Study Report
Reference
Citation | Motivala, 2005 PubMed |
Full Info | Motivala, S.J., Sarfatti, A., Olmos, L. and Irwin, M.R. (2005) Inflammatory markers and sleep disturbance in major depression. Psychosom Med, 67, 187-194.
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Study
Hypothesis or Background |
This study was conducted to determine whether immune activation occurs in major depression, and to evaluate the associations between disordered sleep and markers of inflammation in patients with major depressive disorder.
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Sample Information | major depressive disorder (n = 22) and age-, gender-, and body weight-matched comparison controls (n = 18) |
Method Detail | All-night polysomnography was obtained in patients with acute Diagnostic and Statistical Manual of Mental Disorders, 4th edition major depressive disorder (n = 22) and age-, gender-, and body weight-matched comparison controls (n = 18). After the onset of sleep, nocturnal serum levels of interleukin-6 (IL-6), soluble intercellular adhesion molecule (sICAM), monocyte chemotactic protein (MCP-1), and IL-6 soluble receptor (IL-6sR) were sampled. |
Method Keywords | electroencephalogram (EEG); blood analysis |
Result | As compared with matched controls, depressed patients showed significant (p <.05) nocturnal elevations of circulating levels of IL-6 and sICAM. Both sleep latency and rapid eye movement (REM) density had moderate correlations with IL-6 and sICAM (r's > or = 0.30). Backward regression analyses indicated that sleep latency (beta = 0.34, p <.05) and REM density (beta = 0.27, p = .09) were better predictors of IL-6 than depressive status. Similarly, sleep latency (beta = 0.27, p = .06) and REM density (beta = 0.32, p = .02) were also better predictors of sICAM. |
Conclusions | These findings support the hypothesis that sleep disturbance is associated with elevated levels of the inflammatory markers IL-6 and sICAM. This relationship was not accounted for by other confounding factors such as age and body weight. These findings suggest that the elevations in inflammatory markers found in depressive subjects may be partially the result of disturbances of sleep initiation found in this population. |
Relationships reported by
Motivala, 2005
Component A Approved Name (Name in Paper) |
Component A Type |
Component B Approved Name (Name in Paper) |
Component B Type |
Statistical Result |
Relationship Description |
Result Category (Positive/Negative)) |
MDD
|
syndrome |
Intercellular adhesion molecule 1 (soluble intercellular adhesion molecule (sICAM)) |
protein |
P-value<0.05 |
As compared with matched controls, depressed patients showed significant (p <.05) nocturnal elevations of circulating levels of IL-6 and sICAM. |
Positive
|
Rapid eye movement (REM) sleep (rapid eye movement (REM) sleep)
|
neurobiological system |
Intercellular adhesion molecule 1 (soluble intercellular adhesion molecule (sICAM)) |
protein |
P-value<0.05 |
Both sleep latency and rapid eye movement (REM) density had moderate correlations with IL-6 and sICAM (r's > or = 0.30). Sleep latency (beta = 0.27, p = .06) and REM density (beta = 0.32, p = .02) were also better predictors of sICAM. |
Positive
|
MDD
|
syndrome |
Interleukin-6 (interleukin-6 (IL-6)) |
protein |
P-value<0.05 |
As compared with matched controls, depressed patients showed significant (p <.05) nocturnal elevations of circulating levels of IL-6 and sICAM. |
Positive
|
Rapid eye movement (REM) sleep (rapid eye movement (REM) sleep)
|
neurobiological system |
Interleukin-6 (interleukin-6 (IL-6)) |
protein |
P-value<0.05 |
Both sleep latency and rapid eye movement (REM) density had moderate correlations with IL-6 and sICAM (r's > or = 0.30). Backward regression analyses indicated that sleep latency (beta = 0.34, p <.05) and REM density (beta = 0.27, p = .09) were better predictors of IL-6 than depressive status. |
Positive
|