Sleep apnea linked to depression in men
INFORMATION:
* Please note that numbers in this release may differ slightly from those in the abstract. Many of these investigations are ongoing; the release represents the most up-to-date data available at press time.
Abstract 62529
Obstructive Sleep Apnea (OSA) and Excessive Daytime Sleepiness (EDS) are Associated with Depression in a Community Based Population of Australian Men
Type:
Scientific Abstract
Category:
16.03 - Sleep Disordered Breathing: Epidemiology and Genetics (SRN)
Authors:
C.J. Lang1, S.L. Appleton1, A. Vakulin2, D.R. MEvoy2, G.A. Wittert1, S.A. Martin1, J.F. Grant1, A.W. Taylor1, N.A. Antic2, P. Catcheside2, R. Adams1; 1University of Adelaide - Adelaide, SA/AU, 2Adelaide Institute for Sleep Health - Adelaide, SA/AU; Men Androgen Inflammation Lifestyle and Environment Study (MAILES)
Abstract Body
Rationale: There is still considerable uncertainty regarding an association between OSA and depression in men. We examined the hypotheses that EDS and previously diagnosed and undiagnosed OSA are associated with depression prevalence and incidence in a population-based cohort of community dwelling Australian men.
Methods: Depression was assessed using Beck's Depression Inventory (BDI)/Centre for Epidemiological Studies Depression Scale (CES-D) in 1875 men aged 35-83 years at two time points approximately 5 years apart. A random sample of men without previously diagnosed OSA (n = 857) undertook at home polysomnography (PSG) and completed the Epworth Sleepiness Scale questionnaire. 1660 men without depression at baseline were included in the analysis of incident depression.
Results: Previously undiagnosed severe OSA (adjusted odds ratio [OR] 2.1, 95% CI 1.1-4.0) was associated with depression prevalence in the cross-sectional analyses even after adjustment for confounders and EDS. EDS (adjusted OR 1.1, 95% CI 1.0-1.2) was also associated with depression. Men with previously undiagnosed OSA and EDS had 4.2 times greater odds of depression than subjects without OSA and EDS and 3.5 times greater odds of depression than individuals with either OSA or EDS alone. Both previously diagnosed OSA (OR 2.0, 95% CI 1.15-3.45) and previously undiagnosed severe OSA (AHI ? 30) (OR 2.9, 95% CI 1.19-6.92)) at follow-up were significantly associated with depression onset over a 5 year period. Other PSG parameters including O2 saturation, O2desaturation and arousal index were not associated with depression prevalence or incidence.
Conclusion: Severe OSA and EDS are associated with depression prevalence and onset in men. Clinicians should recognise the risk of OSA in men recently diagnosed with depression, regardless of whether sleepiness is present. However the risk is much higher if both OSA (mild-moderate and severe OSA) and sleepiness are present.