Loading…
Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia
Objective To examine the effect of intravaginal dehydroepiandrosterone (DHEA) on pain at sexual activity (dyspareunia) identified as the most bothersome symptom of vaginal atrophy in postmenopausal women at both screening and day 1. Methods This prospective, randomized, double-blind and placebo-cont...
Saved in:
Published in: | Climacteric : the journal of the International Menopause Society 2011-04, Vol.14 (2), p.282-288 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c444t-a383d7bad64db74adea7aa08f5feb48e9e80553da736618ca1c8786dffdddb2b3 |
---|---|
cites | cdi_FETCH-LOGICAL-c444t-a383d7bad64db74adea7aa08f5feb48e9e80553da736618ca1c8786dffdddb2b3 |
container_end_page | 288 |
container_issue | 2 |
container_start_page | 282 |
container_title | Climacteric : the journal of the International Menopause Society |
container_volume | 14 |
creator | Labrie, F. Archer, D. F. Bouchard, C. Fortier, M. Cusan, L. Gomez, J.-L. Girard, G. Baron, M. Ayotte, N. Moreau, M. Dubé, R. Côté, I. Labrie, C. Lavoie, L. Berger, L. Gilbert, L. Martel, C. Balser, J. |
description | Objective To examine the effect of intravaginal dehydroepiandrosterone (DHEA) on pain at sexual activity (dyspareunia) identified as the most bothersome symptom of vaginal atrophy in postmenopausal women at both screening and day 1.
Methods This prospective, randomized, double-blind and placebo-controlled phase III clinical trial studied the effect of prasterone (DHEA) applied locally in the vagina on the severity of dyspareunia in 114 postmenopausal women who had identified dyspareunia as their most bothersome symptom of vaginal atrophy, while meeting the criteria for superficial cells ≤ 5% and pH > 5.0 at both screening and day 1.
Results At the standard duration of 12 weeks of treatment, increasing doses of 0.25%, 0.5% and 1.0% DHEA decreased the percentage of parabasal cells by 48.6 ± 6.78%, 42.4 ± 7.36% and 54.9 ± 6.60% (p < 0.0001 vs. placebo for all) with no change with placebo (p = 0.769). The effects on superficial cells and pH were also highly significant compared to placebo at all DHEA doses. The severity score of pain at sexual activity decreased by 0.5, 1.4, 1.6 and 1.4 units in the placebo and 0.25%, 0.5% and 1.0% DHEA groups, respectively, with the p value of differences from placebo ranging from 0.0017 to < 0.0001.
Conclusions Intravaginal DHEA, through local estrogen and androgen formation, causes a rapid and highly efficient effect on pain at sexual activity without systemic exposure of the other tissues, thus avoiding the recently reported systemic effects of estrogens. |
doi_str_mv | 10.3109/13697137.2010.535226 |
format | article |
fullrecord | <record><control><sourceid>proquest_infor</sourceid><recordid>TN_cdi_proquest_journals_864546010</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2335880561</sourcerecordid><originalsourceid>FETCH-LOGICAL-c444t-a383d7bad64db74adea7aa08f5feb48e9e80553da736618ca1c8786dffdddb2b3</originalsourceid><addsrcrecordid>eNp9kFFr1jAUhoM43Jz-A5HijQrrTJqkyXejyNA5GHijlxJOm5M1o21q0ir990v5vil6savzEp7zhvMQ8oLRc87o7h3j9U4xrs4rmp8kl1VVPyInTCheUk3F45wzUm7MMXma0i2ljHNWPyHHFauEqJg8IT-uxjnCL7jxI_SFxW61MeDkYcwzzRjDiMWbKcIhvz0roOj8TdevBTrnW4_jXMwRYR62FFxh1zRBxGX08IwcOegTPj_MU_L986dvF1_K66-XVxcfr8tWCDGXwDW3qgFbC9soARZBAVDtpMNGaNyhplJyC4rXNdMtsFYrXVvnrLVN1fBT8nrfO8Xwc8E0m8GnFvseRgxLMloqvcmQmXz1H3kblphvz1AtpKizzAyJPdRmBymiM1P0A8TVMGo2-eZevtnkm738vPby0L00A9o_S_e2M_BhD_jRhTjA7xB7a2ZY-xBdhLH1aat_8Iv3_zR0CP3ctVn33zseLLgDeheo0g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>864546010</pqid></control><display><type>article</type><title>Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia</title><source>Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)</source><creator>Labrie, F. ; Archer, D. F. ; Bouchard, C. ; Fortier, M. ; Cusan, L. ; Gomez, J.-L. ; Girard, G. ; Baron, M. ; Ayotte, N. ; Moreau, M. ; Dubé, R. ; Côté, I. ; Labrie, C. ; Lavoie, L. ; Berger, L. ; Gilbert, L. ; Martel, C. ; Balser, J.</creator><creatorcontrib>Labrie, F. ; Archer, D. F. ; Bouchard, C. ; Fortier, M. ; Cusan, L. ; Gomez, J.-L. ; Girard, G. ; Baron, M. ; Ayotte, N. ; Moreau, M. ; Dubé, R. ; Côté, I. ; Labrie, C. ; Lavoie, L. ; Berger, L. ; Gilbert, L. ; Martel, C. ; Balser, J.</creatorcontrib><description>Objective To examine the effect of intravaginal dehydroepiandrosterone (DHEA) on pain at sexual activity (dyspareunia) identified as the most bothersome symptom of vaginal atrophy in postmenopausal women at both screening and day 1.
Methods This prospective, randomized, double-blind and placebo-controlled phase III clinical trial studied the effect of prasterone (DHEA) applied locally in the vagina on the severity of dyspareunia in 114 postmenopausal women who had identified dyspareunia as their most bothersome symptom of vaginal atrophy, while meeting the criteria for superficial cells ≤ 5% and pH > 5.0 at both screening and day 1.
Results At the standard duration of 12 weeks of treatment, increasing doses of 0.25%, 0.5% and 1.0% DHEA decreased the percentage of parabasal cells by 48.6 ± 6.78%, 42.4 ± 7.36% and 54.9 ± 6.60% (p < 0.0001 vs. placebo for all) with no change with placebo (p = 0.769). The effects on superficial cells and pH were also highly significant compared to placebo at all DHEA doses. The severity score of pain at sexual activity decreased by 0.5, 1.4, 1.6 and 1.4 units in the placebo and 0.25%, 0.5% and 1.0% DHEA groups, respectively, with the p value of differences from placebo ranging from 0.0017 to < 0.0001.
Conclusions Intravaginal DHEA, through local estrogen and androgen formation, causes a rapid and highly efficient effect on pain at sexual activity without systemic exposure of the other tissues, thus avoiding the recently reported systemic effects of estrogens.</description><identifier>ISSN: 1369-7137</identifier><identifier>EISSN: 1473-0804</identifier><identifier>DOI: 10.3109/13697137.2010.535226</identifier><identifier>PMID: 21244215</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Administration, Intravaginal ; ANDROGENS ; Cells ; Dehydroepiandrosterone - administration & dosage ; Dehydroepiandrosterone - therapeutic use ; DHEA ; Dose-Response Relationship, Drug ; Double-Blind Method ; DYSPAREUNIA ; Dyspareunia - drug therapy ; ESTROGENS ; Female ; Humans ; INTRACRINOLOGY ; Medical treatment ; Menopause ; Postmenopause ; PRASTERONE ; Sexual behavior ; Tissues ; Treatment Outcome ; VAGINAL ATROPHY ; Women</subject><ispartof>Climacteric : the journal of the International Menopause Society, 2011-04, Vol.14 (2), p.282-288</ispartof><rights>2011 International Menopause Society 2011</rights><rights>Copyright Taylor & Francis Ltd. Apr 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-a383d7bad64db74adea7aa08f5feb48e9e80553da736618ca1c8786dffdddb2b3</citedby><cites>FETCH-LOGICAL-c444t-a383d7bad64db74adea7aa08f5feb48e9e80553da736618ca1c8786dffdddb2b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21244215$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Labrie, F.</creatorcontrib><creatorcontrib>Archer, D. F.</creatorcontrib><creatorcontrib>Bouchard, C.</creatorcontrib><creatorcontrib>Fortier, M.</creatorcontrib><creatorcontrib>Cusan, L.</creatorcontrib><creatorcontrib>Gomez, J.-L.</creatorcontrib><creatorcontrib>Girard, G.</creatorcontrib><creatorcontrib>Baron, M.</creatorcontrib><creatorcontrib>Ayotte, N.</creatorcontrib><creatorcontrib>Moreau, M.</creatorcontrib><creatorcontrib>Dubé, R.</creatorcontrib><creatorcontrib>Côté, I.</creatorcontrib><creatorcontrib>Labrie, C.</creatorcontrib><creatorcontrib>Lavoie, L.</creatorcontrib><creatorcontrib>Berger, L.</creatorcontrib><creatorcontrib>Gilbert, L.</creatorcontrib><creatorcontrib>Martel, C.</creatorcontrib><creatorcontrib>Balser, J.</creatorcontrib><title>Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia</title><title>Climacteric : the journal of the International Menopause Society</title><addtitle>Climacteric</addtitle><description>Objective To examine the effect of intravaginal dehydroepiandrosterone (DHEA) on pain at sexual activity (dyspareunia) identified as the most bothersome symptom of vaginal atrophy in postmenopausal women at both screening and day 1.
Methods This prospective, randomized, double-blind and placebo-controlled phase III clinical trial studied the effect of prasterone (DHEA) applied locally in the vagina on the severity of dyspareunia in 114 postmenopausal women who had identified dyspareunia as their most bothersome symptom of vaginal atrophy, while meeting the criteria for superficial cells ≤ 5% and pH > 5.0 at both screening and day 1.
Results At the standard duration of 12 weeks of treatment, increasing doses of 0.25%, 0.5% and 1.0% DHEA decreased the percentage of parabasal cells by 48.6 ± 6.78%, 42.4 ± 7.36% and 54.9 ± 6.60% (p < 0.0001 vs. placebo for all) with no change with placebo (p = 0.769). The effects on superficial cells and pH were also highly significant compared to placebo at all DHEA doses. The severity score of pain at sexual activity decreased by 0.5, 1.4, 1.6 and 1.4 units in the placebo and 0.25%, 0.5% and 1.0% DHEA groups, respectively, with the p value of differences from placebo ranging from 0.0017 to < 0.0001.
Conclusions Intravaginal DHEA, through local estrogen and androgen formation, causes a rapid and highly efficient effect on pain at sexual activity without systemic exposure of the other tissues, thus avoiding the recently reported systemic effects of estrogens.</description><subject>Administration, Intravaginal</subject><subject>ANDROGENS</subject><subject>Cells</subject><subject>Dehydroepiandrosterone - administration & dosage</subject><subject>Dehydroepiandrosterone - therapeutic use</subject><subject>DHEA</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>DYSPAREUNIA</subject><subject>Dyspareunia - drug therapy</subject><subject>ESTROGENS</subject><subject>Female</subject><subject>Humans</subject><subject>INTRACRINOLOGY</subject><subject>Medical treatment</subject><subject>Menopause</subject><subject>Postmenopause</subject><subject>PRASTERONE</subject><subject>Sexual behavior</subject><subject>Tissues</subject><subject>Treatment Outcome</subject><subject>VAGINAL ATROPHY</subject><subject>Women</subject><issn>1369-7137</issn><issn>1473-0804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kFFr1jAUhoM43Jz-A5HijQrrTJqkyXejyNA5GHijlxJOm5M1o21q0ir990v5vil6savzEp7zhvMQ8oLRc87o7h3j9U4xrs4rmp8kl1VVPyInTCheUk3F45wzUm7MMXma0i2ljHNWPyHHFauEqJg8IT-uxjnCL7jxI_SFxW61MeDkYcwzzRjDiMWbKcIhvz0roOj8TdevBTrnW4_jXMwRYR62FFxh1zRBxGX08IwcOegTPj_MU_L986dvF1_K66-XVxcfr8tWCDGXwDW3qgFbC9soARZBAVDtpMNGaNyhplJyC4rXNdMtsFYrXVvnrLVN1fBT8nrfO8Xwc8E0m8GnFvseRgxLMloqvcmQmXz1H3kblphvz1AtpKizzAyJPdRmBymiM1P0A8TVMGo2-eZevtnkm738vPby0L00A9o_S_e2M_BhD_jRhTjA7xB7a2ZY-xBdhLH1aat_8Iv3_zR0CP3ctVn33zseLLgDeheo0g</recordid><startdate>201104</startdate><enddate>201104</enddate><creator>Labrie, F.</creator><creator>Archer, D. F.</creator><creator>Bouchard, C.</creator><creator>Fortier, M.</creator><creator>Cusan, L.</creator><creator>Gomez, J.-L.</creator><creator>Girard, G.</creator><creator>Baron, M.</creator><creator>Ayotte, N.</creator><creator>Moreau, M.</creator><creator>Dubé, R.</creator><creator>Côté, I.</creator><creator>Labrie, C.</creator><creator>Lavoie, L.</creator><creator>Berger, L.</creator><creator>Gilbert, L.</creator><creator>Martel, C.</creator><creator>Balser, J.</creator><general>Informa Healthcare</general><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201104</creationdate><title>Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia</title><author>Labrie, F. ; Archer, D. F. ; Bouchard, C. ; Fortier, M. ; Cusan, L. ; Gomez, J.-L. ; Girard, G. ; Baron, M. ; Ayotte, N. ; Moreau, M. ; Dubé, R. ; Côté, I. ; Labrie, C. ; Lavoie, L. ; Berger, L. ; Gilbert, L. ; Martel, C. ; Balser, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-a383d7bad64db74adea7aa08f5feb48e9e80553da736618ca1c8786dffdddb2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Administration, Intravaginal</topic><topic>ANDROGENS</topic><topic>Cells</topic><topic>Dehydroepiandrosterone - administration & dosage</topic><topic>Dehydroepiandrosterone - therapeutic use</topic><topic>DHEA</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>DYSPAREUNIA</topic><topic>Dyspareunia - drug therapy</topic><topic>ESTROGENS</topic><topic>Female</topic><topic>Humans</topic><topic>INTRACRINOLOGY</topic><topic>Medical treatment</topic><topic>Menopause</topic><topic>Postmenopause</topic><topic>PRASTERONE</topic><topic>Sexual behavior</topic><topic>Tissues</topic><topic>Treatment Outcome</topic><topic>VAGINAL ATROPHY</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Labrie, F.</creatorcontrib><creatorcontrib>Archer, D. F.</creatorcontrib><creatorcontrib>Bouchard, C.</creatorcontrib><creatorcontrib>Fortier, M.</creatorcontrib><creatorcontrib>Cusan, L.</creatorcontrib><creatorcontrib>Gomez, J.-L.</creatorcontrib><creatorcontrib>Girard, G.</creatorcontrib><creatorcontrib>Baron, M.</creatorcontrib><creatorcontrib>Ayotte, N.</creatorcontrib><creatorcontrib>Moreau, M.</creatorcontrib><creatorcontrib>Dubé, R.</creatorcontrib><creatorcontrib>Côté, I.</creatorcontrib><creatorcontrib>Labrie, C.</creatorcontrib><creatorcontrib>Lavoie, L.</creatorcontrib><creatorcontrib>Berger, L.</creatorcontrib><creatorcontrib>Gilbert, L.</creatorcontrib><creatorcontrib>Martel, C.</creatorcontrib><creatorcontrib>Balser, J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Climacteric : the journal of the International Menopause Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Labrie, F.</au><au>Archer, D. F.</au><au>Bouchard, C.</au><au>Fortier, M.</au><au>Cusan, L.</au><au>Gomez, J.-L.</au><au>Girard, G.</au><au>Baron, M.</au><au>Ayotte, N.</au><au>Moreau, M.</au><au>Dubé, R.</au><au>Côté, I.</au><au>Labrie, C.</au><au>Lavoie, L.</au><au>Berger, L.</au><au>Gilbert, L.</au><au>Martel, C.</au><au>Balser, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia</atitle><jtitle>Climacteric : the journal of the International Menopause Society</jtitle><addtitle>Climacteric</addtitle><date>2011-04</date><risdate>2011</risdate><volume>14</volume><issue>2</issue><spage>282</spage><epage>288</epage><pages>282-288</pages><issn>1369-7137</issn><eissn>1473-0804</eissn><abstract>Objective To examine the effect of intravaginal dehydroepiandrosterone (DHEA) on pain at sexual activity (dyspareunia) identified as the most bothersome symptom of vaginal atrophy in postmenopausal women at both screening and day 1.
Methods This prospective, randomized, double-blind and placebo-controlled phase III clinical trial studied the effect of prasterone (DHEA) applied locally in the vagina on the severity of dyspareunia in 114 postmenopausal women who had identified dyspareunia as their most bothersome symptom of vaginal atrophy, while meeting the criteria for superficial cells ≤ 5% and pH > 5.0 at both screening and day 1.
Results At the standard duration of 12 weeks of treatment, increasing doses of 0.25%, 0.5% and 1.0% DHEA decreased the percentage of parabasal cells by 48.6 ± 6.78%, 42.4 ± 7.36% and 54.9 ± 6.60% (p < 0.0001 vs. placebo for all) with no change with placebo (p = 0.769). The effects on superficial cells and pH were also highly significant compared to placebo at all DHEA doses. The severity score of pain at sexual activity decreased by 0.5, 1.4, 1.6 and 1.4 units in the placebo and 0.25%, 0.5% and 1.0% DHEA groups, respectively, with the p value of differences from placebo ranging from 0.0017 to < 0.0001.
Conclusions Intravaginal DHEA, through local estrogen and androgen formation, causes a rapid and highly efficient effect on pain at sexual activity without systemic exposure of the other tissues, thus avoiding the recently reported systemic effects of estrogens.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>21244215</pmid><doi>10.3109/13697137.2010.535226</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1369-7137 |
ispartof | Climacteric : the journal of the International Menopause Society, 2011-04, Vol.14 (2), p.282-288 |
issn | 1369-7137 1473-0804 |
language | eng |
recordid | cdi_proquest_journals_864546010 |
source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list) |
subjects | Administration, Intravaginal ANDROGENS Cells Dehydroepiandrosterone - administration & dosage Dehydroepiandrosterone - therapeutic use DHEA Dose-Response Relationship, Drug Double-Blind Method DYSPAREUNIA Dyspareunia - drug therapy ESTROGENS Female Humans INTRACRINOLOGY Medical treatment Menopause Postmenopause PRASTERONE Sexual behavior Tissues Treatment Outcome VAGINAL ATROPHY Women |
title | Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T07%3A06%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intravaginal%20dehydroepiandrosterone%20(prasterone),%20a%20highly%20efficient%20treatment%20of%20dyspareunia&rft.jtitle=Climacteric%20:%20the%20journal%20of%20the%20International%20Menopause%20Society&rft.au=Labrie,%20F.&rft.date=2011-04&rft.volume=14&rft.issue=2&rft.spage=282&rft.epage=288&rft.pages=282-288&rft.issn=1369-7137&rft.eissn=1473-0804&rft_id=info:doi/10.3109/13697137.2010.535226&rft_dat=%3Cproquest_infor%3E2335880561%3C/proquest_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c444t-a383d7bad64db74adea7aa08f5feb48e9e80553da736618ca1c8786dffdddb2b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=864546010&rft_id=info:pmid/21244215&rfr_iscdi=true |