Ak. Goenjian et al., BASAL CORTISOL, DEXAMETHASONE SUPPRESSION OF CORTISOL, AND MHPG IN ADOLESCENTS AFTER THE 1988 EARTHQUAKE IN ARMENIA, The American journal of psychiatry, 153(7), 1996, pp. 929-934
Objective: This study evaluated basal salivary cortisol, 3-methoxy-4-h
ydroxyphenylglycol (MHPG), and cortisol suppression following dexameth
asone administration in adolescents exposed to two levels of earthquak
e-related trauma. Method: Five years after the 1988 earthquake, saliva
samples were obtained from 37 adolescents from two cities in Armenia
at different distances from the epicenter. Baseline saliva samples wer
e obtained at 8:00 a.m., 4:00 p.m., and 11:00 p.m., following which 0.
5 mg of dexamethasone was administered. Nine and 17 hours later, saliv
a samples were again obtained. Subjects were evaluated for posttraumat
ic stress and depressive reactions through use of self-report instrume
nts. Results: Significantly lower mean baseline 8:00 a.m. cortisol lev
els and greater day 2 4:00 p.m. cortisol suppression following dexamet
hasone were observed in the more symptomatic adolescents living in the
city closer to the epicenter. Of the three symptom categories of post
traumatic stress disorder (PTSD), only intrusion (category B) symptoms
were significantly correlated with basal morning cortisol levels and
percent suppression by dexamethasone. The more highly exposed adolesce
nts also exhibited a more rapid decline in MHPG levels over the course
of day 1. Conclusions: The findings indicate that chronic posttraumat
ic stress reactions among adolescents exposed to catastrophic disaster
are associated with hypothalamic-pituitary-adrenal (HPA) axis alterat
ions. The findings are congruent with those previously described in ad
ults with chronic PTSD. Persistent intrusion (category B) symptoms may
constitute continued episodes of distress and evoke repented physiolo
gical stress responses, which, over time, after HPA axis function. The
MHPG findings suggest that there may be diurnal changes associated wi
th severity of posttraumatic stress symptoms.