4.4 Article

]Prevalence of Sleep Disorders in Adults With Down Syndrome: A Comparative Study of Self-Reported, Actigraphic, and Polysomnographic Findings

期刊

JOURNAL OF CLINICAL SLEEP MEDICINE
卷 14, 期 10, 页码 1725-1733

出版社

AMER ACAD SLEEP MEDICINE
DOI: 10.5664/jcsm.7382

关键词

actigraphy; aging; Down syndrome; obstructive sleep apnea; polysomnography; self-reported sleep quality; sleep disruption

资金

  1. Carlos III National Institute of Health of Spain - European Regional Development Fund (ERDF), the European Union Integrated Operational Programme [PI13/01532, PI16/01825, PI11/02526, PI17 (PI17/01019), PI14/01126]
  2. CIBERNED program (Program 1, Alzheimer's disease and other dementias)
  3. Marato TV3 grants [20141210, 20161431]
  4. La Caixa Banking Foundation
  5. Griffols Foundation
  6. Catalan Government [2014SGR-0235]
  7. Catalan Down Syndrome Foundation
  8. Rio Hortega specialized healthcare post-training contract from the Carlos III National Institute of Health, Spain [CM14/00029]
  9. CIBER-BBN
  10. Ministry of Economy and Competitiveness (MINECO), Spain [DPI2017-83989R]
  11. NIH/NIA/NHLBI [R01HL118624, R21AG049348]

向作者/读者索取更多资源

Study Objectives: Sleep problems are often undetected in adults with Down syndrome (DS). Our objective was to determine the prevalence of sleep disorders in adults with DS through self-reported and objective sleep measures. Methods: We performed a community-based cross-sectional study of 54 adults with DS not referred for sleep disorders. Two polysomnography (PSG) sleep studies were performed. Sleep quality was evaluated using the Pittsburgh Sleep Quality Index (PSQI); daytime sleepiness was evaluated using the Epworth Sleepiness Scale (ESS) and the risk for the sleep apnea syndrome (OSA) was identified using the Berlin Questionnaire (BQ). Participants' sleep/wake pattern was assessed from sleep diaries and by wrist actigraphy. PSQI, ESS, and PSG measures were compared with 35 sex-, age-, and body mass index-matched patients in the control groups. Results: In PSG measures, adults with DS showed lower sleep efficiency (69 +/- 17.7 versus 81.6 +/- 11; P < .001), less rapid eye movement sleep (9.4 +/- 5.8 versus 19.4 +/- 5.1; P < .001), a higher prevalence of OSA (78% versus 14%; P < .001), and a higher apnea-hypopnea index (23.5 +/- 24.5 versus 3.8 +/- 10.5; P < .001) than patients in the control group. In the DS group, the questionnaires (mean PSQI 3.7 +/- 2.9; mean ESS 6.3 +/- 4.5 and mean BQ 1 +/- 0) did not reflect the sleep disturbances detected on the PSG. Actigraphy data recorded daytime sleep that was not self-reported (118.2 +/- 104.2 minutes). Conclusions: Adults with DS show severe sleep disruption and a high prevalence of OSA, undetected by self-reported sleep measures. Actigraphy, PSG, and validated simplified devices for screening OSA should be routinely recommended for this population because treatment of sleep disorders can contribute to healthy aging.

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