Long-term cortisol in bipolar disorder: associations with age of onset and psychiatric co-morbidity

Psychoneuroendocrinology. 2012 Dec;37(12):1960-8. doi: 10.1016/j.psyneuen.2012.04.010. Epub 2012 May 24.

Abstract

Introduction: Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis is hypothesized to play a role in the pathogenesis of bipolar disorder (BD). Conflicting results have been reported when saliva or serum was used to measure cortisol levels. A recently developed method is to measure cortisol in scalp hair, with 1cm of scalp hair representing 1 month. We studied whether there are differences in long-term hair cortisol levels between BD patients and healthy individuals and whether there are associations between hair cortisol and disease characteristics.

Methods: Hair samples were collected in 100 BD patients and 195 healthy controls. Long-term cortisol levels were determined in 3 cm hair segments. Saliva samples were collected on two consecutive evenings. Documented disease characteristics were disease state, age of onset and psychiatric co-morbidity.

Results: Hair cortisol levels were not statistically different in BD patients compared to healthy controls (p=0.233) and were not associated with the disease state at the moment of sample collection (p=0.978). In the subgroup of patients with age of onset ≥ 30 years, hair cortisol levels were significantly elevated compared to the subgroup with age of onset <30 years and to healthy controls (p=0.004). Psychiatric co-morbidity was associated with elevated cortisol levels (44.87 versus 31.41 pg/mg hair; p=0.021), with the exclusion of panic disorder, which was associated with decreased cortisol levels (22.13 versus 34.67 pg/mg hair; p=0.019).

Conclusions: Elevated long-term cortisol levels might play a role in a subgroup of patients with BD. There may be differences in pathogenesis of younger and older onset BD suggesting two different disease entities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset*
  • Aged
  • Aged, 80 and over
  • Biomarkers / metabolism
  • Bipolar Disorder / epidemiology*
  • Bipolar Disorder / metabolism*
  • Case-Control Studies
  • Comorbidity
  • Cross-Sectional Studies
  • Female
  • Hair / metabolism
  • Humans
  • Hydrocortisone / metabolism*
  • Hypothalamo-Hypophyseal System / metabolism
  • Male
  • Mental Disorders / epidemiology*
  • Mental Disorders / metabolism
  • Middle Aged
  • Pituitary-Adrenal System / metabolism
  • Psychiatric Status Rating Scales / statistics & numerical data
  • Saliva / metabolism

Substances

  • Biomarkers
  • Hydrocortisone