Movement Disorders (revue)

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Health-related quality of life in multiple system atrophy

Identifieur interne : 001B25 ( PascalFrancis/Corpus ); précédent : 001B24; suivant : 001B26

Health-related quality of life in multiple system atrophy

Auteurs : Anette Schrag ; Felix Geser ; Michaela Stampfer-Kountchev ; Klaus Seppi ; Martin Sawires ; Martin Köllensperger ; Christoph Scherfler ; Niall Quinn ; Maria T. Pellecchia ; Paolo Barone ; Francesca Del Sorbo ; Alberto Albanese ; Karen Ostergaard ; Erik Dupont ; Adriana Cardozo ; Eduardo Tolosa ; Christer F. Nilsson ; Hakan Widner ; Olle Lindvall ; Nir Giladi ; Tanya Gurevich ; Christine Daniels ; Günther Deuschl ; Miguel Coelho ; Cristina Sampaio ; Michael Abele ; Thomas Klockgether ; Nicole Schimke ; Karla M. Eggert ; Wolfgang Oertel ; Ruth Djaldetti ; Carlo Colosimo ; Giuseppe Meco ; Werner Poewe ; Gregor K. Wenning

Source :

RBID : Pascal:06-0352376

Descripteurs français

English descriptors

Abstract

Although multiple system atrophy (MSA) is a neurodegenerative disorder leading to progressive disability and decreased life expectancy, little is known about patients' own evaluation of their illness and factors associated with poor health-related quality of life (Hr-QoL). We, therefore, assessed Hr-QoL and its determinants in MSA. The following scales were applied to 115 patients in the European MSA-Study Group (EMSA-SG) Natural History Study: Medical Outcome Study Short Form (SF-36), EQ-5D, Beck Depression Inventory (BDI), Mini-Mental state examination (MMSE), Unified MSA Rating Scale (UMSARS), Hoehn & Yahr (H&Y) Parkinson's disease staging scale, Composite Autonomic Symptom Scale (COMPASS), and Parkinson's Disease Sleep Scale (PDSS). Forty-six percent of patients had moderate to severe depression (BDI ≥ 17); Hr-QoL scores on the SF-36 and EQ-5D were significantly impaired. Pain, the only domain with similar scores in MSA and published PD patients, was reported more frequently in patients with MSA-P (predominantly parkinsonian motor subtype) than MSA-C (predominantly cerebellar motor subtype; 76% vs. 50%; P = 0.005). Hr-QoL scores correlated most strongly with UMSARS motor, COMPASS, and BDI scores but not with MMSE scores, age at onset, or disease duration. The COMPASS and UMSARS activities of daily living scores were moderate-to-strong predictors for the SF-36 physical summary score and the BDI and UMSARS motor scores for the SF-36 mental summary score. This report is the first study to show that Hr-QoL is significantly impaired in MSA. Although not all possible factors related to impaired Hr-QoL in MSA could be assessed, autonomic dysfunction, motor impairment, and depression were most closely associated with poor Hr-QoL, and therapeutic management, therefore, should concentrate upon these aspects of the disease.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03   1    @0 Mov. disord.
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A08 01  1  ENG  @1 Health-related quality of life in multiple system atrophy
A11 01  1    @1 SCHRAG (Anette)
A11 02  1    @1 GESER (Felix)
A11 03  1    @1 STAMPFER-KOUNTCHEV (Michaela)
A11 04  1    @1 SEPPI (Klaus)
A11 05  1    @1 SAWIRES (Martin)
A11 06  1    @1 KÖLLENSPERGER (Martin)
A11 07  1    @1 SCHERFLER (Christoph)
A11 08  1    @1 QUINN (Niall)
A11 09  1    @1 PELLECCHIA (Maria T.)
A11 10  1    @1 BARONE (Paolo)
A11 11  1    @1 DEL SORBO (Francesca)
A11 12  1    @1 ALBANESE (Alberto)
A11 13  1    @1 OSTERGAARD (Karen)
A11 14  1    @1 DUPONT (Erik)
A11 15  1    @1 CARDOZO (Adriana)
A11 16  1    @1 TOLOSA (Eduardo)
A11 17  1    @1 NILSSON (Christer F.)
A11 18  1    @1 WIDNER (Hakan)
A11 19  1    @1 LINDVALL (Olle)
A11 20  1    @1 GILADI (Nir)
A11 21  1    @1 GUREVICH (Tanya)
A11 22  1    @1 DANIELS (Christine)
A11 23  1    @1 DEUSCHL (Günther)
A11 24  1    @1 COELHO (Miguel)
A11 25  1    @1 SAMPAIO (Cristina)
A11 26  1    @1 ABELE (Michael)
A11 27  1    @1 KLOCKGETHER (Thomas)
A11 28  1    @1 SCHIMKE (Nicole)
A11 29  1    @1 EGGERT (Karla M.)
A11 30  1    @1 OERTEL (Wolfgang)
A11 31  1    @1 DJALDETTI (Ruth)
A11 32  1    @1 COLOSIMO (Carlo)
A11 33  1    @1 MECO (Giuseppe)
A11 34  1    @1 POEWE (Werner)
A11 35  1    @1 WENNING (Gregor K.)
A14 01      @1 Department of Clinical Neurosciences, Royal Free & University College Medical School @2 London @3 GBR @Z 1 aut.
A14 02      @1 Clinical Department of Neurology, Innsbruck Medical University @3 AUT @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 34 aut. @Z 35 aut.
A14 03      @1 University College London, Institute of Neurology, Queen Square @2 London @3 GBR @Z 8 aut.
A14 04      @1 Department of Neurological Sciences, University Federico II @2 Naples @3 ITA @Z 9 aut. @Z 10 aut.
A14 05      @1 Istituto Nazionale Neurologico Carlo Besta, Università Cattolica del Sacro Cuore @2 Milano @3 ITA @Z 11 aut. @Z 12 aut.
A14 06      @1 Aarhus University Hospital, Department of Neurology @2 Aarhus @3 DNK @Z 13 aut. @Z 14 aut.
A14 07      @1 Universitat de Barcelona, Hospital Clinic, Department of Neurology @3 ESP @Z 15 aut. @Z 16 aut.
A14 08      @1 Department of Clinical Neuroscience, Division of Neurology, University of Lund @3 SWE @Z 17 aut. @Z 18 aut. @Z 19 aut.
A14 09      @1 Tel Aviv Sourasky Medical Center, Movement Disorders Unit, Department of Neurology @3 ISR @Z 20 aut. @Z 21 aut.
A14 10      @1 Department of Neurology, Christian-Albrechts University of Kiel @2 Kiel @3 DEU @Z 22 aut. @Z 23 aut.
A14 11      @1 Faculdade de Medicina de Lisboa, Hopital Santa Maria, Centro de Neurosciencias de Lisboa @3 PRT @Z 24 aut. @Z 25 aut.
A14 12      @1 University of Bonn, Department of Neurology @3 DEU @Z 26 aut. @Z 27 aut.
A14 13      @1 Philipps-University Marburg, Department of Neurology @3 DEU @Z 28 aut. @Z 29 aut. @Z 30 aut.
A14 14      @1 Department of Neurology, Rabin Medical Center @2 Petach-Tiqva @3 ISR @Z 31 aut.
A14 15      @1 University of Roma, "La Sapienza, " Department of Neuroscience @3 ITA @Z 32 aut. @Z 33 aut.
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A43 01      @1 INIST @2 20953 @5 354000138863880120
A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
A45       @0 24 ref.
A47 01  1    @0 06-0352376
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 Although multiple system atrophy (MSA) is a neurodegenerative disorder leading to progressive disability and decreased life expectancy, little is known about patients' own evaluation of their illness and factors associated with poor health-related quality of life (Hr-QoL). We, therefore, assessed Hr-QoL and its determinants in MSA. The following scales were applied to 115 patients in the European MSA-Study Group (EMSA-SG) Natural History Study: Medical Outcome Study Short Form (SF-36), EQ-5D, Beck Depression Inventory (BDI), Mini-Mental state examination (MMSE), Unified MSA Rating Scale (UMSARS), Hoehn & Yahr (H&Y) Parkinson's disease staging scale, Composite Autonomic Symptom Scale (COMPASS), and Parkinson's Disease Sleep Scale (PDSS). Forty-six percent of patients had moderate to severe depression (BDI ≥ 17); Hr-QoL scores on the SF-36 and EQ-5D were significantly impaired. Pain, the only domain with similar scores in MSA and published PD patients, was reported more frequently in patients with MSA-P (predominantly parkinsonian motor subtype) than MSA-C (predominantly cerebellar motor subtype; 76% vs. 50%; P = 0.005). Hr-QoL scores correlated most strongly with UMSARS motor, COMPASS, and BDI scores but not with MMSE scores, age at onset, or disease duration. The COMPASS and UMSARS activities of daily living scores were moderate-to-strong predictors for the SF-36 physical summary score and the BDI and UMSARS motor scores for the SF-36 mental summary score. This report is the first study to show that Hr-QoL is significantly impaired in MSA. Although not all possible factors related to impaired Hr-QoL in MSA could be assessed, autonomic dysfunction, motor impairment, and depression were most closely associated with poor Hr-QoL, and therapeutic management, therefore, should concentrate upon these aspects of the disease.
C02 01  X    @0 002B17
C02 02  X    @0 002B17F
C02 03  X    @0 002B17G
C03 01  X  FRE  @0 Système nerveux pathologie @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Atrophie multisystématisée @2 NM @5 02
C03 02  X  ENG  @0 Multiple system atrophy @2 NM @5 02
C03 02  X  SPA  @0 Atrofia multisistematizada @2 NM @5 02
C03 03  X  FRE  @0 Etat dépressif @5 03
C03 03  X  ENG  @0 Depression @5 03
C03 03  X  SPA  @0 Estado depresivo @5 03
C03 04  X  FRE  @0 Qualité vie @5 09
C03 04  X  ENG  @0 Quality of life @5 09
C03 04  X  SPA  @0 Calidad vida @5 09
C03 05  X  FRE  @0 Trouble fonctionnel @5 10
C03 05  X  ENG  @0 Dysfunction @5 10
C03 05  X  SPA  @0 Trastorno funcional @5 10
C07 01  X  FRE  @0 Trouble humeur @5 37
C07 01  X  ENG  @0 Mood disorder @5 37
C07 01  X  SPA  @0 Trastorno humor @5 37
N21       @1 233
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 06-0352376 INIST
ET : Health-related quality of life in multiple system atrophy
AU : SCHRAG (Anette); GESER (Felix); STAMPFER-KOUNTCHEV (Michaela); SEPPI (Klaus); SAWIRES (Martin); KÖLLENSPERGER (Martin); SCHERFLER (Christoph); QUINN (Niall); PELLECCHIA (Maria T.); BARONE (Paolo); DEL SORBO (Francesca); ALBANESE (Alberto); OSTERGAARD (Karen); DUPONT (Erik); CARDOZO (Adriana); TOLOSA (Eduardo); NILSSON (Christer F.); WIDNER (Hakan); LINDVALL (Olle); GILADI (Nir); GUREVICH (Tanya); DANIELS (Christine); DEUSCHL (Günther); COELHO (Miguel); SAMPAIO (Cristina); ABELE (Michael); KLOCKGETHER (Thomas); SCHIMKE (Nicole); EGGERT (Karla M.); OERTEL (Wolfgang); DJALDETTI (Ruth); COLOSIMO (Carlo); MECO (Giuseppe); POEWE (Werner); WENNING (Gregor K.)
AF : Department of Clinical Neurosciences, Royal Free & University College Medical School/London/Royaume-Uni (1 aut.); Clinical Department of Neurology, Innsbruck Medical University/Autriche (2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 34 aut., 35 aut.); University College London, Institute of Neurology, Queen Square/London/Royaume-Uni (8 aut.); Department of Neurological Sciences, University Federico II/Naples/Italie (9 aut., 10 aut.); Istituto Nazionale Neurologico Carlo Besta, Università Cattolica del Sacro Cuore/Milano/Italie (11 aut., 12 aut.); Aarhus University Hospital, Department of Neurology/Aarhus/Danemark (13 aut., 14 aut.); Universitat de Barcelona, Hospital Clinic, Department of Neurology/Espagne (15 aut., 16 aut.); Department of Clinical Neuroscience, Division of Neurology, University of Lund/Suède (17 aut., 18 aut., 19 aut.); Tel Aviv Sourasky Medical Center, Movement Disorders Unit, Department of Neurology/Israël (20 aut., 21 aut.); Department of Neurology, Christian-Albrechts University of Kiel/Kiel/Allemagne (22 aut., 23 aut.); Faculdade de Medicina de Lisboa, Hopital Santa Maria, Centro de Neurosciencias de Lisboa/Portugal (24 aut., 25 aut.); University of Bonn, Department of Neurology/Allemagne (26 aut., 27 aut.); Philipps-University Marburg, Department of Neurology/Allemagne (28 aut., 29 aut., 30 aut.); Department of Neurology, Rabin Medical Center/Petach-Tiqva/Israël (31 aut.); University of Roma, "La Sapienza, " Department of Neuroscience/Italie (32 aut., 33 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 6; Pp. 809-815; Bibl. 24 ref.
LA : Anglais
EA : Although multiple system atrophy (MSA) is a neurodegenerative disorder leading to progressive disability and decreased life expectancy, little is known about patients' own evaluation of their illness and factors associated with poor health-related quality of life (Hr-QoL). We, therefore, assessed Hr-QoL and its determinants in MSA. The following scales were applied to 115 patients in the European MSA-Study Group (EMSA-SG) Natural History Study: Medical Outcome Study Short Form (SF-36), EQ-5D, Beck Depression Inventory (BDI), Mini-Mental state examination (MMSE), Unified MSA Rating Scale (UMSARS), Hoehn & Yahr (H&Y) Parkinson's disease staging scale, Composite Autonomic Symptom Scale (COMPASS), and Parkinson's Disease Sleep Scale (PDSS). Forty-six percent of patients had moderate to severe depression (BDI ≥ 17); Hr-QoL scores on the SF-36 and EQ-5D were significantly impaired. Pain, the only domain with similar scores in MSA and published PD patients, was reported more frequently in patients with MSA-P (predominantly parkinsonian motor subtype) than MSA-C (predominantly cerebellar motor subtype; 76% vs. 50%; P = 0.005). Hr-QoL scores correlated most strongly with UMSARS motor, COMPASS, and BDI scores but not with MMSE scores, age at onset, or disease duration. The COMPASS and UMSARS activities of daily living scores were moderate-to-strong predictors for the SF-36 physical summary score and the BDI and UMSARS motor scores for the SF-36 mental summary score. This report is the first study to show that Hr-QoL is significantly impaired in MSA. Although not all possible factors related to impaired Hr-QoL in MSA could be assessed, autonomic dysfunction, motor impairment, and depression were most closely associated with poor Hr-QoL, and therapeutic management, therefore, should concentrate upon these aspects of the disease.
CC : 002B17; 002B17F; 002B17G
FD : Système nerveux pathologie; Atrophie multisystématisée; Etat dépressif; Qualité vie; Trouble fonctionnel
FG : Trouble humeur
ED : Nervous system diseases; Multiple system atrophy; Depression; Quality of life; Dysfunction
EG : Mood disorder
SD : Sistema nervioso patología; Atrofia multisistematizada; Estado depresivo; Calidad vida; Trastorno funcional
LO : INIST-20953.354000138863880120
ID : 06-0352376

Links to Exploration step

Pascal:06-0352376

Le document en format XML

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<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
<sZ>19 aut.</sZ>
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<inist:fA14 i1="08">
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<s3>SWE</s3>
<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
<sZ>19 aut.</sZ>
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<author>
<name sortKey="Giladi, Nir" sort="Giladi, Nir" uniqKey="Giladi N" first="Nir" last="Giladi">Nir Giladi</name>
<affiliation>
<inist:fA14 i1="09">
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<s3>ISR</s3>
<sZ>20 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
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<author>
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<affiliation>
<inist:fA14 i1="09">
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<s3>ISR</s3>
<sZ>20 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
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<author>
<name sortKey="Daniels, Christine" sort="Daniels, Christine" uniqKey="Daniels C" first="Christine" last="Daniels">Christine Daniels</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Department of Neurology, Christian-Albrechts University of Kiel</s1>
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<s3>DEU</s3>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
</inist:fA14>
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<author>
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<affiliation>
<inist:fA14 i1="10">
<s1>Department of Neurology, Christian-Albrechts University of Kiel</s1>
<s2>Kiel</s2>
<s3>DEU</s3>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Coelho, Miguel" sort="Coelho, Miguel" uniqKey="Coelho M" first="Miguel" last="Coelho">Miguel Coelho</name>
<affiliation>
<inist:fA14 i1="11">
<s1>Faculdade de Medicina de Lisboa, Hopital Santa Maria, Centro de Neurosciencias de Lisboa</s1>
<s3>PRT</s3>
<sZ>24 aut.</sZ>
<sZ>25 aut.</sZ>
</inist:fA14>
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</author>
<author>
<name sortKey="Sampaio, Cristina" sort="Sampaio, Cristina" uniqKey="Sampaio C" first="Cristina" last="Sampaio">Cristina Sampaio</name>
<affiliation>
<inist:fA14 i1="11">
<s1>Faculdade de Medicina de Lisboa, Hopital Santa Maria, Centro de Neurosciencias de Lisboa</s1>
<s3>PRT</s3>
<sZ>24 aut.</sZ>
<sZ>25 aut.</sZ>
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<author>
<name sortKey="Abele, Michael" sort="Abele, Michael" uniqKey="Abele M" first="Michael" last="Abele">Michael Abele</name>
<affiliation>
<inist:fA14 i1="12">
<s1>University of Bonn, Department of Neurology</s1>
<s3>DEU</s3>
<sZ>26 aut.</sZ>
<sZ>27 aut.</sZ>
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</author>
<author>
<name sortKey="Klockgether, Thomas" sort="Klockgether, Thomas" uniqKey="Klockgether T" first="Thomas" last="Klockgether">Thomas Klockgether</name>
<affiliation>
<inist:fA14 i1="12">
<s1>University of Bonn, Department of Neurology</s1>
<s3>DEU</s3>
<sZ>26 aut.</sZ>
<sZ>27 aut.</sZ>
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<author>
<name sortKey="Schimke, Nicole" sort="Schimke, Nicole" uniqKey="Schimke N" first="Nicole" last="Schimke">Nicole Schimke</name>
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<inist:fA14 i1="13">
<s1>Philipps-University Marburg, Department of Neurology</s1>
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<author>
<name sortKey="Eggert, Karla M" sort="Eggert, Karla M" uniqKey="Eggert K" first="Karla M." last="Eggert">Karla M. Eggert</name>
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<inist:fA14 i1="13">
<s1>Philipps-University Marburg, Department of Neurology</s1>
<s3>DEU</s3>
<sZ>28 aut.</sZ>
<sZ>29 aut.</sZ>
<sZ>30 aut.</sZ>
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<author>
<name sortKey="Oertel, Wolfgang" sort="Oertel, Wolfgang" uniqKey="Oertel W" first="Wolfgang" last="Oertel">Wolfgang Oertel</name>
<affiliation>
<inist:fA14 i1="13">
<s1>Philipps-University Marburg, Department of Neurology</s1>
<s3>DEU</s3>
<sZ>28 aut.</sZ>
<sZ>29 aut.</sZ>
<sZ>30 aut.</sZ>
</inist:fA14>
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</author>
<author>
<name sortKey="Djaldetti, Ruth" sort="Djaldetti, Ruth" uniqKey="Djaldetti R" first="Ruth" last="Djaldetti">Ruth Djaldetti</name>
<affiliation>
<inist:fA14 i1="14">
<s1>Department of Neurology, Rabin Medical Center</s1>
<s2>Petach-Tiqva</s2>
<s3>ISR</s3>
<sZ>31 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Colosimo, Carlo" sort="Colosimo, Carlo" uniqKey="Colosimo C" first="Carlo" last="Colosimo">Carlo Colosimo</name>
<affiliation>
<inist:fA14 i1="15">
<s1>University of Roma, "La Sapienza, " Department of Neuroscience</s1>
<s3>ITA</s3>
<sZ>32 aut.</sZ>
<sZ>33 aut.</sZ>
</inist:fA14>
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<author>
<name sortKey="Meco, Giuseppe" sort="Meco, Giuseppe" uniqKey="Meco G" first="Giuseppe" last="Meco">Giuseppe Meco</name>
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<inist:fA14 i1="15">
<s1>University of Roma, "La Sapienza, " Department of Neuroscience</s1>
<s3>ITA</s3>
<sZ>32 aut.</sZ>
<sZ>33 aut.</sZ>
</inist:fA14>
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<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
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<name sortKey="Wenning, Gregor K" sort="Wenning, Gregor K" uniqKey="Wenning G" first="Gregor K." last="Wenning">Gregor K. Wenning</name>
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<inist:fA14 i1="02">
<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<title xml:lang="en" level="a">Health-related quality of life in multiple system atrophy</title>
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<name sortKey="Schrag, Anette" sort="Schrag, Anette" uniqKey="Schrag A" first="Anette" last="Schrag">Anette Schrag</name>
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<inist:fA14 i1="01">
<s1>Department of Clinical Neurosciences, Royal Free & University College Medical School</s1>
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<s3>GBR</s3>
<sZ>1 aut.</sZ>
</inist:fA14>
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<author>
<name sortKey="Geser, Felix" sort="Geser, Felix" uniqKey="Geser F" first="Felix" last="Geser">Felix Geser</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
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<author>
<name sortKey="Stampfer Kountchev, Michaela" sort="Stampfer Kountchev, Michaela" uniqKey="Stampfer Kountchev M" first="Michaela" last="Stampfer-Kountchev">Michaela Stampfer-Kountchev</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
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<name sortKey="Seppi, Klaus" sort="Seppi, Klaus" uniqKey="Seppi K" first="Klaus" last="Seppi">Klaus Seppi</name>
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<inist:fA14 i1="02">
<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
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<name sortKey="Sawires, Martin" sort="Sawires, Martin" uniqKey="Sawires M" first="Martin" last="Sawires">Martin Sawires</name>
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<inist:fA14 i1="02">
<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<name sortKey="Kollensperger, Martin" sort="Kollensperger, Martin" uniqKey="Kollensperger M" first="Martin" last="Köllensperger">Martin Köllensperger</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
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<sZ>34 aut.</sZ>
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<author>
<name sortKey="Scherfler, Christoph" sort="Scherfler, Christoph" uniqKey="Scherfler C" first="Christoph" last="Scherfler">Christoph Scherfler</name>
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<inist:fA14 i1="02">
<s1>Clinical Department of Neurology, Innsbruck Medical University</s1>
<s3>AUT</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
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<name sortKey="Quinn, Niall" sort="Quinn, Niall" uniqKey="Quinn N" first="Niall" last="Quinn">Niall Quinn</name>
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<inist:fA14 i1="03">
<s1>University College London, Institute of Neurology, Queen Square</s1>
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<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
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<author>
<name sortKey="Pellecchia, Maria T" sort="Pellecchia, Maria T" uniqKey="Pellecchia M" first="Maria T." last="Pellecchia">Maria T. Pellecchia</name>
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<inist:fA14 i1="04">
<s1>Department of Neurological Sciences, University Federico II</s1>
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<sZ>9 aut.</sZ>
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</inist:fA14>
</affiliation>
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<author>
<name sortKey="Barone, Paolo" sort="Barone, Paolo" uniqKey="Barone P" first="Paolo" last="Barone">Paolo Barone</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Department of Neurological Sciences, University Federico II</s1>
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<s3>ITA</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Del Sorbo, Francesca" sort="Del Sorbo, Francesca" uniqKey="Del Sorbo F" first="Francesca" last="Del Sorbo">Francesca Del Sorbo</name>
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<inist:fA14 i1="05">
<s1>Istituto Nazionale Neurologico Carlo Besta, Università Cattolica del Sacro Cuore</s1>
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<s3>ITA</s3>
<sZ>11 aut.</sZ>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Albanese, Alberto" sort="Albanese, Alberto" uniqKey="Albanese A" first="Alberto" last="Albanese">Alberto Albanese</name>
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<inist:fA14 i1="05">
<s1>Istituto Nazionale Neurologico Carlo Besta, Università Cattolica del Sacro Cuore</s1>
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<s3>ITA</s3>
<sZ>11 aut.</sZ>
<sZ>12 aut.</sZ>
</inist:fA14>
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<author>
<name sortKey="Ostergaard, Karen" sort="Ostergaard, Karen" uniqKey="Ostergaard K" first="Karen" last="Ostergaard">Karen Ostergaard</name>
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<inist:fA14 i1="06">
<s1>Aarhus University Hospital, Department of Neurology</s1>
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</author>
<author>
<name sortKey="Dupont, Erik" sort="Dupont, Erik" uniqKey="Dupont E" first="Erik" last="Dupont">Erik Dupont</name>
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<inist:fA14 i1="06">
<s1>Aarhus University Hospital, Department of Neurology</s1>
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<sZ>13 aut.</sZ>
<sZ>14 aut.</sZ>
</inist:fA14>
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</author>
<author>
<name sortKey="Cardozo, Adriana" sort="Cardozo, Adriana" uniqKey="Cardozo A" first="Adriana" last="Cardozo">Adriana Cardozo</name>
<affiliation>
<inist:fA14 i1="07">
<s1>Universitat de Barcelona, Hospital Clinic, Department of Neurology</s1>
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<sZ>15 aut.</sZ>
<sZ>16 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Tolosa, Eduardo" sort="Tolosa, Eduardo" uniqKey="Tolosa E" first="Eduardo" last="Tolosa">Eduardo Tolosa</name>
<affiliation>
<inist:fA14 i1="07">
<s1>Universitat de Barcelona, Hospital Clinic, Department of Neurology</s1>
<s3>ESP</s3>
<sZ>15 aut.</sZ>
<sZ>16 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Nilsson, Christer F" sort="Nilsson, Christer F" uniqKey="Nilsson C" first="Christer F." last="Nilsson">Christer F. Nilsson</name>
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<inist:fA14 i1="08">
<s1>Department of Clinical Neuroscience, Division of Neurology, University of Lund</s1>
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<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
<sZ>19 aut.</sZ>
</inist:fA14>
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</author>
<author>
<name sortKey="Widner, Hakan" sort="Widner, Hakan" uniqKey="Widner H" first="Hakan" last="Widner">Hakan Widner</name>
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<inist:fA14 i1="08">
<s1>Department of Clinical Neuroscience, Division of Neurology, University of Lund</s1>
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<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
<sZ>19 aut.</sZ>
</inist:fA14>
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</author>
<author>
<name sortKey="Lindvall, Olle" sort="Lindvall, Olle" uniqKey="Lindvall O" first="Olle" last="Lindvall">Olle Lindvall</name>
<affiliation>
<inist:fA14 i1="08">
<s1>Department of Clinical Neuroscience, Division of Neurology, University of Lund</s1>
<s3>SWE</s3>
<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Giladi, Nir" sort="Giladi, Nir" uniqKey="Giladi N" first="Nir" last="Giladi">Nir Giladi</name>
<affiliation>
<inist:fA14 i1="09">
<s1>Tel Aviv Sourasky Medical Center, Movement Disorders Unit, Department of Neurology</s1>
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<sZ>20 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Gurevich, Tanya" sort="Gurevich, Tanya" uniqKey="Gurevich T" first="Tanya" last="Gurevich">Tanya Gurevich</name>
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<inist:fA14 i1="09">
<s1>Tel Aviv Sourasky Medical Center, Movement Disorders Unit, Department of Neurology</s1>
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<sZ>20 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Daniels, Christine" sort="Daniels, Christine" uniqKey="Daniels C" first="Christine" last="Daniels">Christine Daniels</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Department of Neurology, Christian-Albrechts University of Kiel</s1>
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<s3>DEU</s3>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Deuschl, Gunther" sort="Deuschl, Gunther" uniqKey="Deuschl G" first="Günther" last="Deuschl">Günther Deuschl</name>
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<inist:fA14 i1="10">
<s1>Department of Neurology, Christian-Albrechts University of Kiel</s1>
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<s3>DEU</s3>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
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<author>
<name sortKey="Coelho, Miguel" sort="Coelho, Miguel" uniqKey="Coelho M" first="Miguel" last="Coelho">Miguel Coelho</name>
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<inist:fA14 i1="11">
<s1>Faculdade de Medicina de Lisboa, Hopital Santa Maria, Centro de Neurosciencias de Lisboa</s1>
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<sZ>24 aut.</sZ>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Sampaio, Cristina" sort="Sampaio, Cristina" uniqKey="Sampaio C" first="Cristina" last="Sampaio">Cristina Sampaio</name>
<affiliation>
<inist:fA14 i1="11">
<s1>Faculdade de Medicina de Lisboa, Hopital Santa Maria, Centro de Neurosciencias de Lisboa</s1>
<s3>PRT</s3>
<sZ>24 aut.</sZ>
<sZ>25 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Abele, Michael" sort="Abele, Michael" uniqKey="Abele M" first="Michael" last="Abele">Michael Abele</name>
<affiliation>
<inist:fA14 i1="12">
<s1>University of Bonn, Department of Neurology</s1>
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<sZ>26 aut.</sZ>
<sZ>27 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Klockgether, Thomas" sort="Klockgether, Thomas" uniqKey="Klockgether T" first="Thomas" last="Klockgether">Thomas Klockgether</name>
<affiliation>
<inist:fA14 i1="12">
<s1>University of Bonn, Department of Neurology</s1>
<s3>DEU</s3>
<sZ>26 aut.</sZ>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Schimke, Nicole" sort="Schimke, Nicole" uniqKey="Schimke N" first="Nicole" last="Schimke">Nicole Schimke</name>
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<inist:fA14 i1="13">
<s1>Philipps-University Marburg, Department of Neurology</s1>
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<sZ>28 aut.</sZ>
<sZ>29 aut.</sZ>
<sZ>30 aut.</sZ>
</inist:fA14>
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<div type="abstract" xml:lang="en">Although multiple system atrophy (MSA) is a neurodegenerative disorder leading to progressive disability and decreased life expectancy, little is known about patients' own evaluation of their illness and factors associated with poor health-related quality of life (Hr-QoL). We, therefore, assessed Hr-QoL and its determinants in MSA. The following scales were applied to 115 patients in the European MSA-Study Group (EMSA-SG) Natural History Study: Medical Outcome Study Short Form (SF-36), EQ-5D, Beck Depression Inventory (BDI), Mini-Mental state examination (MMSE), Unified MSA Rating Scale (UMSARS), Hoehn & Yahr (H&Y) Parkinson's disease staging scale, Composite Autonomic Symptom Scale (COMPASS), and Parkinson's Disease Sleep Scale (PDSS). Forty-six percent of patients had moderate to severe depression (BDI ≥ 17); Hr-QoL scores on the SF-36 and EQ-5D were significantly impaired. Pain, the only domain with similar scores in MSA and published PD patients, was reported more frequently in patients with MSA-P (predominantly parkinsonian motor subtype) than MSA-C (predominantly cerebellar motor subtype; 76% vs. 50%; P = 0.005). Hr-QoL scores correlated most strongly with UMSARS motor, COMPASS, and BDI scores but not with MMSE scores, age at onset, or disease duration. The COMPASS and UMSARS activities of daily living scores were moderate-to-strong predictors for the SF-36 physical summary score and the BDI and UMSARS motor scores for the SF-36 mental summary score. This report is the first study to show that Hr-QoL is significantly impaired in MSA. Although not all possible factors related to impaired Hr-QoL in MSA could be assessed, autonomic dysfunction, motor impairment, and depression were most closely associated with poor Hr-QoL, and therapeutic management, therefore, should concentrate upon these aspects of the disease.</div>
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<AU>SCHRAG (Anette); GESER (Felix); STAMPFER-KOUNTCHEV (Michaela); SEPPI (Klaus); SAWIRES (Martin); KÖLLENSPERGER (Martin); SCHERFLER (Christoph); QUINN (Niall); PELLECCHIA (Maria T.); BARONE (Paolo); DEL SORBO (Francesca); ALBANESE (Alberto); OSTERGAARD (Karen); DUPONT (Erik); CARDOZO (Adriana); TOLOSA (Eduardo); NILSSON (Christer F.); WIDNER (Hakan); LINDVALL (Olle); GILADI (Nir); GUREVICH (Tanya); DANIELS (Christine); DEUSCHL (Günther); COELHO (Miguel); SAMPAIO (Cristina); ABELE (Michael); KLOCKGETHER (Thomas); SCHIMKE (Nicole); EGGERT (Karla M.); OERTEL (Wolfgang); DJALDETTI (Ruth); COLOSIMO (Carlo); MECO (Giuseppe); POEWE (Werner); WENNING (Gregor K.)</AU>
<AF>Department of Clinical Neurosciences, Royal Free & University College Medical School/London/Royaume-Uni (1 aut.); Clinical Department of Neurology, Innsbruck Medical University/Autriche (2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 34 aut., 35 aut.); University College London, Institute of Neurology, Queen Square/London/Royaume-Uni (8 aut.); Department of Neurological Sciences, University Federico II/Naples/Italie (9 aut., 10 aut.); Istituto Nazionale Neurologico Carlo Besta, Università Cattolica del Sacro Cuore/Milano/Italie (11 aut., 12 aut.); Aarhus University Hospital, Department of Neurology/Aarhus/Danemark (13 aut., 14 aut.); Universitat de Barcelona, Hospital Clinic, Department of Neurology/Espagne (15 aut., 16 aut.); Department of Clinical Neuroscience, Division of Neurology, University of Lund/Suède (17 aut., 18 aut., 19 aut.); Tel Aviv Sourasky Medical Center, Movement Disorders Unit, Department of Neurology/Israël (20 aut., 21 aut.); Department of Neurology, Christian-Albrechts University of Kiel/Kiel/Allemagne (22 aut., 23 aut.); Faculdade de Medicina de Lisboa, Hopital Santa Maria, Centro de Neurosciencias de Lisboa/Portugal (24 aut., 25 aut.); University of Bonn, Department of Neurology/Allemagne (26 aut., 27 aut.); Philipps-University Marburg, Department of Neurology/Allemagne (28 aut., 29 aut., 30 aut.); Department of Neurology, Rabin Medical Center/Petach-Tiqva/Israël (31 aut.); University of Roma, "La Sapienza, " Department of Neuroscience/Italie (32 aut., 33 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 6; Pp. 809-815; Bibl. 24 ref.</SO>
<LA>Anglais</LA>
<EA>Although multiple system atrophy (MSA) is a neurodegenerative disorder leading to progressive disability and decreased life expectancy, little is known about patients' own evaluation of their illness and factors associated with poor health-related quality of life (Hr-QoL). We, therefore, assessed Hr-QoL and its determinants in MSA. The following scales were applied to 115 patients in the European MSA-Study Group (EMSA-SG) Natural History Study: Medical Outcome Study Short Form (SF-36), EQ-5D, Beck Depression Inventory (BDI), Mini-Mental state examination (MMSE), Unified MSA Rating Scale (UMSARS), Hoehn & Yahr (H&Y) Parkinson's disease staging scale, Composite Autonomic Symptom Scale (COMPASS), and Parkinson's Disease Sleep Scale (PDSS). Forty-six percent of patients had moderate to severe depression (BDI ≥ 17); Hr-QoL scores on the SF-36 and EQ-5D were significantly impaired. Pain, the only domain with similar scores in MSA and published PD patients, was reported more frequently in patients with MSA-P (predominantly parkinsonian motor subtype) than MSA-C (predominantly cerebellar motor subtype; 76% vs. 50%; P = 0.005). Hr-QoL scores correlated most strongly with UMSARS motor, COMPASS, and BDI scores but not with MMSE scores, age at onset, or disease duration. The COMPASS and UMSARS activities of daily living scores were moderate-to-strong predictors for the SF-36 physical summary score and the BDI and UMSARS motor scores for the SF-36 mental summary score. This report is the first study to show that Hr-QoL is significantly impaired in MSA. Although not all possible factors related to impaired Hr-QoL in MSA could be assessed, autonomic dysfunction, motor impairment, and depression were most closely associated with poor Hr-QoL, and therapeutic management, therefore, should concentrate upon these aspects of the disease.</EA>
<CC>002B17; 002B17F; 002B17G</CC>
<FD>Système nerveux pathologie; Atrophie multisystématisée; Etat dépressif; Qualité vie; Trouble fonctionnel</FD>
<FG>Trouble humeur</FG>
<ED>Nervous system diseases; Multiple system atrophy; Depression; Quality of life; Dysfunction</ED>
<EG>Mood disorder</EG>
<SD>Sistema nervioso patología; Atrofia multisistematizada; Estado depresivo; Calidad vida; Trastorno funcional</SD>
<LO>INIST-20953.354000138863880120</LO>
<ID>06-0352376</ID>
</server>
</inist>
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