학술논문

All-Cause Mortality in People with Co-Occurring Insomnia Symptoms and Sleep Apnea: Analysis of the Wisconsin Sleep Cohort
Document Type
article
Source
Nature and Science of Sleep, Vol Volume 14, Pp 1817-1828 (2022)
Subject
sleep disordered breathing
wisconsin sleep cohort
comisa
obstructive sleep apnea
insomnia
respiratory
Psychiatry
RC435-571
Neurophysiology and neuropsychology
QP351-495
Language
English
ISSN
1179-1608
Abstract
Bastien Lechat,1 Kelly A Loffler,1 Douglas M Wallace,2,3 Amy Reynolds,1 Sarah L Appleton,1 Hannah Scott,1 Andrew Vakulin,1,4 Nicole Lovato,1,4 Robert Adams,1,4 Danny J Eckert,1 Peter G Catcheside,1 Alexander Sweetman1,4 1Adelaide Institute for Sleep Health and FHMRI Sleep Health, Flinders University, Adelaide, South Australia, Australia; 2Department of Neurology, Sleep Medicine Division, University of Miami Miller School of Medicine, Miami, FL, USA; 3Neurology Service, Bruce W. Carter Department of Veterans Affairs Medical Centre, Miami, FL, USA; 4National Centre for Sleep Health Services Research: A NHMRC Centre of Research Excellence, Flinders University, Adelaide, South Australia, AustraliaCorrespondence: Bastien Lechat, Adelaide Institute for Sleep Health and Flinders Health and Medical Research Institute: Sleep Health, Level 2A, Mark Oliphant Building, 5 Laffer Drive, Flinders University, Bedford Park, South Australia, 5042, Australia, Email bastien.lechat@flinders.edu.auPurpose: Insomnia symptoms and sleep apnea frequently co-occur and are associated with worse sleep, daytime function, mental health and quality of life, compared to either insomnia or obstructive sleep apnea (OSA) alone. This study aimed to investigate the association of symptoms of co-morbid insomnia and sleep apnea (COMISA) with all-cause mortality.Patients and Methods: Wisconsin Sleep Cohort data were analysed to assess potential associations between COMISA symptoms and all-cause mortality. Nocturnal insomnia symptoms were defined as difficulties initiating sleep, maintaining sleep, and/or early morning awakenings “often” or “almost always”, and/or regular sedative-hypnotic medicine use. OSA was defined as an apnea-hypopnea index ≥ 5/hr sleep. Participants were classified as having neither insomnia symptoms nor OSA, insomnia symptoms alone, OSA alone, or COMISA symptoms. Associations between the four groups and all-cause mortality over 20 years of follow-up were examined via multivariable adjusted Cox regression models.Results: Among 1115 adult participants (mean ± SD age 55 ± 8 years, 53% males), 19.1% had COMISA symptoms. After controlling for sociodemographic and behavioral factors, COMISA symptoms were associated with an increased risk of all-cause mortality compared to no insomnia symptoms or OSA (HR [95% CI]; 1.71 [1.00– 2.93]). OSA alone (0.91 [0.53, 1.57]) and insomnia symptoms alone (1.04 [0.55, 1.97]) were not associated with increased mortality risk.Conclusion: Co-morbid insomnia symptoms and sleep apnea is associated with increased all-cause mortality risk. Future research should investigate mechanisms underpinning COMISA and the effectiveness of different treatment approaches to reduce mortality risk for this common condition.Keywords: sleep disordered breathing, Wisconsin Sleep Cohort, COMISA, obstructive, sleep apnea, insomnia, respiratory