The effects of coculture with autologous cryopreserved endometrial cells on human in vitro fertilization and early embryo morphology : A randomized study
The aim of this study was to examine the influence of endometrial cells on the fertilization rate and early embryonic morphology following routine in vitro fertilization (IVF). Cryopreservation with subsequent thawing allowed the use of autologous somatic cells, thus minimizing the risk of transmiss...
Gespeichert in:
Veröffentlicht in: | Journal of assisted reproduction and genetics 1996-05, Vol.13 (5), p.386-389 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 389 |
---|---|
container_issue | 5 |
container_start_page | 386 |
container_title | Journal of assisted reproduction and genetics |
container_volume | 13 |
creator | NIETO, F. S WATKINS, W. B LOPATA, A BAKER, H. W. G EDGAR, D. H |
description | The aim of this study was to examine the influence of endometrial cells on the fertilization rate and early embryonic morphology following routine in vitro fertilization (IVF). Cryopreservation with subsequent thawing allowed the use of autologous somatic cells, thus minimizing the risk of transmission of infective agents. Interpatient variability was eliminated by randomizing oocytes from each cycle into the control or coculture group.
Two hundred ninety-four oocytes from 24 IVF cycles (21 patients) were included in the study (145 coculture and 149 control). The normal fertilization rate of control oocytes (56.4%) was not significantly different from that of oocytes cocultured with endometrial cells (61.4%). The mean number of blastomeres in cocultured embryos (3.65) was not significantly different from the number in control embryos (3.46) 2 days after insemination, but the proportion of embryos with minimal or no fragmentation was significantly higher in the coculture group [34/84 (40.5%) vs. 17/80 (21.3%); P < 0.01].
The inclusion of cryopreserved autologous endometrial cells in routine clinical IVF procedures does not influence fertilization or the early cleavage rate but may reduce the extent of embryo fragmentation during the early cleavage divisions. |
doi_str_mv | 10.1007/BF02066169 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78226030</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>78226030</sourcerecordid><originalsourceid>FETCH-LOGICAL-c311t-384c2fd45b0fbf2665cd0115d904131956e10892155517ec24be3129d2da58703</originalsourceid><addsrcrecordid>eNpFkcFu1TAQRa0KVNrSDXskLxALpNCxHTsJu7aiBakSm3YdOfaYZ5TED9spSv-Ev8VRn8rKlu6ZI18PIe8YfGYAzcXVDXBQiqnuiJww2YiqEQJelTvItoJatW_IaUq_AKBruTgmx20jOpDihPy93yFF59DkRIOjJphlzEtE-sfnHdVLDmP4GZZETVzDPmLC-IiW4mzDhDl6PVKD41iGZ7pbJj1TP9NHn2OgDmP2o3_S2ZdQz2VKx3GlOA3FRacQ97vNvtIv9JJGvSn9U5GnvNj1LXnt9Jjw_HCekYebr_fX36q7H7ffry_vKiMYy5Voa8OdreUAbnBcKWksMCZtBzUTrJMKGbQdZ1JK1qDh9YCC8c5yq2XbgDgjH5-9-xh-L5hyP_m0VdIzlt5903KuQGzgp2fQxJBSRNfvo590XHsG_baH_v8eCvz-YF2GCe0Levj4kn845DoZPbrS3vj0gglWXl8r8Q8yKZGS</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>78226030</pqid></control><display><type>article</type><title>The effects of coculture with autologous cryopreserved endometrial cells on human in vitro fertilization and early embryo morphology : A randomized study</title><source>MEDLINE</source><source>SpringerNature Complete Journals</source><creator>NIETO, F. S ; WATKINS, W. B ; LOPATA, A ; BAKER, H. W. G ; EDGAR, D. H</creator><creatorcontrib>NIETO, F. S ; WATKINS, W. B ; LOPATA, A ; BAKER, H. W. G ; EDGAR, D. H</creatorcontrib><description>The aim of this study was to examine the influence of endometrial cells on the fertilization rate and early embryonic morphology following routine in vitro fertilization (IVF). Cryopreservation with subsequent thawing allowed the use of autologous somatic cells, thus minimizing the risk of transmission of infective agents. Interpatient variability was eliminated by randomizing oocytes from each cycle into the control or coculture group.
Two hundred ninety-four oocytes from 24 IVF cycles (21 patients) were included in the study (145 coculture and 149 control). The normal fertilization rate of control oocytes (56.4%) was not significantly different from that of oocytes cocultured with endometrial cells (61.4%). The mean number of blastomeres in cocultured embryos (3.65) was not significantly different from the number in control embryos (3.46) 2 days after insemination, but the proportion of embryos with minimal or no fragmentation was significantly higher in the coculture group [34/84 (40.5%) vs. 17/80 (21.3%); P < 0.01].
The inclusion of cryopreserved autologous endometrial cells in routine clinical IVF procedures does not influence fertilization or the early cleavage rate but may reduce the extent of embryo fragmentation during the early cleavage divisions.</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/BF02066169</identifier><identifier>PMID: 8739053</identifier><identifier>CODEN: JARGE4</identifier><language>eng</language><publisher>New York, NY: Kluwer/Plenum</publisher><subject>Adult ; Biological and medical sciences ; Birth control ; Blastomeres - cytology ; Cell Culture Techniques ; Cryopreservation - methods ; Endometrium ; Female ; Fertilization in Vitro - methods ; Gynecology. Andrology. Obstetrics ; Humans ; Male ; Medical sciences ; Oocytes - growth & development ; Oocytes - physiology ; Sterility. Assisted procreation</subject><ispartof>Journal of assisted reproduction and genetics, 1996-05, Vol.13 (5), p.386-389</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-384c2fd45b0fbf2665cd0115d904131956e10892155517ec24be3129d2da58703</citedby><cites>FETCH-LOGICAL-c311t-384c2fd45b0fbf2665cd0115d904131956e10892155517ec24be3129d2da58703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3104146$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8739053$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NIETO, F. S</creatorcontrib><creatorcontrib>WATKINS, W. B</creatorcontrib><creatorcontrib>LOPATA, A</creatorcontrib><creatorcontrib>BAKER, H. W. G</creatorcontrib><creatorcontrib>EDGAR, D. H</creatorcontrib><title>The effects of coculture with autologous cryopreserved endometrial cells on human in vitro fertilization and early embryo morphology : A randomized study</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><description>The aim of this study was to examine the influence of endometrial cells on the fertilization rate and early embryonic morphology following routine in vitro fertilization (IVF). Cryopreservation with subsequent thawing allowed the use of autologous somatic cells, thus minimizing the risk of transmission of infective agents. Interpatient variability was eliminated by randomizing oocytes from each cycle into the control or coculture group.
Two hundred ninety-four oocytes from 24 IVF cycles (21 patients) were included in the study (145 coculture and 149 control). The normal fertilization rate of control oocytes (56.4%) was not significantly different from that of oocytes cocultured with endometrial cells (61.4%). The mean number of blastomeres in cocultured embryos (3.65) was not significantly different from the number in control embryos (3.46) 2 days after insemination, but the proportion of embryos with minimal or no fragmentation was significantly higher in the coculture group [34/84 (40.5%) vs. 17/80 (21.3%); P < 0.01].
The inclusion of cryopreserved autologous endometrial cells in routine clinical IVF procedures does not influence fertilization or the early cleavage rate but may reduce the extent of embryo fragmentation during the early cleavage divisions.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Birth control</subject><subject>Blastomeres - cytology</subject><subject>Cell Culture Techniques</subject><subject>Cryopreservation - methods</subject><subject>Endometrium</subject><subject>Female</subject><subject>Fertilization in Vitro - methods</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Oocytes - growth & development</subject><subject>Oocytes - physiology</subject><subject>Sterility. Assisted procreation</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkcFu1TAQRa0KVNrSDXskLxALpNCxHTsJu7aiBakSm3YdOfaYZ5TED9spSv-Ev8VRn8rKlu6ZI18PIe8YfGYAzcXVDXBQiqnuiJww2YiqEQJelTvItoJatW_IaUq_AKBruTgmx20jOpDihPy93yFF59DkRIOjJphlzEtE-sfnHdVLDmP4GZZETVzDPmLC-IiW4mzDhDl6PVKD41iGZ7pbJj1TP9NHn2OgDmP2o3_S2ZdQz2VKx3GlOA3FRacQ97vNvtIv9JJGvSn9U5GnvNj1LXnt9Jjw_HCekYebr_fX36q7H7ffry_vKiMYy5Voa8OdreUAbnBcKWksMCZtBzUTrJMKGbQdZ1JK1qDh9YCC8c5yq2XbgDgjH5-9-xh-L5hyP_m0VdIzlt5903KuQGzgp2fQxJBSRNfvo590XHsG_baH_v8eCvz-YF2GCe0Levj4kn845DoZPbrS3vj0gglWXl8r8Q8yKZGS</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>NIETO, F. S</creator><creator>WATKINS, W. B</creator><creator>LOPATA, A</creator><creator>BAKER, H. W. G</creator><creator>EDGAR, D. H</creator><general>Kluwer/Plenum</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>19960501</creationdate><title>The effects of coculture with autologous cryopreserved endometrial cells on human in vitro fertilization and early embryo morphology : A randomized study</title><author>NIETO, F. S ; WATKINS, W. B ; LOPATA, A ; BAKER, H. W. G ; EDGAR, D. H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-384c2fd45b0fbf2665cd0115d904131956e10892155517ec24be3129d2da58703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Birth control</topic><topic>Blastomeres - cytology</topic><topic>Cell Culture Techniques</topic><topic>Cryopreservation - methods</topic><topic>Endometrium</topic><topic>Female</topic><topic>Fertilization in Vitro - methods</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Oocytes - growth & development</topic><topic>Oocytes - physiology</topic><topic>Sterility. Assisted procreation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NIETO, F. S</creatorcontrib><creatorcontrib>WATKINS, W. B</creatorcontrib><creatorcontrib>LOPATA, A</creatorcontrib><creatorcontrib>BAKER, H. W. G</creatorcontrib><creatorcontrib>EDGAR, D. H</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>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NIETO, F. S</au><au>WATKINS, W. B</au><au>LOPATA, A</au><au>BAKER, H. W. G</au><au>EDGAR, D. H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of coculture with autologous cryopreserved endometrial cells on human in vitro fertilization and early embryo morphology : A randomized study</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><addtitle>J Assist Reprod Genet</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>13</volume><issue>5</issue><spage>386</spage><epage>389</epage><pages>386-389</pages><issn>1058-0468</issn><eissn>1573-7330</eissn><coden>JARGE4</coden><abstract>The aim of this study was to examine the influence of endometrial cells on the fertilization rate and early embryonic morphology following routine in vitro fertilization (IVF). Cryopreservation with subsequent thawing allowed the use of autologous somatic cells, thus minimizing the risk of transmission of infective agents. Interpatient variability was eliminated by randomizing oocytes from each cycle into the control or coculture group.
Two hundred ninety-four oocytes from 24 IVF cycles (21 patients) were included in the study (145 coculture and 149 control). The normal fertilization rate of control oocytes (56.4%) was not significantly different from that of oocytes cocultured with endometrial cells (61.4%). The mean number of blastomeres in cocultured embryos (3.65) was not significantly different from the number in control embryos (3.46) 2 days after insemination, but the proportion of embryos with minimal or no fragmentation was significantly higher in the coculture group [34/84 (40.5%) vs. 17/80 (21.3%); P < 0.01].
The inclusion of cryopreserved autologous endometrial cells in routine clinical IVF procedures does not influence fertilization or the early cleavage rate but may reduce the extent of embryo fragmentation during the early cleavage divisions.</abstract><cop>New York, NY</cop><pub>Kluwer/Plenum</pub><pmid>8739053</pmid><doi>10.1007/BF02066169</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1058-0468 |
ispartof | Journal of assisted reproduction and genetics, 1996-05, Vol.13 (5), p.386-389 |
issn | 1058-0468 1573-7330 |
language | eng |
recordid | cdi_proquest_miscellaneous_78226030 |
source | MEDLINE; SpringerNature Complete Journals |
subjects | Adult Biological and medical sciences Birth control Blastomeres - cytology Cell Culture Techniques Cryopreservation - methods Endometrium Female Fertilization in Vitro - methods Gynecology. Andrology. Obstetrics Humans Male Medical sciences Oocytes - growth & development Oocytes - physiology Sterility. Assisted procreation |
title | The effects of coculture with autologous cryopreserved endometrial cells on human in vitro fertilization and early embryo morphology : A randomized study |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T10%3A13%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20effects%20of%20coculture%20with%20autologous%20cryopreserved%20endometrial%20cells%20on%20human%20in%20vitro%20fertilization%20and%20early%20embryo%20morphology%20:%20A%20randomized%20study&rft.jtitle=Journal%20of%20assisted%20reproduction%20and%20genetics&rft.au=NIETO,%20F.%20S&rft.date=1996-05-01&rft.volume=13&rft.issue=5&rft.spage=386&rft.epage=389&rft.pages=386-389&rft.issn=1058-0468&rft.eissn=1573-7330&rft.coden=JARGE4&rft_id=info:doi/10.1007/BF02066169&rft_dat=%3Cproquest_cross%3E78226030%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=78226030&rft_id=info:pmid/8739053&rfr_iscdi=true |