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Repeated polysomnography and multiple sleep latency test in narcolepsy type 1 and other hypersomnolence disorders.
Torstensen, Eva Wiberg; Haubjerg Østerby, Niels Christian; Kornum, Birgitte Rahbek; Wanscher, Benedikte; Mignot, Emmanuel; Barløse, Mads; Jennum, Poul Jørgen.
Afiliación
  • Torstensen EW; Danish Center for Sleep Medicine, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark. Electronic address: eva.wiberg.torstensen.01@regionh.dk.
  • Haubjerg Østerby NC; Danish Center for Sleep Medicine, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark. Electronic address: niels.christian.haubjerg.oesterby.01@regionh.dk.
  • Kornum BR; Department of Neuroscience, University of Copenhagen, Denmark. Electronic address: kornum@sund.ku.dk.
  • Wanscher B; Department of Neurology, Medicin 3, Slagelse Hospital, Denmark. Electronic address: bewa@regionsjaelland.dk.
  • Mignot E; Stanford University Center for Sleep Sciences, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA. Electronic address: mignot@stanford.edu.
  • Barløse M; Department of Functional and Diagnostic Imaging, Hvidovre Hospital, Copenhagen, Denmark; Danish Headache Center, Rigshospitalet, Glostrup, Denmark. Electronic address: mads.christian.johannes.barloese@regionh.dk.
  • Jennum PJ; Danish Center for Sleep Medicine, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark. Electronic address: poul.joergen.jennum@regionh.dk.
Sleep Med ; 110: 91-98, 2023 10.
Article en En | MEDLINE | ID: mdl-37544279
ABSTRACT

BACKGROUND:

The diagnosis of narcolepsy is based on clinical information, combined with polysomnography (PSG) and the Multiple Sleep Latency Test (MSLT). PSG and the MSLT are moderately reliable at diagnosing narcolepsy type 1 (NT1) but unreliable for diagnosing narcolepsy type 2 (NT2). This is a problem, especially given the increased risk of a false-positive MSLT in the context of circadian misalignment or sleep deprivation, both of which commonly occur in the general population.

AIM:

We aimed to clarify the accuracy of PSG/MSLT testing in diagnosing NT1 versus controls without sleep disorders. Repeatability and reliability of PSG/MSLT testing and temporal changes in clinical findings of patients with NT1 versus patients with hypersomnolence with normal hypocretin-1 were compared.

METHOD:

84 patients with NT1 and 100 patients with non-NT1-hypersomnolence disorders, all with congruent cerebrospinal fluid hypocretin-1 (CSF-hcrt-1) levels, were included. Twenty-five of the 84 NT1 patients and all the hypersomnolence disorder patients underwent a follow-up evaluation consisting of clinical assessment, PSG, and a modified MSLT. An additional 68 controls with no sleep disorders were assessed at baseline.

CONCLUSION:

Confirming results from previous studies, we found that PSG and our modified MSLT accurately and reliably diagnosed hypocretin-deficient NT1 (accuracy = 0.88, reliability = 0.80). Patients with NT1 had stable clinical and electrophysiological presentations over time that suggested a stable phenotype. In contrast, the PSG/MSLT results of patients with hypersomnolence, and normal CSF-hcrt-1 had poor reliability (0.32) and low repeatability.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de Somnolencia Excesiva / Narcolepsia Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Sleep Med Asunto de la revista: NEUROLOGIA / PSICOFISIOLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de Somnolencia Excesiva / Narcolepsia Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Sleep Med Asunto de la revista: NEUROLOGIA / PSICOFISIOLOGIA Año: 2023 Tipo del documento: Article
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