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SLEEP AND THINKING, MOVING, AND FEELING

SLEEP AND THINKING, MOVING, AND FEELING. Andrew A. Monjan, Ph.D., M.P.H. Chief, Neurobiology of Aging Branch Neuroscience and Neuropsychology of Aging Program National Institute on Aging. BOTTOM LINES. Strong body of data directly interrelating sleep problems with mood disorders

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SLEEP AND THINKING, MOVING, AND FEELING

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  1. SLEEP AND THINKING, MOVING, AND FEELING Andrew A. Monjan, Ph.D., M.P.H. Chief, Neurobiology of Aging Branch Neuroscience and Neuropsychology of Aging Program National Institute on Aging

  2. BOTTOM LINES • Strong body of data directly interrelating sleep problems with mood disorders • Growing data base directly associating sleep disorders with attention and memory problems; cognitive-based therapies improve sleep, and cognitive states may produce disordered sleep • Motor disorders, especially involving the dopaminergic system, may produce sleep disorders; possible association between sleep problems and falls • Sleep and health are directly interrelated

  3. Prevalence of five chronic sleep complaints among elderly men and women Men Women Percent Source: Foley, Monjan, Brown et al. SLEEP 18:425-432, 1995

  4. Prevalence Estimates of Sleep Problems in the Elderly Chronic Sleep Problem Prevalence Any Sleep Complaint 57% Sleep Apnea 24% PLMS 45% RLS 11% Insomnia 29% Early Morning Awakening 19% Ancoli-Israel, et al., 1991; Foley, et al., 1995; Phillips, et al., 2000

  5. INSOMNIAPrevalence by Age Group Percent Age Group Mellinger, et al., 1985; Foley, et al., 1995

  6. INSOMNIAPercent Prevalence and Incidence Percent Foley, et al.,1995;1998

  7. Late Age Sleep Architecture* Middle Age Sleep Architecture1 Stage 1 (5%) Stage 1 7%) REM (16%) REM (25%) Stage 3/4 (9%) Stage 2 (45%) Stage 3/4 (25%) Stage 2 (68%) n=718 1Source: Ancoli-Israel, 1996 *Foley, et al., 2002

  8. NEUROBIOLOGICAL MODEL OF SLEEP FRAGILITY IN LATE-LIFE Cortex (esp. PFC) Cingulate Thalamus Basal Forebrain, Post. Hypothal, Amygdala, Hippocampus Ant. Hyp ARAS Nofzinger, et al.

  9. PROJECTIONS OF THE VENTROLATERAL PREOPTIC NUCLEUS (VLPO) INHIBITING AROUSAL SYSTEMS Sapir, et al., 2001

  10. INFLAMMATORY PATHWAYS MODULATING SLEEP Bryant, et al., 2004

  11. Percent of Adults Who Usually Slept 6 Hours or Less a Night, by Sex and Age: United States, 1985 and 2004 Men Women National Health Interview Survey

  12. NSF, 2003

  13. 2003 Sleep in America PollMethodology Telephone survey of 1,506 adults aged55 to 84 living in the continental USA About 23% of qualified persons agreed to participate Conducted by WB&A Market Research between September 17 and December 10, 2002 Margin of error: no more than + 2.5% for the entire sample Up to 5.6% for sub sample comparisons NSF, 2003

  14. Reported Hours Slept – Older Vs. Younger American Adults NSF, 2003

  15. Sleep Problems and Depression * * NSF, 2003; Foley, et al., 2004

  16. Sleep Problems and Heart Disease * * NSF, 2003; Foley, et al., 2004

  17. Sleep Problems and Lung Disease * * * NSF, 2003; Foley, et al., 2004

  18. Sleep Problems and Stroke * NSF, 2003; Foley, et al., 2004

  19. Sleep Problems and Multiple Medical Conditions NSF, 2003

  20. Insomnia in Older Americans Symptoms Vs. Diagnosis Vs. Treatment Percent _ _ _ National Sleep Foundation, 2003

  21. Sleep Problems and Exercise NSF, 2003

  22. 2003 Sleep in America PollSummary Findings Older adults report getting same amount of sleep as do younger adults Sleep problems in older adults are associated with medical illness, rather than aging per se Individuals with multiple medical problems have a particularly high risk of sleep problems Bodily pain, exercise frequency, ambulatory limitation, and obesity are related to sleep problems in older adults NSF, 2003

  23. Overweight and Obesity National Health Interview Survey

  24. Measured Obesity among People age 65+ Percent Source: National Health and Nutrition Examination Survey, selected years

  25. Sleep Problems and Overweight (Body Mass Index) * * NSF, 2003; Foley, et al., 2004

  26. Implications of short sleep for glucose regulation Environmental/Behavioral Genetic Factors Factors: • Poor Diet • Sedentary Lifestyle • Normal Aging • Chronic Stress • Sleep Loss Insulin Resistance METABOLIC SYNDROME TYPE 2 DIABETIES Van Cauter

  27. GLUCOSE TOLERANCE Kg derived from glucose disappearance curve during IVGTT CLINICAL SIGNIFICANCE 18-27 yr old subjects fully rested 2.40 ± 0.41 18-27 yr old subjects in sleep debt 1.45 ± 0.31 Kg (% per min) Kg (% per min) 21-30 yr old fit subjects (2) Range: 2.20 - 2.90 61-80 yr old adults with impaired glucose tolerance (1) Range: 1.30 - 2.10 (1) from Garcia et al, J Am Geriatr Soc 45: 813-7, 1997. (2) from Prigeon et al, Metabolism 44: 1259-63, 1995. Courtesy of Eve Van Cauter

  28. 45 40 16 +/+ 14 35 Body Weight (g) Clock/Clock 12 30 10 8 10 Week Weight Gain (g) 25 6 4 20 2 Regular High Fat 0 1 2 3 4 5 6 7 8 9 10 Weeks on Diet +/+ Clock/Clock Reg (n=8) Reg (n=9) Fat (n=7) Fat (n=11) Metabolic Phenotypes of the Clock mutant model Turek & Bass, 2006

  29. Function Glucose tolerance Insulin sensitivity C-reactive protein Cardiac sympathetic activity Plasma norepinephrine Evening cortisol levels Plasma TSH levels Plasma leptin levels Mood Vigilance Subjective alertness Sleep Loss Aging SIMILARITIES BETWEEN SLEEP LOSS AND AGING Van Cauter

  30. Sleep Problems and Bodily Pain * NSF, 2003; Foley, et al., 2004

  31. SLEEP AND PAINStudy Design • Subjects meeting diagnostic criteria for co-morbid OA and chronic insomnia were randomized to either: • Standard CBT-I (Eight 2-hour sessions). • Stress Management and Wellness (SMW) intervention. • Neither intervention specifically mentioned pain management; although SMW contained components typically included in behavioral pain interventions. • Problem-solving, goal setting, cognitive approaches to reducing stress and anxiety, interpersonal skills training, and exercise enhancement Vitiello, et al., 2007

  32. Study Design • Subjective sleep quality (two-week log) and self-reported pain (MPQ and SF-36P) were assessed pre and post-treatment for CBT-I and SMW. • CBT-I, but not SMW, subjects were assessed again at one year. • Ten SMW subjects crossed over to CBT-I treatment and were followed up at one year. Vitiello, et al., 2007

  33. Vitiello, et al., 2007

  34. Conclusions • CBT-I improved both immediate and long-term self-reported sleep quality in this sample of older OA patients with co-morbid insomnia. The observation of CBT-I’s long-term impact on sleep in this co-morbid sample is a new finding. • CBT-I, without specifically addressing pain management, reduced both immediate and long-term reported pain in these OA patients. • SMW failed to reduce pain despite containing several components typically included in effective behavioral interventions for management of chronic pain. Vitiello, et al., 2007

  35. Prevalence Rates Of Sleep Disturbances InPersons With Dementia And Their Family Caregivers McCurry, et al. Sleep Medicine Reviews, 2007

  36. SLEEP AND COGNITION (1) • A number of research studies, both cross-sectional and longitudinal, have shown that disturbed sleep has a negative impact on cognitive functioning and quality of life. • Both animal and human studies especially implicate sleep as important for the process of memory consolidation following initial learning. • Many studies have demonstrated the benefit of sleep on the acquisition of a motor skill, with the greatest improvements in recall following the interval in which sleep had occurred (amount of overnight improvement correlated with the amount of NREM and REM sleep experienced), indicating that performance improvements are specifically related to sleep processes.

  37. SLEEP AND COGNITION (2) • It has been proposed that age-related changes in sleep patterns may be linked to changes in the glucocorticoid system, including the hippocampus, which occur with age. • In animal studies, sleep deprivation interferes with the encoding of hippocampal-mediated tasks (even 5-hours of pre-training deprivation disrupts the encoding of avoidance learning). • At the cellular level, sleep deprivation reduces the basic excitability of hippocampal neurons as well as significantly impairing long-term potentiation.

  38. SLEEP AND COGNITION (3) • Thus, there has accumulated a sufficient base of data and converging lines of evidence to suggest that sleep loss associated with aging may be a contributing factor to some of the cognitive decline commonly seen in later life, as well as being a comorbid condition contributing to other metabolic, medical, and behavioral conditions in aging populations.

  39. SOME CONSEQUENCES OF DISORDERED SLEEP IN THE AGING POPULATION • Excessive daytime sleepiness • Attention and memory problems • Depressed mood • Nighttime falls • Overuse of hypnotic drugs and OTC medications • Possible adverse interactions with co-morbid conditions, e.g. sleep apnea and CVD • Lowered quality of life • Metabolic dysfunction

  40. Evidence for Co-Occurrence Cognitive Disability EmotionalDisability Sleep Disorder PhysicalDisability Adapted from Anne Newman

  41. Questions for the Future • What constitutes normal and optimal sleep in the elderly? • Are there different causal mechanisms or co-factors with onset of sleep disorders late in life than earlier in life? • Can sleep loss can increase the stress load, possibly facilitating the development of chronic conditions, such as obesity, diabetes, and hypertension, which have an increased prevalence in low SES groups? • What interventions and therapies are most effective and appropriate for the older population?

  42. Further Questions for the Future • What are the brain mechanisms underlying age-dependent changes in sleep? • What are the relationships between sleep and cognitive functioning in later life? • Are there relationships between sleep, nocturia, and falls? • How does sleep affect aging and disease, and, conversely, how do aging and disease affect sleep?

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