Naltrexone treatment in clomiphene resistant women with polycystic ovary syndrome

BACKGROUND Endogenous opiates may affect various aspects of reproductive and metabolic function in patients with polycystic ovary syndrome (PCOS). This study evaluated long-term inhibition of the opioid system using naltrexone in clomiphene citrate (CC)-resistant women with PCOS. METHODS A group of...

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Veröffentlicht in:Human reproduction (Oxford) 2008-11, Vol.23 (11), p.2564-2569
Hauptverfasser: Ahmed, M.I., Duleba, A.J., El Shahat, O., Ibrahim, M.E., Salem, A.
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container_end_page 2569
container_issue 11
container_start_page 2564
container_title Human reproduction (Oxford)
container_volume 23
creator Ahmed, M.I.
Duleba, A.J.
El Shahat, O.
Ibrahim, M.E.
Salem, A.
description BACKGROUND Endogenous opiates may affect various aspects of reproductive and metabolic function in patients with polycystic ovary syndrome (PCOS). This study evaluated long-term inhibition of the opioid system using naltrexone in clomiphene citrate (CC)-resistant women with PCOS. METHODS A group of 30 infertile females with PCOS were evaluated; all subjects were obese, hyperandrogenic and hyperinsulinemic; 16 patients were amenorrhic and 14 were oligomenorrhic. All subjects received natrexone (50 mg p.o. daily) for 6 months. Patients who did not ovulate after 12 weeks of naltrexone monotherapy, also received CC (starting at 50 mg/day for 5 days and, for non-responders, increasing it up to 150 mg/day). RESULTS Of the 30 women, 3 ovulated during naltrexone monotherapy and 19 of the remaining 27 ovulated during naltrexone + CC therapy. There were no conceptions during naltrexone monotherapy, but 9 of 27 women (33.3%) conceived during naltrexone + CC; there was one missed abortion at 9 weeks, one preterm delivery at 34 weeks and seven term live births. Naltrexone therapy was also followed by significant reductions in BMI, fasting serum insulin, luteinizing hormone (LH), LH/follicle-stimulating hormone ratio and testosterone. CONCLUSIONS In this preliminary trial, naltrexone improved endocrine and metabolic function in women with CC-resistant PCOS. Furthermore, naltrexone restored CC sensitivity in the majority of subjects, resulting in a significant number of pregnancies.
doi_str_mv 10.1093/humrep/den273
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This study evaluated long-term inhibition of the opioid system using naltrexone in clomiphene citrate (CC)-resistant women with PCOS. METHODS A group of 30 infertile females with PCOS were evaluated; all subjects were obese, hyperandrogenic and hyperinsulinemic; 16 patients were amenorrhic and 14 were oligomenorrhic. All subjects received natrexone (50 mg p.o. daily) for 6 months. Patients who did not ovulate after 12 weeks of naltrexone monotherapy, also received CC (starting at 50 mg/day for 5 days and, for non-responders, increasing it up to 150 mg/day). RESULTS Of the 30 women, 3 ovulated during naltrexone monotherapy and 19 of the remaining 27 ovulated during naltrexone + CC therapy. There were no conceptions during naltrexone monotherapy, but 9 of 27 women (33.3%) conceived during naltrexone + CC; there was one missed abortion at 9 weeks, one preterm delivery at 34 weeks and seven term live births. Naltrexone therapy was also followed by significant reductions in BMI, fasting serum insulin, luteinizing hormone (LH), LH/follicle-stimulating hormone ratio and testosterone. CONCLUSIONS In this preliminary trial, naltrexone improved endocrine and metabolic function in women with CC-resistant PCOS. Furthermore, naltrexone restored CC sensitivity in the majority of subjects, resulting in a significant number of pregnancies.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/den273</identifier><identifier>PMID: 18641399</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; Analgesics, Opioid - metabolism ; Biological and medical sciences ; Body Mass Index ; Clomiphene - pharmacology ; clomiphene resistance ; Drug Resistance ; Estrogen Antagonists - pharmacology ; Female ; Gynecology. Andrology. Obstetrics ; Humans ; infertility ; Infertility, Female - drug therapy ; Luteinizing Hormone - metabolism ; Medical sciences ; naltrexone ; Naltrexone - therapeutic use ; Narcotic Antagonists - therapeutic use ; PCOS ; Polycystic Ovary Syndrome - drug therapy ; Pregnancy ; Pregnancy Rate</subject><ispartof>Human reproduction (Oxford), 2008-11, Vol.23 (11), p.2564-2569</ispartof><rights>The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2008</rights><rights>2008 INIST-CNRS</rights><rights>The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. 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This study evaluated long-term inhibition of the opioid system using naltrexone in clomiphene citrate (CC)-resistant women with PCOS. METHODS A group of 30 infertile females with PCOS were evaluated; all subjects were obese, hyperandrogenic and hyperinsulinemic; 16 patients were amenorrhic and 14 were oligomenorrhic. All subjects received natrexone (50 mg p.o. daily) for 6 months. Patients who did not ovulate after 12 weeks of naltrexone monotherapy, also received CC (starting at 50 mg/day for 5 days and, for non-responders, increasing it up to 150 mg/day). RESULTS Of the 30 women, 3 ovulated during naltrexone monotherapy and 19 of the remaining 27 ovulated during naltrexone + CC therapy. There were no conceptions during naltrexone monotherapy, but 9 of 27 women (33.3%) conceived during naltrexone + CC; there was one missed abortion at 9 weeks, one preterm delivery at 34 weeks and seven term live births. Naltrexone therapy was also followed by significant reductions in BMI, fasting serum insulin, luteinizing hormone (LH), LH/follicle-stimulating hormone ratio and testosterone. CONCLUSIONS In this preliminary trial, naltrexone improved endocrine and metabolic function in women with CC-resistant PCOS. Furthermore, naltrexone restored CC sensitivity in the majority of subjects, resulting in a significant number of pregnancies.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Analgesics, Opioid - metabolism</subject><subject>Biological and medical sciences</subject><subject>Body Mass Index</subject><subject>Clomiphene - pharmacology</subject><subject>clomiphene resistance</subject><subject>Drug Resistance</subject><subject>Estrogen Antagonists - pharmacology</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>infertility</subject><subject>Infertility, Female - drug therapy</subject><subject>Luteinizing Hormone - metabolism</subject><subject>Medical sciences</subject><subject>naltrexone</subject><subject>Naltrexone - therapeutic use</subject><subject>Narcotic Antagonists - therapeutic use</subject><subject>PCOS</subject><subject>Polycystic Ovary Syndrome - drug therapy</subject><subject>Pregnancy</subject><subject>Pregnancy Rate</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd-L1DAQx4Mo3t7qo69SBA9f6uZHkyaPcnh3yq6iKIgvIU0nbM-2qUl7e_vfm6NlBV98yEyY-cxk5huEXhD8lmDFNvupCzBsauhpyR6hFSkEzinj-DFaYSpkToggZ-g8xluM01WKp-gs2YIwpVboyyfTjgHufQ9Z8mbsoB-zps9s67tm2EOKB4hNHE2KH3xKZ4dm3GeDb4_2GMfGZv7OhGMWj30dUv4ZeuJMG-H54tfo-9X7b5c3-fbz9YfLd9vcFlyOeY2Nq6GoKw60VAVw5URliK2tUGXlqJRVydIpHLOFxZV02D0UcMqk5daxNbqY-w7B_54gjrprooW2NT34KWqhhKSKiQS--ge89VPo02yaEqJYoXCZoHyGbPAxBnB6CE2X9tIE6weh9Sy0noVO_Mul6VR1UP-lF2UT8HoBTLSmdcH0toknjmJJJOU8cW9mzk_Df99cZky_Afcn2IRfWpSs5Prmx09Nd2JH2Ndr_ZH9Abzrp40</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Ahmed, M.I.</creator><creator>Duleba, A.J.</creator><creator>El Shahat, O.</creator><creator>Ibrahim, M.E.</creator><creator>Salem, A.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20081101</creationdate><title>Naltrexone treatment in clomiphene resistant women with polycystic ovary syndrome</title><author>Ahmed, M.I. ; Duleba, A.J. ; El Shahat, O. ; Ibrahim, M.E. ; Salem, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-d0afde4db5e2794e59f6ba1cdc697bf288b738b74f3c4c0b8f0ffde45238c5cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Analgesics, Opioid - metabolism</topic><topic>Biological and medical sciences</topic><topic>Body Mass Index</topic><topic>Clomiphene - pharmacology</topic><topic>clomiphene resistance</topic><topic>Drug Resistance</topic><topic>Estrogen Antagonists - pharmacology</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>infertility</topic><topic>Infertility, Female - drug therapy</topic><topic>Luteinizing Hormone - metabolism</topic><topic>Medical sciences</topic><topic>naltrexone</topic><topic>Naltrexone - therapeutic use</topic><topic>Narcotic Antagonists - therapeutic use</topic><topic>PCOS</topic><topic>Polycystic Ovary Syndrome - drug therapy</topic><topic>Pregnancy</topic><topic>Pregnancy Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahmed, M.I.</creatorcontrib><creatorcontrib>Duleba, A.J.</creatorcontrib><creatorcontrib>El Shahat, O.</creatorcontrib><creatorcontrib>Ibrahim, M.E.</creatorcontrib><creatorcontrib>Salem, A.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmed, M.I.</au><au>Duleba, A.J.</au><au>El Shahat, O.</au><au>Ibrahim, M.E.</au><au>Salem, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Naltrexone treatment in clomiphene resistant women with polycystic ovary syndrome</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>23</volume><issue>11</issue><spage>2564</spage><epage>2569</epage><pages>2564-2569</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND Endogenous opiates may affect various aspects of reproductive and metabolic function in patients with polycystic ovary syndrome (PCOS). This study evaluated long-term inhibition of the opioid system using naltrexone in clomiphene citrate (CC)-resistant women with PCOS. METHODS A group of 30 infertile females with PCOS were evaluated; all subjects were obese, hyperandrogenic and hyperinsulinemic; 16 patients were amenorrhic and 14 were oligomenorrhic. All subjects received natrexone (50 mg p.o. daily) for 6 months. Patients who did not ovulate after 12 weeks of naltrexone monotherapy, also received CC (starting at 50 mg/day for 5 days and, for non-responders, increasing it up to 150 mg/day). RESULTS Of the 30 women, 3 ovulated during naltrexone monotherapy and 19 of the remaining 27 ovulated during naltrexone + CC therapy. There were no conceptions during naltrexone monotherapy, but 9 of 27 women (33.3%) conceived during naltrexone + CC; there was one missed abortion at 9 weeks, one preterm delivery at 34 weeks and seven term live births. Naltrexone therapy was also followed by significant reductions in BMI, fasting serum insulin, luteinizing hormone (LH), LH/follicle-stimulating hormone ratio and testosterone. CONCLUSIONS In this preliminary trial, naltrexone improved endocrine and metabolic function in women with CC-resistant PCOS. Furthermore, naltrexone restored CC sensitivity in the majority of subjects, resulting in a significant number of pregnancies.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>18641399</pmid><doi>10.1093/humrep/den273</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Analgesics, Opioid - metabolism
Biological and medical sciences
Body Mass Index
Clomiphene - pharmacology
clomiphene resistance
Drug Resistance
Estrogen Antagonists - pharmacology
Female
Gynecology. Andrology. Obstetrics
Humans
infertility
Infertility, Female - drug therapy
Luteinizing Hormone - metabolism
Medical sciences
naltrexone
Naltrexone - therapeutic use
Narcotic Antagonists - therapeutic use
PCOS
Polycystic Ovary Syndrome - drug therapy
Pregnancy
Pregnancy Rate
title Naltrexone treatment in clomiphene resistant women with polycystic ovary syndrome
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