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Preimplantation Genetic Testing for Aneuploidy for Recurrent Pregnancy Loss and Recurrent Implantation Failure in Minimal Ovarian Stimulation Cycle for Women Aged 35–42 Years: Live Birth Rate, Developmental Follow-up of Children, and Embryo Ranking
This study was aimed at exploring the benefits of preimplantation genetic testing for aneuploidy (PGT-A) in ensuring a successful pregnancy in patients with recurrent pregnancy loss (RPL) caused by an abnormal number of chromosomes in the embryo and recurrent implantation failure (RIF). Thirty-two p...
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Published in: | Reproductive sciences (Thousand Oaks, Calif.) Calif.), 2023-03, Vol.30 (3), p.974-983 |
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creator | Kato, Keiichi Kuroda, Tomoko Yamadera-Egawa, Rie Ezoe, Kenji Aoyama, Naoki Usami, Akemi Miki, Tetsuya Yamamoto, Toshiyuki Takeshita, Toshiyuki |
description | This study was aimed at exploring the benefits of preimplantation genetic testing for aneuploidy (PGT-A) in ensuring a successful pregnancy in patients with recurrent pregnancy loss (RPL) caused by an abnormal number of chromosomes in the embryo and recurrent implantation failure (RIF). Thirty-two patients who underwent PGT-A (18 in the RIF protocol and 14 in the RPL protocol) were enrolled in the study, and 2556 patients who did not undergo PGT-A during the same
in vitro
fertilization (IVF) treatment period were enrolled as controls. All patients underwent minimal stimulation cycle IVF. In the RPL protocol, the live birth rate per embryo transfer (ET) and that per patient were higher with PGT-A (80.0% each) than without it (0% each;
P
= 0.0050), and the rate of miscarriages was lower with PGT-A than without it (20.0% vs. 100.0%,
P
= 0.0098). In the RIF protocol, there were no significant differences in the live birth rate per ET and in the rate of miscarriages between groups with and without PGT-A—90.0% vs. 69.2% (
P
= 0.2313) and 0% vs. 10.0% (
P
= 0.3297), respectively. None of the children whose mothers underwent PGT-A presented adverse findings at a 1.5-year developmental check-up. In conclusion, PGT-A in RPL is advantageous for improving the live birth rate per ET and that per patient in minimal stimulation cycle IVF; it reduces the rate of miscarriages. In addition, PGT-A might be more beneficial for embryo selection than the existing morphological grades of blastocysts, resulting in earlier conception. |
doi_str_mv | 10.1007/s43032-022-01073-z |
format | article |
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in vitro
fertilization (IVF) treatment period were enrolled as controls. All patients underwent minimal stimulation cycle IVF. In the RPL protocol, the live birth rate per embryo transfer (ET) and that per patient were higher with PGT-A (80.0% each) than without it (0% each;
P
= 0.0050), and the rate of miscarriages was lower with PGT-A than without it (20.0% vs. 100.0%,
P
= 0.0098). In the RIF protocol, there were no significant differences in the live birth rate per ET and in the rate of miscarriages between groups with and without PGT-A—90.0% vs. 69.2% (
P
= 0.2313) and 0% vs. 10.0% (
P
= 0.3297), respectively. None of the children whose mothers underwent PGT-A presented adverse findings at a 1.5-year developmental check-up. In conclusion, PGT-A in RPL is advantageous for improving the live birth rate per ET and that per patient in minimal stimulation cycle IVF; it reduces the rate of miscarriages. In addition, PGT-A might be more beneficial for embryo selection than the existing morphological grades of blastocysts, resulting in earlier conception.</description><identifier>ISSN: 1933-7191</identifier><identifier>EISSN: 1933-7205</identifier><identifier>DOI: 10.1007/s43032-022-01073-z</identifier><identifier>PMID: 36085548</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Abortion, Habitual - diagnosis ; Abortion, Habitual - genetics ; Abortion, Habitual - therapy ; Aneuploidy ; Birth Rate ; Child ; Embryology ; Female ; Fertilization in Vitro - methods ; Follow-Up Studies ; Genetic Testing - methods ; Genetics: Original Article ; Humans ; Live Birth ; Medicine ; Medicine & Public Health ; Obstetrics/Perinatology/Midwifery ; Ovulation Induction ; Pregnancy ; Pregnancy Rate ; Preimplantation Diagnosis - methods ; Reproductive Medicine ; Retrospective Studies</subject><ispartof>Reproductive sciences (Thousand Oaks, Calif.), 2023-03, Vol.30 (3), p.974-983</ispartof><rights>The Author(s), under exclusive licence to Society for Reproductive Investigation 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2022. The Author(s), under exclusive licence to Society for Reproductive Investigation.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c364t-99a00ef4648e52b98b96cfd5f4b6874d45361e749921067d1ab360b147914d973</cites><orcidid>0000-0002-1394-4532</orcidid></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/36085548$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kato, Keiichi</creatorcontrib><creatorcontrib>Kuroda, Tomoko</creatorcontrib><creatorcontrib>Yamadera-Egawa, Rie</creatorcontrib><creatorcontrib>Ezoe, Kenji</creatorcontrib><creatorcontrib>Aoyama, Naoki</creatorcontrib><creatorcontrib>Usami, Akemi</creatorcontrib><creatorcontrib>Miki, Tetsuya</creatorcontrib><creatorcontrib>Yamamoto, Toshiyuki</creatorcontrib><creatorcontrib>Takeshita, Toshiyuki</creatorcontrib><title>Preimplantation Genetic Testing for Aneuploidy for Recurrent Pregnancy Loss and Recurrent Implantation Failure in Minimal Ovarian Stimulation Cycle for Women Aged 35–42 Years: Live Birth Rate, Developmental Follow-up of Children, and Embryo Ranking</title><title>Reproductive sciences (Thousand Oaks, Calif.)</title><addtitle>Reprod. Sci</addtitle><addtitle>Reprod Sci</addtitle><description>This study was aimed at exploring the benefits of preimplantation genetic testing for aneuploidy (PGT-A) in ensuring a successful pregnancy in patients with recurrent pregnancy loss (RPL) caused by an abnormal number of chromosomes in the embryo and recurrent implantation failure (RIF). Thirty-two patients who underwent PGT-A (18 in the RIF protocol and 14 in the RPL protocol) were enrolled in the study, and 2556 patients who did not undergo PGT-A during the same
in vitro
fertilization (IVF) treatment period were enrolled as controls. All patients underwent minimal stimulation cycle IVF. In the RPL protocol, the live birth rate per embryo transfer (ET) and that per patient were higher with PGT-A (80.0% each) than without it (0% each;
P
= 0.0050), and the rate of miscarriages was lower with PGT-A than without it (20.0% vs. 100.0%,
P
= 0.0098). In the RIF protocol, there were no significant differences in the live birth rate per ET and in the rate of miscarriages between groups with and without PGT-A—90.0% vs. 69.2% (
P
= 0.2313) and 0% vs. 10.0% (
P
= 0.3297), respectively. None of the children whose mothers underwent PGT-A presented adverse findings at a 1.5-year developmental check-up. In conclusion, PGT-A in RPL is advantageous for improving the live birth rate per ET and that per patient in minimal stimulation cycle IVF; it reduces the rate of miscarriages. In addition, PGT-A might be more beneficial for embryo selection than the existing morphological grades of blastocysts, resulting in earlier conception.</description><subject>Abortion, Habitual - diagnosis</subject><subject>Abortion, Habitual - genetics</subject><subject>Abortion, Habitual - therapy</subject><subject>Aneuploidy</subject><subject>Birth Rate</subject><subject>Child</subject><subject>Embryology</subject><subject>Female</subject><subject>Fertilization in Vitro - methods</subject><subject>Follow-Up Studies</subject><subject>Genetic Testing - methods</subject><subject>Genetics: Original Article</subject><subject>Humans</subject><subject>Live Birth</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Obstetrics/Perinatology/Midwifery</subject><subject>Ovulation Induction</subject><subject>Pregnancy</subject><subject>Pregnancy Rate</subject><subject>Preimplantation Diagnosis - methods</subject><subject>Reproductive Medicine</subject><subject>Retrospective Studies</subject><issn>1933-7191</issn><issn>1933-7205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9Uctu1DAUjRCIlsIPsEBesmiKHTsPs5sOnVJpUFEpQqwsJ7mZujh2sJ1B6ar_wB_yGawwkxZ1xcKyrXvOufeekyQvCT4iGJdvPKOYZinO4iG4pOnNo2SfcErTMsP54_s34WQveeb9NcY541n1NNmjBa7ynFX7ye-PDlQ_aGmCDMoadAoGgmrQJfigzAZ11qGFgXHQVrXT7nsBzegcmIAieWOkaSa0tt4jadoHxbOHsiup9OgAKYM-KKN6qdH5VjolDfoUVD_qGbacGg27Jl9sDwYtNtAimv-6_cky9BWk82_RWm0BHSsXrtCFDHCI3sEWtB0iPkTZldXa_kjHAdkOLa-UbuM0h7vZTvraTTayzLe42vPkSSe1hxd390HyeXVyuXyfrs9Pz5aLddrQgoWUc4kxdKxgFeRZzauaF03X5h2ri6pkLctpQaBknGcEF2VLZB3trQkrOWEtL-lB8nrWHZz9PkZbRa98AzqaA3b0IitJVjFOyyJCsxnauOing04MLnrlJkGw-Ju5mDMXMXOxy1zcRNKrO_2x7qH9R7kPOQLoDPCxZDbgxLUdnYk7_0_2D2e4vHA</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Kato, Keiichi</creator><creator>Kuroda, Tomoko</creator><creator>Yamadera-Egawa, Rie</creator><creator>Ezoe, Kenji</creator><creator>Aoyama, Naoki</creator><creator>Usami, Akemi</creator><creator>Miki, Tetsuya</creator><creator>Yamamoto, Toshiyuki</creator><creator>Takeshita, Toshiyuki</creator><general>Springer International Publishing</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>7X8</scope><orcidid>https://orcid.org/0000-0002-1394-4532</orcidid></search><sort><creationdate>20230301</creationdate><title>Preimplantation Genetic Testing for Aneuploidy for Recurrent Pregnancy Loss and Recurrent Implantation Failure in Minimal Ovarian Stimulation Cycle for Women Aged 35–42 Years: Live Birth Rate, Developmental Follow-up of Children, and Embryo Ranking</title><author>Kato, Keiichi ; Kuroda, Tomoko ; Yamadera-Egawa, Rie ; Ezoe, Kenji ; Aoyama, Naoki ; Usami, Akemi ; Miki, Tetsuya ; Yamamoto, Toshiyuki ; Takeshita, Toshiyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c364t-99a00ef4648e52b98b96cfd5f4b6874d45361e749921067d1ab360b147914d973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abortion, Habitual - diagnosis</topic><topic>Abortion, Habitual - genetics</topic><topic>Abortion, Habitual - therapy</topic><topic>Aneuploidy</topic><topic>Birth Rate</topic><topic>Child</topic><topic>Embryology</topic><topic>Female</topic><topic>Fertilization in Vitro - methods</topic><topic>Follow-Up Studies</topic><topic>Genetic Testing - methods</topic><topic>Genetics: Original Article</topic><topic>Humans</topic><topic>Live Birth</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Obstetrics/Perinatology/Midwifery</topic><topic>Ovulation Induction</topic><topic>Pregnancy</topic><topic>Pregnancy Rate</topic><topic>Preimplantation Diagnosis - methods</topic><topic>Reproductive Medicine</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kato, Keiichi</creatorcontrib><creatorcontrib>Kuroda, Tomoko</creatorcontrib><creatorcontrib>Yamadera-Egawa, Rie</creatorcontrib><creatorcontrib>Ezoe, Kenji</creatorcontrib><creatorcontrib>Aoyama, Naoki</creatorcontrib><creatorcontrib>Usami, Akemi</creatorcontrib><creatorcontrib>Miki, Tetsuya</creatorcontrib><creatorcontrib>Yamamoto, Toshiyuki</creatorcontrib><creatorcontrib>Takeshita, Toshiyuki</creatorcontrib><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>Reproductive sciences (Thousand Oaks, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kato, Keiichi</au><au>Kuroda, Tomoko</au><au>Yamadera-Egawa, Rie</au><au>Ezoe, Kenji</au><au>Aoyama, Naoki</au><au>Usami, Akemi</au><au>Miki, Tetsuya</au><au>Yamamoto, Toshiyuki</au><au>Takeshita, Toshiyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preimplantation Genetic Testing for Aneuploidy for Recurrent Pregnancy Loss and Recurrent Implantation Failure in Minimal Ovarian Stimulation Cycle for Women Aged 35–42 Years: Live Birth Rate, Developmental Follow-up of Children, and Embryo Ranking</atitle><jtitle>Reproductive sciences (Thousand Oaks, Calif.)</jtitle><stitle>Reprod. Sci</stitle><addtitle>Reprod Sci</addtitle><date>2023-03-01</date><risdate>2023</risdate><volume>30</volume><issue>3</issue><spage>974</spage><epage>983</epage><pages>974-983</pages><issn>1933-7191</issn><eissn>1933-7205</eissn><abstract>This study was aimed at exploring the benefits of preimplantation genetic testing for aneuploidy (PGT-A) in ensuring a successful pregnancy in patients with recurrent pregnancy loss (RPL) caused by an abnormal number of chromosomes in the embryo and recurrent implantation failure (RIF). Thirty-two patients who underwent PGT-A (18 in the RIF protocol and 14 in the RPL protocol) were enrolled in the study, and 2556 patients who did not undergo PGT-A during the same
in vitro
fertilization (IVF) treatment period were enrolled as controls. All patients underwent minimal stimulation cycle IVF. In the RPL protocol, the live birth rate per embryo transfer (ET) and that per patient were higher with PGT-A (80.0% each) than without it (0% each;
P
= 0.0050), and the rate of miscarriages was lower with PGT-A than without it (20.0% vs. 100.0%,
P
= 0.0098). In the RIF protocol, there were no significant differences in the live birth rate per ET and in the rate of miscarriages between groups with and without PGT-A—90.0% vs. 69.2% (
P
= 0.2313) and 0% vs. 10.0% (
P
= 0.3297), respectively. None of the children whose mothers underwent PGT-A presented adverse findings at a 1.5-year developmental check-up. In conclusion, PGT-A in RPL is advantageous for improving the live birth rate per ET and that per patient in minimal stimulation cycle IVF; it reduces the rate of miscarriages. In addition, PGT-A might be more beneficial for embryo selection than the existing morphological grades of blastocysts, resulting in earlier conception.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>36085548</pmid><doi>10.1007/s43032-022-01073-z</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1394-4532</orcidid></addata></record> |
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subjects | Abortion, Habitual - diagnosis Abortion, Habitual - genetics Abortion, Habitual - therapy Aneuploidy Birth Rate Child Embryology Female Fertilization in Vitro - methods Follow-Up Studies Genetic Testing - methods Genetics: Original Article Humans Live Birth Medicine Medicine & Public Health Obstetrics/Perinatology/Midwifery Ovulation Induction Pregnancy Pregnancy Rate Preimplantation Diagnosis - methods Reproductive Medicine Retrospective Studies |
title | Preimplantation Genetic Testing for Aneuploidy for Recurrent Pregnancy Loss and Recurrent Implantation Failure in Minimal Ovarian Stimulation Cycle for Women Aged 35–42 Years: Live Birth Rate, Developmental Follow-up of Children, and Embryo Ranking |
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