M. Maes et al., INCREASED SERUM INTERLEUKIN-1-RECEPTOR-ANTAGONIST CONCENTRATIONS IN MAJOR DEPRESSION, Journal of affective disorders, 36(1-2), 1995, pp. 29-36
Recently, it has been shown that major depression may be accompanied b
y an increased production of interleukin-lp (IL-1 beta), an acute phas
e (AP) response and simultaneous signs of activation and suppression o
f cell-mediated immunity. The interleukin-1-receptor antagonist (IL-1-
rA) is released in vivo during an AP response and serum levels are inc
reased in many immune disorders. The release of IL-1-rA may limit the
pro-inflammatory effects of IL-1. This study has been carried out to e
xamine serum IL-1-Ra in 68 depressed subjects (21 minor, 25 simple maj
or and 22 melancholic subjects) vs. 22 normal controls. Depressed subj
ects showed significantly higher serum IL-1-rA concentrations than hea
lthy controls. 29% of all depressed subjects had serum IL-1-rA levels
higher than the mean value +2 standard deviations of normal controls;
44% depressed subjects had IL-1-rA values greater than 0.215 ng/ml wit
h a specificity of 90%. In depressed subjects, there was a significant
and positive relationship between serum IL-1-rA and severity of illne
ss. In depression, there were no significant relationships between ser
um IL-1-rA concentrations and indicants of hypothalamic-pituitary-adre
nal (HPA)-axis activity, such as 24-h urinary cortisol and postdexamet
hasone cortisol values. Women had significantly higher serum IL-1-rA l
evels than men. The findings support the thesis that depression is acc
ompanied by an immune-inflammatory response.