Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-23656
Wirtz, P H; Redwine, L S; Linke, S; Hong, S; Rutledge, T; Greenberg, B; Mills, P J (2010). Circulating levels of soluble intercellular adhesion molecule-1 (sICAM-1) independently predict depressive symptom severity after 12 months in heart failure patients. Brain, Behavior, and Immunity, 24(3):366-369.
Objective. To determine whether inflammatory markers prospectively predict depressive symptom severity 12 months later in heart failure (HF) patients. Methods. In 30 HF patients we assessed depressive symptom severity by the Beck depression inventory (BDI) at baseline as well as 12 months later. We measured circulating levels of the soluble intercellular adhesion molecule (sICAM)-1, the cytokine interleukin (IL)-6 and the acute phase protein C-reactive protein (CRP) at baseline assessment. Results. sICAM-1 (r=.38, p=.045) but not CRP or IL-6 correlated with BDI scores 12 months later. Hierarchical linear regression analysis revealed that independent of baseline BDI assessment, cardiovascular risk factors, indicators of HF disease severity, and medication intake, sICAM-1 significantly predicted BDI scores 12 months later. sICAM-1 independently explained between 7% (beta=.26, p=.040) and 10% (beta=.35, p=.045) of the total variance in BDI scores 12 months later. Conclusion. The findings from this exploratory analysis suggest that the adhesion molecule sICAM-1 is an independent predictor of depressive symptoms 12 months later in HF patients. Our prospective findings support the suggested role for inflammation in increasing future depressive symptom severity and extend this linkage for the first time to HF.
|Item Type:||Journal Article, refereed, original work|
|Communities & Collections:||06 Faculty of Arts > Institute of Psychology|
|Uncontrolled Keywords:||heart failure, depression prediction, sICAM-1, CRP, IL-6|
|Date:||01 March 2010|
|Deposited On:||13 Nov 2009 06:34|
|Last Modified:||23 Nov 2012 16:45|
|Funders:||Swiss National Foundation IZKOBO-122843/1 (to PHW)|
|WoS Citation Count:||4|
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