Neuroanatomical differences in brain areas implicated in perceptual and other core features of autism revealed by cortical thickness analysis and voxel-based morphometry
Autism spectrum disorder is a complex neurodevelopmental variant thought to affect 1 in 166 [Fombonne (2003): J Autism Dev Disord 33:365–382]. Individuals with autism demonstrate atypical social interaction, communication, and repetitive behaviors, but can also present enhanced abilities, particular...
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description | Autism spectrum disorder is a complex neurodevelopmental variant thought to affect 1 in 166 [Fombonne (2003): J Autism Dev Disord 33:365–382]. Individuals with autism demonstrate atypical social interaction, communication, and repetitive behaviors, but can also present enhanced abilities, particularly in auditory and visual perception and nonverbal reasoning. Structural brain differences have been reported in autism, in terms of increased total brain volume (particularly in young children with autism), and regional gray/white matter differences in both adults and children with autism, but the reports are inconsistent [Amaral et al. (2008): Trends Neurosci 31:137–145]. These inconsistencies may be due to differences in diagnostic/inclusion criteria, and age and Intelligence Quotient of participants. Here, for the first time, we used two complementary magnetic resonance imaging techniques, cortical thickness analyses, and voxel‐based morphometry (VBM), to investigate the neuroanatomical differences between a homogenous group of young adults with autism of average intelligence but delayed or atypical language development (often referred to as “high‐functioning autism”), relative to a closely matched group of typically developing controls. The cortical thickness and VBM techniques both revealed regional structural brain differences (mostly in terms of gray matter increases) in brain areas implicated in social cognition, communication, and repetitive behaviors, and thus in each of the core atypical features of autism. Gray matter increases were also found in auditory and visual primary and associative perceptual areas. We interpret these results as the first structural brain correlates of atypical auditory and visual perception in autism, in support of the enhanced perceptual functioning model [Mottron et al. (2006): J Autism Dev Disord 36:27–43]. Hum Brain Mapp, 2010. © 2009 Wiley‐Liss, Inc. |
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Individuals with autism demonstrate atypical social interaction, communication, and repetitive behaviors, but can also present enhanced abilities, particularly in auditory and visual perception and nonverbal reasoning. Structural brain differences have been reported in autism, in terms of increased total brain volume (particularly in young children with autism), and regional gray/white matter differences in both adults and children with autism, but the reports are inconsistent [Amaral et al. (2008): Trends Neurosci 31:137–145]. These inconsistencies may be due to differences in diagnostic/inclusion criteria, and age and Intelligence Quotient of participants. Here, for the first time, we used two complementary magnetic resonance imaging techniques, cortical thickness analyses, and voxel‐based morphometry (VBM), to investigate the neuroanatomical differences between a homogenous group of young adults with autism of average intelligence but delayed or atypical language development (often referred to as “high‐functioning autism”), relative to a closely matched group of typically developing controls. The cortical thickness and VBM techniques both revealed regional structural brain differences (mostly in terms of gray matter increases) in brain areas implicated in social cognition, communication, and repetitive behaviors, and thus in each of the core atypical features of autism. Gray matter increases were also found in auditory and visual primary and associative perceptual areas. We interpret these results as the first structural brain correlates of atypical auditory and visual perception in autism, in support of the enhanced perceptual functioning model [Mottron et al. (2006): J Autism Dev Disord 36:27–43]. Hum Brain Mapp, 2010. © 2009 Wiley‐Liss, Inc.</description><identifier>ISSN: 1065-9471</identifier><identifier>EISSN: 1097-0193</identifier><identifier>DOI: 10.1002/hbm.20887</identifier><identifier>PMID: 19790171</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; autism ; Autistic Disorder - complications ; Autistic Disorder - pathology ; Biological and medical sciences ; brain ; Brain - pathology ; Cerebral Cortex - pathology ; cortical thickness ; enhanced perceptual functioning model ; Humans ; Image Processing, Computer-Assisted ; Intelligence ; Intelligence Tests ; Investigative techniques, diagnostic techniques (general aspects) ; Language Disorders - etiology ; Language Disorders - pathology ; Magnetic Resonance Imaging - methods ; Male ; Medical sciences ; MRI ; Nervous system ; Nervous system involvement in other diseases. Miscellaneous ; Neurology ; Organ Size ; Radiodiagnosis. Nmr imagery. 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Brain Mapp</addtitle><description>Autism spectrum disorder is a complex neurodevelopmental variant thought to affect 1 in 166 [Fombonne (2003): J Autism Dev Disord 33:365–382]. Individuals with autism demonstrate atypical social interaction, communication, and repetitive behaviors, but can also present enhanced abilities, particularly in auditory and visual perception and nonverbal reasoning. Structural brain differences have been reported in autism, in terms of increased total brain volume (particularly in young children with autism), and regional gray/white matter differences in both adults and children with autism, but the reports are inconsistent [Amaral et al. (2008): Trends Neurosci 31:137–145]. These inconsistencies may be due to differences in diagnostic/inclusion criteria, and age and Intelligence Quotient of participants. Here, for the first time, we used two complementary magnetic resonance imaging techniques, cortical thickness analyses, and voxel‐based morphometry (VBM), to investigate the neuroanatomical differences between a homogenous group of young adults with autism of average intelligence but delayed or atypical language development (often referred to as “high‐functioning autism”), relative to a closely matched group of typically developing controls. The cortical thickness and VBM techniques both revealed regional structural brain differences (mostly in terms of gray matter increases) in brain areas implicated in social cognition, communication, and repetitive behaviors, and thus in each of the core atypical features of autism. Gray matter increases were also found in auditory and visual primary and associative perceptual areas. We interpret these results as the first structural brain correlates of atypical auditory and visual perception in autism, in support of the enhanced perceptual functioning model [Mottron et al. (2006): J Autism Dev Disord 36:27–43]. Hum Brain Mapp, 2010. © 2009 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Adult</subject><subject>autism</subject><subject>Autistic Disorder - complications</subject><subject>Autistic Disorder - pathology</subject><subject>Biological and medical sciences</subject><subject>brain</subject><subject>Brain - pathology</subject><subject>Cerebral Cortex - pathology</subject><subject>cortical thickness</subject><subject>enhanced perceptual functioning model</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Intelligence</subject><subject>Intelligence Tests</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Language Disorders - etiology</subject><subject>Language Disorders - pathology</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Medical sciences</subject><subject>MRI</subject><subject>Nervous system</subject><subject>Nervous system involvement in other diseases. Miscellaneous</subject><subject>Neurology</subject><subject>Organ Size</subject><subject>Radiodiagnosis. Nmr imagery. Nmr spectrometry</subject><subject>Severity of Illness Index</subject><subject>voxel-based-morphometry</subject><subject>Young Adult</subject><issn>1065-9471</issn><issn>1097-0193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstu1DAUhiMEomVgwQugbBBikdaOkzjeIMEIOkjTsimXnXXsnDCmSRxsZ-g8Em-J58IAC9SNLzrf__8-8kmSp5ScUULy85Xqz3JS1_xeckqJ4Bmhgt3fnqsyEwWnJ8kj778RQmlJ6MPkhAouCOX0NPl5hZOzMECwvdHQpY1pW3Q4aPSpGVLlIK7gEOK1H7vIBGy2lRGdxjFMUQNDk9qwQpdq6zBtEcLkot62KUzB-D51uEboolBttkzYRYWV0TcDeh8NoNt443dOa3uLXabAR7y3blzZHoPbPE4etNB5fHLYZ8nHd2-v54ts-eHi_fz1MtMVzXlW1U1dENFqLUiVK6iFVkRUijdaUCVYmXPeNqqpKVNl0SrGGGmYqISgBWiNbJa82vuOk-qx0TgEB50cnenBbaQFI_-tDGYlv9q1rGpO6mg3S14cDJz9PqEPsjdeY9fBgHbykpdFWdK8pHeTRSkYZ4LcTTKWC1HF_Fnyck9qZ7132B5fToncTouM0yJ30xLZZ3-3-oc8jEcEnh8A8PHHWgeDNv7I5bGJoiq23Pme-2E63Pw_US7eXP6OzvYK4wPeHhXgbmTFGS_l56sLubz8dL34UhA5Z78A8AjqaQ</recordid><startdate>201004</startdate><enddate>201004</enddate><creator>Hyde, Krista L.</creator><creator>Samson, Fabienne</creator><creator>Evans, Alan C.</creator><creator>Mottron, Laurent</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>5PM</scope></search><sort><creationdate>201004</creationdate><title>Neuroanatomical differences in brain areas implicated in perceptual and other core features of autism revealed by cortical thickness analysis and voxel-based morphometry</title><author>Hyde, Krista L. ; Samson, Fabienne ; Evans, Alan C. ; Mottron, Laurent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6127-68d8409fcc9062ba89cb096b7dc91b935277fdbd813b54fb3330d3969914acce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>autism</topic><topic>Autistic Disorder - complications</topic><topic>Autistic Disorder - pathology</topic><topic>Biological and medical sciences</topic><topic>brain</topic><topic>Brain - pathology</topic><topic>Cerebral Cortex - pathology</topic><topic>cortical thickness</topic><topic>enhanced perceptual functioning model</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Intelligence</topic><topic>Intelligence Tests</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Language Disorders - etiology</topic><topic>Language Disorders - pathology</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Medical sciences</topic><topic>MRI</topic><topic>Nervous system</topic><topic>Nervous system involvement in other diseases. Miscellaneous</topic><topic>Neurology</topic><topic>Organ Size</topic><topic>Radiodiagnosis. Nmr imagery. Nmr spectrometry</topic><topic>Severity of Illness Index</topic><topic>voxel-based-morphometry</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hyde, Krista L.</creatorcontrib><creatorcontrib>Samson, Fabienne</creatorcontrib><creatorcontrib>Evans, Alan C.</creatorcontrib><creatorcontrib>Mottron, Laurent</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>PubMed Central (Full Participant titles)</collection><jtitle>Human brain mapping</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hyde, Krista L.</au><au>Samson, Fabienne</au><au>Evans, Alan C.</au><au>Mottron, Laurent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuroanatomical differences in brain areas implicated in perceptual and other core features of autism revealed by cortical thickness analysis and voxel-based morphometry</atitle><jtitle>Human brain mapping</jtitle><addtitle>Hum. Brain Mapp</addtitle><date>2010-04</date><risdate>2010</risdate><volume>31</volume><issue>4</issue><spage>556</spage><epage>566</epage><pages>556-566</pages><issn>1065-9471</issn><eissn>1097-0193</eissn><abstract>Autism spectrum disorder is a complex neurodevelopmental variant thought to affect 1 in 166 [Fombonne (2003): J Autism Dev Disord 33:365–382]. Individuals with autism demonstrate atypical social interaction, communication, and repetitive behaviors, but can also present enhanced abilities, particularly in auditory and visual perception and nonverbal reasoning. Structural brain differences have been reported in autism, in terms of increased total brain volume (particularly in young children with autism), and regional gray/white matter differences in both adults and children with autism, but the reports are inconsistent [Amaral et al. (2008): Trends Neurosci 31:137–145]. These inconsistencies may be due to differences in diagnostic/inclusion criteria, and age and Intelligence Quotient of participants. Here, for the first time, we used two complementary magnetic resonance imaging techniques, cortical thickness analyses, and voxel‐based morphometry (VBM), to investigate the neuroanatomical differences between a homogenous group of young adults with autism of average intelligence but delayed or atypical language development (often referred to as “high‐functioning autism”), relative to a closely matched group of typically developing controls. The cortical thickness and VBM techniques both revealed regional structural brain differences (mostly in terms of gray matter increases) in brain areas implicated in social cognition, communication, and repetitive behaviors, and thus in each of the core atypical features of autism. Gray matter increases were also found in auditory and visual primary and associative perceptual areas. We interpret these results as the first structural brain correlates of atypical auditory and visual perception in autism, in support of the enhanced perceptual functioning model [Mottron et al. (2006): J Autism Dev Disord 36:27–43]. Hum Brain Mapp, 2010. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19790171</pmid><doi>10.1002/hbm.20887</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult autism Autistic Disorder - complications Autistic Disorder - pathology Biological and medical sciences brain Brain - pathology Cerebral Cortex - pathology cortical thickness enhanced perceptual functioning model Humans Image Processing, Computer-Assisted Intelligence Intelligence Tests Investigative techniques, diagnostic techniques (general aspects) Language Disorders - etiology Language Disorders - pathology Magnetic Resonance Imaging - methods Male Medical sciences MRI Nervous system Nervous system involvement in other diseases. Miscellaneous Neurology Organ Size Radiodiagnosis. Nmr imagery. Nmr spectrometry Severity of Illness Index voxel-based-morphometry Young Adult |
title | Neuroanatomical differences in brain areas implicated in perceptual and other core features of autism revealed by cortical thickness analysis and voxel-based morphometry |
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