Movement Disorders (revue)

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Cerebrospinal fluid hypocretin‐1 levels in multiple system atrophy

Identifieur interne : 002F65 ( Main/Exploration ); précédent : 002F64; suivant : 002F66

Cerebrospinal fluid hypocretin‐1 levels in multiple system atrophy

Auteurs : Jose Enrique Martinez-Rodriguez [Espagne] ; Klaus Seppi [Autriche] ; Adriana Cardozo [Espagne] ; Alex Iranzo [Espagne] ; Michaela Stampfer-Kountchev [Autriche] ; Gregor Wenning [Autriche] ; Eduardo Tolosa [Espagne] ; Birgit Högl [Autriche] ; Joan Santamaria [Espagne] ; Werner Poewe [Autriche]

Source :

RBID : ISTEX:9A1C890FE991B101EBEC863232F2035AD7D8B142

English descriptors

Abstract

Hypocretin (orexin) cerebrospinal fluid (CSF) levels have been previously found normal or decreased in Dementia with Lewy bodies and Parkinson disease, two synucleinopathies commonly associated with excessive daytime sleepiness (EDS). We evaluated CSF hypocretin‐1 levels in 15 patients with moderately severe multiple system atrophy (MSA), another synucleinopathy where sleep disorders occur frequently and EDS has been reported, performing additional electrophysiological studies in 5 of them to assess the presence of EDS and sleep onset REM (SOREM) periods. Despite relatively low sleep efficiencies in nocturnal sleep, mean sleep latencies in the Multiple Sleep Latency Test were normal with no SOREM periods. All patients had CSF hypocretin‐1 levels in the normal range (>200 pg/mL) suggesting that the hypocretin system is not altered in MSA, at least in patients with a moderately severe disease. © 2007 Movement Disorder Society

Url:
DOI: 10.1002/mds.21668


Affiliations:


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<div type="abstract" xml:lang="en">Hypocretin (orexin) cerebrospinal fluid (CSF) levels have been previously found normal or decreased in Dementia with Lewy bodies and Parkinson disease, two synucleinopathies commonly associated with excessive daytime sleepiness (EDS). We evaluated CSF hypocretin‐1 levels in 15 patients with moderately severe multiple system atrophy (MSA), another synucleinopathy where sleep disorders occur frequently and EDS has been reported, performing additional electrophysiological studies in 5 of them to assess the presence of EDS and sleep onset REM (SOREM) periods. Despite relatively low sleep efficiencies in nocturnal sleep, mean sleep latencies in the Multiple Sleep Latency Test were normal with no SOREM periods. All patients had CSF hypocretin‐1 levels in the normal range (>200 pg/mL) suggesting that the hypocretin system is not altered in MSA, at least in patients with a moderately severe disease. © 2007 Movement Disorder Society</div>
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