Sleep from the Inside Out
Transcription
Sleep from the Inside Out
Sleep from the Inside Out Disclaimer Appendix 3 Declaration of Vested Interest Form Name of presenter: Heather Murgatroyd , RRT, RPSGT Name of employer: DeVilbiss Healthcare Definition: A presenter may have an interest in or affiliation with an organization, which does not prevent him or her from making a presentation, however, the audience must be informed of this relationship before the presentation of the activity. For this purpose a real or apparent conflict of interest is defined as having a significant financial interest in a product to be discussed directly or indirectly during the presentation; being or having been an employee of a company with such financial interest and/or having had substantial research support by an industry to study the product to be discussed at the presentation. I recognize that I must follow all guidelines and criteria regarding vested interest. [ ] No, I have no real or perceived conflicts of interests that relate to this presentation. (If the response is no, stop here.) [ x ] Yes, I have the following real or perceived conflicts of interest that relate to this presentation: Describe real or perceived conflicts of interest that relate to this presentation I am an employee of DeVilbiss Healthcare and we manufacture respiratory home care equipment. My presentations are not product specific but relate to the principles involved in best utilizing certain technologies in the home environment. Objectives • Define diabetes and how to diagnose. Discuss diabetes and related conditions in relation to Sleep Disordered Breathing. • Define Inflammation and the various markers as related to Sleep Disordered Breathing. • Identify various hormones, their functions, abnormalities and how they relate to Sleep Disordered Breathing. What is Diabetes? A group of diseases marked by high blood glucose • Type 1 – (previously called juvenile diabetes) the body does not produce insulin, the immune system destroys the cells in the pancreas that produce insulin, typically diagnosed in childhood or young adulthood, 5% of all diagnosed diabetes, no known prevention • Type 2 – most common type, 90-95% of cases, body does not produce enough insulin or does not utilize the insulin produced • Gestational – occurs during pregnancy when a non-diabetic woman develops high blood sugar levels, 2-10% of pregnancies http://www.cdc.gov/diabetes/pubs http://www.diabetes.org/diabetes-basics Important Terms • • • • Insulin - a hormone that helps the body use glucose for energy. The beta cells of the pancreas make insulin. People with Type 1 diabetes must take insulin via injection or pump. Glucose - one of the simplest forms of sugar. Blood Glucose - the main sugar found in the blood and the body's main source of energy. Also called blood sugar. A1c – measures average blood glucose for past 2-3 months. Glucose binds to hemoglobin and the amount is proportional to the amount of glucose in the blood. Normal is about 5%. Measuring A1c shows history of blood sugar control. Poorly controlled may show 15% or higher. http://www.diabetes.org/diabetes-basics Type 2 Diabetes Symptoms – • • • • • • • • • • Frequent urination Unusual thirst Extreme hunger Unusual weight loss Extreme fatigue and Irritability Frequent infections Blurred vision Cuts/bruises that are slow to heal Tingling/numbness in the hands/feet Recurring skin, gum, or bladder infections http://www.diabetes.org/diabetes-basics Diagnosing Type 2 Diabetes A1c – blood draw, detects Type 2 and prediabetes, does not require fasting – can be done anytime Fasting plasma glucose test – blood draw, detects diabetes and pre-diabetes, must fast 8 hours prior, most reliable if done in a.m., Oral glucose tolerance test – detects diabetes, pre and gestational, sensitive, must fast 8 hours then drink 75g of glucose dissolved in water and fast an additional 2 hours Random plasma glucose test – blood draw from non-fasting person, values are higher due to assumed meal All tests are not done but a second test must be done to confirm if there are not additional clear symptoms of diabetes Diabetes Care. 2012;35(Supp 1):S12 Complications of Diabetes • • • • • • • • • High blood pressure Heart Disease Stroke Blindness Kidney disease Neuropathy Amputation Dental disease Depression http://www.diabetes.org/diabetes-basics http://www.cdc.gov/diabetes/pubs Cost of Diabetes for 2012 (updated 3/13) • $245 billion: Total costs of diagnosed diabetes in the United States in 2012 • $176 billion for direct medical costs • $69 billion for indirect costs (disability, work loss, premature mortality) http://www.diabetes.org/diabetes-basics Adults 18 years and older • 45-64 age group – 118% increase of diabetes diagnosis – 5.5% to 12.0% Source: 2007–2009 National Health Interview Survey estimates projected to the year 2010. Diabetes is a big deal (2010) • There are 25.8 million people in the United States, or 8.3% of the population, who have diabetes. • Medical expenses are 2 times higher for people with diabetes then for people without. • Diabetes is the 7th leading cause of death in the United States • A person with diabetes is about twice more likely to die then someone else the same age without diabetes. http://www.diabetes.org/diabetes-basics http://www.cdc.gov/diabetes/pubs • We work in Sleep and Respiratory… • Why are we talking about this? Glucose Metabolism • There is an established association between altered glucose metabolism and SDB • What is the mechanism? - Increased sympathetic nervous system activity resulting from intermittent hypoxia, sleep fragmentation and sleep loss – the body releases glucose but does not properly clear it and does not release proper insulin to process. http://journal.publications.chestnet.org/article.aspx?articleid=1085691 • Hypoxemia has been shown to impair glucose metabolism • As the severity of SDB increases there is an association to poor glucose control • Reduced slow wave sleep is associated with poor glucose control • In patients who participated in voluntary sleep deprivation studies, it was shown that is an association between abnormal glucose tolerance and sleep deprivation http://www.journalsleep.org/ViewAbstract.aspx?pid=28399 Insulin Resistance • Maybe part of the Metabolic Syndrome (commonly present) • Precedes T2DM • Condition in which the cells become resistant to a given amount of insulin • More insulin is needed for proper effects • Pancreas produces more to meet the body’s demand and eventually cannot produce enough http://www.medicinenet.com/insulin_resistance/article.htm Islets of Langerhans in the pancreas, where insulin is produced Insulin Resistance and CPAP • Sleep deprivation results in insulin resistance in healthy subjects – which resolves after recovery sleep* • Several studies show treatment with CPAP improves insulin resistance Weinstock et al. studied 50 patients with impaired glucose tolerance and moderate-severe OSA. Results showed participants with severe OSA (> 30/h) had improvement of insulin sensitivity tests after 2 months vs. those receiving sham CPAP. However, improvement was not as significant with less severe OSA patients. Sharma et al. studied 86 patients, (75 with metabolic syndrome) with moderate-severe OSA on CPAP for 3 months and showed a reduction in HbA1C vs those receiving sham CPAP. *SLEEP, Vol. 35, No. 5, 2012 Metabolic Syndrome (aka Syndrome X) • Group of risk factors that occur together • May increase risk of T2DM and coronary artery disease and stroke • Risk factors: ‒ ‒ ‒ ‒ ‒ ‒ Central obesity Insulin resistance aging Lack of exercise genetics Hormone changes http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0004546/ Metabolic Syndrome Having 3 or more of the following: • • • Blood pressure 130/85 mmHg or higher Fasting blood sugar/glucose 100 mg/dl or higher Waist circumference of ‒ ‒ • Low HDL cholesterol ‒ ‒ • 40 + inches for men 35 + inches for women Under 40 mg/dl for men Under 50 mg/dl for women Triglycerides of 150 mg/dl or higher http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH000454 Metabolic Syndrome and SDB • Some discussion of adding OSA to the features of Metabolic Syndrome and calling it “Syndrome Z” • Metabolic Syndrome and OSA have multiple overlapping characteristics • A study by the National Cholesterol Education Program identified in the Adult Treatment Panel III report that Metabolic Syndrome is approximately 40% greater in patients diagnosed with OSA Kostoglou-Athanassiou and Athanassiou. Metabolic syndrome and sleep apnea. 2008. • Sleep disordered breathing may influence the sympathetic nervous system and catecholemine release which may stimulate gluconeogenesis leading to hyperinsulinemia WHAT??!! • When a person has SDB causing arousals, this triggers the “fight or flight” response, which in turn stimulates new glucose production and release causing increased insulin in blood. What can Hyperinsulinemia cause? • High triglycerides (increased risk of heart and stroke) • High plasminogen activator inhibitor activity (PAI-Fx), causing increased risk of clotting • Low HDL cholesterol (increased risk of heart attack and stroke) • High uric acid (gout) • Polycystic ovary syndrome (endocrine disorder with oligoamenorrhea, infertility, hirsutism, obesity, high Leptin levels) • Type 2 diabetes • Obesity • High insulin can also stimulate the kidney to produce angiotension, a substance which increases blood pressure http://www.jewishhospitalcincinnati.com/cholesterol/Research/insulin_resistance.html Diabetes & Sleep Disordered Breathing • Five studies – found 58% - 86% obese diabetic patients also have OSA • Increase severity of OSA associated with increased A1c levels* • Habitual snoring males, whether or not obese, are at greater risk of developing Type 2 Diabetes as compared to non-obese males without habitual snoring or obese males without habitual snoring** *http://www.frontiersin.org/Sleep_and_Chronobiology/10.3389/fneur.2012.00126/full **The role of habitual snoring and obesity in the development of diabetes: a 10-year follow-up study in a male population. Journal of Internal Medicine, 2000;248:13-20 Diabetes & Sleep Disordered Breathing In the Sleep Heart Health Study looking at diabetic participants (DP) vs. non-diabetic participants (NDP), Diabetic participants were observed to have: • • • • Higher overall RDI Lower O2 levels Less time in NREM 3 More time in NREM 1 and 2 Data from the SHHS continues to support the relationship of obesity with both SDB and T2DM. The importance of addressing obesity for patients with either condition is important in the role SDB plays in the exacerbation of cardiovascular disease. Diabetes Care, Vol 26, No 3, March 2003. Diabetes & Sleep Disordered Breathing • In children (5-11) with Type 1 diabetes a study showed more frequent and longer apneas, particularly centrals, when compared to children without T1DM • Youths with diabetes spent less time in N3 and longer periods in N2 then youths without diabetes • PTs with poorly controlled diabetes were shown to have more frequent and longer apneas then those with well controlled diabetes and control subjects Does CPAP help? • Limited research on how treating SDB improves insulin sensitivity and no research on how treating SDB for the prevention of T2DM • Does treatment of OSA help prevent, delay, slow the progression, reduce the severity of Type 2 diabetes, or improve impaired glucose tolerance (also called “prediabetes”)? ‒ ‒ For patients with mild/moderate sleep apnea and obesity – NO For patients with severe sleep apnea YES There are mixed results from studies as they have typically been small studies and done with limited controls A Controlled Trial of CPAP Therapy on Metabolic Control in Individuals with Impaired Glucose Tolerance and Sleep Apnea. Sleep, Vol. 35, No. 5, 2012 Does CPAP help? “Amongst diabetics with sleep breathing disorders, improvement of insulin responsiveness or glycaemia during continuous positive airway pressure (CPAP) treatment has been reported even without a significant change of obesity.” CHEST. 2008;133(2):496-506. doi:10.1378/chest.07-0828 Does CPAP help? Studies show – • Harsch et al. - CPAP on non-diabetic patients improved insulin sensitivity index as quickly as 2 days after start of treatment. • Babu et al. - Reductions in HbA1c almost immediately in patients with abnormally high baselines once on CPAP. Also showed patients with >4 hour/day compliance had reductions in HbA1c which correlated with hours of CPAP use. Levy,P. Bonsignre, MR and J. Eckel. Sleep, sleep-disordered breathing and metabolic consequences. European Respiratory Journal. Vol. 34, No 1. 2009. Does CPAP help? • Lindberg et al. showed reductions in fasting insulin levels and insulin resistance after 3 weeks of CPAP therapy when compared to matched controls not using CPAP. • Weinstock et al. showed that for severe OSA patients (AHI >30/h) active use of CPAP improved insulin sensitivity index from baselines. http://journal.publications.chestnet.org/article.aspx?articleid=1085691 CPAP Therapy and Glucose Control in Sleep Apnea—Weinstock et al SLEEP, Vol. 35, No. 5, 2012. Does CPAP help? Due to conflicting study reports regarding the benefits of CPAP on T2DM, glucose metabolism, insulin resistance, Metabolic Syndrome It is important to know how studies are being conducted. Does CPAP help? Challenges for many of the studies– • Small sample sizes • Limited durations • Obesity role in both T2DM and OSA • Conflicting study results may support that CPAP has a positive effect on some, not all, components of IR, Syndrome X, glucose metabolism Diabetes and sleep deprivation • • • Slow Wave Sleep deprivation also effects glucose tolerance and insulin resistance. In healthy subjects with normal total sleep time but reduced slow wave sleep resulted in decreased insulin sensitivity. There should be an increase in insulin release to compensate, yet this was not seen. As we age, we spend less time in SWS. Could this possibly contribute to the development of T2DM in the elderly? http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2242689/ Inflammation: • Is the body’s response to a harmful stimuli, the means of removing it and start the healing process • Can be acute or chronic • Acute inflammation begins immediately upon injury, lasts a few days and either resolves or becomes… Chronic Inflammation • May last months or years • Is destructive, resulting in tissue damage, fibrosis and necrosis • Many disorders considered to have an inflammatory process: arthritis, acne, sarcoidosis, asthma, colitis • “itis” = inflammation http://en.wikipedia.org/wiki/Inflamation Obesity, OSA and Inflammation • Obesity along with OSA is a strong determinant of systemic inflammation. • Many adipokines (cell messengers) are released by adipose tissue and are linked to inflammation. Obesity increases their production = increased inflammation. • There are synergistic negative effects of OSA and obesity regarding inflammation – more research is needed. Levy,P. Bonsignre, MR and J. Eckel. Sleep, sleep-disordered breathing and metabolic consequences. European Respiratory Journal. Vol. 34, No 1. 2009. Inflammation and OSA • Repetitive hypoxia and re-oxygenation leads to oxidative stress • Oxidative stress is an imbalance which prevents cells from communicating properly. This affects basic functions such as tissue repair and immunity and may result in the development of diseases such as cancer and diabetes. Levy,P. Bonsignre, MR and J. Eckel. Sleep, sleep-disordered breathing and metabolic consequences. European Respiratory Journal. Vol. 34, No 1. 2009. Oxidative Stress and OSA Oxidative Stress is reported to be linked to: • Neurodegenerative diseases • Cardiac diseases • Age-related cancer development • Contribute to aging How is OSA a factor? The repetitive reoxygenation after apneic events may cause a cascade of cell dysfunction contributing to oxidative stress. SLEEP, Vol. 30, No. 3, 2007 • Hypoxia in adipose tissue may cause an inflammatory response - the release of inflammatory adipokines • Growing evidence that hypoxia plays a strong role in gene response and function. Obesity + SDB + Hypoxia = CHRONIC INFLAMMATION Levy,P. Bonsignre, MR and J. Eckel. Sleep, sleep-disordered breathing and metabolic consequences. European Respiratory Journal. Vol. 34, No 1. 2009. Markers of Inflammation • C-reactive protein (CRP) is a biomarker of any inflammation – CPAP has successfully decreased Creactive levels in OSA patients, but did not change in non-obese OSA patients • Short bouts of short sleep duration cause an acute increase in CRP, studies have not shown if there are long-term risks to chronic short sleep duration • Habitual long sleep time (>9 hours) causes an increase in CRP Etzionin, Tamar and Giora Pillar, Sleep, sleep apnea, diabetes and the metabolic syndrome: the role of treatment. SLEEP, Vol. 35, No. 5, 2012. CRP, OSA and Sleep • CRP levels are elevated in OSA patients, particularly moderate – severe OSA • Increased CRP levels correlate with more severe hypoxia, higher day time sleepiness, greater obesity • Within one month of treatment of nasal CPAP, CRP levels decrease http://circ.ahajournals.org/content/107/8/1129.full Markers of Inflammation • Interleukin 6 (IL-6) is a cytokene – relays messages between cells • IL-6 is released in response to burns, trauma, infection • IL-6 enhances the immune system and protects against tissue damage • Too much or too little IL-6 can causes systemic problems – autoimmune disease, malignancies http://www.bio.davidson.edu/Courses/Immunology/Students/Spring2003 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078635/ IL-6, OSA and Sleep • Habitual longer sleep duration (>9 hours) is related to increased IL-6 levels • Sleep deprivation may also increase IL-6 levels – as seen in patients with OSA • Elevated IL-6 is associated with OSA • IL-6 is increased in the upper airway tissue of patients with severe OSA vs mild OSA • Noctural hypoxia is associated with increase production of IL-6 • After 1 month of nasal CPAP, IL-6 levels decreased in one study, another study showed no significant difference after 6 months of good CPAP use http://www.bio.davidson.edu/Courses/Immunology/Students/Spring2003 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078635/ http://circ.ahajournals.org/content/107/8/1129.full Markers of Inflammation • • • • Tumour necrosis factor (TNF-a) is a cytokene – which are important in the regulation of inflammation TNF-a is one of 19 related cytokenes Short sleep duration is directly related to increasing TNF-a levels Partial sleep deprivation for a single night may cause increased THF-a Arnardottir ES; Mackiewica M; Gislason T; Teff KL; Pack Al. Molecular signatures of obstructive sleep apnea in adults: A review and perspective. SLEEP 2009; 32(4): 447-470. TNF-a, OSA and Sleep • See rapid increases in plasma levels of TNF-a following apneic events • TNF-a levels decrease with the application of CPAP • Hours of CPAP use correlate with decrease levels of TNF-a Arnardottir ES et al. Molecular signatures of obstructive sleep apnea in adults: A review and perspective. SLEEP 2009;32(4):447-470. Steiropoulos P et al. Long-term effect of continuous positive airway pressure therapy on inflammation markers of patients with obstructive sleep apnea syndrome. SLEEP 2009;32(4):537-543. A = good complaince > then 4hours per night B = poor complaince < then 4hours per night OSA • Patients with OSA have been shown to have increased levels of TNF-a, CRP and IL-6* • Successful use of CPAP has been shown to decrease the levels of these inflammatory markers* • Note – successful use is not clearly defined • Results are from compliant patients wearing CPAP for 6 months and had no change in BMI Steiropoulos P; Kotsianidis I; Nena E; Tsara V; Gounari E; Hatzizisi O; Kyriazis G; Christaki P; Froudarakis M; Bouros D. Long-term effect of continuous positive airway pressure therapy on inflammation markers of patients with obstructive sleep apnea syndrome. SLEEP 2009;32(4):537543. A = good complaince > then 4hours per night B = poor complaince < then 4hours per night Inflammatory Markers and Weight • Large weight loss (example greater then 40 lbs) successfully reduces some of the inflammatory markers in obese patients – either through traditional diet/exercise or from bariatric surgery, (CRP and IL-6) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2802719/ Hormones • Hormones are chemical messengers in the body. They are sent out by a cell or gland and travel in the body, often in the blood, until they find a receptor cell. • Hormones affect: growth, mood, immunity, metabolism, puberty, reproduction, sexual arousal, hunger/cravings, body’s fight or flight response. There are more then 65 hormones in human body Familiar ones: • Testosterone • Cortisol • Orexin • Epinephrine • Norepinephrine • Melatonin • Dopamine • Insulin • Serotonin • Ghrelin • Leptin • Inhibin • Oxytocin Serotonin • Regulates mood, emotion, sleep, memory, learning and muscle contraction • Produced in brain (90%+) and gut (2%) • Low Serotonin can result in: ‒ ‒ ‒ ‒ Depression Increased pain Irritability SLEEP problems (insomnia, staying asleep) ‒ Constant fatigue http://www.serotoninsyndrome.org/Basics/what-is.html Serotonin and Sleep • Serotonin helps initiate sleep and regulate sleep • Low levels of serotonin may increase sleep onset and effect deep sleep • Serotonin uptake inhibitors, such as paroxetine (paxil), have been show to decrease AHI in NREM sleep* • Mixed-profile serotonin drugs, such as mirtazapine (remeron), have been shown to decrease AHI – however weight gain and sedation are known side-effects of medication so it is not recommend for treatment of OSA** *Effect Of Serotonin Uptake Inhibition On Breathing During Sleep And Daytime Symptoms In Obstructive Sleep Apnea Holger Kraiczi,1 Jan Hedner,1,2 Pia Dahlöf,3 Hasse Ejnell,4 and Jan Carlson 2 Sahlgrenska University Hospital, S 413 45 Göteborg, Sweden **Efficacy of Mirtazapine in Obstructive Sleep Apnea SyndromeDavid W. Carley. PhD1-3; Christopher Olopade, MD2; Ge S. Ruigt, PhD4; Miodrag Radulovacki, MD,PhD2-3 University of Illinois at Chicago, Chicago, IL; 4Translational Research Department, NV Organon, Oss, The Netherlands Serotonin and OSA • Serotonin release stimulates upper airway muscle activity via the hypoglossal nerve. • Withdrawal of serotonin causes atonia in the hypoglossal nerve causing a reduction in upper airway patency • OSA, particularly in REM, is resistant to serotonin therapy* Serotonin uptake inhibition in sleep apnea—Kraiczi et al SLEEP, Vol. 22, No. 1, 1999 *Tonic Respiratory Activity in Sleep and Wakefulness—Orem et al SLEEP, Vol. 25, No. 5, 2002 Can serotoninergic agents treat OSA? A review of various therapies for treatment of OSA found in regards to serotoninergic agents: Study 1 – 20mg of fluoxetine (prozac) for 4 weeks reduced AHI in participants, but not to a statistically significant degree and did not change the number of desaturations. Study 2 – studied the effects of single dose of paroxetine (paxil) on AHI and geneioglossus muscle activity. Found no effect of single dose paroxetine on AHI, but it did increase muscle activity. Study 3 – studies 6 weeks of paroxetine therapy which did result in statistically significant changes in AHI with decreased AHI in NREM sleep and no change in AHI in REM. Overall, did not improve participants subjective sleepiness A Review by Veasey SC, Guilleminault C, Strohl KP et al. Medical therapy for obstructive sleep apnea: a aeview by the medical therapy for obstructive sleep apnea task force of the standards of practice committee of the american academy of sleep medicne. SLEEP 2006;29(8):1036-1044. Ghrelin (discovered in 1999) • Ghrelin is produced in the gi tract – mainly stomach but also hypothalmus, kidney, placenta and pituitary gland, receptors are in the pituitary gland and hypothalmus • Ghrelin stimulates: – Growth hormone – Appetite – promotes hunger, food intake – Gastric activity – stimulates emptying – Decreases fat use which may induce adiposity • Gherlin concentrations are reduced in obese patients • Ghrelin activates same areas of the brain that drug use “rewards” it is critical in brain processing – adapting and learning http://www.vivo.colostate.edu/hbooks/pathphys/endocrine/gi/gh relin.html Ghrelin • “ghre” = grow/growth • Levels are high (increasing hunger sensation) before eating and decrease after eating http://www.vivo.colostate.edu/hbooks/pathphys/endocrine/gi/ghrelin.html Ghrelin and Sleep • Has variable effects on sleep/wake activity • Short sleep = higher ghrelin levels 14.9% higher in 5 hours of sleep vs. 8 hours • Subjects reported higher hunger after just 1 night of total sleep deprivation Schmid, SM et al. A single night of sleep deprivation increases ghrelin levels and feelings of hunger in normal-weight men. 2008 Ghrelin and sleep time Schmid, SM et al. A single night of sleep deprivation increases ghrelin levels and feelings of hunger in normal-weight men. 2008 Ghrelin and Sleep Disordered Breathing • Serum ghrelin levels are higher in patients with OSA as compared to controls • There is a positive correlation to ghrelin levels and AHI • There is a positive correlation between ghrelin levels and Epworth Sleepiness Scale. Ursavas, A et al. Ghrelin, leptin, adiponectin, and resistin levels in sleep apnea syndrome: Role of obesity. Annals of Thoracic Medicine Vol. 5(3) July-September 2010. Does CPAP help? • After 2 days on CPAP, ghrelin levels decreased in most OSA patients. • Serum ghrelin levels while on CPAP were only slightly higher then control group levels. Ursavas, A et al. Ghrelin, leptin, adiponectin, and resistin levels in sleep apnea syndrome: Role of obesity. Annals of Thoracic Medicine Vol. 5(3) July-September 2010. Leptin (discovered 1994) • Leptin – appetite suppressant, helps with weight control, saiety, fat distribution (central obesity “apple shape”) • Leptin resistance is present in obese patients and patients with OSA (even those who are not obese) • Leptin has a positive correlation with AHI • Poor sleep and sleep deprivation causes decreases in Leptin http://www.stanford.edu It’s ALL connected somehow! Remember hyperinsulinemia? How is it related to Leptin? • Leptin, a hormone secreted by fat cells, is an important part of weight regulation. Leptin acts to control food intake and energy expenditure. Leptin concentrations increase with obesity and tend to decrease with weight loss. This is important because leptin levels correlate with insulin levels (both are high in hyperinsulinemia) http://www.jewishhospitalcincinnati.com/cholesterol/Research/insulin_resistance.html Leptin and Sleep duration • Reduced sleep duration is associated with increased morning leptin levels. • Positive association of leptin and self-reported sleep time. Penev, Plamen. Short sleep and circulating adipokine concentrations: does the fat hit the fire? SLEEP. Vol. 34, No.2, 2011. • In a study comparing well rested and sleep deprived individuals, researchers found participants who had too little sleep (four hours or less) consumed more calories and gravitated towards high-fat, high protein foods. "Sleep Deprivation Spurs Hunger" - CNN Health, March 2011 Leptin and OSA In some studies: • Patients with OSA have increased leptin levels when compared to controls of similar weight. • Increases in leptin levels correlate to severity of OSA. Other studies: • Suggest that hypoxemia during sleep is determinant of serum leptin levels more so then OSAS.* • Suggest that confounding factors such as obesity, hypercapnia and sympathetic nervous system activity in OSA patients may also influence leptin levels.* Levy,P. Bonsignre, MR and J. Eckel. Sleep, sleep-disordered breathing and metabolic consequences. European Respiratory Journal. Vol. 34, No 1. 2009. *Ursavas, A et al. Ghrelin, leptin, adiponectin, and resistin levels in sleep apnea syndrome: Role of obesity. Annals of Thoracic Medicine Vol. 5(3) July-September 2010 Leptin and CPAP • Successful treatment with CPAP decreased plasma leptin levels – positive correlation with decreasing AHI • Fasting leptin levels decreased in patients after 8 weeks of CPAP use – even where BMI remained constant* Fasting leptin levels : (○) in obstructive sleep apnoea (OSA) patients (□) controls* Sanner, BM, et al. Influence of treatment on leptin levels in patients with obstructive sleep apnoea. 2004 *http://erj.ersjournals.com/content/22/2/251.full Cortisol • Secreted by the adrenal glands • Known as the “stress hormone” • Makes blood pressure rise • Increases blood sugar levels • Is part of the “fight or flight” response http://www.vaxa.com/sleep-cortisol.cfm Cortisol and Sleep • Cortisol is part of our wakefulness – the cyclical release governs our level of wake • In the morning shortly after waking, cortisol levels increase, promoting wake • In the evening, cortisol levels decrease allowing for relaxation and sleep. • People with insomnia secrete higher cortisol levels in the evening before bedtime. http://www.vaxa.com/sleep-cortisol.cfm Cortisol and Sleep • Chronic stress causes cortisol levels to remain elevated • Can result in poor sleep: – – – – Fragmented Shallow Frequent arousals Delayed sleep onset http://www.vaxa.com/sleep-cortisol.cfm Cortisol & OSA • Untreated OSA is associated with elevated cortisol levels* • Additional to the chronic intermittent hypoxia seen with OSA the frequent arousals cause sympathetic activity leading to elevated cortisol levels *http://jcem.endojournals.org/content/94/11/4234.abstract Arnardottir ES et al. Molecular signatures of obstructive sleep apnea in adults: A review and perspective. SLEEP 2009;32(4):447-470. Autonomic Nervous System Body at rest Fight or Flight Cortisol & CPAP • After 3 months of treatment with CPAP, cortisol levels decrease* • Patients with severe OSA showed decreases in evening cortisol levels after CPAP therapy** • A review of 15 studies of the relationship between cortisol and OSA showed conflicting results. Partially due to cortisol samples only being from one time period, poor controls and infrequent sampling. *http://jcem.endojournals.org/content/94/11/4234.abstract **http://www.ncbi.nlm.nih.gov/pubmed/19375124 http://www.ncbi.nlm.nih.gov/pubmed/21803621 Take away • It’s all connected! • Sleep impacts the whole body. • How can you help your patients connect the dots for healthy sleep? Thank you! Sleep Well! 76