Major depressive disorder (MDD) in adolescents demonstrates resistance
to tricyclic antidepressants and absence of hypercortisolemia, The ef
ficacy of serotonin reuptake inhibitors (SRIs) is uncertain, and respo
nse predictors are unavailable, Abnormal fast feedback and negative fe
edback of the hypothalamic-pituitary-adrenal axis implicates a dampene
d limbic-hippocampal glucocorticoid type II receptor (GC(II)), We hypo
thesized that lymphocyte GC(II) is altered in adolescent MDD and could
serve as a marker for response to SRIs, In an open-label study, adole
scents (n=20) meeting DSM-III-R criteria for MDD showed baseline lymph
ocyte GC(II) sites per cell (sites/cell) values of 793+/-106 versus 2,
563+/-499 (+/-SEM) for matched controls (n=18) (t=3.5; df =36; p<.001)
, GC(II) was bimodally distributed, with SRI responders differing from
nonresponders (t=3.9; df=14; p<.001), GC(II) accurately classified 90
percent of sertraline responders and 80 percent of nonresponders. Onl
y SRI responders showed GC(II) sites/cell upregulated after 6 weeks of
treatment (t=2.1, df=10; p<.05).