| Literature DB >> 26004157 |
Astrid van der Heide1, Ingrid M Hegeman-Kleinn2, Els Peeters3, Gert J Lammers4, Rolf Fronczek5.
Abstract
Narcolepsy type 1 patients typically have undetectable hypocretin-1 levels in the cerebrospinal fluid (CSF), as a result of a selective loss of the hypocretin containing neurons in the hypothalamus. An autoimmune attack targeting hypothalamic hypocretin (orexin) neurons is hypothesised. So far, no direct evidence for an autoimmune attack was found. One of the major limitations of previous studies was that none included patients close to disease onset. We screened serum of 21 narcolepsy type 1 patients close to disease onset (median 11 months), including 8 H1N1 vaccinated patients, for antibodies against hypocretin neurons using immunohistochemistry. No autoantibodies against hypocretin neurons could be detected.Entities:
Keywords: Autoimmune; Cataplexy; Hypothalamus; Immunohistochemistry; Narcolepsy type 1
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Year: 2015 PMID: 26004157 DOI: 10.1016/j.jneuroim.2015.04.008
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478