4.7 Article

Repeated exposure to systemic inflammation and risk of new depressive symptoms among older adults

Journal

TRANSLATIONAL PSYCHIATRY
Volume 7, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/tp.2017.155

Keywords

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Categories

Funding

  1. National Institute on Aging in the United States [RO1AG7644]
  2. British Heart Foundation
  3. MRC ImmunoPsychiatry Consortium [RG71546]
  4. Medical Research Council [MR/K013351/1]
  5. NordForsk
  6. Nordic Programme on Health and Welfare
  7. Economic and Social Research Council professorial fellowship [ES/J023299/1]
  8. consortium of UK government departments
  9. Economic and Social Research Council [ES/J023299/1, 1223506] Funding Source: researchfish
  10. Medical Research Council [G108/603, MR/N029488/1, MR/K013351/1, MR/L014815/1, MR/J002739/1] Funding Source: researchfish
  11. National Institute for Health Research [NF-SI-0513-10051, NF-SI-0616-10074] Funding Source: researchfish
  12. ESRC [ES/J023299/1] Funding Source: UKRI
  13. MRC [MR/N029488/1, MR/K020706/1, G108/603, MR/L014815/1, MR/K013351/1] Funding Source: UKRI

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Evidence on systemic inflammation as a risk factor for future depression is inconsistent, possibly due to a lack of regard for persistency of exposure. We examined whether being inflamed on multiple occasions increases risk of new depressive symptoms using prospective data from a population-based sample of adults aged 50 years or older (the English Longitudinal Study of Ageing). Participants with less than four of eight depressive symptoms in 2004/05 and 2008/09 based on the Eight-item Centre for Epidemiologic Studies Depression scale were analysed. The number of occasions with C-reactive protein >= 3mg l(-1) over the same initial assessments (1 vs 0 occasion, and 2 vs 0 occasions) was examined in relation to change in depressive symptoms between 2008/09 and 2012/13 and odds of developing depressive symptomology (having more than or equal to four of eight symptoms) in 2012/13. In multivariable-adjusted regression models (n = 2068), participants who were inflamed on 1 vs 0 occasion showed no increase in depressive symptoms nor raised odds of developing depressive symptomology; those inflamed on 2 vs 0 occasions showed a 0.10 (95% confidence intervals (CIs) = -0.07, 0.28) symptom increase and 1.60 (95% CI = 1.00, 2.55) times higher odds. In further analyses, 2 vs 0 occasions of inflammation were associated with increased odds of developing depressive symptoms among women (odds ratio (OR) = 2.75, 95% CI = 1.53, 4.95), but not among men (OR = 0.70, 95% CI = 0.29, 1.68); P-for-sex interaction = 0.035. In this cohort study of older adults, repeated but not transient exposure to systemic inflammation was associated with increased risk of future depressive symptoms among women; this subgroup finding requires confirmation of validity.

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