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Home > Journals > Minerva Pneumologica > Past Issues > Minerva Pneumologica 2009 December;48(4) > Minerva Pneumologica 2009 December;48(4):345-76



A Journal on Diseases of the Respiratory System

Official Journal of the Italian Society of Thoracic Endoscopy
Indexed/Abstracted in: EMBASE, Scopus

Frequency: Quarterly

ISSN 0026-4954

Online ISSN 1827-1723


Minerva Pneumologica 2009 December;48(4):345-76




Zarowski M. 1, Ali-Dinar T. 2, Kothare S. V. 2

1 Polysomnography and Sleep Research Unit, Department of Developmental Neurology, Poznan University of Medical Sciences, Poznan, Poland
2 Department of Neurology, Division of Epilepsy and Clinical Neurophysiology, Center for Pediatric Sleep Disorders, Children’s Hospital, Harvard Medical School, Boston, MA, USA

Narcolepsy is a life-long neurological, rapid eye movement (REM) sleep disorder characterized by excessive daytime sleepiness, REM intrusions in wakefulness and sleep, and abnormal sleep-wake cycle regulation. Additional symptoms include sleep maintenance insomnia, REM sleep behavior disorders, obstructive sleep apnea, periodic limb movement, weight gain, migraines, and depression. Narcolepsy is not an uncommon disorder, but is under-recognized. It has an estimated prevalence of 0.05%. The age of onset shows two peaks of presentation: in childhood and in adults. Both genetics and environmental factors may be involved in the development of narcolepsy. The history, combined with polysomnography and Multiple Sleep Latency Test, remain the current gold standard in the diagnosis of narcolepsy. Human leukocyte antigen (HLA) typing shows an association with HLA DQB1*0602 in more than 92% of cases. The levels of Hypocretin-1 are undetectable in the cerebrospinal fluid in most patients with narcolepsy with cataplexy. It is highly specific (99.1%) and sensitive (88.5%) for narcolepsy with cataplexy but can also be positive in the normal population (25-30%). Early recognition and treatment can greatly improve the quality of life of patients with narcolepsy. Treatment of narcolepsy includes non-pharmacological (life style changes) and pharmacological (stimulants, modafinil, sodium oxybate) treatment against hypersomnia and anticataplectic drugs (antidepressants and sodium oxybate). A detail review of the epidemiology, pathophysiology, clinical features, diagnostic evaluations and management of narcolepsy is presented.

language: English


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