Chromosomal abnormality rate in human pre-embryos derived from in vitro fertilization cycles cultured in the presence of Follicular-Fluid Meiosis Activating Sterol (FF-MAS)
BACKGROUND: The objective of the study was to investigate the effect of Follicular-fluid meiosis activating sterol (FF-MAS) when added to the culture media on the incidence of chromosomal abnormalities and pre-embryo development in human pre-embryos. METHODS: 243 women undergoing IVF/ICSI treatment...
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creator | Bergh, Christina Loft, Anne Lundin, Kersti Ziebe, Sören Nilsson, Lars Wikland, Matts Gröndahl, Christian Arce, J.-C. |
description | BACKGROUND: The objective of the study was to investigate the effect of Follicular-fluid meiosis activating sterol (FF-MAS) when added to the culture media on the incidence of chromosomal abnormalities and pre-embryo development in human pre-embryos. METHODS: 243 women undergoing IVF/ICSI treatment donated 353 oocytes in a multicentre, prospective, randomized, double blind, four-arm, controlled trial performed at Danish and Swedish public and private IVF centers. Metaphase II oocytes were randomly assigned to: FF-MAS 5 μM, FF-MAS 20 μM, ethanol 0.2% (vehicle control) or water for injection (inert control). The exposure regimen of FF-MAS to the human oocytes was 4 h prior to fertilization by ICSI and 20 h exposure post ICSI. The primary endpoint was the incidence of numerical chromosomal abnormalities. Secondary endpoints were cleavage rate and pre-embryo quality. RESULT: On the pre-embryo level, no significant differences in chromosomal abnormality rate were observed among the four groups. However, the percentage of uniformly normal pre-embryos was significantly lower in the pooled FF-MAS group (5 μM: 12% and 20 μM: 17%) than in the pooled control group (inert control 32% and vehicle control 42%). A high level of mosaicism (41–60%) was found in all groups. At the blastomere level, the percentage of blastomeres categorized as normal was significantly lower in the FF-MAS 5 μM group (41%) and the FF-MAS 20 μM (29%) group versus the inert (52%) and the vehicle (61%) groups. Significantly reduced cleavage and good quality pre-embryo rates were found in both FF-MAS groups. CONCLUSION: FF-MAS increased the rate of aneuploidy and had detrimental effects on cleavage and pre-embryo development, when exposed both before and after fertilization. |
doi_str_mv | 10.1093/humrep/deh388 |
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METHODS: 243 women undergoing IVF/ICSI treatment donated 353 oocytes in a multicentre, prospective, randomized, double blind, four-arm, controlled trial performed at Danish and Swedish public and private IVF centers. Metaphase II oocytes were randomly assigned to: FF-MAS 5 μM, FF-MAS 20 μM, ethanol 0.2% (vehicle control) or water for injection (inert control). The exposure regimen of FF-MAS to the human oocytes was 4 h prior to fertilization by ICSI and 20 h exposure post ICSI. The primary endpoint was the incidence of numerical chromosomal abnormalities. Secondary endpoints were cleavage rate and pre-embryo quality. RESULT: On the pre-embryo level, no significant differences in chromosomal abnormality rate were observed among the four groups. However, the percentage of uniformly normal pre-embryos was significantly lower in the pooled FF-MAS group (5 μM: 12% and 20 μM: 17%) than in the pooled control group (inert control 32% and vehicle control 42%). A high level of mosaicism (41–60%) was found in all groups. At the blastomere level, the percentage of blastomeres categorized as normal was significantly lower in the FF-MAS 5 μM group (41%) and the FF-MAS 20 μM (29%) group versus the inert (52%) and the vehicle (61%) groups. Significantly reduced cleavage and good quality pre-embryo rates were found in both FF-MAS groups. CONCLUSION: FF-MAS increased the rate of aneuploidy and had detrimental effects on cleavage and pre-embryo development, when exposed both before and after fertilization.</description><identifier>ISSN: 0268-1161</identifier><identifier>ISSN: 1460-2350</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/deh388</identifier><identifier>PMID: 15243006</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; aneuploidy ; Biological and medical sciences ; Blastocyst - cytology ; Blastocyst - physiology ; Blastocyst - ultrastructure ; Blastomeres - cytology ; Blastomeres - physiology ; Cells, Cultured ; Cholestenes - administration & dosage ; Cholestenes - analysis ; Cholestenes - pharmacology ; chromosomal abnormality ; Chromosome Aberrations - statistics & numerical data ; Cleavage Stage, Ovum - drug effects ; Cytogenetic Analysis ; Cytoplasm - ultrastructure ; Dose-Response Relationship, Drug ; Double-Blind Method ; Embryology: invertebrates and vertebrates. Teratology ; Embryonic Development ; Female ; Fertilization ; Fertilization in Vitro ; Follicular Fluid - chemistry ; follicular-fluid meiosis activating sterol MAS ; Fundamental and applied biological sciences. Psychology ; human ; Humans ; Metaphase ; Mosaicism ; oocytes ; Oocytes - drug effects ; Osmolar Concentration</subject><ispartof>Human reproduction (Oxford), 2004-09, Vol.19 (9), p.2109-2117</ispartof><rights>Human Reproduction vol. 19 no. 9 © European Society of Human Reproduction and Embryology 2004; all rights reserved 2004</rights><rights>2004 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Sep 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-b62c7d0ab73b31999993862f81a28568a3ec8334a699c00e8711d0bc35da8d493</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16098888$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15243006$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bergh, Christina</creatorcontrib><creatorcontrib>Loft, Anne</creatorcontrib><creatorcontrib>Lundin, Kersti</creatorcontrib><creatorcontrib>Ziebe, Sören</creatorcontrib><creatorcontrib>Nilsson, Lars</creatorcontrib><creatorcontrib>Wikland, Matts</creatorcontrib><creatorcontrib>Gröndahl, Christian</creatorcontrib><creatorcontrib>Arce, J.-C.</creatorcontrib><creatorcontrib>CEMAS II Study Group</creatorcontrib><title>Chromosomal abnormality rate in human pre-embryos derived from in vitro fertilization cycles cultured in the presence of Follicular-Fluid Meiosis Activating Sterol (FF-MAS)</title><title>Human reproduction (Oxford)</title><addtitle>Hum. Reprod</addtitle><addtitle>Hum. Reprod</addtitle><description>BACKGROUND: The objective of the study was to investigate the effect of Follicular-fluid meiosis activating sterol (FF-MAS) when added to the culture media on the incidence of chromosomal abnormalities and pre-embryo development in human pre-embryos. METHODS: 243 women undergoing IVF/ICSI treatment donated 353 oocytes in a multicentre, prospective, randomized, double blind, four-arm, controlled trial performed at Danish and Swedish public and private IVF centers. Metaphase II oocytes were randomly assigned to: FF-MAS 5 μM, FF-MAS 20 μM, ethanol 0.2% (vehicle control) or water for injection (inert control). The exposure regimen of FF-MAS to the human oocytes was 4 h prior to fertilization by ICSI and 20 h exposure post ICSI. The primary endpoint was the incidence of numerical chromosomal abnormalities. Secondary endpoints were cleavage rate and pre-embryo quality. RESULT: On the pre-embryo level, no significant differences in chromosomal abnormality rate were observed among the four groups. However, the percentage of uniformly normal pre-embryos was significantly lower in the pooled FF-MAS group (5 μM: 12% and 20 μM: 17%) than in the pooled control group (inert control 32% and vehicle control 42%). A high level of mosaicism (41–60%) was found in all groups. At the blastomere level, the percentage of blastomeres categorized as normal was significantly lower in the FF-MAS 5 μM group (41%) and the FF-MAS 20 μM (29%) group versus the inert (52%) and the vehicle (61%) groups. Significantly reduced cleavage and good quality pre-embryo rates were found in both FF-MAS groups. CONCLUSION: FF-MAS increased the rate of aneuploidy and had detrimental effects on cleavage and pre-embryo development, when exposed both before and after fertilization.</description><subject>Adult</subject><subject>aneuploidy</subject><subject>Biological and medical sciences</subject><subject>Blastocyst - cytology</subject><subject>Blastocyst - physiology</subject><subject>Blastocyst - ultrastructure</subject><subject>Blastomeres - cytology</subject><subject>Blastomeres - physiology</subject><subject>Cells, Cultured</subject><subject>Cholestenes - administration & dosage</subject><subject>Cholestenes - analysis</subject><subject>Cholestenes - pharmacology</subject><subject>chromosomal abnormality</subject><subject>Chromosome Aberrations - statistics & numerical data</subject><subject>Cleavage Stage, Ovum - drug effects</subject><subject>Cytogenetic Analysis</subject><subject>Cytoplasm - ultrastructure</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Embryonic Development</subject><subject>Female</subject><subject>Fertilization</subject><subject>Fertilization in Vitro</subject><subject>Follicular Fluid - chemistry</subject><subject>follicular-fluid meiosis activating sterol MAS</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>human</subject><subject>Humans</subject><subject>Metaphase</subject><subject>Mosaicism</subject><subject>oocytes</subject><subject>Oocytes - drug effects</subject><subject>Osmolar Concentration</subject><issn>0268-1161</issn><issn>1460-2350</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0T9v1DAYBvAIgehRGFmRhQSUIdSOE8cZTyeOgloYWqSqi-U4bzgXJw62c-L4THxIHBJRiQG82MPPj_88SfKU4DcEV_R0N3YOhtMGdpTze8mK5AynGS3w_WSFM8ZTQhg5Sh55f4txXHL2MDkiRZZTjNkq-bnZOdtZbztpkKx76-JChwNyMgDSPYr5skeDgxS62h2sRw04vYcGtXHjJPY6OItacEEb_UMGbXukDsqAR2o0YXTRRhZ2MMV46BUg26KtNUZHIF26NaNu0AVo67VHaxX0Psb0X9BlAGcNOtlu04v15evHyYNWGg9Plvk4-bx9e7U5S88_vXu_WZ-nKuc8pDXLVNlgWZe0pqSaBuUsazmRGS8YlxQUpzSXrKoUxsBLQhpcK1o0kjd5RY-TV3Pu4Oy3EXwQnfYKjJE92NGLMv5xPoVG-fKfkjGOaVHgCJ__BW_t6Pr4CpERwjku8YTSGSlnvXfQisHpTrqDIFhMbYu5bTG3Hf2zJXSsO2ju9FJvBC8WIL2SpnWyV9rfOYYrzn8HnczOjsN_z1zuqH2A73-wdF8FK2lZiLPrG3F9dVNsOPsoPtBfseHTVA</recordid><startdate>20040901</startdate><enddate>20040901</enddate><creator>Bergh, Christina</creator><creator>Loft, Anne</creator><creator>Lundin, Kersti</creator><creator>Ziebe, Sören</creator><creator>Nilsson, Lars</creator><creator>Wikland, Matts</creator><creator>Gröndahl, Christian</creator><creator>Arce, J.-C.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20040901</creationdate><title>Chromosomal abnormality rate in human pre-embryos derived from in vitro fertilization cycles cultured in the presence of Follicular-Fluid Meiosis Activating Sterol (FF-MAS)</title><author>Bergh, Christina ; Loft, Anne ; Lundin, Kersti ; Ziebe, Sören ; Nilsson, Lars ; Wikland, Matts ; Gröndahl, Christian ; Arce, J.-C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-b62c7d0ab73b31999993862f81a28568a3ec8334a699c00e8711d0bc35da8d493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>aneuploidy</topic><topic>Biological and medical sciences</topic><topic>Blastocyst - cytology</topic><topic>Blastocyst - physiology</topic><topic>Blastocyst - ultrastructure</topic><topic>Blastomeres - cytology</topic><topic>Blastomeres - physiology</topic><topic>Cells, Cultured</topic><topic>Cholestenes - administration & dosage</topic><topic>Cholestenes - analysis</topic><topic>Cholestenes - pharmacology</topic><topic>chromosomal abnormality</topic><topic>Chromosome Aberrations - statistics & numerical data</topic><topic>Cleavage Stage, Ovum - drug effects</topic><topic>Cytogenetic Analysis</topic><topic>Cytoplasm - ultrastructure</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Embryonic Development</topic><topic>Female</topic><topic>Fertilization</topic><topic>Fertilization in Vitro</topic><topic>Follicular Fluid - chemistry</topic><topic>follicular-fluid meiosis activating sterol MAS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>human</topic><topic>Humans</topic><topic>Metaphase</topic><topic>Mosaicism</topic><topic>oocytes</topic><topic>Oocytes - drug effects</topic><topic>Osmolar Concentration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bergh, Christina</creatorcontrib><creatorcontrib>Loft, Anne</creatorcontrib><creatorcontrib>Lundin, Kersti</creatorcontrib><creatorcontrib>Ziebe, Sören</creatorcontrib><creatorcontrib>Nilsson, Lars</creatorcontrib><creatorcontrib>Wikland, Matts</creatorcontrib><creatorcontrib>Gröndahl, Christian</creatorcontrib><creatorcontrib>Arce, J.-C.</creatorcontrib><creatorcontrib>CEMAS II Study Group</creatorcontrib><collection>Istex</collection><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>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bergh, Christina</au><au>Loft, Anne</au><au>Lundin, Kersti</au><au>Ziebe, Sören</au><au>Nilsson, Lars</au><au>Wikland, Matts</au><au>Gröndahl, Christian</au><au>Arce, J.-C.</au><aucorp>CEMAS II Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromosomal abnormality rate in human pre-embryos derived from in vitro fertilization cycles cultured in the presence of Follicular-Fluid Meiosis Activating Sterol (FF-MAS)</atitle><jtitle>Human reproduction (Oxford)</jtitle><stitle>Hum. Reprod</stitle><addtitle>Hum. Reprod</addtitle><date>2004-09-01</date><risdate>2004</risdate><volume>19</volume><issue>9</issue><spage>2109</spage><epage>2117</epage><pages>2109-2117</pages><issn>0268-1161</issn><issn>1460-2350</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND: The objective of the study was to investigate the effect of Follicular-fluid meiosis activating sterol (FF-MAS) when added to the culture media on the incidence of chromosomal abnormalities and pre-embryo development in human pre-embryos. METHODS: 243 women undergoing IVF/ICSI treatment donated 353 oocytes in a multicentre, prospective, randomized, double blind, four-arm, controlled trial performed at Danish and Swedish public and private IVF centers. Metaphase II oocytes were randomly assigned to: FF-MAS 5 μM, FF-MAS 20 μM, ethanol 0.2% (vehicle control) or water for injection (inert control). The exposure regimen of FF-MAS to the human oocytes was 4 h prior to fertilization by ICSI and 20 h exposure post ICSI. The primary endpoint was the incidence of numerical chromosomal abnormalities. Secondary endpoints were cleavage rate and pre-embryo quality. RESULT: On the pre-embryo level, no significant differences in chromosomal abnormality rate were observed among the four groups. However, the percentage of uniformly normal pre-embryos was significantly lower in the pooled FF-MAS group (5 μM: 12% and 20 μM: 17%) than in the pooled control group (inert control 32% and vehicle control 42%). A high level of mosaicism (41–60%) was found in all groups. At the blastomere level, the percentage of blastomeres categorized as normal was significantly lower in the FF-MAS 5 μM group (41%) and the FF-MAS 20 μM (29%) group versus the inert (52%) and the vehicle (61%) groups. Significantly reduced cleavage and good quality pre-embryo rates were found in both FF-MAS groups. CONCLUSION: FF-MAS increased the rate of aneuploidy and had detrimental effects on cleavage and pre-embryo development, when exposed both before and after fertilization.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>15243006</pmid><doi>10.1093/humrep/deh388</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current) |
subjects | Adult aneuploidy Biological and medical sciences Blastocyst - cytology Blastocyst - physiology Blastocyst - ultrastructure Blastomeres - cytology Blastomeres - physiology Cells, Cultured Cholestenes - administration & dosage Cholestenes - analysis Cholestenes - pharmacology chromosomal abnormality Chromosome Aberrations - statistics & numerical data Cleavage Stage, Ovum - drug effects Cytogenetic Analysis Cytoplasm - ultrastructure Dose-Response Relationship, Drug Double-Blind Method Embryology: invertebrates and vertebrates. Teratology Embryonic Development Female Fertilization Fertilization in Vitro Follicular Fluid - chemistry follicular-fluid meiosis activating sterol MAS Fundamental and applied biological sciences. Psychology human Humans Metaphase Mosaicism oocytes Oocytes - drug effects Osmolar Concentration |
title | Chromosomal abnormality rate in human pre-embryos derived from in vitro fertilization cycles cultured in the presence of Follicular-Fluid Meiosis Activating Sterol (FF-MAS) |
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