4.5 Article

Inflammation, sleep disturbances, and depressed mood among community-dwelling older men

Journal

JOURNAL OF PSYCHOSOMATIC RESEARCH
Volume 76, Issue 5, Pages 368-373

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpsychores.2014.02.005

Keywords

Aging; Depression; Epidemiology; Inflammation; Late-life; Sleep

Categories

Funding

  1. National Institutes of Health
  2. National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
  3. National Institute on Aging (NIA)
  4. National Center for Research Resources (NCRR)
  5. NIH Roadmap for Medical Research [U01 AR45580, U01 AR45614, U01 AR45632, U01 AR45647, U01 AR45654, U01 AR45583, U01 AG18197, U01-AG027810, UL1 TR000128]
  6. National Heart, Lung, and Blood Institute (NHLBI) [R01 HL071194, R01 HL070848, R01 HL070847, R01 HL070842, R01 HL070841, R01 HL070837, R01 HL070838, R01 HL070839]
  7. National Institutes of Health from the National Heart, Lung, and Blood Institute (NHLBI) [HL084183-01]
  8. NIH [K24-AR04884, P50AR060752, P50AR063043]
  9. [T32 AG000181]

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Objective: High rates of sleep disturbances occur in depression. Sleep disturbances are linked to heightened inflammation. We sought to determine if sleep disturbances explain a portion of the putative inflammation - depression association among older adults. In late life, age-related immunoregulation changes may modify the inflammation-depression relationship. Methods: Cross-sectional associations of a panel of serum inflammatory markers with probable depression (measured with the Geriatric Depression Scale) were assessed among 2560 community-dwelling older men. We tested whether inflammatory marker probable depression associations were independent of chronic diseases, as well as objective and subjectively measured sleep disturbances. We also tested whether inflammation-probable depression associations were moderated by age. Results: Inflammatory markers were not independently associated with higher odds of probable depression. A significant age by C-reactive protein (CRP) interaction (p = 0.01) was detected such that the strength of the CRP-probable depression association decreased with age. When stratifying by the median age of 76, elevated odds of probable depression were found for men with CRP levels above the median only among the younger group (OR = 2.08, 95% CI 1.18-3.69). In the final adjusted model, independent effects of chronic diseases and subjective sleep disturbances contributed to a total of 37% attenuation of the original OR (adjusted OR = 1.68, 95% CI 0.911-3.10, p =.09). Conclusions: In late-life, associations between inflammatory markers and mood may be explained by both chronic diseases and subjectively reported sleep disturbances. Our findings indicate that the association of CRP with probable depression diminishes in strength with age. (C) 2014 Elsevier Inc. All rights reserved.

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