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An overview of normal sleep patterns, including sleep stages and changes with aging. It also discusses different types of sleep disorders, such as hypersomnia, insomnia, and parasomnia, and their major clinical and physiological characteristics. The document emphasizes the importance of REM sleep and its functions, as well as the role of neurotransmitters in sleep behavior.
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Summary: Normal Sleep Patterns and Sleep Disorders Kathryn Lovell, PhD, and Christine Liszewski, MD
Objectives:
NORMAL SLEEP PATTERNS
Introduction : In the normal adult there are two main stages of sleep that alternate at about 90-minute intervals. Rapid eye movement (REM) sleep can be roughly described as a period when the brain is active and the body is paralyzed (except for eye movements, middle ear ossicles, and respiration). In non-rapid eye movement (nonREM or NREM) sleep , the brain is less active but the body can move. Non-REM sleep is composed of four stages that are differentiated on the basis of EEG characteristics. When normal individuals first fall asleep, they enter Stage 1 (sleep drowsiness) and then progress through Stages 2, 3, and 4 of NREM sleep. Stages 3 and 4 (deep sleep) are often called slow wave sleep or delta sleep because they are characterized by high amplitude, slow waves (also called delta waves) on EEG. Slow wave sleep may last from a few minutes to an hour, depending on the person’s age, before reversion back to Stage 2 sleep. Shortly after this, the first REM sleep period begins, lasting about 15-20 minutes and is followed by another non-REM cycle. This alternating pattern continues throughout the night, but as the night progresses Stages 3 and 4 are less apparent and the periods of REM sleep grow longer. See graph below for an illustration of the time course. By the criterion of external arousability, REM is the deepest stage of sleep, but by the criterion of internal arousability, REM is the lightest stage of sleep, since a person is more likely to awaken spontaneously from REM sleep than from any other stage.
COMPARISON OF WAKEFULNESS, NON-REM AND REM SLEEP Category EEG characteristics Eye movements Muscle tone (EMG) Waking Low voltage, fast Normal tracking Present Non-REM sleep High voltage, slow (EEG synchronization)
Absent Variable; generally reduced REM sleep Low voltage, fast Specific pattern of rapid eye movements
Absent (except ocular muscles)
The chart shows a typical night's pattern of sleep in a normal young adult. The time spent in REM sleep is indicated by a black bar. The first REM period is usually short. The amount of stage 2 slow wave sleep increases during the night.
Development patterns and changes with aging : One of the most significant determinants of a person’s normal sleep pattern is age. REM sleep occupies about 20-25% of the sleep time in normal young adults. In humans the daily total sleep requirement declines steadily throughout childhood and adolescence, levels off during the middle years, and then often declines further with old age. The need for REM sleep begins in utero. REM sleep fills approximately 80% of the total sleep time of infants born 10 weeks prematurely. In full-term neonates, REM sleep fills 50% of the sleep time. REM sleep declines sharply to about 30-35% of sleep time by age 2 and stabilizes at about 25% by 10 years of age. After that it shows little change until about age 65, when it further declines. The amount of stage 4 slow-wave sleep declines with age and in many people is nearly absent by age 70. As a consequence, older people spend proportionately more time in the lighter stages of slow-wave sleep, from which they awaken more often. Most adults in our culture learn to sleep in one extended period at night. However, the circadian rhythm of sleepiness is actually biphasic and normal afternoon drowsiness is more pronounced in the elderly.
The human sleep pattern changes with age.
Function of REM sleep : Most dreams occur during REM sleep. Deprivation of REM does not lead to serious psychological disturbance, as was once thought. The most important effect of REM deprivation is a dramatic shift in subsequent sleep patterns when the subject is allowed to sleep without interruption. The longer the deprivation, the larger and longer the REM rebound, suggesting that REM sleep is physiologically necessary. However, the purpose of REM sleep or dreaming remains largely unexplained. There is activation of sensory systems during REM sleep. The visual system, particularly the superior colliculus circuit, is intensely activated, and all dreams have visual experiences. Neuroimaging studies of humans have also indicated activation of the limbic system, suggesting a biologic basis of activation of memories and emotions in REM sleep. Thus, the visual cortices and limbic areas to which they project may be operating as a closed system, functionally disconnected from frontal regions in which the highest order integration of visual information takes place. Such “cortical dysynchony” could explain many of the experiential features of dreams, including heightened emotionality, uncritical acceptance of bizarre dream content, a dearth of parallel thoughts or images, temporal disorientation, and the absence of reflective awareness. Studies in animals indicated that those neurons that had been active during the day in encoding spatial position fired at a significantly higher rate in REM sleep than inactive neurons, suggesting that a general function of REM sleep is “off-line” processing of information acquired during the day. The atonia noted in REM sleep is under the control of the magnocellular nucleus of the medulla; this phenomenon is maintained via the reticulospinal tract which mediates inhibition of motor neurons.
Neural mechanisms involved in the sleep-wake cycle : The body’s sleep-wake cycle is usually under the control of circadian rhythms. These rhythms are regulated by the
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motion. A multiple sleep latency test (MSLT) is a measure of daytime sleepiness. The time needed to fall asleep for brief naps during the day is measured.
I. HYPERSOMNIAS (Trouble staying awake – excessive daytime sleepiness)
The most common causes of hypersomnia are insufficient sleep, medications, sleep apnea (central or obstructive), and narcolepsy. Patients may not complain of sleepiness so much as its consequences, including fatigue, headaches, decreased energy, difficulty concentrating, irritability, or an auto accident (“falling asleep at the wheel”).
A. Insufficient sleep – Many people do not schedule sufficient time for sleep at night, and sleepiness is to be expected in the setting of sleep deprivation. This is managed by education the patient about healthy sleep habits.
B. Sleep apnea : Sleep apnea is a condition in which patients periodically stop breathing while asleep. There are two types of sleep apnea- central and obstructive. The most common cause of sleep apnea is due to temporary obstruction of the upper airway. The extreme changes in the concentrations of oxygen and carbon dioxide in the blood that develop after 1 minute or more without air rouse the sleeper, and a few noisy, choking gasps refill the lungs. Obstructive sleep apnea is the most common medical cause of excessive daytime somnolence. Of major importance to the diagnosis is a history of apneic episodes during sleep. Usually the patients are not aware of the episodes because they are brief and arousal is only partial, so the history must be obtained indirectly, typically from a spouse or roommate. Symptoms/signs that are common include loud snoring and pauses in breathing. Additional symptoms include gasping for breath during sleep, dull headaches, and automatic behaviors. Polysomnography is used to confirm the diagnosis and to quantify the severity. The most effective treatment of obstructive sleep apnea (beneficial in over 90% of cases) is nasal continuous positive airway pressure (nasal CPAP), which raises the pressure in the oropharynx, and thus in the upper airway, reversing the pressure gradient across the wall of the airway and propping it open.
C. Narcolepsy : Narcolepsy is a syndrome consisting of excessive daytime sleepiness and disordered regulation of REM sleep, resulting in intrusion of components of REM sleep into NREM sleep and the waking state.
Hypocretin deficiency (demonstrated by low CSF hypocretin-1 levels) is the cause of most narcolepsy-cataplexy cases in animals and humans. Autopsy studies have shown a selective loss of posterior hypothalamic neurons that produce the neuropeptide hypocretin (orexin). (Hypocretins (orexins) are synthesized in the hypothalamus with widespread projections, especially to brainstem nuclei containing norepinephrine, histamine, serotonin and dopamine neurons. Hypocretin neurons integrate metabolic and sleep- and wake-related inputs. ) Additional models hypothesize hyperactivity in the cholinergic system with hypoactivity in the catecholaminergic system.
D. Idiopathic hypersomnia disorders are poorly defined conditions characterized by excessive daytime sleepiness and not diagnosed as narcolepsy (no REM abnormalities during the MSLT).
II. INSOMNIA (Trouble sleeping) : Many different physiological and psychological factors can interfere with sleep. The objective in patient evaluation is to identify the contributing factors and treat those for which therapy is available. Patients with primary insomnia have been shown to have less diurnal sleepiness, higher heart rates, higher core body temperature, and greater metabolic activity than age and gender matched controls. The most severe case of primary insomnia has an insidious onset during childhood and follows a chronic course. It is useful to identify three main patterns of insomnia: sleep-onset delay (trouble falling asleep), early morning arousal (trouble staying asleep), and sleep fragmentation (repeated awakenings). Only one type of sleep-onset delay is described below.
A. Sleep-Onset Delay due to psychophysiologic insomnia: This may be due to anxiety related to life stressors or to depression. Any conditions associated with physical discomfort can also contribute. B. Restless legs syndrome : Restless legs syndrome (RLS) is a sensorimotor disorder often severely affecting sleep, characterized by a strong urge to move the legs accompanied by a strange feeling in the leg; episodes are precipitated by rest with inactivity and the episodes and worse in the evening or night than in the morning. The periodic leg movements (PLM) may occur during sleep (PLMS) and/or while lying or sitting up awake (PLMW). RLS involves a disorder of the transition states between wake and sleep. Although RLS produces chronic loss of sleep, there is no profound frank sleepiness in the daytime. RLS patients report fatigue and trouble concentrating during the day, but do not fall asleep and appear to be overstimulated in the daytime. Early-onset RLS (starting before age 45) appears to result mostly from a pervasive iron metabolism abnormality producing brain iron insufficiency. The impaired iron status produces a hyperdopaminergic state with an exaggerated circadian pattern of DA release. The iron deficiency probably also disrupts other neurotransmitter systems, such as hypocretin (orexin) and histamine. Late-onset RLS (starting after age 45) has more diverse causes, but patients appear to have DA abnormalities similar to those in early-onset RLS cases. RLS etiology appears to have both a genetic and a strong environmental component, with the genetic component more import for early- than for late-onset RLS. The pathogenesis probably involves abnormalities in subcortical CNS dopaminergic systems, with DA receptor dysfunction and increased DA production. Dopaminergic agonists and levodopa provide effective treatment for RLS. The pathophysiology may involve iron
2. Nightmare disorder (Dream Anxiety): This condition consists of repeated awakenings with detailed recall of extended and very frightening dreams. The awakenings are more frequent in the second half of the sleep period. On awakening, the person rapidly becomes alert and oriented.
Comorbidity with Psychiatric Disorders: Sleep and psychiatric disorders are highly comorbid with the highest rates being with anxiety and depression. Studies suggest that the presence of a sleep disturbance may delay recovery from depression. Many antidepressant medications, particularly SSRI’s have been found to improve sleep disturbances in addition to relieving depressive symptoms.
References Bonnet, MH., Arand, DL. (1995). 24 hour metabolic rate in insomniacs and matched normal sleepers. Sleep , 18 , 581-588. Gelb, D.J., Introduction to Clinical Neurology. Boston: Butterworth-Heinemann, 1995. Guilleminault, C. (1989). Clinical features and evaluation of obstructive sleep apnea. In Eds. MH Kryger, T. Roth, & WC Dement (Eds.), Principles and practice of sleep medicine ( pp552-558). Philadelphia: W.B. Saunders Kandel, E.R., Schwartz, J.H., Jessell, T.M., Principles of Neural Science. McGraw-Hill, 2000. Andreason and Black, Introductory Textbook of Psychiatry, Ch. 23: Sleep Disorders, pp. 593-613. Lorenzo, JL. And Barbanjo, MJ. (2000). Monoaminergic selectivity of antidepressive drugs and sleep: neurophysiological implications of depression. Reviews of Neurology , 30: 191- Taheri S, et al., The role of hypocretins (orexins) in sleep regulation and narcolepsy. Ann Rev Neurosci 25:283, Schenck, CH, Mahowald, MW, "REM Sleep Behavior Disorder, in Neurobiology of Disease , S. Gilman, ed, Elsevier 2007 Allen, RP, "Restless Legs syndrome and periodic limb movements in sleep" in Neurobiology of Disease , S. Gilman, ed, Elsevier 2007 Mignot E, Zeitzer JM, "Neurobiology of Narcolepsy and Hypersomnia", in Neurobiology of Disease ,S Gilman, ed, Elsevier
Practice questions
A. The number of afternoon naps decreases B. The amount of stage 4 slow-wave sleep increases C. The total sleep time per day increases markedly D. The percentage of REM sleep decreases
A. REM sleep parasomnia B. NREM sleep parasomnia C. hypersomnia D. insomnia
A. the patient has a sleep-onset REM cycle B. muscle atonia does not occur during REM sleep C. the patient shows only stage 4 sleep D. the patient has frequent apneic episodes during sleep
A. brainstem cholinergic systems B. cortical noradrenergic systems C. subcortical dopamine systems D. cortical GABA systems
A. globus pallidus B. pontine tegmentum C. putamen D. inferior olive
A. high voltage, slow EEG pattern B. paralysis of ocular muscles C. muscle atonia in limbs D. occurs immediately after the first episode of Stage 1 sleep