Objectives
Clinical outcomes are worse for patients with heart failure (HF) and elevated depression symptoms. Depression related sympatho-immune dysregulation may be one mechanism leading to poorer HF prognosis. Sympathetically mediated adrenergic activity is known to regulate immune activity via β-adrenergic receptors (β-ARs). However, studies show conflicting relationships between leukocyte β-AR sensitivity and depression symptoms. The aim of this study was to determine in patients with HF the relationship of leukocyte β-AR sensitivity with two diverse measures of depression, self-report questionnaire versus clinical diagnostic interview.
Methods
Patients with HF (N=73, mean age = 56.3, S.D. = 13.0) completed the Beck Depression Inventory −1A (BDI) and a modified Structured Clinical Interview for the DSM-IV (SCID). Leukocyte β-AR sensitivity was determined from isoproterenol stimulated cyclic AMP levels; plasma norepinephrine and epinephrine were also assessed.
Results
Patients with major depression determined by SCID had significantly higher β-AR sensitivity than non-depressed (F(6, 72) = 9.27, p = .003, η2 = .12). Meanwhile, the BDI revealed a more complex relationship. Minimal, mild, and moderate-to-severe depression symptom groups had significant differences in β-AR sensitivity (F(7, 72) = 7.03, p = .002, η2 = .18), with mild symptoms appearing to correspond with reduced β-AR sensitivity and moderate-to-severe symptoms with higher β-AR sensitivity.
Conclusions
By deconstructing depression measurements a greater depth of information may be garnered to potentially reveal subtypes of depression symptoms and their relation to β-AR sensitivity in HF.