Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations

Purpose The purpose of the study was to compare the morphokinetic parameters of embryos carrying balanced chromosomal translocations with those carrying unbalanced chromosomal translocations using time-lapse microscopy. Methods The study group included 270 embryos that underwent biopsies on day 3 fo...

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Veröffentlicht in:Journal of assisted reproduction and genetics 2019-02, Vol.36 (2), p.315-324
Hauptverfasser: Amir, Hadar, Barbash-Hazan, Shiri, Kalma, Yael, Frumkin, Tsvia, Malcov, Mira, Samara, Nivin, Hasson, Joseph, Reches, Adi, Azem, Foad, Ben-Yosef, Dalit
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container_issue 2
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container_title Journal of assisted reproduction and genetics
container_volume 36
creator Amir, Hadar
Barbash-Hazan, Shiri
Kalma, Yael
Frumkin, Tsvia
Malcov, Mira
Samara, Nivin
Hasson, Joseph
Reches, Adi
Azem, Foad
Ben-Yosef, Dalit
description Purpose The purpose of the study was to compare the morphokinetic parameters of embryos carrying balanced chromosomal translocations with those carrying unbalanced chromosomal translocations using time-lapse microscopy. Methods The study group included 270 embryos that underwent biopsies on day 3 for preimplantation genetic diagnosis (PGD) for chromosomal translocations in our unit between 2013 and 2015. All embryos were incubated under time-lapse microscopy and evaluated for timing of developmental events up to day 5. The timing of these events was compared between balanced and unbalanced embryos, potentially viable and nonviable variants, and maternal versus paternal inheritance of the translocation. Results The PGD analysis found that 209 (77%) of the 270 biopsied embryos carried an unbalanced translocation. Embryos carrying unbalanced translocations, which are expected to lead to implantation failure or miscarriage, cleaved less synchronously and were delayed in time of cleavage to the 4-cell stage (t4) and in time of start of blastulation (tSB) compared with balanced embryos ( P  
doi_str_mv 10.1007/s10815-018-1361-8
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Methods The study group included 270 embryos that underwent biopsies on day 3 for preimplantation genetic diagnosis (PGD) for chromosomal translocations in our unit between 2013 and 2015. All embryos were incubated under time-lapse microscopy and evaluated for timing of developmental events up to day 5. The timing of these events was compared between balanced and unbalanced embryos, potentially viable and nonviable variants, and maternal versus paternal inheritance of the translocation. Results The PGD analysis found that 209 (77%) of the 270 biopsied embryos carried an unbalanced translocation. Embryos carrying unbalanced translocations, which are expected to lead to implantation failure or miscarriage, cleaved less synchronously and were delayed in time of cleavage to the 4-cell stage (t4) and in time of start of blastulation (tSB) compared with balanced embryos ( P  &lt; 0.05). Furthermore, embryos carrying nonviable translocations demonstrated a significant delay at the time of pronuclei fading (tPNf) compared with those carrying potentially viable translocations ( P  &lt; 0.05). Embryos whose unbalanced translocations were of maternal origin were significantly delayed in most of the morphokinetic parameters (including tPNf, t2, t3, t4, t6, t7, t8, cc2, s2, and tSB) compared with embryos carrying balanced translocations ( P  &lt; 0.05). Conclusions Embryos carrying unbalanced chromosomal translocations mainly of maternal origin undergo delayed development and asynchronous cleavage that may lead to implantation failure or miscarriage.</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-018-1361-8</identifier><identifier>PMID: 30421343</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Abortion, Spontaneous - epidemiology ; Abortion, Spontaneous - pathology ; Blastocyst - metabolism ; Blastocyst - pathology ; Chromosome translocations ; Embryo Biology ; Embryo Culture Techniques ; Embryo Implantation - genetics ; Embryo Transfer - methods ; Embryonic Development - genetics ; Embryos ; Female ; Fertilization in Vitro ; Genetic screening ; Gynecology ; Human Genetics ; Humans ; Male ; Medicine ; Medicine &amp; Public Health ; Microscopy ; Miscarriage ; Pregnancy ; Preimplantation Diagnosis ; Reproductive Medicine ; Sperm Injections, Intracytoplasmic - methods ; Translocation, Genetic - genetics</subject><ispartof>Journal of assisted reproduction and genetics, 2019-02, Vol.36 (2), p.315-324</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-p212t-b32c24419ba927cd7315b51fb386e61b2152c6f3cc2c655f3a058d18228f7b563</cites><orcidid>0000-0001-9987-8697</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10815-018-1361-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10815-018-1361-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30421343$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Amir, Hadar</creatorcontrib><creatorcontrib>Barbash-Hazan, Shiri</creatorcontrib><creatorcontrib>Kalma, Yael</creatorcontrib><creatorcontrib>Frumkin, Tsvia</creatorcontrib><creatorcontrib>Malcov, Mira</creatorcontrib><creatorcontrib>Samara, Nivin</creatorcontrib><creatorcontrib>Hasson, Joseph</creatorcontrib><creatorcontrib>Reches, Adi</creatorcontrib><creatorcontrib>Azem, Foad</creatorcontrib><creatorcontrib>Ben-Yosef, Dalit</creatorcontrib><title>Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><addtitle>J Assist Reprod Genet</addtitle><description>Purpose The purpose of the study was to compare the morphokinetic parameters of embryos carrying balanced chromosomal translocations with those carrying unbalanced chromosomal translocations using time-lapse microscopy. Methods The study group included 270 embryos that underwent biopsies on day 3 for preimplantation genetic diagnosis (PGD) for chromosomal translocations in our unit between 2013 and 2015. All embryos were incubated under time-lapse microscopy and evaluated for timing of developmental events up to day 5. The timing of these events was compared between balanced and unbalanced embryos, potentially viable and nonviable variants, and maternal versus paternal inheritance of the translocation. Results The PGD analysis found that 209 (77%) of the 270 biopsied embryos carried an unbalanced translocation. Embryos carrying unbalanced translocations, which are expected to lead to implantation failure or miscarriage, cleaved less synchronously and were delayed in time of cleavage to the 4-cell stage (t4) and in time of start of blastulation (tSB) compared with balanced embryos ( P  &lt; 0.05). Furthermore, embryos carrying nonviable translocations demonstrated a significant delay at the time of pronuclei fading (tPNf) compared with those carrying potentially viable translocations ( P  &lt; 0.05). Embryos whose unbalanced translocations were of maternal origin were significantly delayed in most of the morphokinetic parameters (including tPNf, t2, t3, t4, t6, t7, t8, cc2, s2, and tSB) compared with embryos carrying balanced translocations ( P  &lt; 0.05). Conclusions Embryos carrying unbalanced chromosomal translocations mainly of maternal origin undergo delayed development and asynchronous cleavage that may lead to implantation failure or miscarriage.</description><subject>Abortion, Spontaneous - epidemiology</subject><subject>Abortion, Spontaneous - pathology</subject><subject>Blastocyst - metabolism</subject><subject>Blastocyst - pathology</subject><subject>Chromosome translocations</subject><subject>Embryo Biology</subject><subject>Embryo Culture Techniques</subject><subject>Embryo Implantation - genetics</subject><subject>Embryo Transfer - methods</subject><subject>Embryonic Development - genetics</subject><subject>Embryos</subject><subject>Female</subject><subject>Fertilization in Vitro</subject><subject>Genetic screening</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Microscopy</subject><subject>Miscarriage</subject><subject>Pregnancy</subject><subject>Preimplantation Diagnosis</subject><subject>Reproductive Medicine</subject><subject>Sperm Injections, Intracytoplasmic - methods</subject><subject>Translocation, Genetic - genetics</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkc1LxDAQxYMo7vrxB3iRghcv0UymabNHWfyCBS96DkmarpW2qUm7sP-9WVcRPL2B-fF4M4-QC2A3wFh5G4FJEJSBpIAFUHlA5iBKpCUiO0wzE5KyvJAzchLjB2NsITkekxmynAPmOCfvr03naKuH6LKm0-umX2fBbZxuY1a5Vm9dlXTjWj90rh8zX2euM2HrY2Z1CNsdP_VGt7q3CbXvwXc--k632Rh0H1tv9dj4Pp6RozqZuvMfPSVvD_evyye6enl8Xt6t6MCBj9QgtzzPYWH0gpe2KhGEEVAblIUrwHAQ3BY1WptEiBp1urECybmsSyMKPCXXe98h-M_JxVF1TbSuTQGdn6JKd_MSS2SY0Kt_6IefQp_SfVOQchQsUZc_1GQ6V6khpD-Frfr9YQL4Hohp1a9d-LMBpnZFqX1RKhWldkUpiV8rZ4PV</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Amir, Hadar</creator><creator>Barbash-Hazan, Shiri</creator><creator>Kalma, Yael</creator><creator>Frumkin, Tsvia</creator><creator>Malcov, Mira</creator><creator>Samara, Nivin</creator><creator>Hasson, Joseph</creator><creator>Reches, Adi</creator><creator>Azem, Foad</creator><creator>Ben-Yosef, Dalit</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>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>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9987-8697</orcidid></search><sort><creationdate>20190201</creationdate><title>Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations</title><author>Amir, Hadar ; 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Methods The study group included 270 embryos that underwent biopsies on day 3 for preimplantation genetic diagnosis (PGD) for chromosomal translocations in our unit between 2013 and 2015. All embryos were incubated under time-lapse microscopy and evaluated for timing of developmental events up to day 5. The timing of these events was compared between balanced and unbalanced embryos, potentially viable and nonviable variants, and maternal versus paternal inheritance of the translocation. Results The PGD analysis found that 209 (77%) of the 270 biopsied embryos carried an unbalanced translocation. Embryos carrying unbalanced translocations, which are expected to lead to implantation failure or miscarriage, cleaved less synchronously and were delayed in time of cleavage to the 4-cell stage (t4) and in time of start of blastulation (tSB) compared with balanced embryos ( P  &lt; 0.05). Furthermore, embryos carrying nonviable translocations demonstrated a significant delay at the time of pronuclei fading (tPNf) compared with those carrying potentially viable translocations ( P  &lt; 0.05). Embryos whose unbalanced translocations were of maternal origin were significantly delayed in most of the morphokinetic parameters (including tPNf, t2, t3, t4, t6, t7, t8, cc2, s2, and tSB) compared with embryos carrying balanced translocations ( P  &lt; 0.05). Conclusions Embryos carrying unbalanced chromosomal translocations mainly of maternal origin undergo delayed development and asynchronous cleavage that may lead to implantation failure or miscarriage.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>30421343</pmid><doi>10.1007/s10815-018-1361-8</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9987-8697</orcidid><oa>free_for_read</oa></addata></record>
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subjects Abortion, Spontaneous - epidemiology
Abortion, Spontaneous - pathology
Blastocyst - metabolism
Blastocyst - pathology
Chromosome translocations
Embryo Biology
Embryo Culture Techniques
Embryo Implantation - genetics
Embryo Transfer - methods
Embryonic Development - genetics
Embryos
Female
Fertilization in Vitro
Genetic screening
Gynecology
Human Genetics
Humans
Male
Medicine
Medicine & Public Health
Microscopy
Miscarriage
Pregnancy
Preimplantation Diagnosis
Reproductive Medicine
Sperm Injections, Intracytoplasmic - methods
Translocation, Genetic - genetics
title Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations
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