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Published on: March 1, 2011
Depression, medical illness, and interleukin-1beta in older cardiac patients
J M Lyness1, J A Moynihan, D J Williford
1Department of Psychiatry, University of Rochester Medical Center, New York 14642, USA. Jeffrey_Lyness@urmc.rochester.edu
Insights
Interleukin-1 beta (IL-1beta) levels were not linked to depression in cardiac patients. This cytokine was, however, associated with overall medical illness burden, suggesting a general sickness response rather than a specific link to depression.
Area of Science:
- Immunology
- Psychiatry
- Cardiology
Background:
- Atherosclerosis is hypothesized to contribute to late-life depression via cytokine effects on monoamine systems.
- Pilot data is needed to investigate the association between interleukin-1 beta (IL-1beta) and depression in cardiac patients.
Purpose of the Study:
- To test the hypothesis that serum IL-1beta levels are associated with depression in a cardiac patient group.
Main Methods:
- Thirty-seven cardiac patients underwent evaluations for depression diagnosis (Structured Clinical Interview for DSM-III-R) and symptom severity (Hamilton Rating Scale for Depression).
- Medical illness burden was assessed using the Cumulative Illness Rating Scale.
- Serum IL-1beta levels were quantified using enzyme-linked immunosorbent assay.
Main Results:
- Serum IL-1beta levels showed no significant association with depressive symptom severity or depression diagnosis, even after controlling for medical illness burden, age, and gender.
- A significant positive correlation was observed between IL-1beta levels and medical illness burden.
Conclusions:
- The study did not confirm the hypothesis linking IL-1beta to depression in cardiac patients.
- The correlation between IL-1beta and medical illness burden likely represents a general "sickness response" to various disease states.
- Further research with larger sample sizes and non-cardiac comparison groups is recommended.
Objective:
A model has been proposed in which atherosclerosis contributes to depression in later life by the effects of cytokines on central monoamine systems. We collected pilot data to test the hypothesis that interleukin-1beta (IL-1beta) is associated with depression in a cardiac patient group.
Method:
Thirty-seven subjects completed research evaluations that included depression diagnosis (Structured Clinical Interview for DSM-III-R), depressive symptom severity (Hamilton Rating Scale for Depression), medical illness burden (Cumulative Illness Rating Scale), and serum IL-1beta level measured by enzyme linked immunosorbent assay.
Results:
Serum IL-1beta level was not significantly associated with depressive symptom severity or depression diagnosis, whether or not controlled for medical illness burden, age, and gender. IL-1beta level was significantly correlated with medical illness burden.
Conclusions:
We did not confirm our study hypothesis. The correlation of IL-1beta level with medical illness burden likely reflects its release as part of the "sickness response" in a wide variety of disease states. Further research using a larger sample size and a non-cardiac comparison group is warranted.
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