Hypocretin deficiency develops during onset of human narcolepsy with cataplexy

Andri Savvidou, Stine Knudsen, Mia Olsson-Engman, Steen Gammeltoft, Poul Jennum, Lars Palm

    13 Citationer (Scopus)

    Abstract

    Study Objectives: Although hypothesized through animal studies, a temporal and causal association between hypocretin deficiency and the onset of narcolepsy with cataplexy (NC) has never been proven in humans. Setting: Paediatric Department, Blekinge Hospital, Sweden, and Danish Center for Sleep Medicine, Glostrup Hospital, Denmark. Patient and Results: Two weeks after his second Pandemrix-vaccination, a 10 year old HLA-DQB1*0602-positive boy developed NC. The CSF hypocretin-1 level was 10 pg/ml. However, CSF saved from a pre-narcolepsy episode of Lyme disease revealed a normal hypocretin-1 level (318 pg/ml). Conclusions: We confirm that hypocretin deficiency develops in parallel to the onset of human narcolepsy with cataplexy.

    OriginalsprogEngelsk
    TidsskriftSleep (Online)
    Vol/bind36
    Udgave nummer1
    Sider (fra-til)147-8
    Antal sider2
    ISSN0161-8105
    DOI
    StatusUdgivet - 1 jan. 2013

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