La maladie de Parkinson au Canada (serveur d'exploration)

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Family history of idiopathic REM behavior disorder: A multicenter case-control study

Identifieur interne : 000B43 ( PascalFrancis/Curation ); précédent : 000B42; suivant : 000B44

Family history of idiopathic REM behavior disorder: A multicenter case-control study

Auteurs : Yves Dauvilliers [France] ; Ronald B. Postuma [France, Canada] ; Luigi Ferini-Strambi [Italie] ; Isabelle Arnulf [France] ; Birgit Högl [Autriche] ; Raffaele Manni [Italie] ; Tomoyuki Miyamoto [Japon] ; Wolfgang Oertel [Allemagne] ; Maria Livia Fantini [Italie] ; Monica Puligheddu [Italie] ; Poul Jennum [Danemark] ; Karel Sonka [République tchèque] ; Marco Zucconi [Italie] ; Smeranda Leu-Semenescu [France] ; Birgit Frauscher [Autriche] ; Michele Terzaghi [Italie] ; Masayuki Miyamoto [Japon] ; Marcus Unger [Allemagne] ; Alex Desautels [France] ; Christina Wolfson [Canada] ; Amélie Pelletier [Canada] ; Jacques Montplaisir [France]

Source :

RBID : Pascal:13-0231441

Descripteurs français

English descriptors

Abstract

Objective: To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort. Methods: A total of 316 patients with polysomnography-confirmed iRBD were recruited from 12 RBD study group centers, along with 316 controls matched on sex and age group. All subjects completed a self-administered questionnaire that collected proxy-reported information on family history of tremor, gait trouble, balance trouble, Parkinson disease, memory loss, and Alzheimer disease. The questionnaire also included a single question that asked about possible symptoms of RBD among first-degree relatives (siblings, parents, and children). Results: A positive family history of dream enactment was reported in 13.8% of iRBD cases compared to 4.8% of controls (odds ratio [OR] = 3.9, 95% confidence interval [CI] 2.0-7.7). ORs were increased for both siblings (OR = 6.1, 95% CI 2.1-18.1) and parents (OR = 3.2, 95% CI 1.4-7.8). We found no significant difference in sex, current age (65.3 ± 10.2 vs 66.9 ± 10.2 years), or age at self-reported RBD onset (55.2 ± 11.7 vs 56.6 ± 15.1 years) in possible familial vs sporadic iRBD. No differences were found in family history of tremor, walking and balance troubles, Parkinson disease, memory loss, or Alzheimer disease. Conclusion: We found increased odds of proxy-reported family history of presumed RBD among individuals with confirmed iRBD. This suggests the possibility of a genetic contribution to RBD.
pA  
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A03   1    @0 Neurology
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A06       @2 24
A08 01  1  ENG  @1 Family history of idiopathic REM behavior disorder: A multicenter case-control study
A11 01  1    @1 DAUVILLIERS (Yves)
A11 02  1    @1 POSTUMA (Ronald B.)
A11 03  1    @1 FERINI-STRAMBI (Luigi)
A11 04  1    @1 ARNULF (Isabelle)
A11 05  1    @1 HÖGL (Birgit)
A11 06  1    @1 MANNI (Raffaele)
A11 07  1    @1 MIYAMOTO (Tomoyuki)
A11 08  1    @1 OERTEL (Wolfgang)
A11 09  1    @1 LIVIA FANTINI (Maria)
A11 10  1    @1 PULIGHEDDU (Monica)
A11 11  1    @1 JENNUM (Poul)
A11 12  1    @1 SONKA (Karel)
A11 13  1    @1 ZUCCONI (Marco)
A11 14  1    @1 LEU-SEMENESCU (Smeranda)
A11 15  1    @1 FRAUSCHER (Birgit)
A11 16  1    @1 TERZAGHI (Michele)
A11 17  1    @1 MIYAMOTO (Masayuki)
A11 18  1    @1 UNGER (Marcus)
A11 19  1    @1 DESAUTELS (Alex)
A11 20  1    @1 WOLFSON (Christina)
A11 21  1    @1 PELLETIER (Amélie)
A11 22  1    @1 MONTPLAISIR (Jacques)
A14 01      @1 Department of Neurology, Hôpital Gui de Chauliac, Montpellier, INSERM U1061 @2 Montpellier @3 FRA @Z 1 aut.
A14 02      @1 Centre d'Études Avancées en Médecine du Sommeil, Hôpiral du Sacré-Cœur de Montréal @2 Montréal @3 FRA @Z 2 aut. @Z 19 aut. @Z 22 aut.
A14 03      @1 Department of Neurology, McGill University, Montreal General Hospital @2 Montreal @3 CAN @Z 2 aut.
A14 04      @1 Sleep Disorders Center, Università Vita-Salute San Raffaele @2 Milan @3 ITA @Z 3 aut. @Z 13 aut.
A14 05      @1 Unité des Pathologies du Sommeil, Hôpiral Pitié-Salpêtrière, APHP, and Inserm U975-CRICM-Pierre and Marie Curie University @2 Paris @3 FRA @Z 4 aut. @Z 14 aut.
A14 06      @1 Department of Neurology, Innsbruck Medical University @2 Innsbruck @3 AUT @Z 5 aut. @Z 15 aut.
A14 07      @1 Unit of Sleep Medicine, National Institute of Neurology IRCCS, C. Mondino, Foundation @2 Pavia @3 ITA @Z 6 aut. @Z 16 aut.
A14 08      @1 Department of Neurology, Dokkyo Medical University Koshigaya Hospital @2 Saitama @3 JPN @Z 7 aut. @Z 17 aut.
A14 09      @1 Department of Neurology, Philipps-Universität @2 Marburg @3 DEU @Z 8 aut. @Z 18 aut.
A14 10      @1 Sleep Disorders Center, Department of Neurosciences, University of Turin @2 Turin @3 ITA @Z 9 aut.
A14 11      @1 Sleep Center, Department of Cardiovascular and Neurological Sciences, University of Cagliari @3 ITA @Z 10 aut.
A14 12      @1 Danish Center for Sleep Medicine, University of Copenhagen @3 DNK @Z 11 aut.
A14 13      @1 Department of Neurology First Faculty of Medicine, Charles University and General University Hospital @2 Prague @3 CZE @Z 12 aut.
A14 14      @1 Department of Neurology, Saarland University @2 Homburg/Saar @3 DEU @Z 18 aut.
A14 15      @1 Research Institute of the McGill University Health Center @2 Montreal @3 CAN @Z 20 aut. @Z 21 aut.
A20       @1 2233-2235
A21       @1 2013
A23 01      @0 ENG
A43 01      @1 INIST @2 6345 @5 354000503092290120
A44       @0 0000 @1 © 2013 INIST-CNRS. All rights reserved.
A45       @0 8 ref.
A47 01  1    @0 13-0231441
A60       @1 P
A61       @0 A
A64 01  1    @0 Neurology
A66 01      @0 USA
C01 01    ENG  @0 Objective: To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort. Methods: A total of 316 patients with polysomnography-confirmed iRBD were recruited from 12 RBD study group centers, along with 316 controls matched on sex and age group. All subjects completed a self-administered questionnaire that collected proxy-reported information on family history of tremor, gait trouble, balance trouble, Parkinson disease, memory loss, and Alzheimer disease. The questionnaire also included a single question that asked about possible symptoms of RBD among first-degree relatives (siblings, parents, and children). Results: A positive family history of dream enactment was reported in 13.8% of iRBD cases compared to 4.8% of controls (odds ratio [OR] = 3.9, 95% confidence interval [CI] 2.0-7.7). ORs were increased for both siblings (OR = 6.1, 95% CI 2.1-18.1) and parents (OR = 3.2, 95% CI 1.4-7.8). We found no significant difference in sex, current age (65.3 ± 10.2 vs 66.9 ± 10.2 years), or age at self-reported RBD onset (55.2 ± 11.7 vs 56.6 ± 15.1 years) in possible familial vs sporadic iRBD. No differences were found in family history of tremor, walking and balance troubles, Parkinson disease, memory loss, or Alzheimer disease. Conclusion: We found increased odds of proxy-reported family history of presumed RBD among individuals with confirmed iRBD. This suggests the possibility of a genetic contribution to RBD.
C02 01  X    @0 002B17
C02 02  X    @0 002B17E
C03 01  X  FRE  @0 Pathologie du système nerveux @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 Idiopathique @5 09
C03 02  X  ENG  @0 Idiopathic @5 09
C03 02  X  SPA  @0 Idiopático @5 09
C03 03  X  FRE  @0 Comportement @5 10
C03 03  X  ENG  @0 Behavior @5 10
C03 03  X  SPA  @0 Conducta @5 10
C03 04  X  FRE  @0 Etude multicentrique @5 11
C03 04  X  ENG  @0 Multicenter study @5 11
C03 04  X  SPA  @0 Estudio multicéntrico @5 11
C03 05  X  FRE  @0 Etude cas témoin @5 12
C03 05  X  ENG  @0 Case control study @5 12
C03 05  X  SPA  @0 Estudio caso control @5 12
N21       @1 217
N44 01      @1 OTO
N82       @1 OTO

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Pascal:13-0231441

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<title xml:lang="en" level="a">Family history of idiopathic REM behavior disorder: A multicenter case-control study</title>
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<inist:fA14 i1="04">
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<author>
<name sortKey="Miyamoto, Tomoyuki" sort="Miyamoto, Tomoyuki" uniqKey="Miyamoto T" first="Tomoyuki" last="Miyamoto">Tomoyuki Miyamoto</name>
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<inist:fA14 i1="08">
<s1>Department of Neurology, Dokkyo Medical University Koshigaya Hospital</s1>
<s2>Saitama</s2>
<s3>JPN</s3>
<sZ>7 aut.</sZ>
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</inist:fA14>
<country>Japon</country>
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<name sortKey="Oertel, Wolfgang" sort="Oertel, Wolfgang" uniqKey="Oertel W" first="Wolfgang" last="Oertel">Wolfgang Oertel</name>
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<inist:fA14 i1="09">
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<country>Allemagne</country>
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<name sortKey="Livia Fantini, Maria" sort="Livia Fantini, Maria" uniqKey="Livia Fantini M" first="Maria" last="Livia Fantini">Maria Livia Fantini</name>
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<inist:fA14 i1="10">
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</inist:fA14>
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<inist:fA14 i1="11">
<s1>Sleep Center, Department of Cardiovascular and Neurological Sciences, University of Cagliari</s1>
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</inist:fA14>
<country>Italie</country>
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<name sortKey="Jennum, Poul" sort="Jennum, Poul" uniqKey="Jennum P" first="Poul" last="Jennum">Poul Jennum</name>
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<inist:fA14 i1="12">
<s1>Danish Center for Sleep Medicine, University of Copenhagen</s1>
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<sZ>11 aut.</sZ>
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<country>Danemark</country>
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<name sortKey="Sonka, Karel" sort="Sonka, Karel" uniqKey="Sonka K" first="Karel" last="Sonka">Karel Sonka</name>
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<inist:fA14 i1="13">
<s1>Department of Neurology First Faculty of Medicine, Charles University and General University Hospital</s1>
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<sZ>12 aut.</sZ>
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<country>République tchèque</country>
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<name sortKey="Zucconi, Marco" sort="Zucconi, Marco" uniqKey="Zucconi M" first="Marco" last="Zucconi">Marco Zucconi</name>
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<inist:fA14 i1="04">
<s1>Sleep Disorders Center, Università Vita-Salute San Raffaele</s1>
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<s3>ITA</s3>
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<country>Italie</country>
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<name sortKey="Leu Semenescu, Smeranda" sort="Leu Semenescu, Smeranda" uniqKey="Leu Semenescu S" first="Smeranda" last="Leu-Semenescu">Smeranda Leu-Semenescu</name>
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<inist:fA14 i1="05">
<s1>Unité des Pathologies du Sommeil, Hôpiral Pitié-Salpêtrière, APHP, and Inserm U975-CRICM-Pierre and Marie Curie University</s1>
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<s3>FRA</s3>
<sZ>4 aut.</sZ>
<sZ>14 aut.</sZ>
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<country>France</country>
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<name sortKey="Frauscher, Birgit" sort="Frauscher, Birgit" uniqKey="Frauscher B" first="Birgit" last="Frauscher">Birgit Frauscher</name>
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<inist:fA14 i1="06">
<s1>Department of Neurology, Innsbruck Medical University</s1>
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<s3>AUT</s3>
<sZ>5 aut.</sZ>
<sZ>15 aut.</sZ>
</inist:fA14>
<country>Autriche</country>
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<name sortKey="Terzaghi, Michele" sort="Terzaghi, Michele" uniqKey="Terzaghi M" first="Michele" last="Terzaghi">Michele Terzaghi</name>
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<inist:fA14 i1="07">
<s1>Unit of Sleep Medicine, National Institute of Neurology IRCCS, C. Mondino, Foundation</s1>
<s2>Pavia</s2>
<s3>ITA</s3>
<sZ>6 aut.</sZ>
<sZ>16 aut.</sZ>
</inist:fA14>
<country>Italie</country>
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<name sortKey="Miyamoto, Masayuki" sort="Miyamoto, Masayuki" uniqKey="Miyamoto M" first="Masayuki" last="Miyamoto">Masayuki Miyamoto</name>
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<inist:fA14 i1="08">
<s1>Department of Neurology, Dokkyo Medical University Koshigaya Hospital</s1>
<s2>Saitama</s2>
<s3>JPN</s3>
<sZ>7 aut.</sZ>
<sZ>17 aut.</sZ>
</inist:fA14>
<country>Japon</country>
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<name sortKey="Unger, Marcus" sort="Unger, Marcus" uniqKey="Unger M" first="Marcus" last="Unger">Marcus Unger</name>
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<inist:fA14 i1="09">
<s1>Department of Neurology, Philipps-Universität</s1>
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<sZ>8 aut.</sZ>
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</inist:fA14>
<country>Allemagne</country>
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<inist:fA14 i1="14">
<s1>Department of Neurology, Saarland University</s1>
<s2>Homburg/Saar</s2>
<s3>DEU</s3>
<sZ>18 aut.</sZ>
</inist:fA14>
<country>Allemagne</country>
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<name sortKey="Desautels, Alex" sort="Desautels, Alex" uniqKey="Desautels A" first="Alex" last="Desautels">Alex Desautels</name>
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<inist:fA14 i1="02">
<s1>Centre d'Études Avancées en Médecine du Sommeil, Hôpiral du Sacré-Cœur de Montréal</s1>
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<country>France</country>
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<name sortKey="Wolfson, Christina" sort="Wolfson, Christina" uniqKey="Wolfson C" first="Christina" last="Wolfson">Christina Wolfson</name>
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<inist:fA14 i1="15">
<s1>Research Institute of the McGill University Health Center</s1>
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<name sortKey="Pelletier, Amelie" sort="Pelletier, Amelie" uniqKey="Pelletier A" first="Amélie" last="Pelletier">Amélie Pelletier</name>
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<s1>Research Institute of the McGill University Health Center</s1>
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<name sortKey="Montplaisir, Jacques" sort="Montplaisir, Jacques" uniqKey="Montplaisir J" first="Jacques" last="Montplaisir">Jacques Montplaisir</name>
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<s1>Centre d'Études Avancées en Médecine du Sommeil, Hôpiral du Sacré-Cœur de Montréal</s1>
<s2>Montréal</s2>
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<series>
<title level="j" type="main">Neurology</title>
<title level="j" type="abbreviated">Neurology</title>
<idno type="ISSN">0028-3878</idno>
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<date when="2013">2013</date>
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<title level="j" type="main">Neurology</title>
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<term>Behavior</term>
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<term>Nervous system diseases</term>
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<term>Pathologie du système nerveux</term>
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<div type="abstract" xml:lang="en">Objective: To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort. Methods: A total of 316 patients with polysomnography-confirmed iRBD were recruited from 12 RBD study group centers, along with 316 controls matched on sex and age group. All subjects completed a self-administered questionnaire that collected proxy-reported information on family history of tremor, gait trouble, balance trouble, Parkinson disease, memory loss, and Alzheimer disease. The questionnaire also included a single question that asked about possible symptoms of RBD among first-degree relatives (siblings, parents, and children). Results: A positive family history of dream enactment was reported in 13.8% of iRBD cases compared to 4.8% of controls (odds ratio [OR] = 3.9, 95% confidence interval [CI] 2.0-7.7). ORs were increased for both siblings (OR = 6.1, 95% CI 2.1-18.1) and parents (OR = 3.2, 95% CI 1.4-7.8). We found no significant difference in sex, current age (65.3 ± 10.2 vs 66.9 ± 10.2 years), or age at self-reported RBD onset (55.2 ± 11.7 vs 56.6 ± 15.1 years) in possible familial vs sporadic iRBD. No differences were found in family history of tremor, walking and balance troubles, Parkinson disease, memory loss, or Alzheimer disease. Conclusion: We found increased odds of proxy-reported family history of presumed RBD among individuals with confirmed iRBD. This suggests the possibility of a genetic contribution to RBD.</div>
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<s1>Research Institute of the McGill University Health Center</s1>
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<s0>Objective: To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort. Methods: A total of 316 patients with polysomnography-confirmed iRBD were recruited from 12 RBD study group centers, along with 316 controls matched on sex and age group. All subjects completed a self-administered questionnaire that collected proxy-reported information on family history of tremor, gait trouble, balance trouble, Parkinson disease, memory loss, and Alzheimer disease. The questionnaire also included a single question that asked about possible symptoms of RBD among first-degree relatives (siblings, parents, and children). Results: A positive family history of dream enactment was reported in 13.8% of iRBD cases compared to 4.8% of controls (odds ratio [OR] = 3.9, 95% confidence interval [CI] 2.0-7.7). ORs were increased for both siblings (OR = 6.1, 95% CI 2.1-18.1) and parents (OR = 3.2, 95% CI 1.4-7.8). We found no significant difference in sex, current age (65.3 ± 10.2 vs 66.9 ± 10.2 years), or age at self-reported RBD onset (55.2 ± 11.7 vs 56.6 ± 15.1 years) in possible familial vs sporadic iRBD. No differences were found in family history of tremor, walking and balance troubles, Parkinson disease, memory loss, or Alzheimer disease. Conclusion: We found increased odds of proxy-reported family history of presumed RBD among individuals with confirmed iRBD. This suggests the possibility of a genetic contribution to RBD.</s0>
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<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Idiopathique</s0>
<s5>09</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Idiopathic</s0>
<s5>09</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Idiopático</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Comportement</s0>
<s5>10</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Behavior</s0>
<s5>10</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Conducta</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Etude multicentrique</s0>
<s5>11</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Multicenter study</s0>
<s5>11</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Estudio multicéntrico</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Etude cas témoin</s0>
<s5>12</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Case control study</s0>
<s5>12</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Estudio caso control</s0>
<s5>12</s5>
</fC03>
<fN21>
<s1>217</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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