Narcolepsy Type 1 (with cataplexy) is pathophysiologically characterised by loss of neurons producing which neuropeptide in the lateral hypothalamus?
- A Neuropeptide Y
- B Melanin-concentrating hormone (MCH)
- C Vasoactive intestinal peptide (VIP)
- D Orexin (hypocretin) ✓
Explanation
Narcolepsy Type 1 is characterised by loss of 85–95% of orexin (hypocretin)-producing neurons in the lateral hypothalamus, resulting in undetectable or very low CSF orexin-1 levels (< 110 pg/mL). Orexin normally promotes wakefulness and stabilises sleep-wake transitions; its absence causes pathological intrusions of REM sleep elements into wakefulness (cataplexy, sleep paralysis, hypnagogic hallucinations) and excessive daytime sleepiness. This neuronal loss is believed to be autoimmune (anti-TRIB2 antibodies, HLA-DQB1*06:02 association). Narcolepsy Type 2 lacks cataplexy and typically has normal orexin levels.
Reference: Kaplan & Sadock's Synopsis of Psychiatry, 11th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
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