Developmental Psychiatry Section, Department of Psychiatry, University of Cambridge, Cambridge
Department of Clinical Neurosciences, University of Cambridge, Addenbrookes Hospital, Cambridge
Developmental Psychiatry Section, Department of Psychiatry, University of Cambridge, Cambridge
Department of Physiology, Development and Neurosciences and the Cambridge Centre for Brain Repair, Cambridge Centre for Brain Repair, Cambridge, UK.
Correspondence: Ian M. Goodyer, Developmental Psychiatry Section, Department of Psychiatry, University of Cambridge, Douglas House, 18b Trumpington Road, Cambridge CB2 8AH, UK. Email: ig104{at}cam.ac.uk
This work was funded by a Wellcome Trust programme grant awarded to I.M.G. and J.H. T.J.C. is supported by a Career Scientist Award from the Department of Health.
Background
The short (s) allele of the serotonin transporter gene promoter (5-HTTLPR) may be associated with exposure to social adversities and the subsequent onset of depressive illness in adulthood.
Aims
To test in adolescents at high risk for depression whether the short s allele is associated with levels of morning cortisol and the subsequent onset of a depressive episode.
Method
High-risk adolescents (n = 403) were genotyped for 5-HTTLPR. Salivary samples were obtained on four consecutive school days within 1 h of waking from 393 (97.5%) individuals and 367 (91%) underwent a mental state reassessment at 12 months.
Results
Multilevel analysis revealed higher levels of salivary cortisol in short allele carriers (s/s>s/l>l/l). A subsequent episode of depression was increased in those with higher cortisol and the s allele, and independently by depressive symptoms at entry, in both genders.
Conclusions
The short allele of 5-HTTLPR may moderate the association between morning cortisol and the subsequent onset of a depressive episode.