Longitudinal stability and developmental properties of salivary cortisol levels and circadian rhythms from childhood to adolescence

Dev Psychobiol. 2012 Jul;54(5):493-502. doi: 10.1002/dev.20607. Epub 2011 Sep 27.

Abstract

This study aimed to (1) identify a stable, trait-like component to cortisol and its circadian rhythm, and (2) investigate individual differences in developmental trajectories of HPA-axis maturation. Multiple salivary cortisol samples were collected longitudinally across four assessments from age 9 (3rd grade) through age 15 (9th grade) in a community sample of children (N = 357). Sophisticated statistical models examined cortisol levels and its rhythm over time; effects of age, puberty and gender were primarily considered. In addition to situation-specific and stable short-term or epoch-specific cortisol components, there is a stable, trait-like component of cortisol levels and circadian rhythm across multiple years covering the transition from childhood into adolescence. Youth had higher cortisol and flatter circadian rhythms as they got older and more physically developed. Girls had higher cortisol, stronger circadian rhythms, and greater developmental influences across adolescence. Distinguishing a stable, trait-like component of cortisol level and its circadian rhythm provides the empirical foundation for investigating putative mechanisms underlying individual differences in HPA functioning. The findings also provide important descriptive information about maturational processes influencing HPA-axis development.

Publication types

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

MeSH terms

  • Adolescent
  • Child
  • Circadian Rhythm / physiology*
  • Female
  • Humans
  • Hydrocortisone / metabolism*
  • Hypothalamo-Hypophyseal System / growth & development*
  • Hypothalamo-Hypophyseal System / metabolism
  • Individuality
  • Longitudinal Studies
  • Male
  • Pituitary-Adrenal System / growth & development*
  • Pituitary-Adrenal System / metabolism
  • Puberty / physiology*
  • Saliva / metabolism*
  • Sex Factors
  • Stress, Psychological

Substances

  • Hydrocortisone