Movement Disorders (revue)

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Red flags for multiple system atrophy

Identifieur interne : 002653 ( Main/Exploration ); précédent : 002652; suivant : 002654

Red flags for multiple system atrophy

Auteurs : Martin Köllensperger [Autriche] ; Felix Geser [Autriche] ; Klaus Seppi [Autriche] ; Michaela Stampfer-Kountchev [Autriche] ; Martin Sawires [Autriche] ; Christoph Scherfler [Autriche] ; Sylvia Boesch [Autriche] ; Joerg Mueller [Autriche] ; Vasiliki Koukouni [Royaume-Uni] ; Niall Quinn [Royaume-Uni] ; Maria Teresa Pellecchia [Italie] ; Paolo Barone [Italie] ; Nicole Schimke [Allemagne] ; Richard Dodel [Allemagne] ; Wolfgang Oertel [Allemagne] ; Erik Dupont [Danemark] ; Karen Stergaard [Danemark] ; Christine Daniels [Allemagne] ; Günther Deuschl [Allemagne] ; Tanya Gurevich [Israël] ; Nir Giladi [Israël] ; Miguel Coelho [Portugal] ; Cristina Sampaio [Portugal] ; Christer Nilsson [Suède] ; H Kan Widner [Suède] ; Francesca Del Sorbo [Italie] ; Alberto Albanese [Italie] ; Adriana Cardozo [Espagne] ; Eduardo Tolosa [Espagne] ; Michael Abele [Allemagne] ; Thomas Klockgether [Allemagne] ; Christoph Kamm [Allemagne] ; Thomas Gasser [Allemagne] ; Ruth Djaldetti [Israël] ; Carlo Colosimo [Italie] ; Giuseppe Meco [Italie] ; Anette Schrag [Royaume-Uni] ; Werner Poewe [Autriche] ; Gregor K. Wenning [Autriche]

Source :

RBID : ISTEX:71B6B09D8EA90C87CF4826196DE238FE66B66F9C

Descripteurs français

English descriptors

Abstract

The clinical diagnosis of multiple system atrophy (MSA) is fraught with difficulty and there are no pathognomonic features to discriminate the parkinsonian variant (MSA‐P) from Parkinson's disease (PD). Besides the poor response to levodopa, and the additional presence of pyramidal or cerebellar signs (ataxia) or autonomic failure as major diagnostic criteria, certain other clinical features known as “red flags” or warning signs may raise the clinical suspicion of MSA. To study the diagnostic role of these features in MSA‐P versus PD patients, a standardized red flag check list (RFCL) developed by the European MSA Study Group (EMSA‐SG) was administered to 57 patients with probable MSA‐P and 116 patients with probable PD diagnosed according to established criteria. Those red flags with a specifity over 95% were selected for further analysis. Factor analysis was applied to reduce the number of red flags. The resulting set was then applied to 17 patients with possible MSA‐P who on follow‐up fulfilled criteria of probable MSA‐P. Red flags were grouped into related categories. With two or more of six red flag categories present specificity was 98.3% and sensitivity was 84.2% in our cohort. When applying these criteria to patients with possible MSA‐P, 76.5% of them would have been correctly diagnosed as probable MSA‐P 15.9 (±7.0) months earlier than with the Consensus criteria alone. We propose a combination of two out of six red flag categories as additional diagnostic criteria for probable MSA‐P. © 2008 Movement Disorder Society.

Url:
DOI: 10.1002/mds.21992


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<name sortKey="Giladi, Nir" sort="Giladi, Nir" uniqKey="Giladi N" first="Nir" last="Giladi">Nir Giladi</name>
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<country xml:lang="fr">Israël</country>
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<name sortKey="Coelho, Miguel" sort="Coelho, Miguel" uniqKey="Coelho M" first="Miguel" last="Coelho">Miguel Coelho</name>
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<country xml:lang="fr">Portugal</country>
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<name sortKey="Widner, H Kan" sort="Widner, H Kan" uniqKey="Widner H" first="H Kan" last="Widner">H Kan Widner</name>
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<country xml:lang="fr">Suède</country>
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<name sortKey="Albanese, Alberto" sort="Albanese, Alberto" uniqKey="Albanese A" first="Alberto" last="Albanese">Alberto Albanese</name>
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<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Department of Neurology, University of Barcelona</wicri:regionArea>
<wicri:noRegion>University of Barcelona</wicri:noRegion>
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<author>
<name sortKey="Tolosa, Eduardo" sort="Tolosa, Eduardo" uniqKey="Tolosa E" first="Eduardo" last="Tolosa">Eduardo Tolosa</name>
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<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Department of Neurology, University of Barcelona</wicri:regionArea>
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<author>
<name sortKey="Abele, Michael" sort="Abele, Michael" uniqKey="Abele M" first="Michael" last="Abele">Michael Abele</name>
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<wicri:regionArea>Department of Neurology, University of Bonn</wicri:regionArea>
<wicri:noRegion>University of Bonn</wicri:noRegion>
<wicri:noRegion>University of Bonn</wicri:noRegion>
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<name sortKey="Klockgether, Thomas" sort="Klockgether, Thomas" uniqKey="Klockgether T" first="Thomas" last="Klockgether">Thomas Klockgether</name>
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<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurology, University of Bonn</wicri:regionArea>
<wicri:noRegion>University of Bonn</wicri:noRegion>
<wicri:noRegion>University of Bonn</wicri:noRegion>
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<name sortKey="Kamm, Christoph" sort="Kamm, Christoph" uniqKey="Kamm C" first="Christoph" last="Kamm">Christoph Kamm</name>
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<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurodegenerative Diseases, University of Tübingen, Tübingen</wicri:regionArea>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
<region type="district" nuts="2">District de Tübingen</region>
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<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurodegenerative Diseases, University of Tübingen, Tübingen</wicri:regionArea>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
<region type="district" nuts="2">District de Tübingen</region>
<settlement type="city">Tübingen</settlement>
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</author>
<author>
<name sortKey="Djaldetti, Ruth" sort="Djaldetti, Ruth" uniqKey="Djaldetti R" first="Ruth" last="Djaldetti">Ruth Djaldetti</name>
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<country xml:lang="fr">Israël</country>
<wicri:regionArea>Department of Neurology, Rabin Medical Centre, Petach‐Tiqva</wicri:regionArea>
<wicri:noRegion>Petach‐Tiqva</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Colosimo, Carlo" sort="Colosimo, Carlo" uniqKey="Colosimo C" first="Carlo" last="Colosimo">Carlo Colosimo</name>
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<country xml:lang="fr">Italie</country>
<wicri:regionArea>Department of Neuroscience, University La Sapienza, Rome</wicri:regionArea>
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<settlement type="city">Rome</settlement>
<region nuts="2">Latium</region>
</placeName>
</affiliation>
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<author>
<name sortKey="Meco, Giuseppe" sort="Meco, Giuseppe" uniqKey="Meco G" first="Giuseppe" last="Meco">Giuseppe Meco</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Department of Neuroscience, University La Sapienza, Rome</wicri:regionArea>
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<settlement type="city">Rome</settlement>
<region nuts="2">Latium</region>
</placeName>
</affiliation>
</author>
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<name sortKey="Schrag, Anette" sort="Schrag, Anette" uniqKey="Schrag A" first="Anette" last="Schrag">Anette Schrag</name>
<affiliation wicri:level="3">
<country>Royaume-Uni</country>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
<wicri:orgArea>Institute of Neurology, University College</wicri:orgArea>
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</author>
<author>
<name sortKey="Poewe, Werner" sort="Poewe, Werner" uniqKey="Poewe W" first="Werner" last="Poewe">Werner Poewe</name>
<affiliation wicri:level="1">
<country xml:lang="fr">Autriche</country>
<wicri:regionArea>Department of Neurology, Innsbruck Medical University</wicri:regionArea>
<wicri:noRegion>Innsbruck Medical University</wicri:noRegion>
<placeName>
<settlement type="city">Innsbruck</settlement>
<region nuts="2" type="region">Tyrol (Land)</region>
</placeName>
<orgName type="university">Université de médecine d'Innsbruck</orgName>
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</author>
<author>
<name sortKey="Wenning, Gregor K" sort="Wenning, Gregor K" uniqKey="Wenning G" first="Gregor K." last="Wenning">Gregor K. Wenning</name>
<affiliation wicri:level="1">
<country xml:lang="fr">Autriche</country>
<wicri:regionArea>Section for Clinical Neurobiology, Department of Neurology, Innsbruck Medical University</wicri:regionArea>
<wicri:noRegion>Innsbruck Medical University</wicri:noRegion>
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</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2008-06-15">2008-06-15</date>
<biblScope unit="vol">23</biblScope>
<biblScope unit="issue">8</biblScope>
<biblScope unit="page" from="1093">1093</biblScope>
<biblScope unit="page" to="1099">1099</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">71B6B09D8EA90C87CF4826196DE238FE66B66F9C</idno>
<idno type="DOI">10.1002/mds.21992</idno>
<idno type="ArticleID">MDS21992</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Aged</term>
<term>Cerebellar Ataxia (diagnosis)</term>
<term>Cohort Studies</term>
<term>Diagnosis</term>
<term>Diagnosis, Differential</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Multiple System Atrophy (classification)</term>
<term>Multiple System Atrophy (diagnosis)</term>
<term>Multiple system atrophy</term>
<term>Nervous system diseases</term>
<term>Neurologic Examination (statistics & numerical data)</term>
<term>Parkinson Disease (classification)</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinsonian Disorders (classification)</term>
<term>Parkinsonian Disorders (diagnosis)</term>
<term>Sensitivity and Specificity</term>
<term>Shy-Drager Syndrome (diagnosis)</term>
<term>Sign</term>
<term>diagnosis</term>
<term>multiple system atrophy</term>
<term>red flags</term>
<term>warning signs</term>
</keywords>
<keywords scheme="MESH" qualifier="classification" xml:lang="en">
<term>Multiple System Atrophy</term>
<term>Parkinson Disease</term>
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Cerebellar Ataxia</term>
<term>Multiple System Atrophy</term>
<term>Parkinson Disease</term>
<term>Parkinsonian Disorders</term>
<term>Shy-Drager Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="statistics & numerical data" xml:lang="en">
<term>Neurologic Examination</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Aged</term>
<term>Cohort Studies</term>
<term>Diagnosis, Differential</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Sensitivity and Specificity</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Atrophie multisystématisée</term>
<term>Diagnostic</term>
<term>Pathologie du système nerveux</term>
<term>Signe</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">The clinical diagnosis of multiple system atrophy (MSA) is fraught with difficulty and there are no pathognomonic features to discriminate the parkinsonian variant (MSA‐P) from Parkinson's disease (PD). Besides the poor response to levodopa, and the additional presence of pyramidal or cerebellar signs (ataxia) or autonomic failure as major diagnostic criteria, certain other clinical features known as “red flags” or warning signs may raise the clinical suspicion of MSA. To study the diagnostic role of these features in MSA‐P versus PD patients, a standardized red flag check list (RFCL) developed by the European MSA Study Group (EMSA‐SG) was administered to 57 patients with probable MSA‐P and 116 patients with probable PD diagnosed according to established criteria. Those red flags with a specifity over 95% were selected for further analysis. Factor analysis was applied to reduce the number of red flags. The resulting set was then applied to 17 patients with possible MSA‐P who on follow‐up fulfilled criteria of probable MSA‐P. Red flags were grouped into related categories. With two or more of six red flag categories present specificity was 98.3% and sensitivity was 84.2% in our cohort. When applying these criteria to patients with possible MSA‐P, 76.5% of them would have been correctly diagnosed as probable MSA‐P 15.9 (±7.0) months earlier than with the Consensus criteria alone. We propose a combination of two out of six red flag categories as additional diagnostic criteria for probable MSA‐P. © 2008 Movement Disorder Society.</div>
</front>
</TEI>
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<li>Portugal</li>
<li>Royaume-Uni</li>
<li>Suède</li>
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<li>Hesse (Land)</li>
<li>Latium</li>
<li>Schleswig-Holstein</li>
<li>Tyrol (Land)</li>
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<li>Innsbruck</li>
<li>Kiel</li>
<li>Londres</li>
<li>Marbourg</li>
<li>Rome</li>
<li>Tübingen</li>
</settlement>
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<li>Université de médecine d'Innsbruck</li>
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<name sortKey="Pellecchia, Maria Teresa" sort="Pellecchia, Maria Teresa" uniqKey="Pellecchia M" first="Maria Teresa" last="Pellecchia">Maria Teresa Pellecchia</name>
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<region name="Hesse (Land)">
<name sortKey="Schimke, Nicole" sort="Schimke, Nicole" uniqKey="Schimke N" first="Nicole" last="Schimke">Nicole Schimke</name>
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<name sortKey="Abele, Michael" sort="Abele, Michael" uniqKey="Abele M" first="Michael" last="Abele">Michael Abele</name>
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<name sortKey="Djaldetti, Ruth" sort="Djaldetti, Ruth" uniqKey="Djaldetti R" first="Ruth" last="Djaldetti">Ruth Djaldetti</name>
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