Narcolepsy is a neurological disorder of the sleep-wake cycle characterized by excessive daytime sleepiness, cataplexy, sleep paralysis, and hallucinations upon waking or falling asleep. It most commonly manifests in teens and young adults with excessive daytime sleepiness. Primary narcolepsy is either caused by orexin deficiency (type 1) or is idiopathic (type 2). Secondary narcolepsy can occur as a result of brain damage or other genetic syndromes. Diagnosis requires an established history based on questionnaires or a sleep diary as well as a polysomnogram and multiple sleep latency test or an abnormal orexin A (hypocretin-1) level in the cerebrospinal fluid (CSF). No cure has yet been found, but daytime sleepiness can be managed with CNS stimulants (e.g., modafinil) and a regimen of scheduled naps. Cataplexy, hallucinations, and sleep paralysis are treated with antidepressants or sodium oxybate.
- Prevalence: 25–50:100,000 
- Incidence: ∼ 0.8:100,000 individuals per year
- Sex: ♂ = ♀
- Bimodal distribution: : first peak at 15 years; another smaller peak around age 35
Epidemiological data refers to the US, unless otherwise specified.
Narcolepsy type 1
- Loss of lateral hypothalamic neurons, which produce ; orexin A and orexin B (i.e., hypocretin-1 and hypocretin-2) → severe orexin deficiency → dysregulation of sleep-wake cycles 
- The exact etiology is unknown, but both genetic and environmental factors seem to be implicated.
- Narcolepsy type 2
Excessive daytime sleepiness (EDS): Affected individuals experience an irresistible urge to sleep and sudden, short sleep attacks (< 30 minutes), which may occur in inappropriate situations (e.g., while driving a car).
- One of the earliest manifestations of narcolepsy
- Can occur despite adequate sleep
Abnormal REM sleep
Cataplexy; (60–70% of cases): sudden muscle weakness in a fully conscious person, triggered by strong emotions (e.g., laughing, crying)
- Typically manifests months or even years after EDS
- The loss of muscle tone is similar to that observed during REM sleep.
- Typically manifests as partial cataplexy: isolated weakness of distinct muscle groups (e.g., neck muscles weaken and head tilts forward)
- Usually resolves within a few seconds, at most two minutes
- Sleep paralysis; (∼ 50% of cases): Complete paralysis occurs for 1–2 minutes after waking or before falling asleep (either during a nocturnal or narcoleptic sleep episode, i.e., begins or ends with REM sleep)
- Cataplexy; (60–70% of cases): sudden muscle weakness in a fully conscious person, triggered by strong emotions (e.g., laughing, crying)
- Sleep hallucinations
- Automatic behavior: During narcoleptic episodes, patients often perform routine repetitive tasks automatically without conscious awareness of their environment.
- Other: depression, obesity, impotence or low sex drive, headaches, decreased functional performance
Hypnagogic hallucinations occur while going to sleep.
- Diagnostic criteria 
- Sleep diary
- Narcolepsy questionnaires
- Conducted in a sleep laboratory during sleep, typically over the course of two days
- PSG measures brain waves via electroencephalography (EEG), eye movements via electrooculography (EOG), and muscle activity via electromyography (EMG).
- PSG findings are characterized by EEG beta waves that appear abnormally early after falling asleep (shortened ).
- Multiple sleep latency test (MSLT)
- Measures time needed to fall asleep during daytime naps to assess excessive daytime sleepiness
- Polysomnography is made during the day; five opportunities to nap are provided
- For a conclusive MSLT, patients must have at least six hours of normal sleep as assessed by PSG prior to the test.
- Supports diagnosis if patient both:
- Falls asleep with a mean latency of ≤ 8 minutes
- Shows sleep-onset REM periods (SOREMPs) within 15 minutes after sleep onset in at least 2 out of the 5 opportunities provided
- Decreased CSF orexin A levels: supports diagnosis if ≤ 110 pg/mL or < ⅓ of mean values in healthy persons
- Additional tests
Sleep hygiene recommendations
- Take scheduled naps throughout the day to reduce the urge to sleep.
- Ensure regular sleep periods during the night.
- Avoid substances that disturb the sleep-wake cycle (e.g., alcohol, antipsychotics, opiates).
- Consultations with family and employer (e.g., people with narcolepsy require a place to sleep at their workplace)
Automobile accidents are a concern! Patients should take treatment and be symptom-free to be allowed to drive.
Excessive daytime sleepiness
- Drug of choice: modafinil (nonamphetamine CNS stimulant)
- CNS stimulants
Cataplexy, sleep paralysis, and sleep hallucinations
- SSRIs (e.g, citalopram) or SNRIs (e.g., venlafaxine)
- Nighttime sodium oxybate(a gamma-hydroxybutyrate): highly effective for severe cataplexy ;