Alexander Sweetman , Bastien Lechat , Sarah Appleton , Amy Reynolds , Robert Adams , Yohannes Adama Melaku
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COMISA was defined if participants met criteria for insomnia and high risk OSA. The median (IQR) follow-up for mortality was 8.6 (7.8, 9.8) years. Cox regression models were used to determine the association between COMISA and all-cause mortality, controlling for socio-demographic characteristics, behavioural factors and chronic conditions.</p></div><div><h3>Results</h3><p>The prevalence of no insomnia/OSA, insomnia-alone, OSA-alone, and COMISA were 73.5, 3.0, 20.1, and 3.3%, respectively, and 6.7% of participants died by 11-year follow-up. Compared to participants with no insomnia/OSA, higher mortality risk was observed in participants with COMISA (HR=1.9; 95%CI=1.3-2.8) and insomnia alone (HR=1.5; 95%CI=1.0-2.3) after adjusting for socio-demographic characteristics, and behavioural factors. The relationship between COMISA and mortality persisted after additionally controlling for chronic conditions, sleep duration and sleeping pill use (HR=1.6; 95%CI=1.1-2.3), but the relationship between insomnia-alone and mortality did not (HR=1.4; 95%CI=0.9-2.3).</p></div><div><h3>Conclusion</h3><p>Co-morbid insomnia and high-risk OSA is associated with increased risk of all-cause mortality. More research is needed to identify effective treatments for COMISA.</p></div>","PeriodicalId":74809,"journal":{"name":"Sleep epidemiology","volume":"2 ","pages":"Article 100043"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667343622000245/pdfft?md5=7924d8efb4e5303527d0221e50a6392c&pid=1-s2.0-S2667343622000245-main.pdf","citationCount":"9","resultStr":"{\"title\":\"Association of co-morbid insomnia and sleep apnoea symptoms with all-cause mortality: Analysis of the NHANES 2005-2008 data.\",\"authors\":\"Alexander Sweetman , Bastien Lechat , Sarah Appleton , Amy Reynolds , Robert Adams , Yohannes Adama Melaku\",\"doi\":\"10.1016/j.sleepe.2022.100043\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Co-morbid insomnia and sleep apnoea (COMISA) is a highly prevalent condition associated with negative health outcomes. This population-based study aimed to investigate the association between COMISA and all-cause mortality.</p></div><div><h3>Methods</h3><p>Sleep data in 6,877 participants (Age median [IQR]=45 [33,57], 50.1% male) were drawn from the National Health and Nutrition Examination Survey (2005-2008). Insomnia was defined as difficulties initiating sleep, long awakenings, and/or early morning awakenings on ≥16 nights/month, with daytime impairment. The STOP-Bang questionnaire was used to identify participants at high risk of obstructive sleep apnoea (OSA). COMISA was defined if participants met criteria for insomnia and high risk OSA. The median (IQR) follow-up for mortality was 8.6 (7.8, 9.8) years. Cox regression models were used to determine the association between COMISA and all-cause mortality, controlling for socio-demographic characteristics, behavioural factors and chronic conditions.</p></div><div><h3>Results</h3><p>The prevalence of no insomnia/OSA, insomnia-alone, OSA-alone, and COMISA were 73.5, 3.0, 20.1, and 3.3%, respectively, and 6.7% of participants died by 11-year follow-up. Compared to participants with no insomnia/OSA, higher mortality risk was observed in participants with COMISA (HR=1.9; 95%CI=1.3-2.8) and insomnia alone (HR=1.5; 95%CI=1.0-2.3) after adjusting for socio-demographic characteristics, and behavioural factors. The relationship between COMISA and mortality persisted after additionally controlling for chronic conditions, sleep duration and sleeping pill use (HR=1.6; 95%CI=1.1-2.3), but the relationship between insomnia-alone and mortality did not (HR=1.4; 95%CI=0.9-2.3).</p></div><div><h3>Conclusion</h3><p>Co-morbid insomnia and high-risk OSA is associated with increased risk of all-cause mortality. 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引用次数: 9
摘要
背景:合并症失眠和睡眠呼吸暂停(COMISA)是一种非常普遍的与负面健康结果相关的疾病。这项基于人群的研究旨在调查COMISA与全因死亡率之间的关系。方法选取2005-2008年全国健康与营养检查调查6877名参与者(年龄中位数[IQR]=45[33,57],男性50.1%)的睡眠资料。失眠定义为入睡困难、长时间醒来和/或清晨醒来≥16晚/月,伴有白天障碍。STOP-Bang问卷用于识别阻塞性睡眠呼吸暂停(OSA)高风险的参与者。如果参与者符合失眠和高风险OSA的标准,则定义COMISA。死亡率的中位随访(IQR)为8.6(7.8,9.8)年。使用Cox回归模型确定COMISA与全因死亡率之间的关系,控制社会人口统计学特征、行为因素和慢性病。结果无失眠/OSA、单纯性失眠、单纯性OSA和COMISA患病率分别为73.5%、3.0、20.1%和3.3%,随访11年死亡的比例为6.7%。与没有失眠/OSA的参与者相比,COMISA参与者的死亡风险更高(HR=1.9;95%CI=1.3-2.8)和单纯失眠(HR=1.5;95%CI=1.0-2.3),校正了社会人口统计学特征和行为因素。在另外控制慢性病、睡眠时间和安眠药使用后,COMISA与死亡率的关系仍然存在(HR=1.6;95%CI=1.1-2.3),但单独失眠与死亡率之间没有关系(HR=1.4;95% ci = 0.9 - -2.3)。结论合并症失眠和高危OSA与全因死亡风险增加相关。需要更多的研究来确定COMISA的有效治疗方法。
Association of co-morbid insomnia and sleep apnoea symptoms with all-cause mortality: Analysis of the NHANES 2005-2008 data.
Background
Co-morbid insomnia and sleep apnoea (COMISA) is a highly prevalent condition associated with negative health outcomes. This population-based study aimed to investigate the association between COMISA and all-cause mortality.
Methods
Sleep data in 6,877 participants (Age median [IQR]=45 [33,57], 50.1% male) were drawn from the National Health and Nutrition Examination Survey (2005-2008). Insomnia was defined as difficulties initiating sleep, long awakenings, and/or early morning awakenings on ≥16 nights/month, with daytime impairment. The STOP-Bang questionnaire was used to identify participants at high risk of obstructive sleep apnoea (OSA). COMISA was defined if participants met criteria for insomnia and high risk OSA. The median (IQR) follow-up for mortality was 8.6 (7.8, 9.8) years. Cox regression models were used to determine the association between COMISA and all-cause mortality, controlling for socio-demographic characteristics, behavioural factors and chronic conditions.
Results
The prevalence of no insomnia/OSA, insomnia-alone, OSA-alone, and COMISA were 73.5, 3.0, 20.1, and 3.3%, respectively, and 6.7% of participants died by 11-year follow-up. Compared to participants with no insomnia/OSA, higher mortality risk was observed in participants with COMISA (HR=1.9; 95%CI=1.3-2.8) and insomnia alone (HR=1.5; 95%CI=1.0-2.3) after adjusting for socio-demographic characteristics, and behavioural factors. The relationship between COMISA and mortality persisted after additionally controlling for chronic conditions, sleep duration and sleeping pill use (HR=1.6; 95%CI=1.1-2.3), but the relationship between insomnia-alone and mortality did not (HR=1.4; 95%CI=0.9-2.3).
Conclusion
Co-morbid insomnia and high-risk OSA is associated with increased risk of all-cause mortality. More research is needed to identify effective treatments for COMISA.