The effect of vilazodone on sexual function during the treatment of major depressive disorder

J Sex Med. 2013 Oct;10(10):2465-76. doi: 10.1111/jsm.12004. Epub 2012 Dec 6.

Abstract

Introduction: Sexual dysfunction is common in major depressive disorder (MDD), and many serotonergic antidepressants adversely affect sexual function. Vilazodone, a novel serotonin (5-HT) reuptake inhibitor and 5-HT1A partial agonist approved for MDD, exerts its effects at the 5-HT transporter and at both presynaptic and postsynaptic 5-HT1A receptors. This mechanism may limit sexual dysfunction.

Aim: To summarize effects of vilazodone (40 mg/day, with food) on sexual function in adults with MDD.

Methods: Data sources were three Phase III studies: two 8-week, placebo-controlled studies (NCT00285376 and NCT00683592) and a 52-week open-label study (NCT00644358). Sexual function was assessed by analyzing changes from baseline to end of treatment (EOT) using validated measures.

Main outcome measure: Arizona Sexual Experience Scale or Changes in Sexual Functioning Questionnaire.

Results: Population included 869 patients (vilazodone, 436; placebo, 433) from placebo-controlled studies and 599 patients from the open-label study. Sexual dysfunction prevalence was high (50%, men; 68%, women) before treatment and declined during treatment in vilazodone and placebo groups, indicating improvement on average. At EOT, stable/improved sexual function was observed in ≥91% of patients in placebo-controlled studies; treatment group differences in sexual dysfunction at EOT were not statistically significant for either sex. Differences vs. placebo in changes from baseline of sexual function scores were small and were generally not statistically significant; effect sizes (Cohen's D) were generally of low magnitude. In the placebo-controlled studies, 8.0% of vilazodone-treated patients and 0.9% of placebo-treated patients reported ≥1 sexual-function-related treatment-emergent adverse event (P<0.001).

Conclusion: Half of men and two thirds of women with MDD had sexual dysfunction at baseline; sexual function improved on average in both vilazodone and placebo groups. Results suggest that vilazodone may have a small adverse impact on sexual function in adults with MDD relative to the high prevalence of sexual dysfunction at baseline.

Keywords: Antidepressant; Decreased Sexual Desire; Major Depressive Disorder; Selective Serotonin Reuptake Inhibitor; Sexual Function; Vilazodone.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antidepressive Agents / adverse effects
  • Antidepressive Agents / therapeutic use*
  • Benzofurans / adverse effects
  • Benzofurans / therapeutic use*
  • Depressive Disorder, Major / diagnosis
  • Depressive Disorder, Major / drug therapy*
  • Depressive Disorder, Major / epidemiology
  • Depressive Disorder, Major / psychology
  • Double-Blind Method
  • Female
  • Humans
  • Indoles / adverse effects
  • Indoles / therapeutic use*
  • Male
  • Middle Aged
  • Piperazines / adverse effects
  • Piperazines / therapeutic use*
  • Prevalence
  • Serotonin 5-HT1 Receptor Agonists / adverse effects
  • Serotonin 5-HT1 Receptor Agonists / therapeutic use*
  • Sexual Behavior / drug effects*
  • Sexual Dysfunction, Physiological / diagnosis
  • Sexual Dysfunction, Physiological / drug therapy*
  • Sexual Dysfunction, Physiological / epidemiology
  • Sexual Dysfunction, Physiological / psychology
  • Sexual Dysfunctions, Psychological / diagnosis
  • Sexual Dysfunctions, Psychological / drug therapy*
  • Sexual Dysfunctions, Psychological / epidemiology
  • Sexual Dysfunctions, Psychological / psychology
  • Surveys and Questionnaires
  • Time Factors
  • Treatment Outcome
  • Vilazodone Hydrochloride
  • Young Adult

Substances

  • Antidepressive Agents
  • Benzofurans
  • Indoles
  • Piperazines
  • Serotonin 5-HT1 Receptor Agonists
  • Vilazodone Hydrochloride

Associated data

  • ClinicalTrials.gov/NCT00285376
  • ClinicalTrials.gov/NCT00644358
  • ClinicalTrials.gov/NCT00683592