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The effect of male factors on embryo morphokinetics: a retrospective analysis of 2726 blastocysts
Male infertility may influence fertilization rates, embryo morphology, and implantation rates in in vitro fertilization (IVF) cycles. Oocyte competence plays a major role in embryo development, but there is a limited understanding of the connection between sperm quality, embryo development, and morp...
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Published in: | Journal of assisted reproduction and genetics 2024-10 |
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creator | Pellegrini, Livia Gatti, Simona Navarro, Nuria Hervas, Irene Marcos, Meseguer Viviana, Vásquez Toschi, Marco Galliano, Daniela Cozzolino, Mauro |
description | Male infertility may influence fertilization rates, embryo morphology, and implantation rates in in vitro fertilization (IVF) cycles. Oocyte competence plays a major role in embryo development, but there is a limited understanding of the connection between sperm quality, embryo development, and morphokinetic parameters using donor oocytes. The study evaluated if sperm quality may influence the morphokinetic parameters in IVF cycles.
A retrospective multicentric observational cohort study included 747 ICSI cycles using donor oocytes with fresh or frozen sperm. Embryos were cultured in time-lapse incubators until the blastocyst stage. The population was divided into three groups according to sperm concentration, as control group (> 16 mill/mL), severe oligospermia (0-5 mill/mL), and moderate oligospermia group (5-16 mill/mL).
Morphokinetic analysis showed no difference in the time from the 2-cell to 6-cell stage of embryo development. A significant difference was observed on day 3 of embryo development, specifically at the 7-cell stage (t7), severe oligospermia 53.37 ± 9.81, moderate oligospermia 56.95 ± 9.78, and control 55.1 ± 8.85 h post-insemination (hpi) (p = 0.024), and 8-cell stage (t8), severe oligospermia 55.41 ± 10.83, moderate oligospermia 61.86 ± 12.38 hpi (p |
doi_str_mv | 10.1007/s10815-024-03275-7 |
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A retrospective multicentric observational cohort study included 747 ICSI cycles using donor oocytes with fresh or frozen sperm. Embryos were cultured in time-lapse incubators until the blastocyst stage. The population was divided into three groups according to sperm concentration, as control group (> 16 mill/mL), severe oligospermia (0-5 mill/mL), and moderate oligospermia group (5-16 mill/mL).
Morphokinetic analysis showed no difference in the time from the 2-cell to 6-cell stage of embryo development. A significant difference was observed on day 3 of embryo development, specifically at the 7-cell stage (t7), severe oligospermia 53.37 ± 9.81, moderate oligospermia 56.95 ± 9.78, and control 55.1 ± 8.85 h post-insemination (hpi) (p = 0.024), and 8-cell stage (t8), severe oligospermia 55.41 ± 10.83, moderate oligospermia 61.86 ± 12.38 hpi (p < 0.001), and control 58.61 ± 11.33. Accordingly, the synchrony of the four cleavages going from 4 to 8 cells (s3) was found statistically different among the groups in the severe oligospermia 8.05 ± 9.99, moderate oligospermia 11.66 ± 11.04 hpi, and control 8.55 ± 8.58 (p = 0.009). Morphokinetic time ranges were obtained for t6, t7, t8, and s3 in order to identify the good-quality blastocysts.
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A retrospective multicentric observational cohort study included 747 ICSI cycles using donor oocytes with fresh or frozen sperm. Embryos were cultured in time-lapse incubators until the blastocyst stage. The population was divided into three groups according to sperm concentration, as control group (> 16 mill/mL), severe oligospermia (0-5 mill/mL), and moderate oligospermia group (5-16 mill/mL).
Morphokinetic analysis showed no difference in the time from the 2-cell to 6-cell stage of embryo development. A significant difference was observed on day 3 of embryo development, specifically at the 7-cell stage (t7), severe oligospermia 53.37 ± 9.81, moderate oligospermia 56.95 ± 9.78, and control 55.1 ± 8.85 h post-insemination (hpi) (p = 0.024), and 8-cell stage (t8), severe oligospermia 55.41 ± 10.83, moderate oligospermia 61.86 ± 12.38 hpi (p < 0.001), and control 58.61 ± 11.33. Accordingly, the synchrony of the four cleavages going from 4 to 8 cells (s3) was found statistically different among the groups in the severe oligospermia 8.05 ± 9.99, moderate oligospermia 11.66 ± 11.04 hpi, and control 8.55 ± 8.58 (p = 0.009). Morphokinetic time ranges were obtained for t6, t7, t8, and s3 in order to identify the good-quality blastocysts.
Poor sperm quality is associated with alterations in morphokinetic parameters on day 3 in IVF cycles with donor oocytes, underlining the important role of spermatozoa during embryo development.</description><issn>1058-0468</issn><issn>1573-7330</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtOwzAQRS0EoqXwAyyQl2wCYzuOU3ao4iVVYlPWluOM1UASB9tFyt8TaGE1o9E9V5pDyCWDGwagbiODkskMeJ6B4Epm6ojMmVQiU0LA8bSDLDPIi3JGzmJ8B4BlycUpmYmlUJCrYk7MZosUnUObqHe0My1SZ2zyIVLfU-yqMHra-TBs_UfTY2psvKOGBkzBx2HCmi-kpjftGJv4U8EVL2jVmpi8HWOK5-TEmTbixWEuyNvjw2b1nK1fn15W9-vMsjJPWc7zqnZCcQG1rUC6smAIVgJKx52sOWeMS6WmoywtGsuXwjlVS-DgeCHEglzve4fgP3cYk-6aaLFtTY9-F7VgTKi8lJOBBeH7qJ1-iAGdHkLTmTBqBvpHrd6r1ZNa_atWqwm6OvTvqg7rf-TPpfgGIEJ0Hg</recordid><startdate>20241007</startdate><enddate>20241007</enddate><creator>Pellegrini, Livia</creator><creator>Gatti, Simona</creator><creator>Navarro, Nuria</creator><creator>Hervas, Irene</creator><creator>Marcos, Meseguer</creator><creator>Viviana, Vásquez</creator><creator>Toschi, Marco</creator><creator>Galliano, Daniela</creator><creator>Cozzolino, Mauro</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5929-2357</orcidid></search><sort><creationdate>20241007</creationdate><title>The effect of male factors on embryo morphokinetics: a retrospective analysis of 2726 blastocysts</title><author>Pellegrini, Livia ; Gatti, Simona ; Navarro, Nuria ; Hervas, Irene ; Marcos, Meseguer ; Viviana, Vásquez ; Toschi, Marco ; Galliano, Daniela ; Cozzolino, Mauro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c184t-424bdf37230dcb05f861e0c50e5f2f5d221125771e058ceac293ff7d5020f2633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pellegrini, Livia</creatorcontrib><creatorcontrib>Gatti, Simona</creatorcontrib><creatorcontrib>Navarro, Nuria</creatorcontrib><creatorcontrib>Hervas, Irene</creatorcontrib><creatorcontrib>Marcos, Meseguer</creatorcontrib><creatorcontrib>Viviana, Vásquez</creatorcontrib><creatorcontrib>Toschi, Marco</creatorcontrib><creatorcontrib>Galliano, Daniela</creatorcontrib><creatorcontrib>Cozzolino, Mauro</creatorcontrib><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>Pellegrini, Livia</au><au>Gatti, Simona</au><au>Navarro, Nuria</au><au>Hervas, Irene</au><au>Marcos, Meseguer</au><au>Viviana, Vásquez</au><au>Toschi, Marco</au><au>Galliano, Daniela</au><au>Cozzolino, Mauro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of male factors on embryo morphokinetics: a retrospective analysis of 2726 blastocysts</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><addtitle>J Assist Reprod Genet</addtitle><date>2024-10-07</date><risdate>2024</risdate><issn>1058-0468</issn><issn>1573-7330</issn><eissn>1573-7330</eissn><abstract>Male infertility may influence fertilization rates, embryo morphology, and implantation rates in in vitro fertilization (IVF) cycles. Oocyte competence plays a major role in embryo development, but there is a limited understanding of the connection between sperm quality, embryo development, and morphokinetic parameters using donor oocytes. The study evaluated if sperm quality may influence the morphokinetic parameters in IVF cycles.
A retrospective multicentric observational cohort study included 747 ICSI cycles using donor oocytes with fresh or frozen sperm. Embryos were cultured in time-lapse incubators until the blastocyst stage. The population was divided into three groups according to sperm concentration, as control group (> 16 mill/mL), severe oligospermia (0-5 mill/mL), and moderate oligospermia group (5-16 mill/mL).
Morphokinetic analysis showed no difference in the time from the 2-cell to 6-cell stage of embryo development. A significant difference was observed on day 3 of embryo development, specifically at the 7-cell stage (t7), severe oligospermia 53.37 ± 9.81, moderate oligospermia 56.95 ± 9.78, and control 55.1 ± 8.85 h post-insemination (hpi) (p = 0.024), and 8-cell stage (t8), severe oligospermia 55.41 ± 10.83, moderate oligospermia 61.86 ± 12.38 hpi (p < 0.001), and control 58.61 ± 11.33. Accordingly, the synchrony of the four cleavages going from 4 to 8 cells (s3) was found statistically different among the groups in the severe oligospermia 8.05 ± 9.99, moderate oligospermia 11.66 ± 11.04 hpi, and control 8.55 ± 8.58 (p = 0.009). Morphokinetic time ranges were obtained for t6, t7, t8, and s3 in order to identify the good-quality blastocysts.
Poor sperm quality is associated with alterations in morphokinetic parameters on day 3 in IVF cycles with donor oocytes, underlining the important role of spermatozoa during embryo development.</abstract><cop>Netherlands</cop><pmid>39370476</pmid><doi>10.1007/s10815-024-03275-7</doi><orcidid>https://orcid.org/0000-0002-5929-2357</orcidid></addata></record> |
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title | The effect of male factors on embryo morphokinetics: a retrospective analysis of 2726 blastocysts |
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