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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Veröffentlicht in:Brain (London, England : 1878) England : 1878), 2013-03, Vol.136 (Pt 3), p.905-917
Hauptverfasser: 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
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container_end_page 917
container_issue Pt 3
container_start_page 905
container_title Brain (London, England : 1878)
container_volume 136
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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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&amp;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. 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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. 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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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