Stroke, Vol 24, 52-57, Copyright © 1993 by American Heart Association
M Astrom, T Olsson and K Asplund
BACKGROUND AND PURPOSE: Using the dexamethasone suppression test, we
studied the suppressibility of the cortisol axis and its clinical
determinants at various time points after stroke. A major aim was to
examine the dexamethasone test as a diagnostic tool for the diagnosis of
major depression in stroke patients. METHODS: The dexamethasone suppression
test, major depression, functional ability, and disorientation were
assessed in a cohort of 70 patients with acute stroke and after 3 months (n
= 63) and 3 years (n = 43). RESULTS: Early after stroke, 24% of the
patients were nonsuppressors, with about the same proportion at 3 months
(22%) and 3 years (21%). None of the controls (17 healthy elderly
volunteers) were nonsuppressors. High cortisol levels early after stroke
were significantly associated with functional impairment (r = 0.35; p =
0.003) and disorientation (r = 0.27; p = 0.03). Three years after stroke,
high postdexamethasone cortisol levels were significantly associated with
major depression (r = 0.57; p < 0.001). The sensitivity of the
dexamethasone test was 70% and the specificity 97%. In a longitudinal
analysis of the long-term survivors (n = 42), postdexamethasone cortisol
values at 3 months predicted major depression at 3 years. CONCLUSIONS:
Hypercortisolism is associated with major depression late (3 years) but not
early (0-3 months) after stroke. Patients with hypercortisolism 3 months
after stroke are at risk of major depression later in the course and
warrant careful follow-up from a psychiatric viewpoint.
ARTICLES
Different linkage of depression to hypercortisolism early versus late after stroke. A 3-year longitudinal study
Department of Psychiatry, University Hospital, Umea, Sweden.
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