Failure of tibolone to potentiate the pharmacological effect of fluoxetine in postmenopausal major depression

J Womens Health (Larchmt). 2003 Jan-Feb;12(1):33-9. doi: 10.1089/154099903321154121.

Abstract

Background: Perimenopausal depression has been attributed to physiological progressive estrogen decline. Estrogen and derivatives have some mood-enhancing effects, although studies of using estrogen as an antidepressant have had mixed results. The gonadomimetic drug tibolone stimulates estrogen receptors in a tissue-selective fashion, increasing the gonadal activity without causing some of the usual side effects of other estrogen preparations.

Methods: A total of 31 postmenopausal outpatients with a major depressive disorder (MDD) participated in the study. Sixteen received the antidepressant fluoxetine (20 mg/day) plus tibolone (2.5 mg/day), and 15 received the same dose of fluoxetine plus placebo, assigned in a randomized fashion.

Results: After 8 weeks of treatment, the two groups had a similar level of improvement in their depressive symptoms. Both treatments were well tolerated, without significant side effects. Pretreatment and posttreatment serum hormonal levels did not predict the final response.

Conclusions: Combining tibolone and fluoxetine did not represent a more robust antidepressant response than fluoxetine alone in postmenopausal women with MDD.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Depressive Disorder / blood
  • Depressive Disorder / drug therapy*
  • Double-Blind Method
  • Estrogen Receptor Modulators / therapeutic use*
  • Estrogens / blood
  • Female
  • Fluoxetine / therapeutic use*
  • Humans
  • Mexico
  • Middle Aged
  • Norpregnenes / therapeutic use*
  • Postmenopause*
  • Selective Serotonin Reuptake Inhibitors / therapeutic use*

Substances

  • Estrogen Receptor Modulators
  • Estrogens
  • Norpregnenes
  • Serotonin Uptake Inhibitors
  • Fluoxetine
  • tibolone