Predictive factors of ovarian response and clinical outcome after IVF/ICSI following a rFSH/GnRH antagonist protocol with or without oral contraceptive pre-treatment
BACKGROUND Prediction of ovarian response prior to the first controlled ovarian stimulation (COS) cycle is useful in determining the optimal starting dose of recombinant FSH (rFSH). However, potentially predictive factors may be subject to inter-cycle variability and many patients are pre-treated wi...
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creator | Andersen, A. Nyboe Witjes, H. Gordon, K. Mannaerts, B. |
description | BACKGROUND
Prediction of ovarian response prior to the first controlled ovarian stimulation (COS) cycle is useful in determining the optimal starting dose of recombinant FSH (rFSH). However, potentially predictive factors may be subject to inter-cycle variability and many patients are pre-treated with oral contraceptives (OC) for scheduling purposes. Our objective was to determine predictive factors of ovarian response for patients undergoing COS with rFSH in a gonadotrophin-releasing hormone antagonist protocol and to determine the inter-cycle variability of these factors.
METHODS
In this multinational trial, 442 patients were randomized to receive either OC treatment or no treatment prior to their first COS cycle. For candidate predictive factors, patient characteristics were collected at screening, and endocrine and sonographic data were collected during the early follicular phase of the two subsequent cycles. A treatment regimen of 200 IU rFSH and 0.25 mg ganirelix was applied during the second cycle. Predictive factors of ovarian response and of too low (18 oocytes) ovarian responses were determined using stepwise linear regression and stepwise logistic regression, respectively.
RESULTS
Anti-Müllerian hormone (AMH) and basal FSH were statistically significant predictors of the number of oocytes retrieved and of an excessive ovarian response. For low ovarian response, AMH was the only significant predictive factor. In the non-OC group, the predictive value was higher than in the OC group and higher at the early follicular phase of the stimulation cycle than of the previous cycle. The inter-cycle variation for AMH was low compared with the inter-cycle variation of other hormones. Between the two groups, there were no differences in the number or quality of embryos obtained or transferred, but the implantation rate was significantly lower in the OC group (24.1 versus 30.1%, P= 0.03), resulting in an ongoing pregnancy rate of 26.3% compared with 35.7% in the non-OC group (P= 0.05).
CONCLUSIONS
The best predictive model of ovarian response was in the non-OC group and included both AMH and basal FSH determined at the early follicular phase of the stimulation cycle. In the proceeding cycle, AMH alone had sufficient predictive value since it was not affected by inter-cycle variability or OC pretreatment.
Clinical trial identifier: NCT00778999. |
doi_str_mv | 10.1093/humrep/der318 |
format | Article |
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Prediction of ovarian response prior to the first controlled ovarian stimulation (COS) cycle is useful in determining the optimal starting dose of recombinant FSH (rFSH). However, potentially predictive factors may be subject to inter-cycle variability and many patients are pre-treated with oral contraceptives (OC) for scheduling purposes. Our objective was to determine predictive factors of ovarian response for patients undergoing COS with rFSH in a gonadotrophin-releasing hormone antagonist protocol and to determine the inter-cycle variability of these factors.
METHODS
In this multinational trial, 442 patients were randomized to receive either OC treatment or no treatment prior to their first COS cycle. For candidate predictive factors, patient characteristics were collected at screening, and endocrine and sonographic data were collected during the early follicular phase of the two subsequent cycles. A treatment regimen of 200 IU rFSH and 0.25 mg ganirelix was applied during the second cycle. Predictive factors of ovarian response and of too low (<6 oocytes) or too high (>18 oocytes) ovarian responses were determined using stepwise linear regression and stepwise logistic regression, respectively.
RESULTS
Anti-Müllerian hormone (AMH) and basal FSH were statistically significant predictors of the number of oocytes retrieved and of an excessive ovarian response. For low ovarian response, AMH was the only significant predictive factor. In the non-OC group, the predictive value was higher than in the OC group and higher at the early follicular phase of the stimulation cycle than of the previous cycle. The inter-cycle variation for AMH was low compared with the inter-cycle variation of other hormones. Between the two groups, there were no differences in the number or quality of embryos obtained or transferred, but the implantation rate was significantly lower in the OC group (24.1 versus 30.1%, P= 0.03), resulting in an ongoing pregnancy rate of 26.3% compared with 35.7% in the non-OC group (P= 0.05).
CONCLUSIONS
The best predictive model of ovarian response was in the non-OC group and included both AMH and basal FSH determined at the early follicular phase of the stimulation cycle. In the proceeding cycle, AMH alone had sufficient predictive value since it was not affected by inter-cycle variability or OC pretreatment.
Clinical trial identifier: NCT00778999.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/der318</identifier><identifier>PMID: 21954280</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; Anti-Mullerian Hormone - blood ; Biological and medical sciences ; Clinical Protocols ; Contraceptives, Oral, Hormonal - administration & dosage ; Contraceptives, Oral, Hormonal - therapeutic use ; Female ; Fertilization in Vitro - methods ; Follicle Stimulating Hormone - administration & dosage ; Follicle Stimulating Hormone - blood ; Follicle Stimulating Hormone - therapeutic use ; Gonadotropin-Releasing Hormone - antagonists & inhibitors ; Gynecology. Andrology. Obstetrics ; Hormone Antagonists - administration & dosage ; Hormone Antagonists - therapeutic use ; Humans ; Linear Models ; Logistic Models ; Medical sciences ; Ovulation Induction - methods ; Pregnancy ; Pregnancy Rate ; Sperm Injections, Intracytoplasmic - methods</subject><ispartof>Human reproduction (Oxford), 2011-12, Vol.26 (12), p.3413-3423</ispartof><rights>The Author 2011. 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@oup.com 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-7f6376908bcff0970cd57cf1dcfa139b0d86dbad4b38a26088d44a6c0939011d3</citedby><cites>FETCH-LOGICAL-c394t-7f6376908bcff0970cd57cf1dcfa139b0d86dbad4b38a26088d44a6c0939011d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24790092$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21954280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Andersen, A. Nyboe</creatorcontrib><creatorcontrib>Witjes, H.</creatorcontrib><creatorcontrib>Gordon, K.</creatorcontrib><creatorcontrib>Mannaerts, B.</creatorcontrib><creatorcontrib>Xpect investigators</creatorcontrib><creatorcontrib>on behalf of the Xpect investigators</creatorcontrib><title>Predictive factors of ovarian response and clinical outcome after IVF/ICSI following a rFSH/GnRH antagonist protocol with or without oral contraceptive pre-treatment</title><title>Human reproduction (Oxford)</title><addtitle>Hum Reprod</addtitle><description>BACKGROUND
Prediction of ovarian response prior to the first controlled ovarian stimulation (COS) cycle is useful in determining the optimal starting dose of recombinant FSH (rFSH). However, potentially predictive factors may be subject to inter-cycle variability and many patients are pre-treated with oral contraceptives (OC) for scheduling purposes. Our objective was to determine predictive factors of ovarian response for patients undergoing COS with rFSH in a gonadotrophin-releasing hormone antagonist protocol and to determine the inter-cycle variability of these factors.
METHODS
In this multinational trial, 442 patients were randomized to receive either OC treatment or no treatment prior to their first COS cycle. For candidate predictive factors, patient characteristics were collected at screening, and endocrine and sonographic data were collected during the early follicular phase of the two subsequent cycles. A treatment regimen of 200 IU rFSH and 0.25 mg ganirelix was applied during the second cycle. Predictive factors of ovarian response and of too low (<6 oocytes) or too high (>18 oocytes) ovarian responses were determined using stepwise linear regression and stepwise logistic regression, respectively.
RESULTS
Anti-Müllerian hormone (AMH) and basal FSH were statistically significant predictors of the number of oocytes retrieved and of an excessive ovarian response. For low ovarian response, AMH was the only significant predictive factor. In the non-OC group, the predictive value was higher than in the OC group and higher at the early follicular phase of the stimulation cycle than of the previous cycle. The inter-cycle variation for AMH was low compared with the inter-cycle variation of other hormones. Between the two groups, there were no differences in the number or quality of embryos obtained or transferred, but the implantation rate was significantly lower in the OC group (24.1 versus 30.1%, P= 0.03), resulting in an ongoing pregnancy rate of 26.3% compared with 35.7% in the non-OC group (P= 0.05).
CONCLUSIONS
The best predictive model of ovarian response was in the non-OC group and included both AMH and basal FSH determined at the early follicular phase of the stimulation cycle. In the proceeding cycle, AMH alone had sufficient predictive value since it was not affected by inter-cycle variability or OC pretreatment.
Clinical trial identifier: NCT00778999.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anti-Mullerian Hormone - blood</subject><subject>Biological and medical sciences</subject><subject>Clinical Protocols</subject><subject>Contraceptives, Oral, Hormonal - administration & dosage</subject><subject>Contraceptives, Oral, Hormonal - therapeutic use</subject><subject>Female</subject><subject>Fertilization in Vitro - methods</subject><subject>Follicle Stimulating Hormone - administration & dosage</subject><subject>Follicle Stimulating Hormone - blood</subject><subject>Follicle Stimulating Hormone - therapeutic use</subject><subject>Gonadotropin-Releasing Hormone - antagonists & inhibitors</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Hormone Antagonists - administration & dosage</subject><subject>Hormone Antagonists - therapeutic use</subject><subject>Humans</subject><subject>Linear Models</subject><subject>Logistic Models</subject><subject>Medical sciences</subject><subject>Ovulation Induction - methods</subject><subject>Pregnancy</subject><subject>Pregnancy Rate</subject><subject>Sperm Injections, Intracytoplasmic - methods</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0EokvhyBX5guAS1nayjn1Eq253pUqtWuAaTfynNUrsYDut-ED9nphmgSOnGY1-8-ZpHkJvKflEiazXd_MYzbTWJtZUPEMr2nBSsXpDnqMVYVxUlHJ6gl6l9J2Q0gr-Ep0wKjcNE2SFHq-i0U5ld2-wBZVDTDhYHO4hOvA4mjQFnwwGr7EanHcKBhzmrMJYhjabiA_fduvD9uaAbRiG8OD8LQYcdzf79bm_3pfNDLfBu5TxFEMOKgz4weU7HOJTLWKlLaoq-BxBmenJzBRNlaOBPBqfX6MXFoZk3hzrKfq6O_uy3VcXl-eH7eeLStWyyVVred1ySUSvrCWyJUpvWmWpVhZoLXuiBdc96KavBTBOhNBNA1yVP0pCqa5P0YdFtzj9MZuUu9ElZYYBvAlz6iRlrGWUbQpZLaSKIaVobDdFN0L82VHS_Q6mW4LplmAK_-6oPPej0X_pP0kU4P0RgFR-bCN45dI_rmklIZIV7uPChXn6z81fowGpyg</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Andersen, A. Nyboe</creator><creator>Witjes, H.</creator><creator>Gordon, K.</creator><creator>Mannaerts, B.</creator><general>Oxford University Press</general><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>7X8</scope></search><sort><creationdate>20111201</creationdate><title>Predictive factors of ovarian response and clinical outcome after IVF/ICSI following a rFSH/GnRH antagonist protocol with or without oral contraceptive pre-treatment</title><author>Andersen, A. Nyboe ; Witjes, H. ; Gordon, K. ; Mannaerts, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-7f6376908bcff0970cd57cf1dcfa139b0d86dbad4b38a26088d44a6c0939011d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Anti-Mullerian Hormone - blood</topic><topic>Biological and medical sciences</topic><topic>Clinical Protocols</topic><topic>Contraceptives, Oral, Hormonal - administration & dosage</topic><topic>Contraceptives, Oral, Hormonal - therapeutic use</topic><topic>Female</topic><topic>Fertilization in Vitro - methods</topic><topic>Follicle Stimulating Hormone - administration & dosage</topic><topic>Follicle Stimulating Hormone - blood</topic><topic>Follicle Stimulating Hormone - therapeutic use</topic><topic>Gonadotropin-Releasing Hormone - antagonists & inhibitors</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Hormone Antagonists - administration & dosage</topic><topic>Hormone Antagonists - therapeutic use</topic><topic>Humans</topic><topic>Linear Models</topic><topic>Logistic Models</topic><topic>Medical sciences</topic><topic>Ovulation Induction - methods</topic><topic>Pregnancy</topic><topic>Pregnancy Rate</topic><topic>Sperm Injections, Intracytoplasmic - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andersen, A. Nyboe</creatorcontrib><creatorcontrib>Witjes, H.</creatorcontrib><creatorcontrib>Gordon, K.</creatorcontrib><creatorcontrib>Mannaerts, B.</creatorcontrib><creatorcontrib>Xpect investigators</creatorcontrib><creatorcontrib>on behalf of the Xpect investigators</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andersen, A. Nyboe</au><au>Witjes, H.</au><au>Gordon, K.</au><au>Mannaerts, B.</au><aucorp>Xpect investigators</aucorp><aucorp>on behalf of the Xpect investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictive factors of ovarian response and clinical outcome after IVF/ICSI following a rFSH/GnRH antagonist protocol with or without oral contraceptive pre-treatment</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>26</volume><issue>12</issue><spage>3413</spage><epage>3423</epage><pages>3413-3423</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND
Prediction of ovarian response prior to the first controlled ovarian stimulation (COS) cycle is useful in determining the optimal starting dose of recombinant FSH (rFSH). However, potentially predictive factors may be subject to inter-cycle variability and many patients are pre-treated with oral contraceptives (OC) for scheduling purposes. Our objective was to determine predictive factors of ovarian response for patients undergoing COS with rFSH in a gonadotrophin-releasing hormone antagonist protocol and to determine the inter-cycle variability of these factors.
METHODS
In this multinational trial, 442 patients were randomized to receive either OC treatment or no treatment prior to their first COS cycle. For candidate predictive factors, patient characteristics were collected at screening, and endocrine and sonographic data were collected during the early follicular phase of the two subsequent cycles. A treatment regimen of 200 IU rFSH and 0.25 mg ganirelix was applied during the second cycle. Predictive factors of ovarian response and of too low (<6 oocytes) or too high (>18 oocytes) ovarian responses were determined using stepwise linear regression and stepwise logistic regression, respectively.
RESULTS
Anti-Müllerian hormone (AMH) and basal FSH were statistically significant predictors of the number of oocytes retrieved and of an excessive ovarian response. For low ovarian response, AMH was the only significant predictive factor. In the non-OC group, the predictive value was higher than in the OC group and higher at the early follicular phase of the stimulation cycle than of the previous cycle. The inter-cycle variation for AMH was low compared with the inter-cycle variation of other hormones. Between the two groups, there were no differences in the number or quality of embryos obtained or transferred, but the implantation rate was significantly lower in the OC group (24.1 versus 30.1%, P= 0.03), resulting in an ongoing pregnancy rate of 26.3% compared with 35.7% in the non-OC group (P= 0.05).
CONCLUSIONS
The best predictive model of ovarian response was in the non-OC group and included both AMH and basal FSH determined at the early follicular phase of the stimulation cycle. In the proceeding cycle, AMH alone had sufficient predictive value since it was not affected by inter-cycle variability or OC pretreatment.
Clinical trial identifier: NCT00778999.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>21954280</pmid><doi>10.1093/humrep/der318</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adolescent Adult Anti-Mullerian Hormone - blood Biological and medical sciences Clinical Protocols Contraceptives, Oral, Hormonal - administration & dosage Contraceptives, Oral, Hormonal - therapeutic use Female Fertilization in Vitro - methods Follicle Stimulating Hormone - administration & dosage Follicle Stimulating Hormone - blood Follicle Stimulating Hormone - therapeutic use Gonadotropin-Releasing Hormone - antagonists & inhibitors Gynecology. Andrology. Obstetrics Hormone Antagonists - administration & dosage Hormone Antagonists - therapeutic use Humans Linear Models Logistic Models Medical sciences Ovulation Induction - methods Pregnancy Pregnancy Rate Sperm Injections, Intracytoplasmic - methods |
title | Predictive factors of ovarian response and clinical outcome after IVF/ICSI following a rFSH/GnRH antagonist protocol with or without oral contraceptive pre-treatment |
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