Movement Disorders (revue)

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REM Sleep Behavior Disorder: Motor Manifestations and Pathophysiology

Identifieur interne : 002B22 ( PascalFrancis/Curation ); précédent : 002B21; suivant : 002B23

REM Sleep Behavior Disorder: Motor Manifestations and Pathophysiology

Auteurs : Isabelle Arnulf [France]

Source :

RBID : Pascal:12-0248747

Descripteurs français

English descriptors

Abstract

Patients with REM sleep behavior disorder (RBD) enact violent dreams during REM sleep in the absence of normal muscle atonia. This disorder is highly frequent in patients with synucleinopathies (60%-100% of patients) and rare in patients with other neurodegenerative disorders. The disorder is detected by interview plus video and sleep monitoring. Abnormal movements expose the patients and bed partners to a high risk of injury and sleep disruption. The disorder is usually alleviated with melatonin and clonazepam. Limb movements are mainly minor, jerky, fast, pseudohallucinatory, and repeated, with a limp wrist during apparently grasping movements, although body jerks and complex violent (fights) and nonviolent culturally acquired behaviors are also observed. Notably, parkinsonism disappears during RBD-associated complex behaviors in patients with Parkinson's disease and with multiple system atrophy, suggesting that the upper motor stream bypasses the basal ganglia during REM sleep. Longitudinal studies show that idiopathic RBD predisposes patients to later develop Parkinson's disease, dementia with Lewy bodies, and, more rarely, multiple system atrophy, with a rate of conversion of 46% within 5 years. During this time window, patients concomitantly develop nonmotor signs (decreased olfaction and color vision, orthostatic hypotension, altered visuospatial abilities, increased harm avoidance) and have abnormal test results (decreased putamen dopamine uptake, slower EEG). Patients with idiopathic RBD have higher and faster risk for conversion to Parkinson's disease and dementia with Lewy bodies if abnormalities in dopamine transporter imaging, transcranial sonography, olfaction, and color vision are found at baseline. They constitute a highly specific target for testing neuroprotective agents.
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C01 01    ENG  @0 Patients with REM sleep behavior disorder (RBD) enact violent dreams during REM sleep in the absence of normal muscle atonia. This disorder is highly frequent in patients with synucleinopathies (60%-100% of patients) and rare in patients with other neurodegenerative disorders. The disorder is detected by interview plus video and sleep monitoring. Abnormal movements expose the patients and bed partners to a high risk of injury and sleep disruption. The disorder is usually alleviated with melatonin and clonazepam. Limb movements are mainly minor, jerky, fast, pseudohallucinatory, and repeated, with a limp wrist during apparently grasping movements, although body jerks and complex violent (fights) and nonviolent culturally acquired behaviors are also observed. Notably, parkinsonism disappears during RBD-associated complex behaviors in patients with Parkinson's disease and with multiple system atrophy, suggesting that the upper motor stream bypasses the basal ganglia during REM sleep. Longitudinal studies show that idiopathic RBD predisposes patients to later develop Parkinson's disease, dementia with Lewy bodies, and, more rarely, multiple system atrophy, with a rate of conversion of 46% within 5 years. During this time window, patients concomitantly develop nonmotor signs (decreased olfaction and color vision, orthostatic hypotension, altered visuospatial abilities, increased harm avoidance) and have abnormal test results (decreased putamen dopamine uptake, slower EEG). Patients with idiopathic RBD have higher and faster risk for conversion to Parkinson's disease and dementia with Lewy bodies if abnormalities in dopamine transporter imaging, transcranial sonography, olfaction, and color vision are found at baseline. They constitute a highly specific target for testing neuroprotective agents.
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C03 01  X  FRE  @0 Trouble du sommeil @5 01
C03 01  X  ENG  @0 Sleep disorder @5 01
C03 01  X  SPA  @0 Trastorno sueño @5 01
C03 02  X  FRE  @0 Trouble moteur @5 02
C03 02  X  ENG  @0 Motor system disorder @5 02
C03 02  X  SPA  @0 Trastorno motor @5 02
C03 03  X  FRE  @0 Maladie de Parkinson @2 NM @5 03
C03 03  X  ENG  @0 Parkinson disease @2 NM @5 03
C03 03  X  SPA  @0 Parkinson enfermedad @2 NM @5 03
C03 04  X  FRE  @0 Pathologie du système nerveux @5 04
C03 04  X  ENG  @0 Nervous system diseases @5 04
C03 04  X  SPA  @0 Sistema nervioso patología @5 04
C03 05  X  FRE  @0 Sommeil paradoxal @5 09
C03 05  X  ENG  @0 Rapid eye movement sleep @5 09
C03 05  X  SPA  @0 Sueño paradojal @5 09
C03 06  X  FRE  @0 Comportement @5 10
C03 06  X  ENG  @0 Behavior @5 10
C03 06  X  SPA  @0 Conducta @5 10
C03 07  X  FRE  @0 Physiopathologie @5 11
C03 07  X  ENG  @0 Pathophysiology @5 11
C03 07  X  SPA  @0 Fisiopatología @5 11
C07 01  X  FRE  @0 Cycle veille sommeil @5 37
C07 01  X  ENG  @0 Sleep wake cycle @5 37
C07 01  X  SPA  @0 Ciclo sueño vigilia @5 37
C07 02  X  FRE  @0 Trouble neurologique @5 39
C07 02  X  ENG  @0 Neurological disorder @5 39
C07 02  X  SPA  @0 Trastorno neurológico @5 39
C07 03  X  FRE  @0 Pathologie de l'encéphale @5 40
C07 03  X  ENG  @0 Cerebral disorder @5 40
C07 03  X  SPA  @0 Encéfalo patología @5 40
C07 04  X  FRE  @0 Syndrome extrapyramidal @5 41
C07 04  X  ENG  @0 Extrapyramidal syndrome @5 41
C07 04  X  SPA  @0 Extrapiramidal síndrome @5 41
C07 05  X  FRE  @0 Maladie dégénérative @5 42
C07 05  X  ENG  @0 Degenerative disease @5 42
C07 05  X  SPA  @0 Enfermedad degenerativa @5 42
C07 06  X  FRE  @0 Pathologie du système nerveux central @5 43
C07 06  X  ENG  @0 Central nervous system disease @5 43
C07 06  X  SPA  @0 Sistema nervosio central patología @5 43
N21       @1 191
N44 01      @1 OTO
N82       @1 OTO

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Pascal:12-0248747

Le document en format XML

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