Publication

Inflammation is associated with future depressive symptoms among older adults

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  • 05/23/2025
Type of Material
Authors
    Erin Bondy, Washington University in St. LouisSara A Norton, Washington University in St. LouisMichaela Voss, Washington University in St. LouisRebecca B Marks, Washington University in St. LouisMichael J Boudreaux, Washington University in St. LouisMichael Treadway, Emory UniversityThomas F Oltmanns, Washington University in St. LouisRyan Bogdan, Washington University in St. Louis
Language
  • English
Date
  • 2021-05-01
Publisher
  • Elsevier Inc
Publication Version
Copyright Statement
  • © 2021 The Authors
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 13
Grant/Funding Information
  • The SPAN study is funded by R01-AG045231 and R01-AG061162.
  • EB was supported by F31-MH123105. SN, MV, MB, TFO, and RB were supported by R01-AG045231 & R01-AG061162.
  • RB received additional support from R01-HD083614, R01-AG052564, R21-AA027827, R01-DA046224, R56-AG059265, R34-DA050272, R01-AG061162 and the Klingenstein Third Generation Foundation.
  • Within the past three years MTT has received consulting fees from Avanir Pharmaceuticals and BlackThorn Therapeutics. No funding or sponsorship was provided by these companies for the current work, and all views expressed herein are solely those of the authors.
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Abstract
  • Inflammation has been reliably associated with depression. However, the directionality of this association is poorly understood, with evidence that elevated inflammation may promote and precede the development of depression, as well as arise following its expression. Using data from older adults (N ​= ​1,072, ages 60–73) who participated in the ongoing longitudinal St. Louis Personality and Aging Network (SPAN) study, we examined whether inflammatory markers (interleukin-6: IL-6, C-reactive protein: CRP, and tumor necrosis factor α: TNFα) and depression were prospectively predictive of one another. Fasting serum samples and self-reports of depressive symptoms (Beck Depression Inventory-II) were obtained from participants at 2 sessions approximately 2 years apart. Structural equation models as well as regressions that accounted for a host of potentially confounding covariates and depression at baseline revealed that baseline IL-6 and CRP, but not baseline TNFα were associated with elevated depressive symptoms at the follow-up session (IL-6: β ​= ​0.080, p ​= ​0.036; CRP: β ​= ​0.083, p ​= ​0.03; TNFα: β ​= ​0.039, p ​= ​0.314). However, there was no association between baseline depressive symptoms and follow-up inflammatory markers (βs ​= ​−0.12 to −0.006, all ps ​> ​0.05). Collectively, these data suggest that inflammation prospectively predicts depression, but depression does not predict inflammation in older age. These data add to a growing literature suggesting that inflammatory signaling may plausibly promote the development of depression.
Author Notes
  • Ryan Bogdan, CB 1125, Psychological and Brain Sciences, Bldg Room 453, Washington University in St. Louis, One Brookings Drive, St. Louis, MO, 63130, USA. Email: rbogdan@wustl.edu
Keywords
Research Categories
  • Psychology, General

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