TY - JOUR
T1 - Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy
AU - Members of the VVA Prasterone Research Group
AU - Labrie, Fernand
AU - Derogatis, Leonard
AU - Archer, David F.
AU - Koltun, William
AU - Vachon, Andrée
AU - Young, Douglas
AU - Frenette, Louise
AU - Portman, David
AU - Montesino, Marlene
AU - Côté, Isabelle
AU - Parent, Julie
AU - Lavoie, Lyne
AU - Beauregard, Adam
AU - Martel, Céline
AU - Vaillancourt, Mario
AU - Balser, John
AU - Moyneur, Érick
AU - Ackerman, Ronald T.
AU - Andruczyk, Eugene
AU - Aqua, Keith
AU - Archer, David F.
AU - Belle-Isle, Jasmin
AU - Blank, Steven
AU - Blouin, François
AU - Chavoustie, Steven E.
AU - Bouchard, Céline
AU - Cooper, Theodore
AU - Cusan, Leonello
AU - Donovan, Arthur J.
AU - Drosman, Steven
AU - Eder, Scott E.
AU - Elfassi, émile
AU - Euband, Charles Dale
AU - Fikry, Sameh
AU - Gervais, Benoît
AU - Goldberg, Cynthia
AU - Grainger, David A.
AU - Janzen, Jeannette
AU - Komer, Lawrence D.
AU - Kroll, Robin
AU - Lederman, Samuel N.
AU - London, Andrew
AU - McClinton, Joe D.
AU - O'Mahony, Michael F.J.
AU - O'Mahony, William F.
AU - Poindexter, Alfred
AU - Portman, David J.
AU - Sussman, Steven
AU - Thériault, Guy
AU - Upp, Linda
N1 - Funding Information:
The study was sponsored by EndoCeutics. The study sponsor was involved in the design, data analysis (with two external consulting firms for statistics, namely Veristat and Statlog) and writing of the manuscript.
Publisher Copyright:
© 2015 International Society for Sexual Medicine.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - Introduction: Previous data have shown that intravaginal dehydroepiandrosterone (DHEA, prasterone) improved all the domains of sexual function, an effect most likely related to the local formation of androgens from DHEA. Aims: To confirm in a placebo-controlled, prospective, double-blind and randomized study the benefits of daily intravaginal DHEA for 12 weeks on sexual function using the Female Sexual Function Index (FSFI) questionnaire. Methods: Placebo was administered daily to 157 women while 325 women received 0.50% (6.5mg) DHEA daily for 12 weeks. All women were postmenopausal meeting the criteria of vulvovaginal atrophy (VVA), namely moderate to severe dyspareunia as their most bothersome symptom of VVA in addition to having ≤5% of vaginal superficial cells and vaginal pH>5.0. The FSFI questionnaire was filled at baseline (screening and day 1), 6 weeks and 12 weeks. Comparison between DHEA and placebo of the changes from baseline to 12 weeks was made using the analysis of covariance test, with treatment group as the main factor and baseline value as the covariate. Main Outcome Measures: The six domains and total score of the FSFI questionnaire were evaluated. Results: The FSFI domain desire increased over placebo by 0.24 unit (+49.0%, P=0.0105), arousal by 0.42 unit (+56.8%, P=0.0022), lubrication by 0.57 unit (+36.1%, P=0.0005), orgasm by 0.32 unit (+33.0%, P=0.047), satisfaction by 0.44 unit (+48.3%, P=0.0012), and pain at sexual activity by 0.62 unit (+39.2%, P=0.001). The total FSFI score, on the other hand, has shown a superiority of 2.59 units in the DHEA group over placebo or a 41.3% greater change than placebo (P=0.0006 over placebo). Conclusion: The present data show that all the six domains of the FSFI are improved over placebo (from P=0.047 to 0.0005), thus confirming the previously observed benefits of intravaginal DHEA on female sexual dysfunction by an action exerted exclusively at the level of the vagina, in the absence of biologically significant changes of serum steroids levels.
AB - Introduction: Previous data have shown that intravaginal dehydroepiandrosterone (DHEA, prasterone) improved all the domains of sexual function, an effect most likely related to the local formation of androgens from DHEA. Aims: To confirm in a placebo-controlled, prospective, double-blind and randomized study the benefits of daily intravaginal DHEA for 12 weeks on sexual function using the Female Sexual Function Index (FSFI) questionnaire. Methods: Placebo was administered daily to 157 women while 325 women received 0.50% (6.5mg) DHEA daily for 12 weeks. All women were postmenopausal meeting the criteria of vulvovaginal atrophy (VVA), namely moderate to severe dyspareunia as their most bothersome symptom of VVA in addition to having ≤5% of vaginal superficial cells and vaginal pH>5.0. The FSFI questionnaire was filled at baseline (screening and day 1), 6 weeks and 12 weeks. Comparison between DHEA and placebo of the changes from baseline to 12 weeks was made using the analysis of covariance test, with treatment group as the main factor and baseline value as the covariate. Main Outcome Measures: The six domains and total score of the FSFI questionnaire were evaluated. Results: The FSFI domain desire increased over placebo by 0.24 unit (+49.0%, P=0.0105), arousal by 0.42 unit (+56.8%, P=0.0022), lubrication by 0.57 unit (+36.1%, P=0.0005), orgasm by 0.32 unit (+33.0%, P=0.047), satisfaction by 0.44 unit (+48.3%, P=0.0012), and pain at sexual activity by 0.62 unit (+39.2%, P=0.001). The total FSFI score, on the other hand, has shown a superiority of 2.59 units in the DHEA group over placebo or a 41.3% greater change than placebo (P=0.0006 over placebo). Conclusion: The present data show that all the six domains of the FSFI are improved over placebo (from P=0.047 to 0.0005), thus confirming the previously observed benefits of intravaginal DHEA on female sexual dysfunction by an action exerted exclusively at the level of the vagina, in the absence of biologically significant changes of serum steroids levels.
KW - Androgens
KW - Arousal
KW - Dehydroepiandrosterone (DHEA)
KW - Desire
KW - Female Sexual Dysfunction
KW - Female Sexual Function Index (FSFI)
KW - Intracrinology
KW - Postmenopause
KW - Prasterone
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U2 - 10.1111/jsm.13045
DO - 10.1111/jsm.13045
M3 - Article
C2 - 26597311
AN - SCOPUS:84952876373
SN - 1743-6095
VL - 12
SP - 2401
EP - 2412
JO - Journal of Sexual Medicine
JF - Journal of Sexual Medicine
IS - 12
ER -