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Sleep Disorders Medicine In Psychiatry. Alan B. Douglass MD, FRCPC, Dip. ABPN, Dip. Amer. Board of Sleep Medicine Asst. Professor, Dept of Psychiatry, University of Ottawa Medical Director, Sleep Disorders Service, Royal Ottawa Hospital. Introduction.
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Sleep Disorders MedicineIn Psychiatry Alan B. Douglass MD, FRCPC, Dip. ABPN, Dip. Amer. Board of Sleep Medicine Asst. Professor, Dept of Psychiatry, University of Ottawa Medical Director, Sleep Disorders Service, Royal Ottawa Hospital
Introduction • A large proportion of insomnia cases involve elements of: • Depression • Anxiety Disorder • Bipolar Disorder • Current diagnostic reference – Internat’l Classification of Sleep Disorders (ICSD) • Resembles DSM-IV-TR, but more specific diagnostic criteria
Stg% Table of Stg. %
Wake => Sleep Transition Table of Stg. % Wake => Sleep Transition R & K 1968
Stage 2 Sleep R & K 1968
REM sleep onset Onset of REM R & K 1968
Sleep Restriction MSLT
Monoamines controlled by Orexin SCNclock DA(+) ~ Orexin / Hypocretin Histamine (+) 5HT(+) NA (+)
Clinical Applicability – Apnea • Sleep apnea and depression share clinical features; apnea can produce secondary depression • Serious sleep apnea can cause sufficient sleep impairment to suggest dementia • Serious snoring in demented patient could suggest treatable illness • Apnea or PLMD can cause sleep deprivation, then relapse of mania or depression
SYMPTOMS Late evening / night Legs cramp, squirm, move by themselves Multiple awakenings “Charley Horses” Can’t tolerate legs being immobilized Majority elderly TREATMENT Check Fe, ferritin, B12, folate Dopamine agonists (L-DOPA, ropinirole, pramipexole) Benzodiazepines or opiates now 2nd line Quinine obsolete RLS – PLMD: Sx and Tx
RLS – PLMD: neurochemistry • Likely due to iron deficiency in basal ganglia (Fe is co-factor in enzymes that synthesize DA). • May predict onset of “syn-nuclein-opathies” (REM behaviour disorder, PSP, Parkinson’s, Lewy Body dementia).
Narcolepsy: age of onset Silber 2004, p.97.
Narcolepsy “Tetrad” • True sleep attacks • Falls asleep without warning, unusual situations • Cataplexy • Flaccid muscle paralysis; eyes and diaphragm OK; pt. remains awake but paralyzed. • Hypnagogic / Hypnopompic hallucinations • “Multimodal” – visual, tactile, auditory, smell. Often highly emotional, sexual, frightening • Sleep Paralysis • Awakes unable to move anything but eyes. Can’t breathe voluntarily or talk. HH often occur.
Narcolepsy Treatment • SLEEPINESS: • Stimulants (noradrenaline receptor agonists): d-amphetamine (Dexedrine), methylphenidate (Ritalin), modafinil (Alertec). • CATPLEXY: • Antidepressants that increase serotonin and / or noradrenaline and block Ach.
Worm in lateral hypothalamus causing narcolepsy.(neurocysticercosis)J. Clin. Sleep Med. 1(1) 2005, p. 41.
Sleep Abnormalities in Psychiatry Benca, 1992 • Meta-analysis of sleep in all major psychiatric disorders showed affective disorders had the largest and most consistent differences from controls. Kaneko, 1981 • Extremely short nocturnal REM latency is common to both psychiatric disorders and narcolepsy
Psychiatric Sleep Measurements Most polysomnographic measurements are the same as for a clinical study (“epoch”= 30 sec.): • Sleep Latency (SL) – sleep onset measured as first three contiguous epochs of Stage 1 sleep • REM Latency (RL) – time from sleep onset to first epoch of REM sleep • REM Latency Minus Awake (RLMA) – RL subtracting any interposed epochs of wake • Eye Movement Density in REM Sleep (REM Density, RD) – the actual number of eye movements divided by minutes spent in REM
RL and RLMA • REM Latency is shortened by the cholinergic agonists arecoline, pilocarpine, physostigmine • Prolonged by anti-cholinergics (benztropine, trihexyphenidyl, diphenhydramine • RL correlates inversely with age • RLMA – superior statistical properties; smaller variance, more normal distribution
MDD • Long initial insomnia, early morning wakening • Shallow sleep, easily awakened • Non-refreshing sleep • Antidepressants are REM suppressants • Increase neurotransmission in serotonergic and adrenergic monoamine pathways • REM is under tonic inhibition by monoamines • Monoamine nuclei are under control of OREXIN from lateral hypothalamus
MDD (cont) • Some powerful sleep mechanism underlies the expression of depression • Total sleep deprivation or selective REM deprivation dramatically improves mood of severely depressed patients • Benefit lost after one night’s sleep or nap • Amount of Non-REM sleep in nap predicts worsening of mood
Alcoholism • Acute administration of alcohol produces REM suppression, then: Hallucination – visual, gustatory, tactile dream-like imagery Actually REM sleep without physiological paralysis Withdrawal after chronic alcohol intoxication
Narcolepsy versus Schizophrenia Apparent “Schizophrenic” Hallucinations Actually Daytime REM sleep intrusion Narcolepsy • 90% aassociation of narcolepsy with a DNA fragment (DQB1*0602) allows “inverse” screening of schizophrenics for narcolepsy • Narcolepsy is detectable in sleep lab (MSLT) but pt. must be medication-free for at least 3 weeks.
Bipolar Disorder vs. Depression Excessive sleeping Crushing fatigue Extreme appetite Actually Depressed Phase of Bipolar Disorder “Atypical Depression” DDX: Narcolepsy, Idiopathic Hypersomnolence
Bipolar Disorder (cont) • “Switch process” from depression to mania often occurs at night • Significantly reduced sleep on that night is often seen • REM deprivation may be the key factor in the switch • May also explain seasonal cyclicity of some bipolars (shorter sleep in Spring)
Narcolepsy + Apparent Schizophrenic Hallucinations Actually Hypnagogic Hallucinations Bipolar Disorder Bipolar Disorder + Narcolepsy Narcolepsy gives mis-Dx: psychotic bipolar, schizo-affective
REM Latency (RL) • Short RL not specific for depression • Seen also in schizophrenia, bipolar disorder, schizoaffective disorder, alcoholism, and borderline personality disorder • Puzzle: RL abnormalities not correlated with any shared clinical feature of these illnesses • Psychotic bipolar depression has the shortest RL values observed (10 – 40 min.)
REM Latency (cont) MDD - Short RL, usually < 65 minutes (normal controls > 80 minutes) • Short RL predicts eventual successful antidepressant response in MDD • Psychotic MDD patients have shorter mean RL than non-psychotic MDD Depression, schizophrenia – RL inversely correlated to symptom severity • Bipolar – RL short in depressive phase • RL abnormalities exist in relatives of bipolar patients Sleep abnormalities are state rather than trait markers – normalize with treatment
Sleep Efficiency (SE) • SE in MDD less than normals, but equal to insomniacs • 75-150 mg doxepin qHS improves SE; mirtazepine also very effective • SE also poor in schizophrenia • Normalizes after adequate antipsychotic drug treatment
Clinical Applicability • Bipolar Mania - Initial insomnia is the most persistent symptom in treated bipolar patients, even when euthymic. • Higher levels of mood stabilizer eliminate insomnia without need for sleep lab referral • Alcohol Withdrawal DTs - REM rebounds strongly after cessation of drinking • Absence of customary REM paralysis allows patient to act out dreams (similar to REM behavior disorder patients)
Clinical Applicability • Depressed Bipolar patient with hypersomnia (“atypical depression”) can be mistaken for Idiopathic Hypersomnolence, or even narcolepsy. • Cataplexy is the key differential symptom – only present in narcolepsy