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Published on: December 2, 2015
A prospective evaluation of the directionality of the depression-inflammation relationship
Jesse C Stewart1, Kevin L Rand, Matthew F Muldoon
1Department of Psychology, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USA. matsunag@fujita-hu.ac.jp
Insights
Depression may precede inflammation, increasing coronary artery disease risk. This study found depressive symptoms predicted higher interleukin-6 (IL-6) levels over six years in healthy older adults.
Area of Science:
- Cardiovascular disease research
- Psychoneuroimmunology
- Gerontology
Background:
- Cross-sectional studies link depression to elevated inflammatory markers like IL-6 and CRP.
- Prospective studies are needed to clarify the directionality of the depression-inflammation relationship.
Purpose of the Study:
- To investigate the longitudinal associations between depressive symptoms and inflammatory markers (IL-6, CRP) in healthy older adults.
- To determine if depression predicts future inflammation or vice versa.
Main Methods:
- A 6-year prospective cohort study of 263 healthy older adults.
- Baseline and follow-up assessments included the Beck Depression Inventory-II (BDI-II) and serum IL-6 and CRP levels.
- Path analyses were used to evaluate longitudinal associations.
Main Results:
- Baseline depressive symptoms (BDI-II) predicted a significant 6-year increase in IL-6 levels.
- Body-mass index was a stronger predictor of IL-6 change than depressive symptoms.
- No significant longitudinal association was found between IL-6 and depressive symptoms, or between CRP and depressive symptoms.
Conclusions:
- Depressive symptoms may precede and exacerbate inflammation relevant to coronary artery disease in healthy older adults.
- Depression may contribute to cardiovascular risk through inflammatory pathways.
Abstract:
Cross-sectional studies have found that individuals with depressive disorders or symptoms have elevated levels of inflammatory markers predictive of coronary artery disease, including interleukin-6 (IL-6) and C-reactive protein (CRP). Due to the paucity of prospective studies, however, the directionality of the depression-inflammation relationship is unclear. We evaluated the longitudinal associations between depressive symptoms and both IL-6 and CRP among 263 healthy, older men and women enrolled in the Pittsburgh Healthy Heart Project, a 6-year prospective cohort study. During the baseline and follow-up visits, participants completed the Beck Depression Inventory-II (BDI-II) to assess depressive symptoms and underwent blood draws to quantify serum IL-6 and CRP. Path analyses revealed that baseline BDI-II (beta=0.18, p=0.01, DeltaR(2)=0.02) was a predictor of 6-year change in IL-6, even after adjustment for demographic, biomedical, and behavioral factors as well as other negative emotions. Of all the factors examined, only body-mass index was a stronger predictor of IL-6 change than depressive symptoms. In contrast to these results, baseline IL-6 did not predict 6-year change in BDI-II. Evidence of a weak bidirectional relationship between BDI-II and CRP was also observed; however, neither of these longitudinal associations was significant. The present findings indicate that depressive symptoms may precede and augment some inflammatory processes relevant to coronary artery disease among healthy, older adults. Therefore, our results imply that depression may lead to inflammation and that inflammation may be one of the mechanisms through which depression contributes to cardiovascular risk.
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