Cleavage kinetics analysis of human embryos predicts development to blastocyst and implantation

Abstract Cleavage kinetics of human embryos is indicative of ability to develop to blastocyst and implant. Recent advances in time-lapse microscopy have opened new and important research opportunities. In this study involving infertile couples requiring standard IVF/intracytoplasmic sperm injection...

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Veröffentlicht in:Reproductive biomedicine online 2012-11, Vol.25 (5), p.474-480
Hauptverfasser: Dal Canto, Mariabeatrice, Coticchio, Giovanni, Mignini Renzini, Mario, De Ponti, Elena, Novara, Paola Vittoria, Brambillasca, Fausta, Comi, Ruggero, Fadini, Rubens
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container_issue 5
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container_title Reproductive biomedicine online
container_volume 25
creator Dal Canto, Mariabeatrice
Coticchio, Giovanni
Mignini Renzini, Mario
De Ponti, Elena
Novara, Paola Vittoria
Brambillasca, Fausta
Comi, Ruggero
Fadini, Rubens
description Abstract Cleavage kinetics of human embryos is indicative of ability to develop to blastocyst and implant. Recent advances in time-lapse microscopy have opened new and important research opportunities. In this study involving infertile couples requiring standard IVF/intracytoplasmic sperm injection treatment, zygotes were cultured by integrated embryo-culture time-lapse microscopy to analyse cleavage times from the 2- to the 8-cell stages in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after 8-cell stage, times of cleavage to 7- and 8-cell stages of embryos developing to blastocyst were shorter (56.5 ± 8.1 versus 58.8 ± 10.4 h, P = 0.03 and 61.0 ± 9.4 versus 65.2 ± 13.0 h, P = 0.0008, respectively). In embryos developing to blastocyst, absence of blastocoele expansion on day 5 was associated with progressive cleavage delay. Implanting embryos developed to 8-cell stage in a shorter period compared with those unable to implant (54.9 ± 5.2 and 58.0 ± 7.2 h, respectively, P = 0.035). In conclusion, cleavage from 2- to 8-cell stage occurs progressively earlier in embryos with the ability to develop to blastocyst, expand and implant. Conventional observation times on days 2 and 3 are inappropriate for accurate embryo evaluation. The speed at which human embryos cleave is known to be suggestive of their ability to develop in vitro to the blastocyst stage and implant after transfer into the uterus. Recent advances in time-lapse microscopy, which allows acquisition of images every 15–20 min, have opened new and important research opportunities. In a retrospective study involving infertile couples requiring standard IVF or intracytoplasmic sperm injection treatment, fertilized oocytes were cultured by an integrated embryo-culture time-lapse microscopy system in order to perform an analysis of cleavage times from the 2- to the 8-cell stage in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after the 8-cell stage, times of cleavage to the 7- and 8-cell stage of embryos that developed to blastocyst were significantly shorter (56.5 ± 8.1 h versus 58.8 ± 10.4 h and 61.0 ± 9.4 h versus 65.2 ± 13.0 h, respectively). In embryos developing to the blastocyst stage, absence of blastocoele expansion on day 5 was associated with a progressive cleavage delay. Implanting embryos developed to the 8-cell stage in a shorter period compared to those unable to implant (5
doi_str_mv 10.1016/j.rbmo.2012.07.016
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Recent advances in time-lapse microscopy have opened new and important research opportunities. In this study involving infertile couples requiring standard IVF/intracytoplasmic sperm injection treatment, zygotes were cultured by integrated embryo-culture time-lapse microscopy to analyse cleavage times from the 2- to the 8-cell stages in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after 8-cell stage, times of cleavage to 7- and 8-cell stages of embryos developing to blastocyst were shorter (56.5 ± 8.1 versus 58.8 ± 10.4 h, P = 0.03 and 61.0 ± 9.4 versus 65.2 ± 13.0 h, P = 0.0008, respectively). In embryos developing to blastocyst, absence of blastocoele expansion on day 5 was associated with progressive cleavage delay. Implanting embryos developed to 8-cell stage in a shorter period compared with those unable to implant (54.9 ± 5.2 and 58.0 ± 7.2 h, respectively, P = 0.035). In conclusion, cleavage from 2- to 8-cell stage occurs progressively earlier in embryos with the ability to develop to blastocyst, expand and implant. Conventional observation times on days 2 and 3 are inappropriate for accurate embryo evaluation. The speed at which human embryos cleave is known to be suggestive of their ability to develop in vitro to the blastocyst stage and implant after transfer into the uterus. Recent advances in time-lapse microscopy, which allows acquisition of images every 15–20 min, have opened new and important research opportunities. In a retrospective study involving infertile couples requiring standard IVF or intracytoplasmic sperm injection treatment, fertilized oocytes were cultured by an integrated embryo-culture time-lapse microscopy system in order to perform an analysis of cleavage times from the 2- to the 8-cell stage in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after the 8-cell stage, times of cleavage to the 7- and 8-cell stage of embryos that developed to blastocyst were significantly shorter (56.5 ± 8.1 h versus 58.8 ± 10.4 h and 61.0 ± 9.4 h versus 65.2 ± 13.0 h, respectively). In embryos developing to the blastocyst stage, absence of blastocoele expansion on day 5 was associated with a progressive cleavage delay. Implanting embryos developed to the 8-cell stage in a shorter period compared to those unable to implant (54.9 ± 5.2 h and 58.0 ± 7.2 h, respectively, P = 0.035). In conclusion, cleavage from the 2- to the 8-cell stage occurs progressively earlier in embryos with the ability to develop to blastocyst, expand and implant. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c477t-dcdd2dd8e73b715aba011b7cefc231308deeb57d202cfef09c48eb825b72b50a3</citedby><cites>FETCH-LOGICAL-c477t-dcdd2dd8e73b715aba011b7cefc231308deeb57d202cfef09c48eb825b72b50a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.rbmo.2012.07.016$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22995750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dal Canto, Mariabeatrice</creatorcontrib><creatorcontrib>Coticchio, Giovanni</creatorcontrib><creatorcontrib>Mignini Renzini, Mario</creatorcontrib><creatorcontrib>De Ponti, Elena</creatorcontrib><creatorcontrib>Novara, Paola Vittoria</creatorcontrib><creatorcontrib>Brambillasca, Fausta</creatorcontrib><creatorcontrib>Comi, Ruggero</creatorcontrib><creatorcontrib>Fadini, Rubens</creatorcontrib><title>Cleavage kinetics analysis of human embryos predicts development to blastocyst and implantation</title><title>Reproductive biomedicine online</title><addtitle>Reprod Biomed Online</addtitle><description>Abstract Cleavage kinetics of human embryos is indicative of ability to develop to blastocyst and implant. Recent advances in time-lapse microscopy have opened new and important research opportunities. In this study involving infertile couples requiring standard IVF/intracytoplasmic sperm injection treatment, zygotes were cultured by integrated embryo-culture time-lapse microscopy to analyse cleavage times from the 2- to the 8-cell stages in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after 8-cell stage, times of cleavage to 7- and 8-cell stages of embryos developing to blastocyst were shorter (56.5 ± 8.1 versus 58.8 ± 10.4 h, P = 0.03 and 61.0 ± 9.4 versus 65.2 ± 13.0 h, P = 0.0008, respectively). In embryos developing to blastocyst, absence of blastocoele expansion on day 5 was associated with progressive cleavage delay. Implanting embryos developed to 8-cell stage in a shorter period compared with those unable to implant (54.9 ± 5.2 and 58.0 ± 7.2 h, respectively, P = 0.035). In conclusion, cleavage from 2- to 8-cell stage occurs progressively earlier in embryos with the ability to develop to blastocyst, expand and implant. Conventional observation times on days 2 and 3 are inappropriate for accurate embryo evaluation. The speed at which human embryos cleave is known to be suggestive of their ability to develop in vitro to the blastocyst stage and implant after transfer into the uterus. Recent advances in time-lapse microscopy, which allows acquisition of images every 15–20 min, have opened new and important research opportunities. In a retrospective study involving infertile couples requiring standard IVF or intracytoplasmic sperm injection treatment, fertilized oocytes were cultured by an integrated embryo-culture time-lapse microscopy system in order to perform an analysis of cleavage times from the 2- to the 8-cell stage in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after the 8-cell stage, times of cleavage to the 7- and 8-cell stage of embryos that developed to blastocyst were significantly shorter (56.5 ± 8.1 h versus 58.8 ± 10.4 h and 61.0 ± 9.4 h versus 65.2 ± 13.0 h, respectively). In embryos developing to the blastocyst stage, absence of blastocoele expansion on day 5 was associated with a progressive cleavage delay. Implanting embryos developed to the 8-cell stage in a shorter period compared to those unable to implant (54.9 ± 5.2 h and 58.0 ± 7.2 h, respectively, P = 0.035). In conclusion, cleavage from the 2- to the 8-cell stage occurs progressively earlier in embryos with the ability to develop to blastocyst, expand and implant. Conventional observation times on day 2 and 3 are appropriate for accurate embryo evaluation.</description><subject>Adult</subject><subject>blastocyst</subject><subject>Blastocyst - cytology</subject><subject>Cell Division</subject><subject>cleavage</subject><subject>Embryo Culture Techniques</subject><subject>Embryo Implantation</subject><subject>Embryo Transfer</subject><subject>Embryonic Development</subject><subject>embryos</subject><subject>Female</subject><subject>Fertilization in Vitro</subject><subject>Humans</subject><subject>implantation</subject><subject>IVF</subject><subject>Obstetrics and Gynecology</subject><subject>Pregnancy</subject><subject>Time Factors</subject><subject>Time-Lapse Imaging</subject><subject>time-lapse microscopy</subject><issn>1472-6483</issn><issn>1472-6491</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v1DAQxS0EakvpF-CAfOSywXaSdSIhJLSiBakSB-Bs-c8EvHXi4HFWyrfH0ZYeOHDyaPR-T573CHnNWcUZ3787VsmMsRKMi4rJqqyekSveSLHbNz1__jR39SV5iXhkjHesqy_IpRB938qWXRF1CKBP-ifQBz9B9hapnnRY0SONA_21jHqiMJq0RqRzAudtRurgBCHOI0yZ5khN0JijXTEX2FE_zkFPWWcfp1fkxaADws3je01-3H76fvi8u_969-Xw8X5nGynzzlnnhHMdyNpI3mqjGedGWhisqHnNOgdgWukEE3aAgfW26cB0ojVSmJbp-pq8PfvOKf5eALMaPVoI5SMQF1Sc1_1eCN60RSrOUpsiYoJBzcmPOq2KM7UFq45qC1ZtwSomVVkV6M2j_2JGcE_I3ySL4P1ZAOXKk4ek0HqYbEksgc3KRf9__w__4Db4yVsdHmAFPMYllVrKHQoLo75t1W7NcsFYs2d9_Qf4qKFX</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Dal Canto, Mariabeatrice</creator><creator>Coticchio, Giovanni</creator><creator>Mignini Renzini, Mario</creator><creator>De Ponti, Elena</creator><creator>Novara, Paola Vittoria</creator><creator>Brambillasca, Fausta</creator><creator>Comi, Ruggero</creator><creator>Fadini, Rubens</creator><general>Elsevier Ltd</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></search><sort><creationdate>20121101</creationdate><title>Cleavage kinetics analysis of human embryos predicts development to blastocyst and implantation</title><author>Dal Canto, Mariabeatrice ; Coticchio, Giovanni ; Mignini Renzini, Mario ; De Ponti, Elena ; Novara, Paola Vittoria ; Brambillasca, Fausta ; Comi, Ruggero ; Fadini, Rubens</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c477t-dcdd2dd8e73b715aba011b7cefc231308deeb57d202cfef09c48eb825b72b50a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>blastocyst</topic><topic>Blastocyst - cytology</topic><topic>Cell Division</topic><topic>cleavage</topic><topic>Embryo Culture Techniques</topic><topic>Embryo Implantation</topic><topic>Embryo Transfer</topic><topic>Embryonic Development</topic><topic>embryos</topic><topic>Female</topic><topic>Fertilization in Vitro</topic><topic>Humans</topic><topic>implantation</topic><topic>IVF</topic><topic>Obstetrics and Gynecology</topic><topic>Pregnancy</topic><topic>Time Factors</topic><topic>Time-Lapse Imaging</topic><topic>time-lapse microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dal Canto, Mariabeatrice</creatorcontrib><creatorcontrib>Coticchio, Giovanni</creatorcontrib><creatorcontrib>Mignini Renzini, Mario</creatorcontrib><creatorcontrib>De Ponti, Elena</creatorcontrib><creatorcontrib>Novara, Paola Vittoria</creatorcontrib><creatorcontrib>Brambillasca, Fausta</creatorcontrib><creatorcontrib>Comi, Ruggero</creatorcontrib><creatorcontrib>Fadini, Rubens</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 biomedicine online</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dal Canto, Mariabeatrice</au><au>Coticchio, Giovanni</au><au>Mignini Renzini, Mario</au><au>De Ponti, Elena</au><au>Novara, Paola Vittoria</au><au>Brambillasca, Fausta</au><au>Comi, Ruggero</au><au>Fadini, Rubens</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cleavage kinetics analysis of human embryos predicts development to blastocyst and implantation</atitle><jtitle>Reproductive biomedicine online</jtitle><addtitle>Reprod Biomed Online</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>25</volume><issue>5</issue><spage>474</spage><epage>480</epage><pages>474-480</pages><issn>1472-6483</issn><eissn>1472-6491</eissn><abstract>Abstract Cleavage kinetics of human embryos is indicative of ability to develop to blastocyst and implant. Recent advances in time-lapse microscopy have opened new and important research opportunities. In this study involving infertile couples requiring standard IVF/intracytoplasmic sperm injection treatment, zygotes were cultured by integrated embryo-culture time-lapse microscopy to analyse cleavage times from the 2- to the 8-cell stages in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after 8-cell stage, times of cleavage to 7- and 8-cell stages of embryos developing to blastocyst were shorter (56.5 ± 8.1 versus 58.8 ± 10.4 h, P = 0.03 and 61.0 ± 9.4 versus 65.2 ± 13.0 h, P = 0.0008, respectively). In embryos developing to blastocyst, absence of blastocoele expansion on day 5 was associated with progressive cleavage delay. Implanting embryos developed to 8-cell stage in a shorter period compared with those unable to implant (54.9 ± 5.2 and 58.0 ± 7.2 h, respectively, P = 0.035). In conclusion, cleavage from 2- to 8-cell stage occurs progressively earlier in embryos with the ability to develop to blastocyst, expand and implant. Conventional observation times on days 2 and 3 are inappropriate for accurate embryo evaluation. The speed at which human embryos cleave is known to be suggestive of their ability to develop in vitro to the blastocyst stage and implant after transfer into the uterus. Recent advances in time-lapse microscopy, which allows acquisition of images every 15–20 min, have opened new and important research opportunities. In a retrospective study involving infertile couples requiring standard IVF or intracytoplasmic sperm injection treatment, fertilized oocytes were cultured by an integrated embryo-culture time-lapse microscopy system in order to perform an analysis of cleavage times from the 2- to the 8-cell stage in relation to the ability to develop to blastocyst, expand and implant. In comparison to embryos arresting after the 8-cell stage, times of cleavage to the 7- and 8-cell stage of embryos that developed to blastocyst were significantly shorter (56.5 ± 8.1 h versus 58.8 ± 10.4 h and 61.0 ± 9.4 h versus 65.2 ± 13.0 h, respectively). In embryos developing to the blastocyst stage, absence of blastocoele expansion on day 5 was associated with a progressive cleavage delay. Implanting embryos developed to the 8-cell stage in a shorter period compared to those unable to implant (54.9 ± 5.2 h and 58.0 ± 7.2 h, respectively, P = 0.035). In conclusion, cleavage from the 2- to the 8-cell stage occurs progressively earlier in embryos with the ability to develop to blastocyst, expand and implant. Conventional observation times on day 2 and 3 are appropriate for accurate embryo evaluation.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>22995750</pmid><doi>10.1016/j.rbmo.2012.07.016</doi><tpages>7</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adult
blastocyst
Blastocyst - cytology
Cell Division
cleavage
Embryo Culture Techniques
Embryo Implantation
Embryo Transfer
Embryonic Development
embryos
Female
Fertilization in Vitro
Humans
implantation
IVF
Obstetrics and Gynecology
Pregnancy
Time Factors
Time-Lapse Imaging
time-lapse microscopy
title Cleavage kinetics analysis of human embryos predicts development to blastocyst and implantation
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