(Klein Gilles) - Centre Hospitalier de Luxembourg Department of Neurosciences
(Burghaus Lothar) - University Hospital of Cologne Department of Neurology
(Vaillant Michel) - CRP Sante Competences Center for Methodology and Statistics
(Pieri Vannina) - Centre Hospitalier de Luxembourg Department of Neurosciences
(Fink Gereon R) - University Hospital of Cologne Department of Neurology
(Diederich Nico) - Centre Hospitalier de Luxembourg Department of Neurosciences
Abstract
Background and Purpose: Excessive daytime sleepiness and sudden sleep attacks are the main features of narcolepsy, but rapid-eye-movement sleep behavior disorder (RBD), hyposmia, and depression can also occur. The latter symptoms are nonmotor features in idiopathic Parkinson¡¯s disease (IPD). In the present study, IPD-proven diagnostic tools were tested to determine whether they are also applicable in the assessment of narcolepsy.
Methods: This was a case-control study comparing 15 patients with narcolepsy (PN) and 15 control subjects (CS) using the Scales for Outcomes in Parkinson¡¯s Autonomic Test (SCOPA-AUT), Parkinson¡¯s Disease Nonmotor Symptoms (PDNMS), University of Pennsylvania Smell Test, Farnsworth-Munsell 100 Hue test, Beck Depression Inventory, and the RBD screening questionnaire.
Results: Both the PN and CS exhibited mild hyposmia and no deficits in visual tests. Frequent dysautonomia in all domains except sexuality was found for the PN. The total SCOPA-AUT score was higher for the PN (18.47¡¾10.08, mean¡¾SD) than for the CS (4.40¡¾3.09), as was the PDNMS score (10.53¡¾4.78 and 1.80¡¾2.31, respectively). RBD was present in 87% of the PN and 0% of the CS. The PN were more depressed than the CS. The differences between the PN and CS for all of these variables were statistically significant (all p<0.05).
Conclusions: The results of this study provide evidence for the presence of dysautonomia and confirm the comorbidities of depression and RBD in narcolepsy patients. The spectrum, which is comparable to the nonmotor complex in IPD, suggests wide-ranging, clinically detectable dysfunction beyond the narcoleptic core syndrome.
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autonomic failure, multisystem disorder, narcolepsy, Parkinson¡¯s disease
KMID :
1130620140100040314
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