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Doctors issue warning as common sleep habit is linked to risk of early death in major study
Doctors issue warning as common sleep habit is linked to risk of early death in major study

Daily Mail​

time10 hours ago

  • Health
  • Daily Mail​

Doctors issue warning as common sleep habit is linked to risk of early death in major study

Daytime napping may be linked to a higher risk of early death, according to a major new study. The discovery was made by researchers who tracking the sleep habits of more than 86,000 healthy middle-aged adults. They found that those who regularly napped—particularly in the early afternoon—were more likely to die prematurely than those who did not. The study, presented at the SLEEP 2025 conference, found the risk of death rose by up to 20 per cent among frequent nappers. Experts say daytime sleepiness may be a warning sign of disrupted or poor-quality night-time rest, and could point to underlying health problems such as sleep disorders, dementia, or heart failure. Professor James Rowley, from Rush University Medical Center in Chicago, who was not involved in the research, said the findings should influence how doctors ask patients about sleep. 'The major take-home message is that if a doctor asks about a patient's sleep habits, they should also be asking about napping,' he told Medscape Medical News. 'In other words, doctors should be asking their patients, 'Do you nap in the day?' The study focused on middle-aged adults who did not work night shifts and had no major health problems at the outset. This helped to rule out other explanations for excessive daytime sleepiness and suggesting that the link with earlier death may not simply be due to existing illness or lifestyle factors. The participant's sleep was assessed over a week-long period, using actigraphy—a method for monitoring a person's sleep-wake patterns using a small, watch-like device called an actigraph. Daytime napping was defined as sleep between 9am and 7pm. On average, participants napped for around 24 minutes, with approximately a third of naps taken in the morning, between 9 and 11am. During a follow-up period of 11 years, 5,189 of the participants died and overall, researchers noted that as people got older, they slept for longer later in the day. After adjusting for potentially confounding lifestyle factors such as smoking, alcohol use and nighttime sleep duration, results showed that a less consistent napping routine was associated with a 14 per cent increased risk of mortality. Scientists found the highest risk of death was seen in people who slept for the longest during the day, with people who nap between 11am and 1pm experiencing a seven per cent increased risk. Lead researcher, Professor Chenlu Gao, from Harvard Medical School, said: 'Our study fills a gap in knowledge by showing that it's not just whether someone naps but how long, how variable, and when they nap may be meaningful indicators of future health risk. 'While many studies have examined the links between sleep and mortality, they have largely focused on nighttime sleep. 'However, napping is an important component of the 24-hour-sleep-wake cycle and may carry its own health implications. 'Our findings suggest that certain patterns of napping could serve as early indications of declining health.' The researchers warned that further research is needed to better understand the biological pathways underlying these associations. They noted that longer or more irregular naps could reflect underlying health problems such as heart disease, type 2 diabetes, depression and dementia. Other studies suggest the explanation may lie with the impact on our circadian rhythms—the natural sleep-wake cycles that determine a host of bodily functions. The experts, from the Karolinska Institute in Stockholm, also argued that being asleep during the daytime could impact the brain's ability to clear waste that builds up during the day. The findings come after a landmark study last year suggested almost half of all cases of Alzheimer's disease—the most common cause of dementia—could be prevented by tackling 14 lifestyle factors. These included hearing loss, high cholesterol, vision loss and lack of exercise. Experts claimed the study, published in the prestigious journal The Lancet, provided more hope than 'ever before' that the disorder that blights the lives of millions can be prevented. Alzheimer's Disease affects 982,000 people in the UK. Alzheimer's Research UK analysis found 74,261 people died from dementia in 2022 compared with 69,178 a year earlier, making it the country's biggest killer. One 2019 estimate put the annual death toll at 70,000 people a year with the health issues caused costing the NHS £700million each year to treat. The WHO puts the annual global death toll from physical inactivity at around 2million per year, making it in the running to be among the top 10 leading causes of global death and disability.

Daytime Sleepiness Tied to Risk for Early Death in Women
Daytime Sleepiness Tied to Risk for Early Death in Women

Medscape

time13-06-2025

  • Health
  • Medscape

Daytime Sleepiness Tied to Risk for Early Death in Women

SEATTLE — Excessive daytime sleepiness (EDS) was associated with a significantly increased risk for all-cause mortality in women, results of a large observational study showed. After adjusting for health and demographic factors, women aged 50 and 65 years with high scores on the Epworth Sleepiness Scale (ESS) were 16% more likely to die from any cause than their counterparts who had normal levels of sleepiness on this tool. This association was not found in younger women or in those over age 65 years. 'Identifying middle age as a critical period suggests clinicians should prioritize an Epworth Sleepiness Scale assessment and excessive daytime sleepiness management in women approaching their 50s and early 60s,' lead author Arash Maghsoudi, PhD, with Baylor College of Medicine in Houston, said in a news release. The findings were presented on June 9 at SLEEP 2025. Data Gap in Women EDS has been associated with all-cause mortality in previous studies, which primarily focused on men. Maghsoudi and colleagues analyzed the medical records of 40,250 female veterans (mean age, 48 years) from 1999 to 2022, focusing on individuals with sleep-related International Classification of Diseases, 9th/10th Revision codes, or those who had received clinical sleep services. They used a validated natural language processing tool to extract ESS scores from clinical notes, with scores categorized as normal (0-10) or high (11-24). Participants were further stratified into three age groups: Young (< 50 years), middle-aged (≥ 50 to < 65 years), and older adults (≥ 65 years). The results were adjusted for age, race, ethnicity, BMI, and Charlson Comorbidity Index. In the overall cohort, the adjusted odds ratio for all-cause mortality in those with high ESS scores compared to those with normal ESS scores was not statistically significant. However, when stratified by age, middle-aged women with high ESS scores had a significantly higher likelihood of all-cause mortality (adjusted odds ratio, 1.16), with no significant associations seen in the younger or older age groups. The researchers said further studies are needed to explore potential mechanisms, including sex-specific responses to sleepiness and the role of age in this association. 'Intriguing' Data Commenting on this research for Medscape Medical News , Indira Gurubhagavatula, MD, MPH, director of the Sleep Medicine Fellowship and professor of medicine at the University of Pennsylvania Perelman School of Medicine in Philadelphia, said the finding that subjectively reported EDS in middle-aged women is associated with mortality strengthens the American Academy of Sleep Medicine (AASM) position that 'sleepiness matters.' The AASM recently published a position statement highlighting how sleepiness can interfere with daily functioning and serve as a marker for other conditions such as mental health problems, sleep disorders, or side effects of medications, as previously reported by Medscape Medical News . 'For these reasons, it is important for clinicians to ask their patients about sleepiness,' said Gurubhagavatula, a spokesperson for AASM. 'The Epworth Sleepiness Scale is a method to get quick, subjective responses and can help guide next steps in clinical evaluation. Improving sleepiness by treating the underlying cause can help restore daytime functioning at home and work, reduce risks of chronic health conditions, and improve people's quality of life,' Gurubhagavatula said. She noted that mechanistic reasons for the relationship between sleepiness and mortality in middle-aged women remain unknown. 'We need more studies to investigate the causal factors that would explain why this association exists,' she added. That said, 'the adjusted odds ratio is just above 1 (average 1.16) in the middle age group. If this is confirmed to be true, even though the risk seems small at an individual level, when you consider it across an entire population, the risk burden to society may be significant,' Gurubhagavatula told Medscape Medical News . She also cautioned that the study involved women veterans, whose risks for sleepiness and mortality may be different than those in other populations. Moreover, the results may not necessarily generalize to other groups. 'The bottom line is that the report is intriguing and calls for more studies to confirm this finding and help explain the mechanism,' Gurubhagavatula concluded.

Axsome Therapeutics Showcases Innovation in Sleep Medicine with Multiple Presentations for AXS-12 and Solriamfetol at SLEEP 2025
Axsome Therapeutics Showcases Innovation in Sleep Medicine with Multiple Presentations for AXS-12 and Solriamfetol at SLEEP 2025

Hamilton Spectator

time11-06-2025

  • Health
  • Hamilton Spectator

Axsome Therapeutics Showcases Innovation in Sleep Medicine with Multiple Presentations for AXS-12 and Solriamfetol at SLEEP 2025

NEW YORK, June 11, 2025 (GLOBE NEWSWIRE) — Axsome Therapeutics, Inc. (NASDAQ: AXSM), a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) disorders, today announced seven presentations, including two featured oral plenary sessions, on AXS-12 and solriamfetol, at SLEEP 2025, the 39th annual meeting of the Associated Professional Sleep Societies (APSS), being held June 8-11, 2025, in Seattle, Washington. Details for the presentations are as follows: AXS-12 Title: ENCORE: Topline Results of a Phase 3 Open-Label Extension and Randomized-Withdrawal Trial of AXS-12 in Narcolepsy Lead Author: Richard Bogan, MD, FCCP, FAASM, Associate Clinical Professor at the University of South Carolina School of Medicine in Columbia, SC Poster Presentation Date and Time: Wednesday, June 11, 10 - 11:45 a.m. PT Poster Session: P-51 Poster Number: 405 Title: Impact of AXS-12 on Symptom Severity and Functional Impairment in Narcolepsy: Results from the Phase 3 SYMPHONY Trial Lead Author: Michael Thorpy, MD, Director of the Sleep-Wake Disorders Center at the Montefiore Medical Center and Professor of Neurology at Albert Einstein College of Medicine, New York, NY Oral Presentation Date and Time: Wednesday, June 11, 3:45 - 4 p.m. PT Oral Session: O-24 Poster Presentation Date and Time: Wednesday, June 11, 10 - 11:45 a.m. PT Poster Session: P-51 Poster Number: 390 Title: Residual Symptom Burden in Patients with Narcolepsy Satisfied with Treatment: Subgroup Analysis from the CRESCENDO Survey Lead Author: Michael Thorpy, MD, Director of the Sleep-Wake Disorders Center at the Montefiore Medical Center and Professor of Neurology at Albert Einstein College of Medicine, New York, NY Oral Presentation Date and Time: Wednesday, June 11, 4 - 4:15 p.m. PT Oral Session: O-24 Poster Presentation Date and Time: Wednesday, June 11, 10 - 11:45 a.m. PT Poster Session: P-51 Poster Number: 391 Solriamfetol Title: Effects of Solriamfetol on Neuropsychological Outcomes in Patients with Obstructive Sleep Apnea in the Real-World SURWEY Study Lead Author: Yaroslav Winter, MD, Mainz Comprehensive Epilepsy and Sleep Medicine Center, Department of Neurology, Johannes Gutenberg-University, Mainz, Germany Poster Presentation Date and Time: Wednesday, June 11, 10 - 11:45 a.m. PT Poster Session: P-50 Poster Number: 366 Title: Real-World Use of Solriamfetol for Excessive Daytime Sleepiness in Patients with Obstructive Sleep Apnea in the US Lead Author: Yang Zhao, PhD, Axsome Therapeutics Poster Presentation Date and Time: Wednesday, June 11, 10 - 11:45 a.m. PT Poster Session: P-50 Poster Number: 369 About AXS-12 AXS-12 (reboxetine) is a highly selective and potent norepinephrine reuptake inhibitor and cortical dopamine modulator under development for the treatment of narcolepsy. AXS-12 is thought to modulate noradrenergic activity to promote maintain tone during wakefulness, and noradrenergic and cortical dopamine signaling to promote wakefulness and enhance cognition. AXS-12 has been granted U.S. Food and Drug Administration (FDA) Orphan Drug Designation for the treatment of narcolepsy. AXS-12 is covered by issued patents providing protection to at least 2039. AXS-12 is an investigational drug product not approved by the FDA. About Solriamfetol Solriamfetol is a dopamine and norepinephrine reuptake inhibitor (DNRI), TAAR1 agonist, and 5-HT1A agonist being developed for the treatment of attention deficit hyperactivity disorder (ADHD), major depressive disorder (MDD), binge eating disorder (BED), and excessive sleepiness associated with shift work disorder (SWD). About Axsome Therapeutics Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at and follow us on LinkedIn and X . Forward Looking Statements Certain matters discussed in this press release are 'forward-looking statements'. The Company may, in some cases, use terms such as 'predicts,' 'believes,' 'potential,' 'continue,' 'estimates,' 'anticipates,' 'expects,' 'plans,' 'intends,' 'may,' 'could,' 'might,' 'will,' 'should' or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. In particular, the Company's statements regarding trends and potential future results are examples of such forward-looking statements. The forward-looking statements include risks and uncertainties, including, but not limited to, the commercial success of the Company's SUNOSI®, AUVELITY®, and SYMBRAVO® products and the success of the Company's efforts to obtain any additional indication(s) with respect to solriamfetol and/or AXS-05; the Company's ability to maintain and expand payer coverage; the success, timing and cost of the Company's ongoing clinical trials and anticipated clinical trials for the Company's current product candidates, including statements regarding the timing of initiation, pace of enrollment and completion of the trials (including the Company's ability to fully fund the Company's disclosed clinical trials, which assumes no material changes to the Company's currently projected revenues or expenses), futility analyses and receipt of interim results, which are not necessarily indicative of the final results of the Company's ongoing clinical trials, and/or data readouts, and the number or type of studies or nature of results necessary to support the filing of a new drug application ('NDA') for any of the Company's current product candidates; the Company's ability to fund additional clinical trials to continue the advancement of the Company's product candidates; the timing of and the Company's ability to obtain and maintain U.S. Food and Drug Administration ('FDA') or other regulatory authority approval of, or other action with respect to, the Company's product candidates, including statements regarding the timing of any NDA submission; the Company's ability to successfully defend its intellectual property or obtain the necessary licenses at a cost acceptable to the Company, if at all; the Company's ability to successfully resolve any intellectual property litigation, and even if such disputes are settled, whether the applicable federal agencies will approve of such settlements; the successful implementation of the Company's research and development programs and collaborations; the success of the Company's license agreements; the acceptance by the market of the Company's products and product candidates, if approved; the Company's anticipated capital requirements, including the amount of capital required for the commercialization of SUNOSI, AUVELITY, and SYMBRAVO and for the Company's commercial launch of its other product candidates, if approved, and the potential impact on the Company's anticipated cash runway; the Company's ability to convert sales to recognized revenue and maintain a favorable gross to net sales; unforeseen circumstances or other disruptions to normal business operations arising from or related to domestic political climate, geo-political conflicts or a global pandemic and other factors, including general economic conditions and regulatory developments, not within the Company's control. The factors discussed herein could cause actual results and developments to be materially different from those expressed in or implied by such statements. The forward-looking statements are made only as of the date of this press release and the Company undertakes no obligation to publicly update such forward-looking statements to reflect subsequent events or circumstances. Investors: Mark Jacobson Chief Operating Officer (212) 332-3243 mjacobson@ Media: Darren Opland Director, Corporate Communications (929) 837-1065 dopland@

How having a sleepy teen could save your kid from a future heart attack
How having a sleepy teen could save your kid from a future heart attack

Yahoo

time10-06-2025

  • Health
  • Yahoo

How having a sleepy teen could save your kid from a future heart attack

For parents with a sleepy teenager, less variable sleep patterns could be a sign of a healthier future for their child. Teens who had better sleep habits at age 15 were found to have improved heart health seven years later, researchers at the American Academy of Sleep Medicine said on Monday. The healthy sleep habits include falling asleep and waking up earlier, spending a lower percentage of time in bed awake, and having lower variability in total sleep time and sleep onset. Average total sleep time did not predict future cardiovascular health. In teens, cardiac incidents are rare, but they can occur. Approximately 2,000 young and seemingly healthy people under the age of 25 die each year of sudden cardiac arrest, according to the Centers for Disease Control and Prevention. Heart attacks in people under 40 have been increasing over the past decade, the Cleveland Clinic notes. 'Given the importance of sleep health for physical health and well-being in the short-term, we were not surprised to see a lasting association between adolescent sleep timing, sleep maintenance efficiency, and sleep variability with cardiovascular health in young adulthood,' Dr. Gina Marie Mathew, a senior post-doctoral associate in public health at Stony Brook Renaissance School of Medicine, explained in a statement. 'It was unexpected, however, that with and without adjustment for potentially confounding factors, total sleep time during adolescence was not a significant predictor of cardiovascular health during young adulthood,' she added. 'This single null finding, of course, does not indicate that total sleep time is unimportant. Rather, when paired with other studies, these findings underscore the complexity of sleep health and the need to consider multiple sleep dimensions as potential targets for promoting and maintaining cardiovascular health.' Mathew was the lead data analyst and author of the National Institutes of Health-backed research that was presented on Sunday at the SLEEP 2025 annual meeting. To reach these conclusions, the researchers analyzed data from Princeton and Columbia University's Future of Families and Child Wellbeing Study: the longest-running and only contemporary U.S. birth cohort study of young adults based on a national sample. Their data included 307 adults, the majority of whom were girls. At age 15, participants wore a device on their wrist for a week to measure sleep variables. At age 22, their cardiovascular health was assessed using their diet, physical activity, exposure to nicotine, body mass index, and measurements of fats in the blood, blood sugar, and blood pressure. They were scored based on these factors using the American Heart Association's Life's Essential 8. Teens between the ages of 13 and 18 years old should sleep eight to 10 hours regularly to promote optimal health, the academy said. Getting the recommended number of hours is associated with improved attention, behavior, memory, mental and physical health, and other positive outcomes. However, Mathew pointed out that the results highlight the need for a more comprehensive approach to address the relationship between adolescent sleep health and cardiovascular health. 'Future research and recommendations should emphasize the importance of multiple dimensions of sleep health, including earlier sleep timing, higher sleep maintenance efficiency, and lower sleep variability as protective factors for long-term heart health,' she said.

Jazz Pharmaceuticals presents late-breaking phase 4 data showcasing Xywav
Jazz Pharmaceuticals presents late-breaking phase 4 data showcasing Xywav

Business Insider

time10-06-2025

  • Business
  • Business Insider

Jazz Pharmaceuticals presents late-breaking phase 4 data showcasing Xywav

Jazz Pharmaceuticals (JAZZ) 'announced late-breaking Phase 4 data evaluating treatment benefits of Xywav oral solution in people with narcolepsy. These results are two of Jazz's four late-breaking abstracts presented today as oral presentations at SLEEP 2025. The four late-breaking abstracts, selected for their scientific quality and innovation, comprise all industry-sponsored late-breaking oral presentations selected by the Associated Professional Sleep Societies. Xywav is the only low-sodium oxybate approved by the U.S. Food and Drug Administration for the treatment of cataplexy or excessive daytime sleepiness in patients 7 years of age and older with narcolepsy and for adults with idiopathic hypersomnia. The Xywav label recommends a nightly dose of 6-9 grams per night.' Confident Investing Starts Here:

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