and linguistic dimensions simultaneously. Secondly, we aimed to determine the neuroanatomical correlates of changes along these different dimensions. We recorded, transcribed and analysed speech samples for 50 patients with primary progressive aphasia, along with neurodegenerative and normal control groups. Patients were scanned with magnetic resonance imaging, and voxel-based morphometry was used to identify regions where atrophy correlated significantly with motor speech and linguistic features. Speech samples in patients with the non-fluent variant were characterized by slow rate, distortions, syntactic errors and reduced complexity. In contrast, patients with the semantic variant exhibited normal rate and very few speech or syntactic errors, but showed increased proportions of closed class words, pronouns and verbs, and higher frequency nouns, reflecting lexical retrieval deficits. In patients with the logopenic variant, speech rate (a common proxy for fluency) was intermediate between the other two variants, but distortions and syntactic errors were less common than in the non-fluent variant, while lexical access was less impaired than in the semantic variant. Reduced speech rate was linked with atrophy to a wide range of both anterior and posterior language regions, but specific deficits had more circumscribed anatomical correlates. Frontal regions were associated with motor speech and syntactic processes, anterior and inferior temporal regions with lexical retrieval, and posterior temporal regions with phonological errors and several other types of disruptions to fluency. These findings demonstrate that a multidimensional quantification of connected speech production is necessa |
doi_str_mv | 10.1093/brain/awq129 |
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The connected speech of patients with primary progressive aphasia has often been dichotomized simply as ‘fluent’ or ‘non-fluent’, however fluency is a multidimensional construct that encompasses features such as speech rate, phrase length, articulatory agility and syntactic structure, which are not always impacted in parallel. In this study, our first objective was to improve the characterization of connected speech production in each variant of primary progressive aphasia, by quantifying speech output along a number of motor speech and linguistic dimensions simultaneously. Secondly, we aimed to determine the neuroanatomical correlates of changes along these different dimensions. We recorded, transcribed and analysed speech samples for 50 patients with primary progressive aphasia, along with neurodegenerative and normal control groups. Patients were scanned with magnetic resonance imaging, and voxel-based morphometry was used to identify regions where atrophy correlated significantly with motor speech and linguistic features. Speech samples in patients with the non-fluent variant were characterized by slow rate, distortions, syntactic errors and reduced complexity. In contrast, patients with the semantic variant exhibited normal rate and very few speech or syntactic errors, but showed increased proportions of closed class words, pronouns and verbs, and higher frequency nouns, reflecting lexical retrieval deficits. In patients with the logopenic variant, speech rate (a common proxy for fluency) was intermediate between the other two variants, but distortions and syntactic errors were less common than in the non-fluent variant, while lexical access was less impaired than in the semantic variant. Reduced speech rate was linked with atrophy to a wide range of both anterior and posterior language regions, but specific deficits had more circumscribed anatomical correlates. Frontal regions were associated with motor speech and syntactic processes, anterior and inferior temporal regions with lexical retrieval, and posterior temporal regions with phonological errors and several other types of disruptions to fluency. These findings demonstrate that a multidimensional quantification of connected speech production is necessary to characterize the differences between the speech patterns of each primary progressive aphasic variant adequately, and to reveal associations between particular aspects of connected speech and specific components of the neural network for speech production.</description><identifier>ISSN: 0006-8950</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/awq129</identifier><identifier>PMID: 20542982</identifier><identifier>CODEN: BRAIAK</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Aged ; Aphasia, Primary Progressive - complications ; Aphasia, Primary Progressive - diagnosis ; Aphasia, Primary Progressive - physiopathology ; Biological and medical sciences ; Brain Mapping - methods ; Female ; Frontotemporal Dementia - complications ; Frontotemporal Dementia - diagnosis ; Frontotemporal Dementia - physiopathology ; Humans ; logopenic progressive aphasia ; Male ; Medical sciences ; Middle Aged ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Nerve Net - pathology ; Nerve Net - physiopathology ; Neurology ; Original ; primary progressive aphasia ; progressive non-fluent aphasia ; semantic dementia ; Speech - physiology ; speech production ; Speech Production Measurement - methods</subject><ispartof>Brain (London, England : 1878), 2010-07, Vol.133 (7), p.2069-2088</ispartof><rights>2015 INIST-CNRS</rights><rights>The Author (2010). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-cd0edf25caaa0444cee868580341d3e3601e2212a58426ee311e612a63c2a7c53</citedby><cites>FETCH-LOGICAL-c515t-cd0edf25caaa0444cee868580341d3e3601e2212a58426ee311e612a63c2a7c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22985093$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20542982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilson, Stephen M.</creatorcontrib><creatorcontrib>Henry, Maya L.</creatorcontrib><creatorcontrib>Besbris, Max</creatorcontrib><creatorcontrib>Ogar, Jennifer M.</creatorcontrib><creatorcontrib>Dronkers, Nina F.</creatorcontrib><creatorcontrib>Jarrold, William</creatorcontrib><creatorcontrib>Miller, Bruce L.</creatorcontrib><creatorcontrib>Gorno-Tempini, Maria Luisa</creatorcontrib><title>Connected speech production in three variants of primary progressive aphasia</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>Primary progressive aphasia is a clinical syndrome defined by progressive deficits isolated to speech and/or language, and can be classified into non-fluent, semantic and logopenic variants based on motor speech, linguistic and cognitive features. The connected speech of patients with primary progressive aphasia has often been dichotomized simply as ‘fluent’ or ‘non-fluent’, however fluency is a multidimensional construct that encompasses features such as speech rate, phrase length, articulatory agility and syntactic structure, which are not always impacted in parallel. In this study, our first objective was to improve the characterization of connected speech production in each variant of primary progressive aphasia, by quantifying speech output along a number of motor speech and linguistic dimensions simultaneously. Secondly, we aimed to determine the neuroanatomical correlates of changes along these different dimensions. We recorded, transcribed and analysed speech samples for 50 patients with primary progressive aphasia, along with neurodegenerative and normal control groups. Patients were scanned with magnetic resonance imaging, and voxel-based morphometry was used to identify regions where atrophy correlated significantly with motor speech and linguistic features. Speech samples in patients with the non-fluent variant were characterized by slow rate, distortions, syntactic errors and reduced complexity. In contrast, patients with the semantic variant exhibited normal rate and very few speech or syntactic errors, but showed increased proportions of closed class words, pronouns and verbs, and higher frequency nouns, reflecting lexical retrieval deficits. In patients with the logopenic variant, speech rate (a common proxy for fluency) was intermediate between the other two variants, but distortions and syntactic errors were less common than in the non-fluent variant, while lexical access was less impaired than in the semantic variant. Reduced speech rate was linked with atrophy to a wide range of both anterior and posterior language regions, but specific deficits had more circumscribed anatomical correlates. Frontal regions were associated with motor speech and syntactic processes, anterior and inferior temporal regions with lexical retrieval, and posterior temporal regions with phonological errors and several other types of disruptions to fluency. These findings demonstrate that a multidimensional quantification of connected speech production is necessary to characterize the differences between the speech patterns of each primary progressive aphasic variant adequately, and to reveal associations between particular aspects of connected speech and specific components of the neural network for speech production.</description><subject>Aged</subject><subject>Aphasia, Primary Progressive - complications</subject><subject>Aphasia, Primary Progressive - diagnosis</subject><subject>Aphasia, Primary Progressive - physiopathology</subject><subject>Biological and medical sciences</subject><subject>Brain Mapping - methods</subject><subject>Female</subject><subject>Frontotemporal Dementia - complications</subject><subject>Frontotemporal Dementia - diagnosis</subject><subject>Frontotemporal Dementia - physiopathology</subject><subject>Humans</subject><subject>logopenic progressive aphasia</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Nerve Net - pathology</subject><subject>Nerve Net - physiopathology</subject><subject>Neurology</subject><subject>Original</subject><subject>primary progressive aphasia</subject><subject>progressive non-fluent aphasia</subject><subject>semantic dementia</subject><subject>Speech - physiology</subject><subject>speech production</subject><subject>Speech Production Measurement - methods</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c-LEzEUB_AgiltXb55lLuLFcV9-zsxF0OK6QlHwB4iX8DbzZhudJt1kWvW_N7W16mlPIbwPX17yZewhh2ccOnl2mdCHM_x-zUV3i824MlALrs1tNgMAU7edhhN2L-evAFxJYe6yEwFaia4VM7aYxxDITdRXeU3kltU6xX7jJh9D5UM1LRNRtcXkMUy5ikOZ-xWmnzt3lShnv6UK10vMHu-zOwOOmR4czlP26fzVx_lFvXj3-s38xaJ2muupdj1QPwjtEBGUUo6oNa1uQSreS5IGOAnBBepWCUMkOSdTrkY6gY3T8pQ93-euN5cr6h2FKeFoD5vZiN7-Pwl-aa_i1oq2E52CEvDkEJDi9YbyZFc-OxpHDBQ32TZatuUPu-ZmqVQDIIW8WUqpGm3kTj7dS5dizomG4-Yc7K5T-7tTu--08Ef_vvaI_5RYwOMDwOxwHBIG5_NfV5AuqcXVe-fzRD-Oc0zfrGlko-3F5y928fL8bfeh0_a9_AVBLLu3</recordid><startdate>20100701</startdate><enddate>20100701</enddate><creator>Wilson, Stephen M.</creator><creator>Henry, Maya L.</creator><creator>Besbris, Max</creator><creator>Ogar, Jennifer M.</creator><creator>Dronkers, Nina F.</creator><creator>Jarrold, William</creator><creator>Miller, Bruce L.</creator><creator>Gorno-Tempini, Maria Luisa</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</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>7TK</scope><scope>7T9</scope><scope>5PM</scope></search><sort><creationdate>20100701</creationdate><title>Connected speech production in three variants of primary progressive aphasia</title><author>Wilson, Stephen M. ; Henry, Maya L. ; Besbris, Max ; Ogar, Jennifer M. ; Dronkers, Nina F. ; Jarrold, William ; Miller, Bruce L. ; Gorno-Tempini, Maria Luisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-cd0edf25caaa0444cee868580341d3e3601e2212a58426ee311e612a63c2a7c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aged</topic><topic>Aphasia, Primary Progressive - complications</topic><topic>Aphasia, Primary Progressive - diagnosis</topic><topic>Aphasia, Primary Progressive - physiopathology</topic><topic>Biological and medical sciences</topic><topic>Brain Mapping - methods</topic><topic>Female</topic><topic>Frontotemporal Dementia - complications</topic><topic>Frontotemporal Dementia - diagnosis</topic><topic>Frontotemporal Dementia - physiopathology</topic><topic>Humans</topic><topic>logopenic progressive aphasia</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Nerve Net - pathology</topic><topic>Nerve Net - physiopathology</topic><topic>Neurology</topic><topic>Original</topic><topic>primary progressive aphasia</topic><topic>progressive non-fluent aphasia</topic><topic>semantic dementia</topic><topic>Speech - physiology</topic><topic>speech production</topic><topic>Speech Production Measurement - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilson, Stephen M.</creatorcontrib><creatorcontrib>Henry, Maya L.</creatorcontrib><creatorcontrib>Besbris, Max</creatorcontrib><creatorcontrib>Ogar, Jennifer M.</creatorcontrib><creatorcontrib>Dronkers, Nina F.</creatorcontrib><creatorcontrib>Jarrold, William</creatorcontrib><creatorcontrib>Miller, Bruce L.</creatorcontrib><creatorcontrib>Gorno-Tempini, Maria Luisa</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>Neurosciences Abstracts</collection><collection>Linguistics and Language Behavior Abstracts (LLBA)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain (London, England : 1878)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilson, Stephen M.</au><au>Henry, Maya L.</au><au>Besbris, Max</au><au>Ogar, Jennifer M.</au><au>Dronkers, Nina F.</au><au>Jarrold, William</au><au>Miller, Bruce L.</au><au>Gorno-Tempini, Maria Luisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Connected speech production in three variants of primary progressive aphasia</atitle><jtitle>Brain (London, England : 1878)</jtitle><addtitle>Brain</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>133</volume><issue>7</issue><spage>2069</spage><epage>2088</epage><pages>2069-2088</pages><issn>0006-8950</issn><eissn>1460-2156</eissn><coden>BRAIAK</coden><abstract>Primary progressive aphasia is a clinical syndrome defined by progressive deficits isolated to speech and/or language, and can be classified into non-fluent, semantic and logopenic variants based on motor speech, linguistic and cognitive features. The connected speech of patients with primary progressive aphasia has often been dichotomized simply as ‘fluent’ or ‘non-fluent’, however fluency is a multidimensional construct that encompasses features such as speech rate, phrase length, articulatory agility and syntactic structure, which are not always impacted in parallel. In this study, our first objective was to improve the characterization of connected speech production in each variant of primary progressive aphasia, by quantifying speech output along a number of motor speech and linguistic dimensions simultaneously. Secondly, we aimed to determine the neuroanatomical correlates of changes along these different dimensions. We recorded, transcribed and analysed speech samples for 50 patients with primary progressive aphasia, along with neurodegenerative and normal control groups. Patients were scanned with magnetic resonance imaging, and voxel-based morphometry was used to identify regions where atrophy correlated significantly with motor speech and linguistic features. Speech samples in patients with the non-fluent variant were characterized by slow rate, distortions, syntactic errors and reduced complexity. In contrast, patients with the semantic variant exhibited normal rate and very few speech or syntactic errors, but showed increased proportions of closed class words, pronouns and verbs, and higher frequency nouns, reflecting lexical retrieval deficits. In patients with the logopenic variant, speech rate (a common proxy for fluency) was intermediate between the other two variants, but distortions and syntactic errors were less common than in the non-fluent variant, while lexical access was less impaired than in the semantic variant. Reduced speech rate was linked with atrophy to a wide range of both anterior and posterior language regions, but specific deficits had more circumscribed anatomical correlates. Frontal regions were associated with motor speech and syntactic processes, anterior and inferior temporal regions with lexical retrieval, and posterior temporal regions with phonological errors and several other types of disruptions to fluency. These findings demonstrate that a multidimensional quantification of connected speech production is necessary to characterize the differences between the speech patterns of each primary progressive aphasic variant adequately, and to reveal associations between particular aspects of connected speech and specific components of the neural network for speech production.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>20542982</pmid><doi>10.1093/brain/awq129</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aphasia, Primary Progressive - complications Aphasia, Primary Progressive - diagnosis Aphasia, Primary Progressive - physiopathology Biological and medical sciences Brain Mapping - methods Female Frontotemporal Dementia - complications Frontotemporal Dementia - diagnosis Frontotemporal Dementia - physiopathology Humans logopenic progressive aphasia Male Medical sciences Middle Aged Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Nerve Net - pathology Nerve Net - physiopathology Neurology Original primary progressive aphasia progressive non-fluent aphasia semantic dementia Speech - physiology speech production Speech Production Measurement - methods |
title | Connected speech production in three variants of primary progressive aphasia |
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