Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Huang, Y.-S.
Right arrow Articles by Guilleminault, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Huang, Y.-S.
Right arrow Articles by Guilleminault, C.
Related Collections
Right arrow Adolescence
Right arrow Other hypersomnias
NEUROLOGY 2008;70:795-801
© 2008 American Academy of Neurology

Polysomnography in Kleine-Levin syndrome

Yu-Shu Huang, MD, Yu-Hsuan Lin, MD and Christian Guilleminault, MD, BiolD

From the Sleep Center and Child Psychiatry Department (Y.-S.H., Y.-H.L.), Chang Gung Memorial Hospital Taipei, Taiwan; and Stanford University Sleep Disorders Clinic (C.G.), Stanford, CA.

Address correspondence and reprint requests to Dr. Christian Guilleminault, Stanford University Sleep Medicine Program, 401 Quarry Rd Suite 3301, Stanford, CA 94305 cguil{at}stanford.edu

Background: Cause and pathogenesis of the Kleine-Levin syndrome (KLS), a recurrent hypersomnia affecting mainly male adolescents, remain unknown, with only scant information on the sleep characteristics during episodes. We describe findings obtained with polysomnography (PSG) and Multiple Sleep Latency Test (MSLT) and correlation obtained between clinical and PSG findings from different episodes.

Method: Nineteen patients (17 male) were investigated with PSG and MSLT. Ten patients had data during both symptomatic episode and asymptomatic interval. The analyses considered day of onset of symptoms and relationship between this time of onset and day of recording during the symptomatic period.

Results: When PSG was performed early (before the end of the first half of the symptomatic period), an important reduction in slow wave sleep (SWS) was always present with progressive return to normal during the second half (with percentages very similar to those monitored during the asymptomatic period) despite persistence of clinical symptoms. REM sleep remained normal in the first half of the episode but decreased in the second half: the differences between first and second half of episodes were significant for SWS (p = 0.014) and REM sleep (p = 0.027). The overall mean sleep latency at MSLT was 9.51 ± 4.82 minutes and 7 of 17 patients had two or more sleep onset REM periods during the symptomatic period.

Conclusion: Important changes in sleep occur over time during the symptomatic period, with clear impairment of slow wave sleep at symptom onset. But Multiple Sleep Latency Test (MSLT) is of little help in defining sleep problems and findings from the MSLT do not correlate with symptom onset.

Abbreviations: EOG = electro-oculogram; ESS = Epworth Sleepiness Scale; ICSD-2 = International Classification of Sleep Disorders, 2nd ed.; KLS = Kleine-Levin syndrome; MSLT = Multiple Sleep Latency Test; PSG = polysomnography; SOREM = sleep onset in REM; SWS = slow wave sleep; VAS = visual analogue scale; WASO = wake time after sleep onset.


Disclosure: The authors report no conflicts of interest.

Received July 17, 2007. Accepted in final form October 2, 2007.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by AAN Enterprises, Inc.