Narcolepsy
Also known as: Narcolepsy Type 1, Narcolepsy Type 2
Narcolepsy is a chronic neurological disorder that impairs the brain's ability to regulate sleep-wake cycles, causing overwhelming daytime drowsiness and sudden attacks of sleep. Type 1 narcolepsy includes cataplexy (sudden loss of muscle tone triggered by emotions), while Type 2 does not. The condition is caused by a deficiency of the neurotransmitter hypocretin (orexin) and typically begins in childhood or young adulthood.
Symptoms
Causes
- Loss of hypocretin (orexin)-producing neurons in the hypothalamus
- Autoimmune destruction possibly triggered by infection (H1N1, streptococcus)
- Genetic factors (strong association with HLA-DQB1*0602)
- Rarely, brain injuries or tumors affecting the hypothalamus
Risk Factors
- Family history of narcolepsy
- Age 10–30 at symptom onset
- Carrying the HLA-DQB1*0602 gene variant
- History of certain infections (H1N1 influenza, streptococcal infections)
Diagnosis
- Polysomnography (overnight sleep study)
- Multiple Sleep Latency Test (MSLT) showing rapid-onset REM sleep
- Measurement of hypocretin levels in cerebrospinal fluid (for Type 1)
- Sleep diary and Epworth Sleepiness Scale assessment
Treatment
- Wake-promoting agents (modafinil, armodafinil, solriamfetol)
- Sodium oxybate (Xyrem) for cataplexy and disrupted nighttime sleep
- Pitolisant (histamine-3 receptor inverse agonist)
- Scheduled short naps during the day
- Antidepressants (venlafaxine, fluoxetine) for cataplexy in some patients
- Lifestyle modifications (regular sleep schedule, good sleep hygiene)
Prevention
- No known prevention for narcolepsy
- Early diagnosis and treatment can significantly improve quality of life
When to See a Doctor
- Persistent excessive daytime sleepiness interfering with work or school
- Episodes of sudden muscle weakness with strong emotions
- Falling asleep involuntarily during activities like driving or talking
- Sleep paralysis or vivid hallucinations during sleep transitions
Frequently Asked Questions
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