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The novel hypothalamic neuropeptides orexins, or hypocretins, have gained much attention as potent modulators of various different physiological functions.1 Deficient orexin neurotransmission may be responsible for excessive somnolence, as shown in several conditions related to secondary narcolepsy, through direct or indirect damage to the posterior hypothalamus and its connections.2 We have studied for the first time the longitudinal changes of hypocretin-1 concentrations in cerebrospinal fluid (CSF) in patients with acute haemorrhagic brain injury.
Nine patients from a previously reported cohort3 and 21 controls (seven women and five men, median age 38 years, range 17 to 70) with other neurological disease were enrolled in the study (table 1). The patient group included five subjects with intracerebral haemorrhage and five with subarachnoid haemorrhage (table 1). All patients had extraventricular drains inserted within a median of two days of disease onset (range 2 to 36) as a treatment procedure because of increasing signs of hydrocephalus. Morning CSF samples were collected twice: first between day 1 and day 2 after catheter insertion, and second between day 4 and day 10. Patients were assessed using the Glasgow coma scale (GCS) at …
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Competing interests: none declared