Rapid eye movement sleep disturbances in Huntington disease

I. Arnulf; J. Nielsen; E. Lohmann; J. Schieffer; E. Wild; P. Jennum; E. Konofal; M. Walker; D. Oudiette; S. Tabrizi; A. Durr

Rapid eye movement sleep disturbances in Huntington disease

I. Arnulf, J. Nielsen, E. Lohmann, J. Schieffer, E. Wild, P. Jennum, E. Konofal, M. Walker, D. Oudiette, S. Tabrizi, A. Durr

154 Citationer (Scopus)

Abstract

Background: Sleep disorders including insomnia, movements during sleep, and daytime sleepiness are common but poorly studied in Huntington disease (HD). Objective: To evaluate the HD sleep-wake phenotype (including abnormal motor activity during sleep) in patients with various HD stages and the length of CAG repeals. Because a mild hypocretin deficiency has been found in the brains of some patients with HD (hereinafter referred to as HD patients), we also tested the HD patients for narcolepsy. Design and Patients: Twenty-five HD patients (including 2 premanifest carriers) underwent clinical interview, nighttime video and sleep monitoring, and daytime multiple sleep latency tests. Their results were compared with those of patients with narcolepsy and control patients. Results: The HD patients had frequent insomnia, earlier sleep onset, lower sleep efficiency, increased stage I sleep, delayed and shortened rapid eye movement (REM) sleep, and increased periodic leg movements. Three HD patients (12%) had REM sleep behavior disorders. No sleep abnormality correlated with CAG repeat length. Reduced REM sleep duration (but not REM sleep behavior disorders) was present in premanifest carriers and patients with very mild HD and worsened with disease severity. In contrast to narcoleptic patients, HD patients had no cataplexy, hypnagogic hallucinations, or sleep paralysis. Four HD patients had abnormally low (< 8 minutes) daytime sleep latencies, but none had multiple sleep-onset REM periods. Conclusions: The sleep phenotype of HD includes insomnia, advanced sleep phase, periodic leg movements, REM sleep behavior disorders, and reduced REM sleep but not narcolepsy. Reduced REM sleep may precede chorea. Mutant huntingtin may exert an effect on REM sleep and motor control during sleep
Udgivelsesdato: 2008/4

Originalsprog	Engelsk
Tidsskrift	Archives of Neurology
Vol/bind	65
Udgave nummer	4
Sider (fra-til)	482-488
Antal sider	6
ISSN	0003-9942
Status	Udgivet - 2008

Citationsformater

@article{389e27308bd411de8bc9000ea68e967b,

title = "Rapid eye movement sleep disturbances in Huntington disease",

abstract = "Background: Sleep disorders including insomnia, movements during sleep, and daytime sleepiness are common but poorly studied in Huntington disease (HD). Objective: To evaluate the HD sleep-wake phenotype (including abnormal motor activity during sleep) in patients with various HD stages and the length of CAG repeals. Because a mild hypocretin deficiency has been found in the brains of some patients with HD (hereinafter referred to as HD patients), we also tested the HD patients for narcolepsy. Design and Patients: Twenty-five HD patients (including 2 premanifest carriers) underwent clinical interview, nighttime video and sleep monitoring, and daytime multiple sleep latency tests. Their results were compared with those of patients with narcolepsy and control patients. Results: The HD patients had frequent insomnia, earlier sleep onset, lower sleep efficiency, increased stage I sleep, delayed and shortened rapid eye movement (REM) sleep, and increased periodic leg movements. Three HD patients (12%) had REM sleep behavior disorders. No sleep abnormality correlated with CAG repeat length. Reduced REM sleep duration (but not REM sleep behavior disorders) was present in premanifest carriers and patients with very mild HD and worsened with disease severity. In contrast to narcoleptic patients, HD patients had no cataplexy, hypnagogic hallucinations, or sleep paralysis. Four HD patients had abnormally low (< 8 minutes) daytime sleep latencies, but none had multiple sleep-onset REM periods. Conclusions: The sleep phenotype of HD includes insomnia, advanced sleep phase, periodic leg movements, REM sleep behavior disorders, and reduced REM sleep but not narcolepsy. Reduced REM sleep may precede chorea. Mutant huntingtin may exert an effect on REM sleep and motor control during sleep Udgivelsesdato: 2008/4",

author = "I. Arnulf and J. Nielsen and E. Lohmann and J. Schieffer and E. Wild and P. Jennum and E. Konofal and M. Walker and D. Oudiette and S. Tabrizi and A. Durr",

note = "Times Cited: 0ArticleEnglishArnulf, IHop La Pitie Salpetriere, 47-83 Blvd Hop, F-75651 Paris 13, FranceCited References Count: 33286GZAMER MEDICAL ASSOC515 N STATE ST, CHICAGO, IL 60610-0946 USACHICAGO",

year = "2008",

language = "English",

volume = "65",

pages = "482--488",

journal = "JAMA Neurology",

issn = "2168-6149",

publisher = "The JAMA Network",

number = "4",

}

TY - JOUR

T1 - Rapid eye movement sleep disturbances in Huntington disease

AU - Arnulf, I.

AU - Nielsen, J.

AU - Lohmann, E.

AU - Schieffer, J.

AU - Wild, E.

AU - Jennum, P.

AU - Konofal, E.

AU - Walker, M.

AU - Oudiette, D.

AU - Tabrizi, S.

AU - Durr, A.

N1 - Times Cited: 0ArticleEnglishArnulf, IHop La Pitie Salpetriere, 47-83 Blvd Hop, F-75651 Paris 13, FranceCited References Count: 33286GZAMER MEDICAL ASSOC515 N STATE ST, CHICAGO, IL 60610-0946 USACHICAGO

PY - 2008

Y1 - 2008

N2 - Background: Sleep disorders including insomnia, movements during sleep, and daytime sleepiness are common but poorly studied in Huntington disease (HD). Objective: To evaluate the HD sleep-wake phenotype (including abnormal motor activity during sleep) in patients with various HD stages and the length of CAG repeals. Because a mild hypocretin deficiency has been found in the brains of some patients with HD (hereinafter referred to as HD patients), we also tested the HD patients for narcolepsy. Design and Patients: Twenty-five HD patients (including 2 premanifest carriers) underwent clinical interview, nighttime video and sleep monitoring, and daytime multiple sleep latency tests. Their results were compared with those of patients with narcolepsy and control patients. Results: The HD patients had frequent insomnia, earlier sleep onset, lower sleep efficiency, increased stage I sleep, delayed and shortened rapid eye movement (REM) sleep, and increased periodic leg movements. Three HD patients (12%) had REM sleep behavior disorders. No sleep abnormality correlated with CAG repeat length. Reduced REM sleep duration (but not REM sleep behavior disorders) was present in premanifest carriers and patients with very mild HD and worsened with disease severity. In contrast to narcoleptic patients, HD patients had no cataplexy, hypnagogic hallucinations, or sleep paralysis. Four HD patients had abnormally low (< 8 minutes) daytime sleep latencies, but none had multiple sleep-onset REM periods. Conclusions: The sleep phenotype of HD includes insomnia, advanced sleep phase, periodic leg movements, REM sleep behavior disorders, and reduced REM sleep but not narcolepsy. Reduced REM sleep may precede chorea. Mutant huntingtin may exert an effect on REM sleep and motor control during sleep Udgivelsesdato: 2008/4

AB - Background: Sleep disorders including insomnia, movements during sleep, and daytime sleepiness are common but poorly studied in Huntington disease (HD). Objective: To evaluate the HD sleep-wake phenotype (including abnormal motor activity during sleep) in patients with various HD stages and the length of CAG repeals. Because a mild hypocretin deficiency has been found in the brains of some patients with HD (hereinafter referred to as HD patients), we also tested the HD patients for narcolepsy. Design and Patients: Twenty-five HD patients (including 2 premanifest carriers) underwent clinical interview, nighttime video and sleep monitoring, and daytime multiple sleep latency tests. Their results were compared with those of patients with narcolepsy and control patients. Results: The HD patients had frequent insomnia, earlier sleep onset, lower sleep efficiency, increased stage I sleep, delayed and shortened rapid eye movement (REM) sleep, and increased periodic leg movements. Three HD patients (12%) had REM sleep behavior disorders. No sleep abnormality correlated with CAG repeat length. Reduced REM sleep duration (but not REM sleep behavior disorders) was present in premanifest carriers and patients with very mild HD and worsened with disease severity. In contrast to narcoleptic patients, HD patients had no cataplexy, hypnagogic hallucinations, or sleep paralysis. Four HD patients had abnormally low (< 8 minutes) daytime sleep latencies, but none had multiple sleep-onset REM periods. Conclusions: The sleep phenotype of HD includes insomnia, advanced sleep phase, periodic leg movements, REM sleep behavior disorders, and reduced REM sleep but not narcolepsy. Reduced REM sleep may precede chorea. Mutant huntingtin may exert an effect on REM sleep and motor control during sleep Udgivelsesdato: 2008/4

M3 - Journal article

SN - 2168-6149

VL - 65

SP - 482

EP - 488

JO - JAMA Neurology

JF - JAMA Neurology

IS - 4

ER -