Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6
Spinocerebellar ataxias are dominantly inherited disorders that are associated with progressive brain degeneration, mainly affecting the cerebellum and brainstem. As part of the multicentre European integrated project on spinocerebellar ataxias study, 37 patients with spinocerebellar ataxia-1, 19 wi...
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creator | REETZ, Kathrin COSTA, Ana S GRISOLI, Marina DÜRR, Alexandra VAN DE WARRENBURG, Bart P TIMMANN, Dagmar PANDOLFO, Massimo BAUER, Peter JACOBI, Heike HAUSER, Till-Karsten KLOCKGETHER, Thomas SCHULZ, Jörg B MIRZAZADE, Shahram LEHMANN, Anna JUZEK, Agnes RAKOWICZ, Maria BOGUSLAWSKA, Romana SCHÖLS, Ludger LINNEMANN, Christoph MARIOTTI, Caterina |
description | Spinocerebellar ataxias are dominantly inherited disorders that are associated with progressive brain degeneration, mainly affecting the cerebellum and brainstem. As part of the multicentre European integrated project on spinocerebellar ataxias study, 37 patients with spinocerebellar ataxia-1, 19 with spinocerebellar ataxia-3 and seven with spinocerebellar ataxia-6 were clinically examined and underwent magnetic resonance imaging at baseline and after a 2-year follow-up. All patients were compared with age-matched and gender-matched healthy control subjects. Magnetic resonance imaging analysis included three-dimensional volumetry and observer-independent longitudinal voxel-based morphometry. Volumetry revealed loss of brainstem, cerebellar and basal ganglia volume in all genotypes. Most sensitive to change was the pontine volume in spinocerebellar ataxia-1, striatal volume in spinocerebellar ataxia-3 and caudate volume in spinocerebellar ataxia-6. Sensitivity to change, as measured by standard response mean, of the respective MRI measures was greater than that of the most sensitive clinical measure, the Scale for the Assessment and Rating of Ataxia. Longitudinal voxel-based morphometry revealed greatest grey matter loss in the cerebellum and brainstem in spinocerebellar ataxia-1, in the putamen and pallidum in spinocerebellar ataxia-3 and in the cerebellum, thalamus, putamen and pallidum in spinocerebellar ataxia-6. There was a mild correlation between CAG repeat length and volume loss of the bilateral cerebellum and the pons in spinocerebellar ataxia-1. Quantitative volumetry and voxel-based morphometry imaging demonstrated genotype-specific patterns of atrophy progression in spinocerebellar ataxias-1, 3 and 6, and they showed a high sensitivity to detect change that was superior to clinical scales. These structural magnetic resonance imaging findings have the potential to serve as surrogate markers, which might help to delineate quantifiable endpoints and non-invasive methods for rapid and reliable data acquisition, encouraging their use in clinical trials. |
doi_str_mv | 10.1093/brain/aws369 |
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As part of the multicentre European integrated project on spinocerebellar ataxias study, 37 patients with spinocerebellar ataxia-1, 19 with spinocerebellar ataxia-3 and seven with spinocerebellar ataxia-6 were clinically examined and underwent magnetic resonance imaging at baseline and after a 2-year follow-up. All patients were compared with age-matched and gender-matched healthy control subjects. Magnetic resonance imaging analysis included three-dimensional volumetry and observer-independent longitudinal voxel-based morphometry. Volumetry revealed loss of brainstem, cerebellar and basal ganglia volume in all genotypes. Most sensitive to change was the pontine volume in spinocerebellar ataxia-1, striatal volume in spinocerebellar ataxia-3 and caudate volume in spinocerebellar ataxia-6. Sensitivity to change, as measured by standard response mean, of the respective MRI measures was greater than that of the most sensitive clinical measure, the Scale for the Assessment and Rating of Ataxia. Longitudinal voxel-based morphometry revealed greatest grey matter loss in the cerebellum and brainstem in spinocerebellar ataxia-1, in the putamen and pallidum in spinocerebellar ataxia-3 and in the cerebellum, thalamus, putamen and pallidum in spinocerebellar ataxia-6. There was a mild correlation between CAG repeat length and volume loss of the bilateral cerebellum and the pons in spinocerebellar ataxia-1. Quantitative volumetry and voxel-based morphometry imaging demonstrated genotype-specific patterns of atrophy progression in spinocerebellar ataxias-1, 3 and 6, and they showed a high sensitivity to detect change that was superior to clinical scales. These structural magnetic resonance imaging findings have the potential to serve as surrogate markers, which might help to delineate quantifiable endpoints and non-invasive methods for rapid and reliable data acquisition, encouraging their use in clinical trials.</description><identifier>ISSN: 0006-8950</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/aws369</identifier><identifier>PMID: 23423669</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Ataxin ; Atrophy ; Atrophy - pathology ; Basal ganglia ; Biological and medical sciences ; Brain ; Brain - pathology ; Brain stem ; Cerebellum ; Clinical trials ; Data acquisition ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Disease Progression ; Female ; Genotype ; Genotypes ; Globus pallidus ; Hereditary diseases ; Humans ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Middle Aged ; Morphometry ; Neostriatum ; Neuroimaging ; Neurology ; Pons ; Putamen ; Spinocerebellar Ataxias - complications ; Spinocerebellar Ataxias - genetics ; Spinocerebellar Ataxias - pathology ; Thalamus ; Trinucleotide repeats</subject><ispartof>Brain (London, England : 1878), 2013-03, Vol.136 (Pt 3), p.905-917</ispartof><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-2f7b4937dc92ece214566b5e10fa13802e0646ad4d314b97a3d8f98db8ab80313</citedby><cites>FETCH-LOGICAL-c458t-2f7b4937dc92ece214566b5e10fa13802e0646ad4d314b97a3d8f98db8ab80313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27157968$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23423669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>REETZ, Kathrin</creatorcontrib><creatorcontrib>COSTA, Ana S</creatorcontrib><creatorcontrib>GRISOLI, Marina</creatorcontrib><creatorcontrib>DÜRR, Alexandra</creatorcontrib><creatorcontrib>VAN DE WARRENBURG, Bart P</creatorcontrib><creatorcontrib>TIMMANN, Dagmar</creatorcontrib><creatorcontrib>PANDOLFO, Massimo</creatorcontrib><creatorcontrib>BAUER, Peter</creatorcontrib><creatorcontrib>JACOBI, Heike</creatorcontrib><creatorcontrib>HAUSER, Till-Karsten</creatorcontrib><creatorcontrib>KLOCKGETHER, Thomas</creatorcontrib><creatorcontrib>SCHULZ, Jörg B</creatorcontrib><creatorcontrib>MIRZAZADE, Shahram</creatorcontrib><creatorcontrib>LEHMANN, Anna</creatorcontrib><creatorcontrib>JUZEK, Agnes</creatorcontrib><creatorcontrib>RAKOWICZ, Maria</creatorcontrib><creatorcontrib>BOGUSLAWSKA, Romana</creatorcontrib><creatorcontrib>SCHÖLS, Ludger</creatorcontrib><creatorcontrib>LINNEMANN, Christoph</creatorcontrib><creatorcontrib>MARIOTTI, Caterina</creatorcontrib><creatorcontrib>axia Study Group Investigators</creatorcontrib><creatorcontrib>the Ataxia Study Group Investigators</creatorcontrib><title>Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>Spinocerebellar ataxias are dominantly inherited disorders that are associated with progressive brain degeneration, mainly affecting the cerebellum and brainstem. As part of the multicentre European integrated project on spinocerebellar ataxias study, 37 patients with spinocerebellar ataxia-1, 19 with spinocerebellar ataxia-3 and seven with spinocerebellar ataxia-6 were clinically examined and underwent magnetic resonance imaging at baseline and after a 2-year follow-up. All patients were compared with age-matched and gender-matched healthy control subjects. Magnetic resonance imaging analysis included three-dimensional volumetry and observer-independent longitudinal voxel-based morphometry. Volumetry revealed loss of brainstem, cerebellar and basal ganglia volume in all genotypes. Most sensitive to change was the pontine volume in spinocerebellar ataxia-1, striatal volume in spinocerebellar ataxia-3 and caudate volume in spinocerebellar ataxia-6. Sensitivity to change, as measured by standard response mean, of the respective MRI measures was greater than that of the most sensitive clinical measure, the Scale for the Assessment and Rating of Ataxia. Longitudinal voxel-based morphometry revealed greatest grey matter loss in the cerebellum and brainstem in spinocerebellar ataxia-1, in the putamen and pallidum in spinocerebellar ataxia-3 and in the cerebellum, thalamus, putamen and pallidum in spinocerebellar ataxia-6. There was a mild correlation between CAG repeat length and volume loss of the bilateral cerebellum and the pons in spinocerebellar ataxia-1. Quantitative volumetry and voxel-based morphometry imaging demonstrated genotype-specific patterns of atrophy progression in spinocerebellar ataxias-1, 3 and 6, and they showed a high sensitivity to detect change that was superior to clinical scales. These structural magnetic resonance imaging findings have the potential to serve as surrogate markers, which might help to delineate quantifiable endpoints and non-invasive methods for rapid and reliable data acquisition, encouraging their use in clinical trials.</description><subject>Adult</subject><subject>Ataxin</subject><subject>Atrophy</subject><subject>Atrophy - pathology</subject><subject>Basal ganglia</subject><subject>Biological and medical sciences</subject><subject>Brain</subject><subject>Brain - pathology</subject><subject>Brain stem</subject><subject>Cerebellum</subject><subject>Clinical trials</subject><subject>Data acquisition</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Globus pallidus</subject><subject>Hereditary diseases</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Morphometry</subject><subject>Neostriatum</subject><subject>Neuroimaging</subject><subject>Neurology</subject><subject>Pons</subject><subject>Putamen</subject><subject>Spinocerebellar Ataxias - complications</subject><subject>Spinocerebellar Ataxias - genetics</subject><subject>Spinocerebellar Ataxias - pathology</subject><subject>Thalamus</subject><subject>Trinucleotide repeats</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1P3DAQhq2qqCy0N87Il0o9EPBXHPuIVuVDQuIAnKOJMylGWSd4sq323zfLbuHayztzePRqNA9jJ1KcS-H1RZMhpgv4Q9r6T2whjRWFkqX9zBZCCFs4X4pDdkT0IoQ0Wtkv7FBpo7S1fsFerzEN02bEgkYMsYuBjzBNmBPxoeMw5WF83vAxD78yEsUhccjIV8MchIniFH8jn54h8dDHFAP0vMXtijwm_rC8lGfb1BxSu13sV3bQQU_4bT-P2dPVz8flTXF3f327vLwrgindVKiuaozXVRu8woBKmtLapkQpOpDaCYXCGgutabU0ja9At67zrm0cNE5oqY_Zj13vfPvrGmmqV5EC9j0kHNZUSy2d9UZV5n9QZa0slZvRsx0a8kCUsavHHFeQN7UU9dZH_eaj3vmY8dN987pZYfsO_xMwA9_3AND8uy5DCpE-uEqWlbdO_wXH_pPW</recordid><startdate>20130301</startdate><enddate>20130301</enddate><creator>REETZ, Kathrin</creator><creator>COSTA, Ana S</creator><creator>GRISOLI, Marina</creator><creator>DÜRR, Alexandra</creator><creator>VAN DE WARRENBURG, Bart P</creator><creator>TIMMANN, Dagmar</creator><creator>PANDOLFO, Massimo</creator><creator>BAUER, Peter</creator><creator>JACOBI, Heike</creator><creator>HAUSER, Till-Karsten</creator><creator>KLOCKGETHER, Thomas</creator><creator>SCHULZ, Jörg B</creator><creator>MIRZAZADE, Shahram</creator><creator>LEHMANN, Anna</creator><creator>JUZEK, Agnes</creator><creator>RAKOWICZ, Maria</creator><creator>BOGUSLAWSKA, Romana</creator><creator>SCHÖLS, Ludger</creator><creator>LINNEMANN, Christoph</creator><creator>MARIOTTI, Caterina</creator><general>Oxford University Press</general><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></search><sort><creationdate>20130301</creationdate><title>Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6</title><author>REETZ, Kathrin ; COSTA, Ana S ; GRISOLI, Marina ; DÜRR, Alexandra ; VAN DE WARRENBURG, Bart P ; TIMMANN, Dagmar ; PANDOLFO, Massimo ; BAUER, Peter ; JACOBI, Heike ; HAUSER, Till-Karsten ; KLOCKGETHER, Thomas ; SCHULZ, Jörg B ; MIRZAZADE, Shahram ; LEHMANN, Anna ; JUZEK, Agnes ; RAKOWICZ, Maria ; BOGUSLAWSKA, Romana ; SCHÖLS, Ludger ; LINNEMANN, Christoph ; MARIOTTI, Caterina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-2f7b4937dc92ece214566b5e10fa13802e0646ad4d314b97a3d8f98db8ab80313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Ataxin</topic><topic>Atrophy</topic><topic>Atrophy - pathology</topic><topic>Basal ganglia</topic><topic>Biological and medical sciences</topic><topic>Brain</topic><topic>Brain - pathology</topic><topic>Brain stem</topic><topic>Cerebellum</topic><topic>Clinical trials</topic><topic>Data acquisition</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Genotype</topic><topic>Genotypes</topic><topic>Globus pallidus</topic><topic>Hereditary diseases</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Morphometry</topic><topic>Neostriatum</topic><topic>Neuroimaging</topic><topic>Neurology</topic><topic>Pons</topic><topic>Putamen</topic><topic>Spinocerebellar Ataxias - complications</topic><topic>Spinocerebellar Ataxias - genetics</topic><topic>Spinocerebellar Ataxias - pathology</topic><topic>Thalamus</topic><topic>Trinucleotide repeats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>REETZ, Kathrin</creatorcontrib><creatorcontrib>COSTA, Ana S</creatorcontrib><creatorcontrib>GRISOLI, Marina</creatorcontrib><creatorcontrib>DÜRR, Alexandra</creatorcontrib><creatorcontrib>VAN DE WARRENBURG, Bart P</creatorcontrib><creatorcontrib>TIMMANN, Dagmar</creatorcontrib><creatorcontrib>PANDOLFO, Massimo</creatorcontrib><creatorcontrib>BAUER, Peter</creatorcontrib><creatorcontrib>JACOBI, Heike</creatorcontrib><creatorcontrib>HAUSER, Till-Karsten</creatorcontrib><creatorcontrib>KLOCKGETHER, Thomas</creatorcontrib><creatorcontrib>SCHULZ, Jörg B</creatorcontrib><creatorcontrib>MIRZAZADE, Shahram</creatorcontrib><creatorcontrib>LEHMANN, Anna</creatorcontrib><creatorcontrib>JUZEK, Agnes</creatorcontrib><creatorcontrib>RAKOWICZ, Maria</creatorcontrib><creatorcontrib>BOGUSLAWSKA, Romana</creatorcontrib><creatorcontrib>SCHÖLS, Ludger</creatorcontrib><creatorcontrib>LINNEMANN, Christoph</creatorcontrib><creatorcontrib>MARIOTTI, Caterina</creatorcontrib><creatorcontrib>axia Study Group Investigators</creatorcontrib><creatorcontrib>the Ataxia Study Group Investigators</creatorcontrib><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><jtitle>Brain (London, England : 1878)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>REETZ, Kathrin</au><au>COSTA, Ana S</au><au>GRISOLI, Marina</au><au>DÜRR, Alexandra</au><au>VAN DE WARRENBURG, Bart P</au><au>TIMMANN, Dagmar</au><au>PANDOLFO, Massimo</au><au>BAUER, Peter</au><au>JACOBI, Heike</au><au>HAUSER, Till-Karsten</au><au>KLOCKGETHER, Thomas</au><au>SCHULZ, Jörg B</au><au>MIRZAZADE, Shahram</au><au>LEHMANN, Anna</au><au>JUZEK, Agnes</au><au>RAKOWICZ, Maria</au><au>BOGUSLAWSKA, Romana</au><au>SCHÖLS, Ludger</au><au>LINNEMANN, Christoph</au><au>MARIOTTI, Caterina</au><aucorp>axia Study Group Investigators</aucorp><aucorp>the Ataxia Study Group Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6</atitle><jtitle>Brain (London, England : 1878)</jtitle><addtitle>Brain</addtitle><date>2013-03-01</date><risdate>2013</risdate><volume>136</volume><issue>Pt 3</issue><spage>905</spage><epage>917</epage><pages>905-917</pages><issn>0006-8950</issn><eissn>1460-2156</eissn><abstract>Spinocerebellar ataxias are dominantly inherited disorders that are associated with progressive brain degeneration, mainly affecting the cerebellum and brainstem. As part of the multicentre European integrated project on spinocerebellar ataxias study, 37 patients with spinocerebellar ataxia-1, 19 with spinocerebellar ataxia-3 and seven with spinocerebellar ataxia-6 were clinically examined and underwent magnetic resonance imaging at baseline and after a 2-year follow-up. All patients were compared with age-matched and gender-matched healthy control subjects. Magnetic resonance imaging analysis included three-dimensional volumetry and observer-independent longitudinal voxel-based morphometry. Volumetry revealed loss of brainstem, cerebellar and basal ganglia volume in all genotypes. Most sensitive to change was the pontine volume in spinocerebellar ataxia-1, striatal volume in spinocerebellar ataxia-3 and caudate volume in spinocerebellar ataxia-6. Sensitivity to change, as measured by standard response mean, of the respective MRI measures was greater than that of the most sensitive clinical measure, the Scale for the Assessment and Rating of Ataxia. Longitudinal voxel-based morphometry revealed greatest grey matter loss in the cerebellum and brainstem in spinocerebellar ataxia-1, in the putamen and pallidum in spinocerebellar ataxia-3 and in the cerebellum, thalamus, putamen and pallidum in spinocerebellar ataxia-6. There was a mild correlation between CAG repeat length and volume loss of the bilateral cerebellum and the pons in spinocerebellar ataxia-1. Quantitative volumetry and voxel-based morphometry imaging demonstrated genotype-specific patterns of atrophy progression in spinocerebellar ataxias-1, 3 and 6, and they showed a high sensitivity to detect change that was superior to clinical scales. These structural magnetic resonance imaging findings have the potential to serve as surrogate markers, which might help to delineate quantifiable endpoints and non-invasive methods for rapid and reliable data acquisition, encouraging their use in clinical trials.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>23423669</pmid><doi>10.1093/brain/aws369</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Ataxin Atrophy Atrophy - pathology Basal ganglia Biological and medical sciences Brain Brain - pathology Brain stem Cerebellum Clinical trials Data acquisition Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Disease Progression Female Genotype Genotypes Globus pallidus Hereditary diseases Humans Magnetic Resonance Imaging Male Medical sciences Middle Aged Morphometry Neostriatum Neuroimaging Neurology Pons Putamen Spinocerebellar Ataxias - complications Spinocerebellar Ataxias - genetics Spinocerebellar Ataxias - pathology Thalamus Trinucleotide repeats |
title | Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6 |
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