Structural white matter abnormalities in patients with idiopathic dystonia
We investigated whether structural white matter abnormalities, in the form of disruption of axonal coherence and integrity as measured with diffusion tensor imaging (DTI), constitute an underlying pathological mechanism of idiopathic dystonia (ID), independent of genotype status. We studied seven su...
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Veröffentlicht in: | Movement disorders 2007-06, Vol.22 (8), p.1110-1116 |
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description | We investigated whether structural white matter abnormalities, in the form of disruption of axonal coherence and integrity as measured with diffusion tensor imaging (DTI), constitute an underlying pathological mechanism of idiopathic dystonia (ID), independent of genotype status. We studied seven subjects with ID: all had cervical dystonia as their main symptom (one patient also had spasmodic dysphonia and two patients had concurrent generalized dystonia, both DYT1‐negative). We compared DTI MR images of patients with 10 controls, evaluating differences in mean diffusivity (MD) and fractional anisotropy (FA). ID was associated with increased FA values in the thalamus and adjacent white matter, and in the white matter underlying the middle frontal gyrus. ID was also associated with increase in MD in adjacent white matter to the pallidum and putamen bilaterally, left caudate, and in subcortical hemispheric regions, including the postcentral gyrus. Abnormal FA and MD in patients with ID indicate that abnormal axonal coherence and integrity contribute to the pathophysiology of dystonia. These findings suggest that ID is not only a functional disorder, but also associated with structural brain changes. Impaired connectivity and disrupted flow of information may contribute to the impairment of motor planning and regulation in dystonia. © 2006 Movement Disorder Society |
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We studied seven subjects with ID: all had cervical dystonia as their main symptom (one patient also had spasmodic dysphonia and two patients had concurrent generalized dystonia, both DYT1‐negative). We compared DTI MR images of patients with 10 controls, evaluating differences in mean diffusivity (MD) and fractional anisotropy (FA). ID was associated with increased FA values in the thalamus and adjacent white matter, and in the white matter underlying the middle frontal gyrus. ID was also associated with increase in MD in adjacent white matter to the pallidum and putamen bilaterally, left caudate, and in subcortical hemispheric regions, including the postcentral gyrus. Abnormal FA and MD in patients with ID indicate that abnormal axonal coherence and integrity contribute to the pathophysiology of dystonia. These findings suggest that ID is not only a functional disorder, but also associated with structural brain changes. Impaired connectivity and disrupted flow of information may contribute to the impairment of motor planning and regulation in dystonia. © 2006 Movement Disorder Society</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.21295</identifier><identifier>PMID: 17230463</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Axons - physiology ; Biological and medical sciences ; Brain - abnormalities ; Brain - physiopathology ; Diagnosis, Differential ; Diffusion Magnetic Resonance Imaging ; diffusion tensor imaging ; Diseases of striated muscles. Neuromuscular diseases ; dystonia ; Dystonic Disorders - diagnosis ; Dystonic Disorders - genetics ; Dystonic Disorders - physiopathology ; Female ; Genotype ; Humans ; Male ; Medical sciences ; Middle Aged ; MRI ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurology ; pathophysiology ; Severity of Illness Index ; white matter</subject><ispartof>Movement disorders, 2007-06, Vol.22 (8), p.1110-1116</ispartof><rights>Copyright © 2006 Movement Disorder Society</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4225-bc9f2ab0bb392ab77740a6b2eeaaa0f65459d57cbb94de052471ce3474e8d95f3</citedby><cites>FETCH-LOGICAL-c4225-bc9f2ab0bb392ab77740a6b2eeaaa0f65459d57cbb94de052471ce3474e8d95f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmds.21295$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmds.21295$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18883320$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17230463$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonilha, Leonardo</creatorcontrib><creatorcontrib>de Vries, Paulien M.</creatorcontrib><creatorcontrib>Vincent, Diana J.</creatorcontrib><creatorcontrib>Rorden, Chris</creatorcontrib><creatorcontrib>Morgan, Paul S.</creatorcontrib><creatorcontrib>Hurd, Mark W.</creatorcontrib><creatorcontrib>Besenski, Nada</creatorcontrib><creatorcontrib>Bergmann, Kenneth J.</creatorcontrib><creatorcontrib>Hinson, Vanessa K.</creatorcontrib><title>Structural white matter abnormalities in patients with idiopathic dystonia</title><title>Movement disorders</title><addtitle>Mov. Disord</addtitle><description>We investigated whether structural white matter abnormalities, in the form of disruption of axonal coherence and integrity as measured with diffusion tensor imaging (DTI), constitute an underlying pathological mechanism of idiopathic dystonia (ID), independent of genotype status. We studied seven subjects with ID: all had cervical dystonia as their main symptom (one patient also had spasmodic dysphonia and two patients had concurrent generalized dystonia, both DYT1‐negative). We compared DTI MR images of patients with 10 controls, evaluating differences in mean diffusivity (MD) and fractional anisotropy (FA). ID was associated with increased FA values in the thalamus and adjacent white matter, and in the white matter underlying the middle frontal gyrus. ID was also associated with increase in MD in adjacent white matter to the pallidum and putamen bilaterally, left caudate, and in subcortical hemispheric regions, including the postcentral gyrus. Abnormal FA and MD in patients with ID indicate that abnormal axonal coherence and integrity contribute to the pathophysiology of dystonia. These findings suggest that ID is not only a functional disorder, but also associated with structural brain changes. Impaired connectivity and disrupted flow of information may contribute to the impairment of motor planning and regulation in dystonia. © 2006 Movement Disorder Society</description><subject>Adult</subject><subject>Aged</subject><subject>Axons - physiology</subject><subject>Biological and medical sciences</subject><subject>Brain - abnormalities</subject><subject>Brain - physiopathology</subject><subject>Diagnosis, Differential</subject><subject>Diffusion Magnetic Resonance Imaging</subject><subject>diffusion tensor imaging</subject><subject>Diseases of striated muscles. Neuromuscular diseases</subject><subject>dystonia</subject><subject>Dystonic Disorders - diagnosis</subject><subject>Dystonic Disorders - genetics</subject><subject>Dystonic Disorders - physiopathology</subject><subject>Female</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>MRI</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurology</subject><subject>pathophysiology</subject><subject>Severity of Illness Index</subject><subject>white matter</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E1P3DAQBmALFcEWOPQPVLm0EoeAx45j51jRAl3xIUQrjtbYcbSGfCy2o-3--4buUk5VT2NZz8wrvYR8AHoClLLTro4nDFgldsgMBIdcMSHfkRlVSuQclNgn72N8pBRAQLlH9kEyTouSz8j8PoXRpjFgm60WPrmsw5RcyND0Q-iw9cm7mPk-W-L06lPMVj4tMl_7YfpZeJvV65iG3uMh2W2wje5oOw_Iz_NvP84u86vbi-9nX65yWzAmcmOrhqGhxvBqmlLKgmJpmHOISJtSFKKqhbTGVEXtqGCFBOt4IQun6ko0_IB83txdhuF5dDHpzkfr2hZ7N4xRlwqoKqH6L2QATElBJ3i8gTYMMQbX6GXwHYa1BqpfGtZTw_pPw5P9uD06ms7Vb3Jb6QQ-bQFGi20TsLc-vjmlFOfsJfR041a-det_J-rrr_ev0flmw8fkfv3dwPCkS8ml0A83F_pG3bH55Rz0nP8GOkGiDg</recordid><startdate>20070615</startdate><enddate>20070615</enddate><creator>Bonilha, Leonardo</creator><creator>de Vries, Paulien M.</creator><creator>Vincent, Diana J.</creator><creator>Rorden, Chris</creator><creator>Morgan, Paul S.</creator><creator>Hurd, Mark W.</creator><creator>Besenski, Nada</creator><creator>Bergmann, Kenneth J.</creator><creator>Hinson, Vanessa K.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</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>7TK</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>20070615</creationdate><title>Structural white matter abnormalities in patients with idiopathic dystonia</title><author>Bonilha, Leonardo ; de Vries, Paulien M. ; Vincent, Diana J. ; Rorden, Chris ; Morgan, Paul S. ; Hurd, Mark W. ; Besenski, Nada ; Bergmann, Kenneth J. ; Hinson, Vanessa K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4225-bc9f2ab0bb392ab77740a6b2eeaaa0f65459d57cbb94de052471ce3474e8d95f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Axons - physiology</topic><topic>Biological and medical sciences</topic><topic>Brain - abnormalities</topic><topic>Brain - physiopathology</topic><topic>Diagnosis, Differential</topic><topic>Diffusion Magnetic Resonance Imaging</topic><topic>diffusion tensor imaging</topic><topic>Diseases of striated muscles. Neuromuscular diseases</topic><topic>dystonia</topic><topic>Dystonic Disorders - diagnosis</topic><topic>Dystonic Disorders - genetics</topic><topic>Dystonic Disorders - physiopathology</topic><topic>Female</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>MRI</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neurology</topic><topic>pathophysiology</topic><topic>Severity of Illness Index</topic><topic>white matter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonilha, Leonardo</creatorcontrib><creatorcontrib>de Vries, Paulien M.</creatorcontrib><creatorcontrib>Vincent, Diana J.</creatorcontrib><creatorcontrib>Rorden, Chris</creatorcontrib><creatorcontrib>Morgan, Paul S.</creatorcontrib><creatorcontrib>Hurd, Mark W.</creatorcontrib><creatorcontrib>Besenski, Nada</creatorcontrib><creatorcontrib>Bergmann, Kenneth J.</creatorcontrib><creatorcontrib>Hinson, Vanessa K.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonilha, Leonardo</au><au>de Vries, Paulien M.</au><au>Vincent, Diana J.</au><au>Rorden, Chris</au><au>Morgan, Paul S.</au><au>Hurd, Mark W.</au><au>Besenski, Nada</au><au>Bergmann, Kenneth J.</au><au>Hinson, Vanessa K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural white matter abnormalities in patients with idiopathic dystonia</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov. Disord</addtitle><date>2007-06-15</date><risdate>2007</risdate><volume>22</volume><issue>8</issue><spage>1110</spage><epage>1116</epage><pages>1110-1116</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>We investigated whether structural white matter abnormalities, in the form of disruption of axonal coherence and integrity as measured with diffusion tensor imaging (DTI), constitute an underlying pathological mechanism of idiopathic dystonia (ID), independent of genotype status. We studied seven subjects with ID: all had cervical dystonia as their main symptom (one patient also had spasmodic dysphonia and two patients had concurrent generalized dystonia, both DYT1‐negative). We compared DTI MR images of patients with 10 controls, evaluating differences in mean diffusivity (MD) and fractional anisotropy (FA). ID was associated with increased FA values in the thalamus and adjacent white matter, and in the white matter underlying the middle frontal gyrus. ID was also associated with increase in MD in adjacent white matter to the pallidum and putamen bilaterally, left caudate, and in subcortical hemispheric regions, including the postcentral gyrus. Abnormal FA and MD in patients with ID indicate that abnormal axonal coherence and integrity contribute to the pathophysiology of dystonia. These findings suggest that ID is not only a functional disorder, but also associated with structural brain changes. Impaired connectivity and disrupted flow of information may contribute to the impairment of motor planning and regulation in dystonia. © 2006 Movement Disorder Society</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17230463</pmid><doi>10.1002/mds.21295</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Axons - physiology Biological and medical sciences Brain - abnormalities Brain - physiopathology Diagnosis, Differential Diffusion Magnetic Resonance Imaging diffusion tensor imaging Diseases of striated muscles. Neuromuscular diseases dystonia Dystonic Disorders - diagnosis Dystonic Disorders - genetics Dystonic Disorders - physiopathology Female Genotype Humans Male Medical sciences Middle Aged MRI Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Neurology pathophysiology Severity of Illness Index white matter |
title | Structural white matter abnormalities in patients with idiopathic dystonia |
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