Serotonin transporter polymorphism predicts waking cortisol in young girls

Psychoneuroendocrinology. 2009 Jun;34(5):681-6. doi: 10.1016/j.psyneuen.2008.11.006. Epub 2009 Jan 6.

Abstract

Major Depressive Disorder (MDD) is one of the most prevalent and costly of all psychiatric disorders. The hypothalamic pituitary adrenal (HPA)-axis, which regulates the hormonal response to stress, has been found to be disrupted in depression. HPA dysregulation may represent an important risk factor for depression. To examine a possible genetic underpinning of this risk factor without the confound of current or lifetime depression, we genotyped 84 never-disordered young girls, over a third of whom were at elevated risk for depression, to assess the association between a polymorphism in the promoter region of the serotonin transporter (5-HTT) gene and diurnal variation in HPA-axis activity. This 5-HTT-linked polymorphic region (5-HTTLPR) has been previously found to interact with stress to increase risk for depression. We found 5-HTTLPR to be significantly associated with diurnal cortisol levels: girls who were homozygous for the short-allele had higher levels of waking (but not afternoon or evening) cortisol than did their long-allele counterparts. This finding suggests that genetic susceptibility to HPA-axis dysregulation, especially apparent in levels of waking cortisol, is detectable in individuals as young as 9 years of age.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Arousal / genetics*
  • Arousal / physiology
  • Child
  • Circadian Rhythm / genetics
  • Circadian Rhythm / physiology
  • Depressive Disorder, Major / diagnosis
  • Depressive Disorder, Major / genetics
  • Depressive Disorder, Major / metabolism
  • Depressive Disorder, Major / physiopathology
  • Female
  • Genetic Linkage
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Hydrocortisone / genetics
  • Hydrocortisone / metabolism*
  • Hypothalamo-Hypophyseal System / metabolism
  • Hypothalamo-Hypophyseal System / physiopathology
  • Pituitary-Adrenal System / metabolism
  • Pituitary-Adrenal System / physiopathology
  • Polymorphism, Genetic*
  • Prognosis
  • Serotonin Plasma Membrane Transport Proteins / genetics*

Substances

  • Serotonin Plasma Membrane Transport Proteins
  • Hydrocortisone