4.6 Article

The pro-inflammatory profile of depressed patients is (partly) related to obesity

Journal

JOURNAL OF PSYCHIATRIC RESEARCH
Volume 70, Issue -, Pages 91-97

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpsychires.2015.09.001

Keywords

Depression; Inflammation; Cytokine; C-reactive protein; Leptin; Adiponectin

Categories

Funding

  1. NIH National Center for Research Resources [5UL1RR025777-03, 5KL2RR025776-03, 5TL1RR025775-03]
  2. Brain & Behavior Research Foundation and Pamlab, Inc.

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Many people with major depressive disorder (MDD) show evidence of systemic inflammation, including elevations in inflammatory factors, but the cause is unclear. The purpose of this analysis was to determine if obesity might contribute to the pro-inflammatory state in MDD patients. Blood was obtained from 135 MDD patients and 50 controls. Serum was extracted and assayed for interleukin (IL) - 1 beta, IL-2, IL-5, IL-6, IL-8, IL-10, IL-12p70, IL-17, interferon-gamma (IFN gamma), tumor necrosis factor alpha (TNF alpha), C-reactive protein (CRP), leptin, and adiponectin using single- or multi-plex human immunoassay kits. The primary analysis contrasted IL-6, TNF alpha, and CRP between MDD and control groups with body mass index (BMI) as a covariate. The other analytes were compared in an exploratory fashion. IL-6 (but not TNF alpha or CRP) showed significant differences between MDD and controls even after covarying for BMI. Obese controls and obese MDD groups were significantly higher in IL-6 than both lean groups, but the two obese groups did not differ from each other. In the exploratory analyses, the IL-2 level showed robust and significant differences between MDD and controls even after covarying for BMI. Both lean and obese MDD were higher than lean and obese controls. Adiponectin levels were also lower in the MDD sample than controls. Prior findings of higher IL-6, and CRP in MDD patients may be explained, at least in part, based on obesity. High IL-2, however, was associated with depression and not obesity. The results have significant implications for the understanding of pathophysiology and, potentially treatment of MDD. (C) 2015 Elsevier Ltd. All rights reserved.

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