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Lack of Influence of Dyspareunia on the Beneficial Effect of Intravaginal Prasterone (Dehydroepiandrosterone, DHEA) on Sexual Dysfunction in Postmenopausal Women
- Source :
- The Journal of Sexual Medicine. 11:1766-1785
- Publication Year :
- 2014
- Publisher :
- Oxford University Press (OUP), 2014.
-
Abstract
- Introduction We have previously observed that intravaginal prasterone (dehydroepiandrosterone, DHEA) improved all domains of female sexual dysfunction (FSD). Aim Investigate the influence of moderate/severe pain at sexual activity (dyspareunia) (MSD) at baseline on FSD following prasterone administration. Methods The effect of daily administration of prasterone (0, 3.25 mg, 6.5 mg or 13 mg) for 12 weeks on FSD in 215 postmenopausal women with or without MSD at baseline was evaluated in a prospective, randomized, double‐blind, and placebo‐controlled phase III clinical trial. Main Outcome Measures Differences were examined on desire, arousal and orgasm. Results Comparable benefits were observed in women not having MSD (n = 56) vs. those having MSD (n = 159). The benefits over placebo in prasterone‐treated women for desire, avoiding intimacy and vaginal dryness as well as for the total sexual domain of the MENQOL (Menopause Specific Quality of Life) questionnaire, ranged between 18.0% and 38.2% with P values of P = 0.01), 118% ( P = 0.001) and 31.1% ( P = 0.03) were observed over placebo, respectively, while similar differences (58.0%, 67.6% and 32.1%) did not reach statistical significance in the MSD− group having up to only 44 prasterone‐treated women compared with 119 in the MSD+ group. Conclusions No MSD at baseline does not apparently affect the effects of intravaginal prasterone on sexual dysfunction. Knowing the absence of significant effects of estrogens on FSD, the present data suggest that vulvovaginal atrophy (VVA) and vulvovaginal sexual dysfunction (VVSD) are two different consequences of sex steroid deficiency at menopause which can respond independently. In addition, the present data seriously question the justification of pain being part of FSD as well as the separation of FSD into separate domains. Labrie F, Archer D, Bouchard C, Fortier M, Cusan L, Gomez J‐L, Girard G, Baron M, Ayotte N, Moreau M, Dube R, Cote I, Labrie C, Lavoie L, Gilbert L, Martel C, and Balser J. Lack of influence of dyspareunia on the beneficial effect of intravaginal prasterone (dehydroepiandrosterone, DHEA) on sexual dysfunction in postmenopausal women. J Sex Med 2014;11:1766–1785.
- Subjects :
- Adult
medicine.medical_specialty
Sexual Behavior
Urology
Endocrinology, Diabetes and Metabolism
media_common.quotation_subject
Vaginal Diseases
Female sexual dysfunction
Dehydroepiandrosterone
Orgasm
Placebo
Nerve Fibers
Endocrinology
Double-Blind Method
Surveys and Questionnaires
Statistical significance
medicine
Humans
Prospective Studies
Sexual Dysfunctions, Psychological
Aged
media_common
Gynecology
business.industry
Suppositories
Estrogens
Middle Aged
medicine.disease
Postmenopause
Menopause
Administration, Intravaginal
Psychiatry and Mental health
Dyspareunia
medicine.anatomical_structure
Sexual dysfunction
Reproductive Medicine
Vagina
Androgens
Quality of Life
Female
medicine.symptom
Arousal
business
Subjects
Details
- ISSN :
- 17436095
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- The Journal of Sexual Medicine
- Accession number :
- edsair.doi.dedup.....4c41c9a7d974e5c5e2a5da7c180bf76d