La maladie de Parkinson en France (serveur d'exploration)

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Parkinson's disease and sleepiness: An integral part of PD

Identifieur interne : 001116 ( PascalFrancis/Corpus ); précédent : 001115; suivant : 001117

Parkinson's disease and sleepiness: An integral part of PD

Auteurs : I. Arnulf ; E. Konofal ; M. Merino-Andreu ; J. L. Houeto ; V. Mesnage ; M. L. Welter ; L. Lacomblez ; J. L. Golmard ; J. P. Derenne ; Y. Agid

Source :

RBID : Pascal:02-0298578

Descripteurs français

English descriptors

Abstract

Objective: To investigate the potential causes of excessive daytime sleepiness in patients with PD-poor sleep quality, abnormal sleep-wakefulness control, and treatment with dopaminergic agents. Methods: The authors performed night-time polysomnography and daytime multiple sleep latency tests in 54 consecutive levodopa-treated patients with PD referred for sleepiness, 27 of whom were also receiving dopaminergic agonists. Results: Sleep latency was 6.3 ± 0.6 minutes (normal >8 minutes), and the Epworth Sleepiness score was 14.3 ± 4.1 (normal <10). A narcolepsy-like phenotype (≥2 sleep-onset REM periods) was found in 39% of the patients, who were sleepier (4.6 ± 0.9 minutes) than the other 61% of patients (7.4 ± 0.7 minutes). Periodic leg movement syndromes were rare (15%, range 16 to 43/h), but obstructive sleep apnea-hypopnea syndromes were frequent (20% of patients had an apnea-hypopnea index >15/h; range 15.1 to 50.0). Severity of sleepiness was weakly correlated with Epworth Sleepiness score (r = -0.34) and daily dose of levodopa (r = 0.30) but not with dopamine-agonist treatment, age, disease duration, parkinsonian motor disability, total sleep time, periodic leg movement, apnea-hypopnea, or arousal indices. Conclusions: In patients with PD preselected for sleepiness, severity of sleepiness was not dependent on nocturnal sleep abnormalities, motor and cognitive impairment, or antiparkinsonian treatment. The results suggest that sleepiness-sudden onset of sleep-does not result from pharmacotherapy but is related to the pathology of PD.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0028-3878
A02 01      @0 NEURAI
A03   1    @0 Neurology
A05       @2 58
A06       @2 7
A08 01  1  ENG  @1 Parkinson's disease and sleepiness: An integral part of PD
A11 01  1    @1 ARNULF (I.)
A11 02  1    @1 KONOFAL (E.)
A11 03  1    @1 MERINO-ANDREU (M.)
A11 04  1    @1 HOUETO (J. L.)
A11 05  1    @1 MESNAGE (V.)
A11 06  1    @1 WELTER (M. L.)
A11 07  1    @1 LACOMBLEZ (L.)
A11 08  1    @1 GOLMARD (J. L.)
A11 09  1    @1 DERENNE (J. P.)
A11 10  1    @1 AGID (Y.)
A14 01      @1 Fédération des Pathologies du Sommeil, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris @3 FRA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 9 aut.
A14 02      @1 Centre d'Investigation Clinique, Fédération de Neurologie and Inserm U289, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris @3 FRA @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 10 aut.
A14 03      @1 Service de Neuropharmacologie, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris @3 FRA @Z 7 aut.
A14 04      @1 Service d'Informatique Médicale, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris @3 FRA @Z 8 aut.
A20       @1 1019-1024
A21       @1 2002
A23 01      @0 ENG
A43 01      @1 INIST @2 6345 @5 354000107955740060
A44       @0 0000 @1 © 2002 INIST-CNRS. All rights reserved.
A45       @0 27 ref.
A47 01  1    @0 02-0298578
A60       @1 P
A61       @0 A
A64 01  1    @0 Neurology
A66 01      @0 USA
C01 01    ENG  @0 Objective: To investigate the potential causes of excessive daytime sleepiness in patients with PD-poor sleep quality, abnormal sleep-wakefulness control, and treatment with dopaminergic agents. Methods: The authors performed night-time polysomnography and daytime multiple sleep latency tests in 54 consecutive levodopa-treated patients with PD referred for sleepiness, 27 of whom were also receiving dopaminergic agonists. Results: Sleep latency was 6.3 ± 0.6 minutes (normal >8 minutes), and the Epworth Sleepiness score was 14.3 ± 4.1 (normal <10). A narcolepsy-like phenotype (≥2 sleep-onset REM periods) was found in 39% of the patients, who were sleepier (4.6 ± 0.9 minutes) than the other 61% of patients (7.4 ± 0.7 minutes). Periodic leg movement syndromes were rare (15%, range 16 to 43/h), but obstructive sleep apnea-hypopnea syndromes were frequent (20% of patients had an apnea-hypopnea index >15/h; range 15.1 to 50.0). Severity of sleepiness was weakly correlated with Epworth Sleepiness score (r = -0.34) and daily dose of levodopa (r = 0.30) but not with dopamine-agonist treatment, age, disease duration, parkinsonian motor disability, total sleep time, periodic leg movement, apnea-hypopnea, or arousal indices. Conclusions: In patients with PD preselected for sleepiness, severity of sleepiness was not dependent on nocturnal sleep abnormalities, motor and cognitive impairment, or antiparkinsonian treatment. The results suggest that sleepiness-sudden onset of sleep-does not result from pharmacotherapy but is related to the pathology of PD.
C02 01  X    @0 002B17G
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C03 01  X  ENG  @0 Parkinson disease @5 01
C03 01  X  SPA  @0 Parkinson enfermedad @5 01
C03 02  X  FRE  @0 Somnolence @5 04
C03 02  X  ENG  @0 Somnolence @5 04
C03 02  X  SPA  @0 Somnolencia @5 04
C03 03  X  FRE  @0 Trouble sommeil @5 07
C03 03  X  ENG  @0 Sleep disorder @5 07
C03 03  X  SPA  @0 Trastorno sueño @5 07
C03 04  X  FRE  @0 Etiologie @5 17
C03 04  X  ENG  @0 Etiology @5 17
C03 04  X  SPA  @0 Etiología @5 17
C03 05  X  FRE  @0 Homme @5 20
C03 05  X  ENG  @0 Human @5 20
C03 05  X  SPA  @0 Hombre @5 20
C07 01  X  FRE  @0 Système nerveux pathologie @5 37
C07 01  X  ENG  @0 Nervous system diseases @5 37
C07 01  X  SPA  @0 Sistema nervioso patología @5 37
C07 02  X  FRE  @0 Système nerveux central pathologie @5 38
C07 02  X  ENG  @0 Central nervous system disease @5 38
C07 02  X  SPA  @0 Sistema nervosio central patología @5 38
C07 03  X  FRE  @0 Encéphale pathologie @5 39
C07 03  X  ENG  @0 Cerebral disorder @5 39
C07 03  X  SPA  @0 Encéfalo patología @5 39
C07 04  X  FRE  @0 Extrapyramidal syndrome @5 40
C07 04  X  ENG  @0 Extrapyramidal syndrome @5 40
C07 04  X  SPA  @0 Extrapiramidal síndrome @5 40
C07 05  X  FRE  @0 Maladie dégénérative @5 41
C07 05  X  ENG  @0 Degenerative disease @5 41
C07 05  X  SPA  @0 Enfermedad degenerativa @5 41
C07 06  X  FRE  @0 Trouble neurologique @5 54
C07 06  X  ENG  @0 Neurological disorder @5 54
C07 06  X  SPA  @0 Trastorno neurológico @5 54
N21       @1 169
N82       @1 PSI

Format Inist (serveur)

NO : PASCAL 02-0298578 INIST
ET : Parkinson's disease and sleepiness: An integral part of PD
AU : ARNULF (I.); KONOFAL (E.); MERINO-ANDREU (M.); HOUETO (J. L.); MESNAGE (V.); WELTER (M. L.); LACOMBLEZ (L.); GOLMARD (J. L.); DERENNE (J. P.); AGID (Y.)
AF : Fédération des Pathologies du Sommeil, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris/France (1 aut., 2 aut., 3 aut., 9 aut.); Centre d'Investigation Clinique, Fédération de Neurologie and Inserm U289, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris/France (4 aut., 5 aut., 6 aut., 10 aut.); Service de Neuropharmacologie, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris/France (7 aut.); Service d'Informatique Médicale, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris/France (8 aut.)
DT : Publication en série; Niveau analytique
SO : Neurology; ISSN 0028-3878; Coden NEURAI; Etats-Unis; Da. 2002; Vol. 58; No. 7; Pp. 1019-1024; Bibl. 27 ref.
LA : Anglais
EA : Objective: To investigate the potential causes of excessive daytime sleepiness in patients with PD-poor sleep quality, abnormal sleep-wakefulness control, and treatment with dopaminergic agents. Methods: The authors performed night-time polysomnography and daytime multiple sleep latency tests in 54 consecutive levodopa-treated patients with PD referred for sleepiness, 27 of whom were also receiving dopaminergic agonists. Results: Sleep latency was 6.3 ± 0.6 minutes (normal >8 minutes), and the Epworth Sleepiness score was 14.3 ± 4.1 (normal <10). A narcolepsy-like phenotype (≥2 sleep-onset REM periods) was found in 39% of the patients, who were sleepier (4.6 ± 0.9 minutes) than the other 61% of patients (7.4 ± 0.7 minutes). Periodic leg movement syndromes were rare (15%, range 16 to 43/h), but obstructive sleep apnea-hypopnea syndromes were frequent (20% of patients had an apnea-hypopnea index >15/h; range 15.1 to 50.0). Severity of sleepiness was weakly correlated with Epworth Sleepiness score (r = -0.34) and daily dose of levodopa (r = 0.30) but not with dopamine-agonist treatment, age, disease duration, parkinsonian motor disability, total sleep time, periodic leg movement, apnea-hypopnea, or arousal indices. Conclusions: In patients with PD preselected for sleepiness, severity of sleepiness was not dependent on nocturnal sleep abnormalities, motor and cognitive impairment, or antiparkinsonian treatment. The results suggest that sleepiness-sudden onset of sleep-does not result from pharmacotherapy but is related to the pathology of PD.
CC : 002B17G
FD : Parkinson maladie; Somnolence; Trouble sommeil; Etiologie; Homme
FG : Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Trouble neurologique
ED : Parkinson disease; Somnolence; Sleep disorder; Etiology; Human
EG : Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Neurological disorder
SD : Parkinson enfermedad; Somnolencia; Trastorno sueño; Etiología; Hombre
LO : INIST-6345.354000107955740060
ID : 02-0298578

Links to Exploration step

Pascal:02-0298578

Le document en format XML

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<div type="abstract" xml:lang="en">Objective: To investigate the potential causes of excessive daytime sleepiness in patients with PD-poor sleep quality, abnormal sleep-wakefulness control, and treatment with dopaminergic agents. Methods: The authors performed night-time polysomnography and daytime multiple sleep latency tests in 54 consecutive levodopa-treated patients with PD referred for sleepiness, 27 of whom were also receiving dopaminergic agonists. Results: Sleep latency was 6.3 ± 0.6 minutes (normal >8 minutes), and the Epworth Sleepiness score was 14.3 ± 4.1 (normal <10). A narcolepsy-like phenotype (≥2 sleep-onset REM periods) was found in 39% of the patients, who were sleepier (4.6 ± 0.9 minutes) than the other 61% of patients (7.4 ± 0.7 minutes). Periodic leg movement syndromes were rare (15%, range 16 to 43/h), but obstructive sleep apnea-hypopnea syndromes were frequent (20% of patients had an apnea-hypopnea index >15/h; range 15.1 to 50.0). Severity of sleepiness was weakly correlated with Epworth Sleepiness score (r = -0.34) and daily dose of levodopa (r = 0.30) but not with dopamine-agonist treatment, age, disease duration, parkinsonian motor disability, total sleep time, periodic leg movement, apnea-hypopnea, or arousal indices. Conclusions: In patients with PD preselected for sleepiness, severity of sleepiness was not dependent on nocturnal sleep abnormalities, motor and cognitive impairment, or antiparkinsonian treatment. The results suggest that sleepiness-sudden onset of sleep-does not result from pharmacotherapy but is related to the pathology of PD.</div>
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