Effect of estrogen priming through luteal phase and stimulation phase in poor responders in in-vitro fertilization

Purpose To verify whether a novel protocol administering E 2 during the luteal phase of the preceding cycle and during ovarian stimulation in GnRH antagonist cycle could enhance follicular response and hence improve outcomes in poor responders. Methods In this retrospective analysis, a total of 155...

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Veröffentlicht in:Journal of assisted reproduction and genetics 2012-03, Vol.29 (3), p.225-230
Hauptverfasser: Chang, Eun Mi, Han, Ji Eun, Won, Hyung Jae, Kim, You Shin, Yoon, Tae Ki, Lee, Woo Sik
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container_issue 3
container_start_page 225
container_title Journal of assisted reproduction and genetics
container_volume 29
creator Chang, Eun Mi
Han, Ji Eun
Won, Hyung Jae
Kim, You Shin
Yoon, Tae Ki
Lee, Woo Sik
description Purpose To verify whether a novel protocol administering E 2 during the luteal phase of the preceding cycle and during ovarian stimulation in GnRH antagonist cycle could enhance follicular response and hence improve outcomes in poor responders. Methods In this retrospective analysis, a total of 155 poor responder patients subjected to IVF/ICSI were analyzed. All the patients had history of more than one prior IVF cycle failure with poor response (less than 5 oocytes retrieved and/or maximal E 2 level less than 500 pg/mL) by using conventional long agonist or antagonist protocol. In luteal E2 treatment protocol ( n  = 86), oral estradiol valerate 4 mg/day was initiated on luteal day 21 and either stopped at menstrual cycle day 3 (Protocol A, n  = 28) or continued during the period of ovarian stimulation until the day of hCG injection (Protocol B, n  = 58). IVF parameters and pregnancy outcome of luteal E2 treatments group were compared with a standard GnRH antagonist protocol ( n  = 69) which the patients received no hormonal pretreatment. Results Compared to standard GnRH antagonist protocol, cancellation rate was lower with luteal E2 group (15.1% vs 37.7%, p  
doi_str_mv 10.1007/s10815-011-9685-7
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Methods In this retrospective analysis, a total of 155 poor responder patients subjected to IVF/ICSI were analyzed. All the patients had history of more than one prior IVF cycle failure with poor response (less than 5 oocytes retrieved and/or maximal E 2 level less than 500 pg/mL) by using conventional long agonist or antagonist protocol. In luteal E2 treatment protocol ( n  = 86), oral estradiol valerate 4 mg/day was initiated on luteal day 21 and either stopped at menstrual cycle day 3 (Protocol A, n  = 28) or continued during the period of ovarian stimulation until the day of hCG injection (Protocol B, n  = 58). IVF parameters and pregnancy outcome of luteal E2 treatments group were compared with a standard GnRH antagonist protocol ( n  = 69) which the patients received no hormonal pretreatment. Results Compared to standard GnRH antagonist protocol, cancellation rate was lower with luteal E2 group (15.1% vs 37.7%, p  &lt; 0.01). Moreover, patients treated with luteal estrogen resulted in an increased number of oocytes retrieved (4.5 ± 2.9 vs 3.2 ± 1.9; p  &lt; 0.01). A trend toward increase in number of normally fertilized embryos (2.9 ± 2.1vs 2.3 ± 1.9; p  = 0.043), and increased prevalence of good quality embryos (51.2% vs 25%; p  = 0.047) were noted. Comparing protocol A and B, there were no significant difference between embryologic data, however there were slight increase in ongoing pregnancy rate in protocol B compared to A (27.1% vs 20%, p  = 0.357), although statistical significance was not achieved. Conclusion Estrogen priming through luteal phase and stimulation phase improved ovarian responsiveness and this may lead to an increase in pregnancy rate in poor responders with failed cycle.</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-011-9685-7</identifier><identifier>PMID: 22160464</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Adult ; Assisted Reproduction Technologies ; Cohort analysis ; Cohort Studies ; Data processing ; Drug Resistance ; Ectogenesis - drug effects ; Embryos ; Estradiol ; Estradiol - administration &amp; dosage ; Estradiol - analogs &amp; derivatives ; Estradiol - blood ; Estradiol - pharmacology ; Estrogens ; Estrogens - administration &amp; dosage ; Estrogens - blood ; Estrogens - pharmacology ; Female ; Fertility ; Fertilization ; Fertilization in Vitro ; Gonadotropin-releasing hormone ; Gonadotropin-Releasing Hormone - antagonists &amp; inhibitors ; Gynecology ; Hormone Antagonists - pharmacology ; Human Genetics ; Humans ; In vitro fertilization ; Infertility - blood ; Infertility - therapy ; Luteal Phase - drug effects ; Medicine ; Medicine &amp; Public Health ; Menstrual cycle ; Menstruation ; Oocytes ; Ovaries ; Ovulation - drug effects ; Ovulation Induction - methods ; Pregnancy ; Pregnancy Outcome ; Pregnancy Rate ; Reproductive Medicine ; Retrospective Studies ; Statistics ; Ultrasonic imaging</subject><ispartof>Journal of assisted reproduction and genetics, 2012-03, Vol.29 (3), p.225-230</ispartof><rights>Springer Science+Business Media, LLC 2011</rights><rights>Springer Science+Business Media, LLC 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c566t-d87a6fd1833410ff13e0f6289fcf615c959f7f4e93592454fccfc8110240ef873</citedby><cites>FETCH-LOGICAL-c566t-d87a6fd1833410ff13e0f6289fcf615c959f7f4e93592454fccfc8110240ef873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288134/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288134/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22160464$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Eun Mi</creatorcontrib><creatorcontrib>Han, Ji Eun</creatorcontrib><creatorcontrib>Won, Hyung Jae</creatorcontrib><creatorcontrib>Kim, You Shin</creatorcontrib><creatorcontrib>Yoon, Tae Ki</creatorcontrib><creatorcontrib>Lee, Woo Sik</creatorcontrib><title>Effect of estrogen priming through luteal phase and stimulation phase in poor responders in in-vitro fertilization</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><addtitle>J Assist Reprod Genet</addtitle><description>Purpose To verify whether a novel protocol administering E 2 during the luteal phase of the preceding cycle and during ovarian stimulation in GnRH antagonist cycle could enhance follicular response and hence improve outcomes in poor responders. Methods In this retrospective analysis, a total of 155 poor responder patients subjected to IVF/ICSI were analyzed. All the patients had history of more than one prior IVF cycle failure with poor response (less than 5 oocytes retrieved and/or maximal E 2 level less than 500 pg/mL) by using conventional long agonist or antagonist protocol. In luteal E2 treatment protocol ( n  = 86), oral estradiol valerate 4 mg/day was initiated on luteal day 21 and either stopped at menstrual cycle day 3 (Protocol A, n  = 28) or continued during the period of ovarian stimulation until the day of hCG injection (Protocol B, n  = 58). IVF parameters and pregnancy outcome of luteal E2 treatments group were compared with a standard GnRH antagonist protocol ( n  = 69) which the patients received no hormonal pretreatment. Results Compared to standard GnRH antagonist protocol, cancellation rate was lower with luteal E2 group (15.1% vs 37.7%, p  &lt; 0.01). Moreover, patients treated with luteal estrogen resulted in an increased number of oocytes retrieved (4.5 ± 2.9 vs 3.2 ± 1.9; p  &lt; 0.01). A trend toward increase in number of normally fertilized embryos (2.9 ± 2.1vs 2.3 ± 1.9; p  = 0.043), and increased prevalence of good quality embryos (51.2% vs 25%; p  = 0.047) were noted. Comparing protocol A and B, there were no significant difference between embryologic data, however there were slight increase in ongoing pregnancy rate in protocol B compared to A (27.1% vs 20%, p  = 0.357), although statistical significance was not achieved. Conclusion Estrogen priming through luteal phase and stimulation phase improved ovarian responsiveness and this may lead to an increase in pregnancy rate in poor responders with failed cycle.</description><subject>Adult</subject><subject>Assisted Reproduction Technologies</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Data processing</subject><subject>Drug Resistance</subject><subject>Ectogenesis - drug effects</subject><subject>Embryos</subject><subject>Estradiol</subject><subject>Estradiol - administration &amp; dosage</subject><subject>Estradiol - analogs &amp; derivatives</subject><subject>Estradiol - blood</subject><subject>Estradiol - pharmacology</subject><subject>Estrogens</subject><subject>Estrogens - administration &amp; dosage</subject><subject>Estrogens - blood</subject><subject>Estrogens - pharmacology</subject><subject>Female</subject><subject>Fertility</subject><subject>Fertilization</subject><subject>Fertilization in Vitro</subject><subject>Gonadotropin-releasing hormone</subject><subject>Gonadotropin-Releasing Hormone - antagonists &amp; inhibitors</subject><subject>Gynecology</subject><subject>Hormone Antagonists - pharmacology</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>In vitro fertilization</subject><subject>Infertility - blood</subject><subject>Infertility - therapy</subject><subject>Luteal Phase - drug effects</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Menstrual cycle</subject><subject>Menstruation</subject><subject>Oocytes</subject><subject>Ovaries</subject><subject>Ovulation - drug effects</subject><subject>Ovulation Induction - methods</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Pregnancy Rate</subject><subject>Reproductive Medicine</subject><subject>Retrospective Studies</subject><subject>Statistics</subject><subject>Ultrasonic imaging</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kUuPFSEQhYnROOPoD3BjiBtXKMWrYWNiJuMjmcSNrgnS0JdJX7hC9yT666W91_GRuKJS9dWBw0HoKdCXQOnwqgHVIAkFIEZpSYZ76BzkwMnAOb3fayo1oULpM_SotRtKqdGMP0RnjIHqfXGO6lWMwS-4RBzaUssUMj7UtE95wsuulnXa4XldgpvxYedawC6PuC1pv85uSSWfuqkXpVRcQzuUPIbatlbK5DZ1URxDXdKcvv9ceYweRDe38OR0XqDPb68-Xb4n1x_ffbh8c028VGohox6ciiNozgXQGIEHGhXTJvqoQHojTRyiCIZLw4QU0fvoNQBlgoaoB36BXh91D-uXfRh9yEt1s93cufrNFpfs35OcdnYqt5YzrYGLLvDiJFDL17V_j92n5sM8uxzK2qyRQnFDte7k83_Im7LW3N1Zw_jAhALVIThCvpbWaoh3TwFqtzztMU_b87Rbnnbz8OxPD3cbvwLsADsCrY_yFOrvm_-v-gOBT63f</recordid><startdate>20120301</startdate><enddate>20120301</enddate><creator>Chang, Eun Mi</creator><creator>Han, Ji Eun</creator><creator>Won, Hyung Jae</creator><creator>Kim, You Shin</creator><creator>Yoon, Tae Ki</creator><creator>Lee, Woo Sik</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20120301</creationdate><title>Effect of estrogen priming through luteal phase and stimulation phase in poor responders in in-vitro fertilization</title><author>Chang, Eun Mi ; 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Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Eun Mi</au><au>Han, Ji Eun</au><au>Won, Hyung Jae</au><au>Kim, You Shin</au><au>Yoon, Tae Ki</au><au>Lee, Woo Sik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of estrogen priming through luteal phase and stimulation phase in poor responders in in-vitro fertilization</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><stitle>J Assist Reprod Genet</stitle><addtitle>J Assist Reprod Genet</addtitle><date>2012-03-01</date><risdate>2012</risdate><volume>29</volume><issue>3</issue><spage>225</spage><epage>230</epage><pages>225-230</pages><issn>1058-0468</issn><eissn>1573-7330</eissn><abstract>Purpose To verify whether a novel protocol administering E 2 during the luteal phase of the preceding cycle and during ovarian stimulation in GnRH antagonist cycle could enhance follicular response and hence improve outcomes in poor responders. Methods In this retrospective analysis, a total of 155 poor responder patients subjected to IVF/ICSI were analyzed. All the patients had history of more than one prior IVF cycle failure with poor response (less than 5 oocytes retrieved and/or maximal E 2 level less than 500 pg/mL) by using conventional long agonist or antagonist protocol. In luteal E2 treatment protocol ( n  = 86), oral estradiol valerate 4 mg/day was initiated on luteal day 21 and either stopped at menstrual cycle day 3 (Protocol A, n  = 28) or continued during the period of ovarian stimulation until the day of hCG injection (Protocol B, n  = 58). IVF parameters and pregnancy outcome of luteal E2 treatments group were compared with a standard GnRH antagonist protocol ( n  = 69) which the patients received no hormonal pretreatment. Results Compared to standard GnRH antagonist protocol, cancellation rate was lower with luteal E2 group (15.1% vs 37.7%, p  &lt; 0.01). Moreover, patients treated with luteal estrogen resulted in an increased number of oocytes retrieved (4.5 ± 2.9 vs 3.2 ± 1.9; p  &lt; 0.01). A trend toward increase in number of normally fertilized embryos (2.9 ± 2.1vs 2.3 ± 1.9; p  = 0.043), and increased prevalence of good quality embryos (51.2% vs 25%; p  = 0.047) were noted. Comparing protocol A and B, there were no significant difference between embryologic data, however there were slight increase in ongoing pregnancy rate in protocol B compared to A (27.1% vs 20%, p  = 0.357), although statistical significance was not achieved. Conclusion Estrogen priming through luteal phase and stimulation phase improved ovarian responsiveness and this may lead to an increase in pregnancy rate in poor responders with failed cycle.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>22160464</pmid><doi>10.1007/s10815-011-9685-7</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Springer Nature - Complete Springer Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Adult
Assisted Reproduction Technologies
Cohort analysis
Cohort Studies
Data processing
Drug Resistance
Ectogenesis - drug effects
Embryos
Estradiol
Estradiol - administration & dosage
Estradiol - analogs & derivatives
Estradiol - blood
Estradiol - pharmacology
Estrogens
Estrogens - administration & dosage
Estrogens - blood
Estrogens - pharmacology
Female
Fertility
Fertilization
Fertilization in Vitro
Gonadotropin-releasing hormone
Gonadotropin-Releasing Hormone - antagonists & inhibitors
Gynecology
Hormone Antagonists - pharmacology
Human Genetics
Humans
In vitro fertilization
Infertility - blood
Infertility - therapy
Luteal Phase - drug effects
Medicine
Medicine & Public Health
Menstrual cycle
Menstruation
Oocytes
Ovaries
Ovulation - drug effects
Ovulation Induction - methods
Pregnancy
Pregnancy Outcome
Pregnancy Rate
Reproductive Medicine
Retrospective Studies
Statistics
Ultrasonic imaging
title Effect of estrogen priming through luteal phase and stimulation phase in poor responders in in-vitro fertilization
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