Background: Research on depression has identified hyperactivity of the HPA axis as a
potential contributory factor to the intergenerational transmission of affective symptoms. However,
this has not yet been examined in the context of social phobia. The current study compared HPA axis
activity in response to a universal social stressor (starting school) in children of 2 groups of women:
one with social phobia and one with no history of anxiety (comparison group). To determine specificity
of effects of maternal social phobia, a third group of children were also examined whose mothers had
generalised anxiety disorder (GAD).
Method: Children provided salivary cortisol samples in the morning, afternoon and at bedtime across 3
time-blocks surrounding the school start: a month before starting school (baseline), the first week at
school (stress response), and the end of the first school term (stress recovery). Child behavioural
inhibition at 14 months was also assessed to explore the influence of early temperament on later stress
responses.
Results: All children displayed an elevation in morning and afternoon cortisol from baseline during the
first week at school, which remained elevated until the end of the first term. Children in the social
phobia group, however, also displayed an equivalent elevation in bedtime cortisol, which was not
observed for comparison children or for children of mothers with GAD. Children in the social phobia
group who were classified as 'inhibited' at 14 months displayed significantly higher afternoon cortisol
levels overall.
Summary: A persistent stress response to school in the morning and afternoon is typical for all
children, but children of mothers with social phobia also display atypical elevations in evening cortisol
levels when at school - signalling long-term disruption of the circadian rhythm in HPA axis activity.
This is the first study to report HPA axis disruption in children at risk of developing social phobia, and
future research should aim to determine whether this represents a pathway for symptom
development, taking early temperament into account