Movement Disorders (revue)

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Depression comorbidity in spinocerebellar ataxia

Identifieur interne : 000522 ( Istex/Corpus ); précédent : 000521; suivant : 000523

Depression comorbidity in spinocerebellar ataxia

Auteurs : Tanja Schmitz-Hübsch ; Mathieu Coudert ; Sophie Tezenas Du Montcel ; Paola Giunti ; Robyn Labrum ; Alexandra Dürr ; Pascale Ribai ; Perrine Charles ; Christoph Linnemann ; Ludger Schöls ; Maryla Rakowicz ; Rafal Rola ; Elszbieta Zdzienicka ; Roberto Fancellu ; Caterina Mariotti ; Lazlo Baliko ; Bela Melegh ; Alessandro Filla ; Elena Salvatore ; Bart P. C. Van De Warrenburg ; Sandra Szymanski ; Jon Infante ; Dagmar Timmann ; Sylvia Boesch ; Chantal Depondt ; Jun-Suk Kang ; Jörg B. Schulz ; Thomas Klopstock ; Nicole Lossnitzer ; Bernd Löwe ; Caroline Frick ; Daniela Rottl Nder ; Thomas E. Schlaepfer ; Thomas Klockgether

Source :

RBID : ISTEX:50B77A4B4C970763DCD1BFCBA3F272B70C8B5985

English descriptors

Abstract

This is a description of the prevalence and profile of depressive symptoms in dominant spinocerebellar ataxia (SCA). Depressive symptoms were assessed in a convenience sample of 526 genetically confirmed and clinically affected patients (117 SCA1, 163 SCA2, 139 SCA3, and 107 SCA6) using the Patient Health Questionnaire (PHQ). In addition, depressive status according to the examiner and the use of antidepressants was recorded. Depression self‐assessment was compared with an interview‐based psychiatric assessment in a subset of 26 patients. Depression prevalence estimates were 17.1% according to the PHQ algorithm and 15.4% when assessed clinically. The sensitivity of clinical impression compared with PHQ classification was low (0.35), whereas diagnostic accuracy of PHQ compared with psychiatric interview in the subset was high. Antidepressants were used by 17.7% of patients and in >10% of patients without current clinically relevant depressive symptoms. Depression profile in SCA did not differ from a sample of patients with major depressive disorder except for the movement‐related item. Neither depression prevalence nor use of antidepressants differed between genetic subtypes, with only sleep disturbance more common in SCA3. In a multivariate analysis, ataxia severity and female sex independently predicted depressive status in SCA. The PHQ algorithmic classification is appropriate for use in SCA but should stimulate further psychiatric evaluation if depression is indicated. Despite a higher risk for depression with more severe disease, the relation of depressive symptoms to SCA neurodegeneration remains to be shown. © 2011 Movement Disorder Society

Url:
DOI: 10.1002/mds.23698

Links to Exploration step

ISTEX:50B77A4B4C970763DCD1BFCBA3F272B70C8B5985

Le document en format XML

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<name sortKey="Schmitz Bsch, Tanja" sort="Schmitz Bsch, Tanja" uniqKey="Schmitz Bsch T" first="Tanja" last="Schmitz-Hübsch">Tanja Schmitz-Hübsch</name>
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<mods:affiliation>Department of Neurology, University Hospital of Bonn, Bonn, Germany</mods:affiliation>
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<mods:affiliation>Modeling in Clinical Research, EA 3974, University Pierre et Marie Curie, Paris, France</mods:affiliation>
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<name sortKey="Tezenas Du Montcel, Sophie" sort="Tezenas Du Montcel, Sophie" uniqKey="Tezenas Du Montcel S" first="Sophie" last="Tezenas Du Montcel">Sophie Tezenas Du Montcel</name>
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<mods:affiliation>Modeling in Clinical Research, EA 3974, University Pierre et Marie Curie, Paris, France</mods:affiliation>
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<name sortKey="Giunti, Paola" sort="Giunti, Paola" uniqKey="Giunti P" first="Paola" last="Giunti">Paola Giunti</name>
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<name sortKey="Labrum, Robyn" sort="Labrum, Robyn" uniqKey="Labrum R" first="Robyn" last="Labrum">Robyn Labrum</name>
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<name sortKey="Durr, Alexandra" sort="Durr, Alexandra" uniqKey="Durr A" first="Alexandra" last="Dürr">Alexandra Dürr</name>
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<name sortKey="Ribai, Pascale" sort="Ribai, Pascale" uniqKey="Ribai P" first="Pascale" last="Ribai">Pascale Ribai</name>
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<name sortKey="Charles, Perrine" sort="Charles, Perrine" uniqKey="Charles P" first="Perrine" last="Charles">Perrine Charles</name>
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<name sortKey="Linnemann, Christoph" sort="Linnemann, Christoph" uniqKey="Linnemann C" first="Christoph" last="Linnemann">Christoph Linnemann</name>
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<name sortKey="Schols, Ludger" sort="Schols, Ludger" uniqKey="Schols L" first="Ludger" last="Schöls">Ludger Schöls</name>
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<name sortKey="Rakowicz, Maryla" sort="Rakowicz, Maryla" uniqKey="Rakowicz M" first="Maryla" last="Rakowicz">Maryla Rakowicz</name>
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<name sortKey="Rola, Rafal" sort="Rola, Rafal" uniqKey="Rola R" first="Rafal" last="Rola">Rafal Rola</name>
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<name sortKey="Zdzienicka, Elszbieta" sort="Zdzienicka, Elszbieta" uniqKey="Zdzienicka E" first="Elszbieta" last="Zdzienicka">Elszbieta Zdzienicka</name>
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<name sortKey="Fancellu, Roberto" sort="Fancellu, Roberto" uniqKey="Fancellu R" first="Roberto" last="Fancellu">Roberto Fancellu</name>
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<name sortKey="Mariotti, Caterina" sort="Mariotti, Caterina" uniqKey="Mariotti C" first="Caterina" last="Mariotti">Caterina Mariotti</name>
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<name sortKey="Baliko, Lazlo" sort="Baliko, Lazlo" uniqKey="Baliko L" first="Lazlo" last="Baliko">Lazlo Baliko</name>
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<mods:affiliation>Department of Neurology and Stroke, County Hospital, Veszprém, Hungary</mods:affiliation>
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<name sortKey="Melegh, Bela" sort="Melegh, Bela" uniqKey="Melegh B" first="Bela" last="Melegh">Bela Melegh</name>
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<mods:affiliation>Department of Medical Genetics and Child Development, University of Pécs, Hungary</mods:affiliation>
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<name sortKey="Filla, Alessandro" sort="Filla, Alessandro" uniqKey="Filla A" first="Alessandro" last="Filla">Alessandro Filla</name>
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<name sortKey="Salvatore, Elena" sort="Salvatore, Elena" uniqKey="Salvatore E" first="Elena" last="Salvatore">Elena Salvatore</name>
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<mods:affiliation>Department of Neurology, University of Naples, Naples, Italy</mods:affiliation>
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<name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name>
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<mods:affiliation>Department of Neurology, Donders Centre for Neuroscience, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands</mods:affiliation>
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<name sortKey="Szymanski, Sandra" sort="Szymanski, Sandra" uniqKey="Szymanski S" first="Sandra" last="Szymanski">Sandra Szymanski</name>
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<mods:affiliation>Department of Neurology, St. Josef Hospital, University Hospital of Bochum, Bochum, Germany</mods:affiliation>
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<name sortKey="Infante, Jon" sort="Infante, Jon" uniqKey="Infante J" first="Jon" last="Infante">Jon Infante</name>
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<mods:affiliation>Department of Neurology, University Hospital “Marqués de Valdecilla,” CIBERNED, Santander, Spain</mods:affiliation>
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<name sortKey="Timmann, Dagmar" sort="Timmann, Dagmar" uniqKey="Timmann D" first="Dagmar" last="Timmann">Dagmar Timmann</name>
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<mods:affiliation>Department of Neurology, University Hospital of Essen, Essen, Germany</mods:affiliation>
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<name sortKey="Boesch, Sylvia" sort="Boesch, Sylvia" uniqKey="Boesch S" first="Sylvia" last="Boesch">Sylvia Boesch</name>
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<mods:affiliation>Department of Neurology, University of Innsbruck, Innsbruck, Austria</mods:affiliation>
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<name sortKey="Depondt, Chantal" sort="Depondt, Chantal" uniqKey="Depondt C" first="Chantal" last="Depondt">Chantal Depondt</name>
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<mods:affiliation>Department of Neurology, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium</mods:affiliation>
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<author>
<name sortKey="Kang, Jun Uk" sort="Kang, Jun Uk" uniqKey="Kang J" first="Jun-Suk" last="Kang">Jun-Suk Kang</name>
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<mods:affiliation>Department of Neurology, University of Frankfurt, Frankfurt/M, Germany</mods:affiliation>
</affiliation>
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<author>
<name sortKey="Schulz, Jorg B" sort="Schulz, Jorg B" uniqKey="Schulz J" first="Jörg B." last="Schulz">Jörg B. Schulz</name>
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<mods:affiliation>Department of Neurology, University Clinic, RTHW Aachen, Aachen, Germany</mods:affiliation>
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<name sortKey="Klopstock, Thomas" sort="Klopstock, Thomas" uniqKey="Klopstock T" first="Thomas" last="Klopstock">Thomas Klopstock</name>
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<mods:affiliation>Department of Neurology, Friedrich‐Baur‐Institute, University Hospital of Ludwig‐Maximilians‐University, München, Germany</mods:affiliation>
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<name sortKey="Lossnitzer, Nicole" sort="Lossnitzer, Nicole" uniqKey="Lossnitzer N" first="Nicole" last="Lossnitzer">Nicole Lossnitzer</name>
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<mods:affiliation>Department of Psychosomatic and General Internal Medicine, Medical University Hospital Heidelberg, Heidelberg, Germany</mods:affiliation>
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<name sortKey="Lowe, Bernd" sort="Lowe, Bernd" uniqKey="Lowe B" first="Bernd" last="Löwe">Bernd Löwe</name>
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<mods:affiliation>Department of Psychosomatic Medicine and Psychotherapy, University Medical Center Hamburg‐Eppendorf and Hamburg‐Eilbek (Schön Clinics), Hamburg, Germany</mods:affiliation>
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<name sortKey="Frick, Caroline" sort="Frick, Caroline" uniqKey="Frick C" first="Caroline" last="Frick">Caroline Frick</name>
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<mods:affiliation>Department of Psychiatry and Psychotherapy, University Clinic Bonn, Bonn, Germany</mods:affiliation>
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<name sortKey="Rottl Nder, Daniela" sort="Rottl Nder, Daniela" uniqKey="Rottl Nder D" first="Daniela" last="Rottl Nder">Daniela Rottl Nder</name>
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<mods:affiliation>Department of Psychiatry and Psychotherapy, University Clinic Bonn, Bonn, Germany</mods:affiliation>
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<name sortKey="Schlaepfer, Thomas E" sort="Schlaepfer, Thomas E" uniqKey="Schlaepfer T" first="Thomas E." last="Schlaepfer">Thomas E. Schlaepfer</name>
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<mods:affiliation>Department of Psychiatry and Psychotherapy, University Clinic Bonn, Bonn, Germany</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Department of Psychiatry and Behavioral Science, Johns Hopkins University, Baltimore, Maryland, USA</mods:affiliation>
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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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<mods:affiliation>Department of Neurology, University Hospital of Bonn, Bonn, Germany</mods:affiliation>
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<title level="a" type="main" xml:lang="en">Depression comorbidity in spinocerebellar ataxia</title>
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<name sortKey="Schmitz Bsch, Tanja" sort="Schmitz Bsch, Tanja" uniqKey="Schmitz Bsch T" first="Tanja" last="Schmitz-Hübsch">Tanja Schmitz-Hübsch</name>
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<mods:affiliation>Department of Neurology, University Hospital of Bonn, Bonn, Germany</mods:affiliation>
</affiliation>
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<author>
<name sortKey="Coudert, Mathieu" sort="Coudert, Mathieu" uniqKey="Coudert M" first="Mathieu" last="Coudert">Mathieu Coudert</name>
<affiliation>
<mods:affiliation>Department of Biostatistics and Medical Informatics, Hôpital de la Pitié‐Salpêtrière, Assistance Publique‐Hôpitaux, Paris, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Modeling in Clinical Research, EA 3974, University Pierre et Marie Curie, Paris, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Tezenas Du Montcel, Sophie" sort="Tezenas Du Montcel, Sophie" uniqKey="Tezenas Du Montcel S" first="Sophie" last="Tezenas Du Montcel">Sophie Tezenas Du Montcel</name>
<affiliation>
<mods:affiliation>Department of Biostatistics and Medical Informatics, Hôpital de la Pitié‐Salpêtrière, Assistance Publique‐Hôpitaux, Paris, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Modeling in Clinical Research, EA 3974, University Pierre et Marie Curie, Paris, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Giunti, Paola" sort="Giunti, Paola" uniqKey="Giunti P" first="Paola" last="Giunti">Paola Giunti</name>
<affiliation>
<mods:affiliation>Department of Molecular Neuroscience, Institute of Neurology, Queen Square, London, United Kingdom</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Labrum, Robyn" sort="Labrum, Robyn" uniqKey="Labrum R" first="Robyn" last="Labrum">Robyn Labrum</name>
<affiliation>
<mods:affiliation>Division of Neurogenetics, National Hospital of Neurology and Neurosurgery, Queen Square, London, United Kingdom</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Durr, Alexandra" sort="Durr, Alexandra" uniqKey="Durr A" first="Alexandra" last="Dürr">Alexandra Dürr</name>
<affiliation>
<mods:affiliation>INSERM, UMR_S679 Neurologie & Thérapeutique Expérimentale, Paris, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>AP‐HP, Hôpital de la Salpêtrière, Department of Genetics and Cytogenetics, Paris, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Ribai, Pascale" sort="Ribai, Pascale" uniqKey="Ribai P" first="Pascale" last="Ribai">Pascale Ribai</name>
<affiliation>
<mods:affiliation>INSERM, UMR_S679 Neurologie & Thérapeutique Expérimentale, Paris, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>AP‐HP, Hôpital de la Salpêtrière, Department of Genetics and Cytogenetics, Paris, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Charles, Perrine" sort="Charles, Perrine" uniqKey="Charles P" first="Perrine" last="Charles">Perrine Charles</name>
<affiliation>
<mods:affiliation>INSERM, UMR_S679 Neurologie & Thérapeutique Expérimentale, Paris, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>AP‐HP, Hôpital de la Salpêtrière, Department of Genetics and Cytogenetics, Paris, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Linnemann, Christoph" sort="Linnemann, Christoph" uniqKey="Linnemann C" first="Christoph" last="Linnemann">Christoph Linnemann</name>
<affiliation>
<mods:affiliation>Department of Neurology and Hertie‐Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Schols, Ludger" sort="Schols, Ludger" uniqKey="Schols L" first="Ludger" last="Schöls">Ludger Schöls</name>
<affiliation>
<mods:affiliation>Department of Neurology and Hertie‐Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Rakowicz, Maryla" sort="Rakowicz, Maryla" uniqKey="Rakowicz M" first="Maryla" last="Rakowicz">Maryla Rakowicz</name>
<affiliation>
<mods:affiliation>Department of Clinical Neurophysiology, Institute of Psychiatry and Neurology, Warsaw, Poland</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Rola, Rafal" sort="Rola, Rafal" uniqKey="Rola R" first="Rafal" last="Rola">Rafal Rola</name>
<affiliation>
<mods:affiliation>First Department of Neurology, Institute of Psychiatry and Neurology, Warsaw, Poland</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Zdzienicka, Elszbieta" sort="Zdzienicka, Elszbieta" uniqKey="Zdzienicka E" first="Elszbieta" last="Zdzienicka">Elszbieta Zdzienicka</name>
<affiliation>
<mods:affiliation>Department of Genetics, Institute of Psychiatry and Neurology, Warsaw, Poland</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Fancellu, Roberto" sort="Fancellu, Roberto" uniqKey="Fancellu R" first="Roberto" last="Fancellu">Roberto Fancellu</name>
<affiliation>
<mods:affiliation>Department of Biochemistry and Genetics, Fondazione‐IRCCS, Istituto Neurologico Carlo Besta, Milan, Italy</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Mariotti, Caterina" sort="Mariotti, Caterina" uniqKey="Mariotti C" first="Caterina" last="Mariotti">Caterina Mariotti</name>
<affiliation>
<mods:affiliation>Department of Biochemistry and Genetics, Fondazione‐IRCCS, Istituto Neurologico Carlo Besta, Milan, Italy</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Baliko, Lazlo" sort="Baliko, Lazlo" uniqKey="Baliko L" first="Lazlo" last="Baliko">Lazlo Baliko</name>
<affiliation>
<mods:affiliation>Department of Neurology and Stroke, County Hospital, Veszprém, Hungary</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Melegh, Bela" sort="Melegh, Bela" uniqKey="Melegh B" first="Bela" last="Melegh">Bela Melegh</name>
<affiliation>
<mods:affiliation>Department of Medical Genetics and Child Development, University of Pécs, Hungary</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Filla, Alessandro" sort="Filla, Alessandro" uniqKey="Filla A" first="Alessandro" last="Filla">Alessandro Filla</name>
<affiliation>
<mods:affiliation>Department of Neurology, University of Naples, Naples, Italy</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Salvatore, Elena" sort="Salvatore, Elena" uniqKey="Salvatore E" first="Elena" last="Salvatore">Elena Salvatore</name>
<affiliation>
<mods:affiliation>Department of Neurology, University of Naples, Naples, Italy</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name>
<affiliation>
<mods:affiliation>Department of Neurology, Donders Centre for Neuroscience, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Szymanski, Sandra" sort="Szymanski, Sandra" uniqKey="Szymanski S" first="Sandra" last="Szymanski">Sandra Szymanski</name>
<affiliation>
<mods:affiliation>Department of Neurology, St. Josef Hospital, University Hospital of Bochum, Bochum, Germany</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Infante, Jon" sort="Infante, Jon" uniqKey="Infante J" first="Jon" last="Infante">Jon Infante</name>
<affiliation>
<mods:affiliation>Department of Neurology, University Hospital “Marqués de Valdecilla,” CIBERNED, Santander, Spain</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Timmann, Dagmar" sort="Timmann, Dagmar" uniqKey="Timmann D" first="Dagmar" last="Timmann">Dagmar Timmann</name>
<affiliation>
<mods:affiliation>Department of Neurology, University Hospital of Essen, Essen, Germany</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Boesch, Sylvia" sort="Boesch, Sylvia" uniqKey="Boesch S" first="Sylvia" last="Boesch">Sylvia Boesch</name>
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<div type="abstract" xml:lang="en">This is a description of the prevalence and profile of depressive symptoms in dominant spinocerebellar ataxia (SCA). Depressive symptoms were assessed in a convenience sample of 526 genetically confirmed and clinically affected patients (117 SCA1, 163 SCA2, 139 SCA3, and 107 SCA6) using the Patient Health Questionnaire (PHQ). In addition, depressive status according to the examiner and the use of antidepressants was recorded. Depression self‐assessment was compared with an interview‐based psychiatric assessment in a subset of 26 patients. Depression prevalence estimates were 17.1% according to the PHQ algorithm and 15.4% when assessed clinically. The sensitivity of clinical impression compared with PHQ classification was low (0.35), whereas diagnostic accuracy of PHQ compared with psychiatric interview in the subset was high. Antidepressants were used by 17.7% of patients and in >10% of patients without current clinically relevant depressive symptoms. Depression profile in SCA did not differ from a sample of patients with major depressive disorder except for the movement‐related item. Neither depression prevalence nor use of antidepressants differed between genetic subtypes, with only sleep disturbance more common in SCA3. In a multivariate analysis, ataxia severity and female sex independently predicted depressive status in SCA. The PHQ algorithmic classification is appropriate for use in SCA but should stimulate further psychiatric evaluation if depression is indicated. Despite a higher risk for depression with more severe disease, the relation of depressive symptoms to SCA neurodegeneration remains to be shown. © 2011 Movement Disorder Society</div>
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<forename type="first">Thomas E.</forename>
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<title level="j">Movement Disorders</title>
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<p>This is a description of the prevalence and profile of depressive symptoms in dominant spinocerebellar ataxia (SCA). Depressive symptoms were assessed in a convenience sample of 526 genetically confirmed and clinically affected patients (117 SCA1, 163 SCA2, 139 SCA3, and 107 SCA6) using the Patient Health Questionnaire (PHQ). In addition, depressive status according to the examiner and the use of antidepressants was recorded. Depression self‐assessment was compared with an interview‐based psychiatric assessment in a subset of 26 patients. Depression prevalence estimates were 17.1% according to the PHQ algorithm and 15.4% when assessed clinically. The sensitivity of clinical impression compared with PHQ classification was low (0.35), whereas diagnostic accuracy of PHQ compared with psychiatric interview in the subset was high. Antidepressants were used by 17.7% of patients and in >10% of patients without current clinically relevant depressive symptoms. Depression profile in SCA did not differ from a sample of patients with major depressive disorder except for the movement‐related item. Neither depression prevalence nor use of antidepressants differed between genetic subtypes, with only sleep disturbance more common in SCA3. In a multivariate analysis, ataxia severity and female sex independently predicted depressive status in SCA. The PHQ algorithmic classification is appropriate for use in SCA but should stimulate further psychiatric evaluation if depression is indicated. Despite a higher risk for depression with more severe disease, the relation of depressive symptoms to SCA neurodegeneration remains to be shown. © 2011 Movement Disorder Society</p>
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<p>This is a description of the prevalence and profile of depressive symptoms in dominant spinocerebellar ataxia (SCA). Depressive symptoms were assessed in a convenience sample of 526 genetically confirmed and clinically affected patients (117 SCA1, 163 SCA2, 139 SCA3, and 107 SCA6) using the Patient Health Questionnaire (PHQ). In addition, depressive status according to the examiner and the use of antidepressants was recorded. Depression self‐assessment was compared with an interview‐based psychiatric assessment in a subset of 26 patients. Depression prevalence estimates were 17.1% according to the PHQ algorithm and 15.4% when assessed clinically. The sensitivity of clinical impression compared with PHQ classification was low (0.35), whereas diagnostic accuracy of PHQ compared with psychiatric interview in the subset was high. Antidepressants were used by 17.7% of patients and in >10% of patients without current clinically relevant depressive symptoms. Depression profile in SCA did not differ from a sample of patients with major depressive disorder except for the movement‐related item. Neither depression prevalence nor use of antidepressants differed between genetic subtypes, with only sleep disturbance more common in SCA3. In a multivariate analysis, ataxia severity and female sex independently predicted depressive status in SCA. The PHQ algorithmic classification is appropriate for use in SCA but should stimulate further psychiatric evaluation if depression is indicated. Despite a higher risk for depression with more severe disease, the relation of depressive symptoms to SCA neurodegeneration remains to be shown. © 2011 Movement Disorder Society</p>
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<abstract lang="en">This is a description of the prevalence and profile of depressive symptoms in dominant spinocerebellar ataxia (SCA). Depressive symptoms were assessed in a convenience sample of 526 genetically confirmed and clinically affected patients (117 SCA1, 163 SCA2, 139 SCA3, and 107 SCA6) using the Patient Health Questionnaire (PHQ). In addition, depressive status according to the examiner and the use of antidepressants was recorded. Depression self‐assessment was compared with an interview‐based psychiatric assessment in a subset of 26 patients. Depression prevalence estimates were 17.1% according to the PHQ algorithm and 15.4% when assessed clinically. The sensitivity of clinical impression compared with PHQ classification was low (0.35), whereas diagnostic accuracy of PHQ compared with psychiatric interview in the subset was high. Antidepressants were used by 17.7% of patients and in >10% of patients without current clinically relevant depressive symptoms. Depression profile in SCA did not differ from a sample of patients with major depressive disorder except for the movement‐related item. Neither depression prevalence nor use of antidepressants differed between genetic subtypes, with only sleep disturbance more common in SCA3. In a multivariate analysis, ataxia severity and female sex independently predicted depressive status in SCA. The PHQ algorithmic classification is appropriate for use in SCA but should stimulate further psychiatric evaluation if depression is indicated. Despite a higher risk for depression with more severe disease, the relation of depressive symptoms to SCA neurodegeneration remains to be shown. © 2011 Movement Disorder Society</abstract>
<note type="additional physical form">Author Roles and Disclosures</note>
<note type="content">*Relevant conflicts of interest/financial disclosures: Nothing to report.</note>
<note type="content">*The study was supported by grant EUROSCA/LSHM‐CT‐2004‐503304 from the European Union (to T. Schmitz‐Hübsch, S. Tezenas du Montcel, P. Giunti, L. Schöls, M. Rakowicz, R. Rola, E. Zdzienicka, R. Fancellu, C. Mariotti, B. Melegh, A. Filla, B.P.C. van de Warrenburg, J. Infante, S. Boesch, C. Depondt, J.‐S. Kang, J. Schulz, T. Klockgether), grant GeneMove/01 GM 0503 from the German Ministry of Education and Research (to D. Timmann, L. Schöls, J.‐S. Kang, J. Schulz, T. Klopstock, T. Klockgether), and grant 3 PO5B 019 24 from the Polish Ministry of Scientific Research and Information Technology (to R. Rola).</note>
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